---
_id: '2358'
abstract:
- lang: eng
text: A study was conducted on the one-dimensional (1D) bosons in three-dimensional
(3D) traps. A rigorous analysis was carried out on the parameter regions in which
various types of 1D or 3D behavior occurred in the ground state. The four parameter
regions include density, transverse, longitudinal dimensions and scattering length.
author:
- first_name: Élliott
full_name: Lieb, Élliott H
last_name: Lieb
- first_name: Robert
full_name: Robert Seiringer
id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
last_name: Seiringer
orcid: 0000-0002-6781-0521
- first_name: Jakob
full_name: Yngvason, Jakob
last_name: Yngvason
citation:
ama: Lieb É, Seiringer R, Yngvason J. One-dimensional Bosons in three-dimensional
traps. Physical Review Letters. 2003;91(15):1504011-1504014. doi:10.1103/PhysRevLett.91.150401
apa: Lieb, É., Seiringer, R., & Yngvason, J. (2003). One-dimensional Bosons
in three-dimensional traps. Physical Review Letters. American Physical
Society. https://doi.org/10.1103/PhysRevLett.91.150401
chicago: Lieb, Élliott, Robert Seiringer, and Jakob Yngvason. “One-Dimensional Bosons
in Three-Dimensional Traps.” Physical Review Letters. American Physical
Society, 2003. https://doi.org/10.1103/PhysRevLett.91.150401.
ieee: É. Lieb, R. Seiringer, and J. Yngvason, “One-dimensional Bosons in three-dimensional
traps,” Physical Review Letters, vol. 91, no. 15. American Physical Society,
pp. 1504011–1504014, 2003.
ista: Lieb É, Seiringer R, Yngvason J. 2003. One-dimensional Bosons in three-dimensional
traps. Physical Review Letters. 91(15), 1504011–1504014.
mla: Lieb, Élliott, et al. “One-Dimensional Bosons in Three-Dimensional Traps.”
Physical Review Letters, vol. 91, no. 15, American Physical Society, 2003,
pp. 1504011–14, doi:10.1103/PhysRevLett.91.150401.
short: É. Lieb, R. Seiringer, J. Yngvason, Physical Review Letters 91 (2003) 1504011–1504014.
date_created: 2018-12-11T11:57:12Z
date_published: 2003-10-10T00:00:00Z
date_updated: 2021-01-12T06:57:00Z
day: '10'
doi: 10.1103/PhysRevLett.91.150401
extern: 1
intvolume: ' 91'
issue: '15'
main_file_link:
- open_access: '1'
url: http://arxiv.org/abs/cond-mat/0304071
month: '10'
oa: 1
page: 1504011 - 1504014
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '4571'
quality_controlled: 0
status: public
title: One-dimensional Bosons in three-dimensional traps
type: journal_article
volume: 91
year: '2003'
...
---
_id: '2414'
author:
- first_name: Uli
full_name: Uli Wagner
id: 36690CA2-F248-11E8-B48F-1D18A9856A87
last_name: Wagner
orcid: 0000-0002-1494-0568
citation:
ama: Wagner U. On k-Sets and Their Applications. 2003. doi:10.3929/ethz-a-004708408
apa: Wagner, U. (2003). On k-Sets and Their Applications. ETH Zurich. https://doi.org/10.3929/ethz-a-004708408
chicago: Wagner, Uli. “On K-Sets and Their Applications.” ETH Zurich, 2003. https://doi.org/10.3929/ethz-a-004708408.
ieee: U. Wagner, “On k-Sets and Their Applications,” ETH Zurich, 2003.
ista: Wagner U. 2003. On k-Sets and Their Applications. ETH Zurich.
mla: Wagner, Uli. On K-Sets and Their Applications. ETH Zurich, 2003, doi:10.3929/ethz-a-004708408.
short: U. Wagner, On K-Sets and Their Applications, ETH Zurich, 2003.
date_created: 2018-12-11T11:57:31Z
date_published: 2003-01-01T00:00:00Z
date_updated: 2021-01-12T06:57:20Z
day: '01'
doi: 10.3929/ethz-a-004708408
extern: 1
month: '01'
publication_status: published
publisher: ETH Zurich
publist_id: '4511'
quality_controlled: 0
status: public
title: On k-Sets and Their Applications
type: dissertation
year: '2003'
...
---
_id: '2424'
abstract:
- lang: eng
text: We introduce the adaptive neighborhood graph as a data structure for modeling
a smooth manifold M embedded in some (potentially very high-dimensional) Euclidean
space ℝd. We assume that M is known to us only through a finite sample P ⊂ M,
as it is often the case in applications. The adaptive neighborhood graph is a
geometric graph on P. Its complexity is at most min{2O(k)(n, n2}, where n = |P|
and k = dim M, as opposed to the n⌈d/2⌉ complexity of the Delaunay triangulation,
which is often used to model manifolds. We show that we can provably correctly
infer the connectivity of M and the dimension of M from the adaptive neighborhood
graph provided a certain standard sampling condition is fulfilled. The running
time of the dimension detection algorithm is d2O(k7 log k) for each connected
component of M. If the dimension is considered constant, this is a constant-time
operation, and the adaptive neighborhood graph is of linear size. Moreover, the
exponential dependence of the constants is only on the intrinsic dimension k,
not on the ambient dimension d. This is of particular interest if the co-dimension
is high, i.e., if k is much smaller than d, as is the case in many applications.
The adaptive neighborhood graph also allows us to approximate the geodesic distances
between the points in P.
author:
- first_name: Joachim
full_name: Giesen, Joachim
last_name: Giesen
- first_name: Uli
full_name: Uli Wagner
id: 36690CA2-F248-11E8-B48F-1D18A9856A87
last_name: Wagner
orcid: 0000-0002-1494-0568
citation:
ama: 'Giesen J, Wagner U. Shape dimension and intrinsic metric from samples of manifolds
with high co-dimension. In: ACM; 2003:329-337. doi:10.1145/777792.777841'
apa: 'Giesen, J., & Wagner, U. (2003). Shape dimension and intrinsic metric
from samples of manifolds with high co-dimension (pp. 329–337). Presented at the
SoCG: Symposium on Computational Geometry, ACM. https://doi.org/10.1145/777792.777841'
chicago: Giesen, Joachim, and Uli Wagner. “Shape Dimension and Intrinsic Metric
from Samples of Manifolds with High Co-Dimension,” 329–37. ACM, 2003. https://doi.org/10.1145/777792.777841.
ieee: 'J. Giesen and U. Wagner, “Shape dimension and intrinsic metric from samples
of manifolds with high co-dimension,” presented at the SoCG: Symposium on Computational
Geometry, 2003, pp. 329–337.'
ista: 'Giesen J, Wagner U. 2003. Shape dimension and intrinsic metric from samples
of manifolds with high co-dimension. SoCG: Symposium on Computational Geometry,
329–337.'
mla: Giesen, Joachim, and Uli Wagner. Shape Dimension and Intrinsic Metric from
Samples of Manifolds with High Co-Dimension. ACM, 2003, pp. 329–37, doi:10.1145/777792.777841.
short: J. Giesen, U. Wagner, in:, ACM, 2003, pp. 329–337.
conference:
name: 'SoCG: Symposium on Computational Geometry'
date_created: 2018-12-11T11:57:35Z
date_published: 2003-06-01T00:00:00Z
date_updated: 2021-01-12T06:57:24Z
day: '01'
doi: 10.1145/777792.777841
extern: 1
month: '06'
page: 329 - 337
publication_status: published
publisher: ACM
publist_id: '4501'
quality_controlled: 0
status: public
title: Shape dimension and intrinsic metric from samples of manifolds with high co-dimension
type: conference
year: '2003'
...
---
_id: '2423'
abstract:
- lang: eng
text: A finite set N ⊃ Rd is a weak ε-net for an n-point set X ⊃ Rd (with respect
to convex sets) if N intersects every convex set K with |K ∩ X| ≥ εn. We give
an alternative, and arguably simpler, proof of the fact, first shown by Chazelle
et al. [7], that every point set X in Rd admits a weak ε-net of cardinality O(ε-d
polylog(1/ε)). Moreover, for a number of special point sets (e.g., for points
on the moment curve), our method gives substantially better bounds. The construction
yields an algorithm to construct such weak ε-nets in time O(n ln(1/ε)). We also
prove, by a different method, a near-linear upper bound for points uniformly distributed
on the (d - 1)-dimensional sphere.
author:
- first_name: Jiří
full_name: Matoušek, Jiří
last_name: Matoušek
- first_name: Uli
full_name: Uli Wagner
id: 36690CA2-F248-11E8-B48F-1D18A9856A87
last_name: Wagner
orcid: 0000-0002-1494-0568
citation:
ama: 'Matoušek J, Wagner U. New constructions of weak epsilon-nets. In: ACM; 2003:129-135.
doi:10.1145/777792.777813'
apa: 'Matoušek, J., & Wagner, U. (2003). New constructions of weak epsilon-nets
(pp. 129–135). Presented at the SoCG: Symposium on Computational Geometry, ACM.
https://doi.org/10.1145/777792.777813'
chicago: Matoušek, Jiří, and Uli Wagner. “New Constructions of Weak Epsilon-Nets,”
129–35. ACM, 2003. https://doi.org/10.1145/777792.777813.
ieee: 'J. Matoušek and U. Wagner, “New constructions of weak epsilon-nets,” presented
at the SoCG: Symposium on Computational Geometry, 2003, pp. 129–135.'
ista: 'Matoušek J, Wagner U. 2003. New constructions of weak epsilon-nets. SoCG:
Symposium on Computational Geometry, 129–135.'
mla: Matoušek, Jiří, and Uli Wagner. New Constructions of Weak Epsilon-Nets.
ACM, 2003, pp. 129–35, doi:10.1145/777792.777813.
short: J. Matoušek, U. Wagner, in:, ACM, 2003, pp. 129–135.
conference:
name: 'SoCG: Symposium on Computational Geometry'
date_created: 2018-12-11T11:57:34Z
date_published: 2003-06-01T00:00:00Z
date_updated: 2021-01-12T06:57:24Z
day: '01'
doi: 10.1145/777792.777813
extern: 1
month: '06'
page: 129 - 135
publication_status: published
publisher: ACM
publist_id: '4502'
quality_controlled: 0
status: public
title: New constructions of weak epsilon-nets
type: conference
year: '2003'
...
---
_id: '2422'
abstract:
- lang: eng
text: We prove a lower bound of 0.3288(4 n) for the rectilinear crossing number
cr̄(Kn) of a complete graph on n vertices, or in other words, for the minimum
number of convex quadrilaterals in any set of n points in general position in
the Euclidean plane. As we see it, the main contribution of this paper is not
so much the concrete numerical improvement over earlier bounds, as the novel method
of proof, which is not based on bounding cr̄(Kn) for some small n.
author:
- first_name: Uli
full_name: Uli Wagner
id: 36690CA2-F248-11E8-B48F-1D18A9856A87
last_name: Wagner
orcid: 0000-0002-1494-0568
citation:
ama: 'Wagner U. On the rectilinear crossing number of complete graphs. In: SIAM;
2003:583-588.'
apa: 'Wagner, U. (2003). On the rectilinear crossing number of complete graphs (pp.
583–588). Presented at the SODA: Symposium on Discrete Algorithms, SIAM.'
chicago: Wagner, Uli. “On the Rectilinear Crossing Number of Complete Graphs,” 583–88.
SIAM, 2003.
ieee: 'U. Wagner, “On the rectilinear crossing number of complete graphs,” presented
at the SODA: Symposium on Discrete Algorithms, 2003, pp. 583–588.'
ista: 'Wagner U. 2003. On the rectilinear crossing number of complete graphs. SODA:
Symposium on Discrete Algorithms, 583–588.'
mla: Wagner, Uli. On the Rectilinear Crossing Number of Complete Graphs.
SIAM, 2003, pp. 583–88.
short: U. Wagner, in:, SIAM, 2003, pp. 583–588.
conference:
name: 'SODA: Symposium on Discrete Algorithms'
date_created: 2018-12-11T11:57:34Z
date_published: 2003-01-01T00:00:00Z
date_updated: 2021-01-12T06:57:24Z
day: '01'
extern: 1
main_file_link:
- open_access: '0'
url: http://dl.acm.org/citation.cfm?id=644206
month: '01'
page: 583 - 588
publication_status: published
publisher: SIAM
publist_id: '4503'
quality_controlled: 0
status: public
title: On the rectilinear crossing number of complete graphs
type: conference
year: '2003'
...
---
_id: '2623'
abstract:
- lang: eng
text: Patients with Hodgkin's disease can develop paraneoplastic cerebellar ataxia
because of the generation of autoantibodies against mGluR1 (mGluR1-Abs). Yet,
the pathophysiological mechanisms underlying their motor coordination deficits
remain to be elucidated. Here, we show that application of IgG purified from the
patients' serum to cerebellar slices of mice acutely reduces the basal activity
of Purkinje cells, whereas application to the flocculus of mice in vivo evokes
acute disturbances in the performance of their compensatory eye movements. In
addition, the mGluR1-Abs block induction of long-term depression in cultured mouse
Purkinje cells, whereas the cerebellar motor learning behavior of the patients
is affected in that they show impaired adaptation of their saccadic eye movements.
Finally, postmortem analysis of the cerebellum of a paraneoplastic cerebellar
ataxia patient showed that the number of Purkinje cells was significantly reduced
by approximately two thirds compared with three controls. We conclude that autoantibodies
against mGluR1 can cause cerebellar motor coordination deficits caused by a combination
of rapid effects on both acute and plastic responses of Purkinje cells and chronic
degenerative effects.
author:
- first_name: Michiel
full_name: Coesmans, Michiel P
last_name: Coesmans
- first_name: Peter
full_name: Sillevis-Smitt, Peter A
last_name: Sillevis Smitt
- first_name: David
full_name: Linden, David J
last_name: Linden
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Tomoo
full_name: Hirano, Tomoo
last_name: Hirano
- first_name: Yoshinori
full_name: Yamakawa, Yoshinori
last_name: Yamakawa
- first_name: Adriaan
full_name: Van Alphen, Adriaan M
last_name: Van Alphen
- first_name: Chongde
full_name: Luo, Chongde
last_name: Luo
- first_name: Jos
full_name: Van Der Geest, Jos N
last_name: Van Der Geest
- first_name: Johan
full_name: Kros, Johan M
last_name: Kros
- first_name: Carlo
full_name: Gaillard, Carlo A
last_name: Gaillard
- first_name: Maarten
full_name: Frens, Maarten A
last_name: Frens
- first_name: Chris
full_name: De Zeeuw, Chris I
last_name: De Zeeuw
citation:
ama: Coesmans M, Sillevis Smitt P, Linden D, et al. Mechanisms underlying cerebellar
motor deficits due to mGluR1-autoantibodies. Annals of Neurology. 2003;53(3):325-336.
doi:10.1002/ana.10451
apa: Coesmans, M., Sillevis Smitt, P., Linden, D., Shigemoto, R., Hirano, T., Yamakawa,
Y., … De Zeeuw, C. (2003). Mechanisms underlying cerebellar motor deficits due
to mGluR1-autoantibodies. Annals of Neurology. Wiley-Blackwell. https://doi.org/10.1002/ana.10451
chicago: Coesmans, Michiel, Peter Sillevis Smitt, David Linden, Ryuichi Shigemoto,
Tomoo Hirano, Yoshinori Yamakawa, Adriaan Van Alphen, et al. “Mechanisms Underlying
Cerebellar Motor Deficits Due to MGluR1-Autoantibodies.” Annals of Neurology.
Wiley-Blackwell, 2003. https://doi.org/10.1002/ana.10451.
ieee: M. Coesmans et al., “Mechanisms underlying cerebellar motor deficits
due to mGluR1-autoantibodies,” Annals of Neurology, vol. 53, no. 3. Wiley-Blackwell,
pp. 325–336, 2003.
ista: Coesmans M, Sillevis Smitt P, Linden D, Shigemoto R, Hirano T, Yamakawa Y,
Van Alphen A, Luo C, Van Der Geest J, Kros J, Gaillard C, Frens M, De Zeeuw C.
2003. Mechanisms underlying cerebellar motor deficits due to mGluR1-autoantibodies.
Annals of Neurology. 53(3), 325–336.
mla: Coesmans, Michiel, et al. “Mechanisms Underlying Cerebellar Motor Deficits
Due to MGluR1-Autoantibodies.” Annals of Neurology, vol. 53, no. 3, Wiley-Blackwell,
2003, pp. 325–36, doi:10.1002/ana.10451.
short: M. Coesmans, P. Sillevis Smitt, D. Linden, R. Shigemoto, T. Hirano, Y. Yamakawa,
A. Van Alphen, C. Luo, J. Van Der Geest, J. Kros, C. Gaillard, M. Frens, C. De
Zeeuw, Annals of Neurology 53 (2003) 325–336.
date_created: 2018-12-11T11:58:44Z
date_published: 2003-03-01T00:00:00Z
date_updated: 2021-01-12T06:58:39Z
day: '01'
doi: 10.1002/ana.10451
extern: 1
intvolume: ' 53'
issue: '3'
month: '03'
page: 325 - 336
publication: Annals of Neurology
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4274'
quality_controlled: 0
status: public
title: Mechanisms underlying cerebellar motor deficits due to mGluR1-autoantibodies
type: journal_article
volume: 53
year: '2003'
...
---
_id: '2625'
abstract:
- lang: eng
text: Metabotropic glutamate receptor 1 (mGluR1) plays a crucial role in synaptic
plasticity and motor learning in the cerebellum. We have studied activity-dependent
changes in mGluR1 function in mouse cultured Purkinje neurons. Depolarizing stimulation
potentiated Ca2+ and current responses to an mGluR1 agonist for several hours
in the cultured Purkinje neurons. It also blocked internalization of mGluR1 and
increased the number of mGluR1s on the cell membrane. We found that depolarization
simultaneously increased transcription of Homer1a in Purkinje neurons. Homer1a
inhibited internalization and increased cell-surface expression of mGluR1 when
coexpressed in human embryonic kidney (HEK)-293 cells. Depolarization-induced
Homer1a expression in Purkinje neurons was blocked by a mitogen-activated protein
kinase (MAPK) inhibitor. Changes in internalization and mGluR1-mediated Ca2+ response
were also blocked by inhibition of MAPK activity, suggesting that localization
and activity of mGluR1 were regulated in the same signalling pathway as Homer1a
expression. It is thus suggested that depolarization of the Purkinje neuron leads
to the increment in mGluR1 responsiveness through MAPK activity and induction
of Homer1a expression, which increases active mGluR1 on the cell surface by blocking
internalization of mGluR1.
author:
- first_name: Itsunari
full_name: Minami, Itsunari
last_name: Minami
- first_name: Mineko
full_name: Kengaku, Mineko
last_name: Kengaku
- first_name: Sillevis
full_name: Smitt, Sillevis P
last_name: Smitt
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Tomoo
full_name: Hirano, Tomoo
last_name: Hirano
citation:
ama: Minami I, Kengaku M, Smitt S, Shigemoto R, Hirano T. Long-term potentiation
of mGluR1 activity by depolarization-induced Homer1a in mouse cerebellar Purkinje
neurons. European Journal of Neuroscience. 2003;17(5):1023-1032. doi:10.1046/j.1460-9568.2003.02499.x
apa: Minami, I., Kengaku, M., Smitt, S., Shigemoto, R., & Hirano, T. (2003).
Long-term potentiation of mGluR1 activity by depolarization-induced Homer1a in
mouse cerebellar Purkinje neurons. European Journal of Neuroscience. Wiley-Blackwell.
https://doi.org/10.1046/j.1460-9568.2003.02499.x
chicago: Minami, Itsunari, Mineko Kengaku, Sillevis Smitt, Ryuichi Shigemoto, and
Tomoo Hirano. “Long-Term Potentiation of MGluR1 Activity by Depolarization-Induced
Homer1a in Mouse Cerebellar Purkinje Neurons.” European Journal of Neuroscience.
Wiley-Blackwell, 2003. https://doi.org/10.1046/j.1460-9568.2003.02499.x.
ieee: I. Minami, M. Kengaku, S. Smitt, R. Shigemoto, and T. Hirano, “Long-term potentiation
of mGluR1 activity by depolarization-induced Homer1a in mouse cerebellar Purkinje
neurons,” European Journal of Neuroscience, vol. 17, no. 5. Wiley-Blackwell,
pp. 1023–1032, 2003.
ista: Minami I, Kengaku M, Smitt S, Shigemoto R, Hirano T. 2003. Long-term potentiation
of mGluR1 activity by depolarization-induced Homer1a in mouse cerebellar Purkinje
neurons. European Journal of Neuroscience. 17(5), 1023–1032.
mla: Minami, Itsunari, et al. “Long-Term Potentiation of MGluR1 Activity by Depolarization-Induced
Homer1a in Mouse Cerebellar Purkinje Neurons.” European Journal of Neuroscience,
vol. 17, no. 5, Wiley-Blackwell, 2003, pp. 1023–32, doi:10.1046/j.1460-9568.2003.02499.x.
short: I. Minami, M. Kengaku, S. Smitt, R. Shigemoto, T. Hirano, European Journal
of Neuroscience 17 (2003) 1023–1032.
date_created: 2018-12-11T11:58:44Z
date_published: 2003-03-01T00:00:00Z
date_updated: 2021-01-12T06:58:39Z
day: '01'
doi: 10.1046/j.1460-9568.2003.02499.x
extern: 1
intvolume: ' 17'
issue: '5'
month: '03'
page: 1023 - 1032
publication: European Journal of Neuroscience
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4273'
quality_controlled: 0
status: public
title: Long-term potentiation of mGluR1 activity by depolarization-induced Homer1a
in mouse cerebellar Purkinje neurons
type: journal_article
volume: 17
year: '2003'
...
---
_id: '2626'
abstract:
- lang: eng
text: The expression pattern of metabotropic glutamate receptor Iα (mGluR1α) was
immunohistochemically investigated in substantia nigra dopaminergic neurons of
the macaque monkey. In normal monkeys, mGluR1α immunoreactivity was weakly observed
in the dorsal tier of the substantia nigra pars compacta (SNc-d) where calbindin-D28k-containing
dopaminergic neurons invulnerable to parkinsonian degeneration are specifically
located. On the other hand, mGluR1α was strongly expressed in the ventral tier
of the substantia nigra pars cornpacta (SNc-v). In monkeys treated with the parkinsonism-inducing
drug, I-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), mGluR1α expression
was decreased in dopaminergic neurons in the SNc-v that were spared its toxic
action. These results suggest that mGluR1α expression may be involved at least
partly in the vulnerability of dopaminergic neurons to parkinsonian insults.
author:
- first_name: Katsuyuki
full_name: Kaneda, Katsuyuki
last_name: Kaneda
- first_name: Michiko
full_name: Imanishi, Michiko
last_name: Imanishi
- first_name: Atsushi
full_name: Nambu, Atsushi
last_name: Nambu
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Masahiko
full_name: Takada, Masahiko
last_name: Takada
citation:
ama: Kaneda K, Imanishi M, Nambu A, Shigemoto R, Takada M. Differential expression
patterns of mGluR1α in monkey nigral dopamine neurons. Neuroreport. 2003;14(7):947-950.
doi:10.1097/01.wnr.0000074344.81633.e4
apa: Kaneda, K., Imanishi, M., Nambu, A., Shigemoto, R., & Takada, M. (2003).
Differential expression patterns of mGluR1α in monkey nigral dopamine neurons.
Neuroreport. Lippincott, Williams & Wilkins. https://doi.org/10.1097/01.wnr.0000074344.81633.e4
chicago: Kaneda, Katsuyuki, Michiko Imanishi, Atsushi Nambu, Ryuichi Shigemoto,
and Masahiko Takada. “Differential Expression Patterns of MGluR1α in Monkey Nigral
Dopamine Neurons.” Neuroreport. Lippincott, Williams & Wilkins, 2003.
https://doi.org/10.1097/01.wnr.0000074344.81633.e4.
ieee: K. Kaneda, M. Imanishi, A. Nambu, R. Shigemoto, and M. Takada, “Differential
expression patterns of mGluR1α in monkey nigral dopamine neurons,” Neuroreport,
vol. 14, no. 7. Lippincott, Williams & Wilkins, pp. 947–950, 2003.
ista: Kaneda K, Imanishi M, Nambu A, Shigemoto R, Takada M. 2003. Differential expression
patterns of mGluR1α in monkey nigral dopamine neurons. Neuroreport. 14(7), 947–950.
mla: Kaneda, Katsuyuki, et al. “Differential Expression Patterns of MGluR1α in Monkey
Nigral Dopamine Neurons.” Neuroreport, vol. 14, no. 7, Lippincott, Williams
& Wilkins, 2003, pp. 947–50, doi:10.1097/01.wnr.0000074344.81633.e4.
short: K. Kaneda, M. Imanishi, A. Nambu, R. Shigemoto, M. Takada, Neuroreport 14
(2003) 947–950.
date_created: 2018-12-11T11:58:45Z
date_published: 2003-05-01T00:00:00Z
date_updated: 2021-01-12T06:58:40Z
day: '01'
doi: 10.1097/01.wnr.0000074344.81633.e4
extern: 1
intvolume: ' 14'
issue: '7'
month: '05'
page: 947 - 950
publication: Neuroreport
publication_status: published
publisher: Lippincott, Williams & Wilkins
publist_id: '4272'
quality_controlled: 0
status: public
title: Differential expression patterns of mGluR1α in monkey nigral dopamine neurons
type: journal_article
volume: 14
year: '2003'
...
---
_id: '2627'
abstract:
- lang: eng
text: Despite its implications for higher order functions of the brain, little is
currently known about the molecular basis of left-right asymmetry of the brain.
Here we report that synaptic distribution of N-methyl-D-aspartate (NMDA) receptor
GluRε2 (NR2B) subunits in the adult mouse hippocampus is asymmetrical between
the left and right and between the apical and basal dendrites of single neurons.
These asymmetrical allocations of ε2 subunits differentiate the properties of
NMDA receptors and synaptic plasticity between the left and right hippocampus.
These results provide a molecular basis for the structural and functional asymmetry
of the mature brain.
author:
- first_name: Ryosuke
full_name: Kawakami, Ryosuke
last_name: Kawakami
- first_name: Yoshiaki
full_name: Shinohara, Yoshiaki
last_name: Shinohara
- first_name: Yuichiro
full_name: Kato, Yuichiro
last_name: Kato
- first_name: Hiroyuki
full_name: Sugiyama, Hiroyuki
last_name: Sugiyama
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Isao
full_name: Ito, Isao
last_name: Ito
citation:
ama: Kawakami R, Shinohara Y, Kato Y, Sugiyama H, Shigemoto R, Ito I. Asymmetrical
allocation of NMDA receptor ε2 subunits in hippocampal circuitry. Science.
2003;300(5621):990-994. doi:10.1126/science.1082609
apa: Kawakami, R., Shinohara, Y., Kato, Y., Sugiyama, H., Shigemoto, R., & Ito,
I. (2003). Asymmetrical allocation of NMDA receptor ε2 subunits in hippocampal
circuitry. Science. American Association for the Advancement of Science.
https://doi.org/10.1126/science.1082609
chicago: Kawakami, Ryosuke, Yoshiaki Shinohara, Yuichiro Kato, Hiroyuki Sugiyama,
Ryuichi Shigemoto, and Isao Ito. “Asymmetrical Allocation of NMDA Receptor Ε2
Subunits in Hippocampal Circuitry.” Science. American Association for the
Advancement of Science, 2003. https://doi.org/10.1126/science.1082609.
ieee: R. Kawakami, Y. Shinohara, Y. Kato, H. Sugiyama, R. Shigemoto, and I. Ito,
“Asymmetrical allocation of NMDA receptor ε2 subunits in hippocampal circuitry,”
Science, vol. 300, no. 5621. American Association for the Advancement of
Science, pp. 990–994, 2003.
ista: Kawakami R, Shinohara Y, Kato Y, Sugiyama H, Shigemoto R, Ito I. 2003. Asymmetrical
allocation of NMDA receptor ε2 subunits in hippocampal circuitry. Science. 300(5621),
990–994.
mla: Kawakami, Ryosuke, et al. “Asymmetrical Allocation of NMDA Receptor Ε2 Subunits
in Hippocampal Circuitry.” Science, vol. 300, no. 5621, American Association
for the Advancement of Science, 2003, pp. 990–94, doi:10.1126/science.1082609.
short: R. Kawakami, Y. Shinohara, Y. Kato, H. Sugiyama, R. Shigemoto, I. Ito, Science
300 (2003) 990–994.
date_created: 2018-12-11T11:58:45Z
date_published: 2003-05-09T00:00:00Z
date_updated: 2021-01-12T06:58:40Z
day: '09'
doi: 10.1126/science.1082609
extern: 1
intvolume: ' 300'
issue: '5621'
month: '05'
page: 990 - 994
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '4271'
quality_controlled: 0
status: public
title: Asymmetrical allocation of NMDA receptor ε2 subunits in hippocampal circuitry
type: journal_article
volume: 300
year: '2003'
...
---
_id: '2629'
abstract:
- lang: eng
text: The release of neurotransmitters is modulated by presynaptic metabotropic
glutamate receptors (mGluRs), which show a highly selective expression and subcellular
location in glutamatergic terminals in the hippocampus. Using immunocytochemistry,
we investigated whether one of the receptors, mGluR7, whose level of expression
is governed by the postsynaptic target, was present in GABAergic terminals and
whether such terminals targeted particular cells. A total of 165 interneuron dendritic
profiles receiving 466 synapses (82% mGluR7a-positive) were analysed. The presynaptic
active zones of most GAD-(77%) or GABA-positive (94%) synaptic boutons on interneurons
innervated by mGluR7a-enriched glutamatergic terminals (mGluR7a-decorated) were
immunopositive for mGluR7a. GABAergic terminals on pyramidal cells and most other
interneurons in str. oriens were mGluR7a-immunonegative. The mGluR7a-decorated
cells were mostly somatostatin- and mGluR1α-immunopositive neurons in str. oriens
and the alveus. Their GABAergic input mainly originated from VIP-positive terminals,
90% of which expressed high levels of mGluR7a in the presynaptic active zone.
Parvalbumin-positive synaptic terminals were rare on mGluR7a-decorated cells,
but on these neurons 73% of them were mGluR7a-immunopositive. Some type II synapses
innervating interneurons were immunopositive for mGluR7b, as were some type I
synapses. Because not all target cells of VIP-positive neurons are known it has
not been possible to determine whether mGluR7 is expressed in a target-cell-specific
manner in the terminals of single GABAergic cells. The activation of mGluR7 may
decrease GABA release to mGluR7-decorated cells at times of high pyramidal cell
activity, which elevates extracellular glutamate levels. Alternatively, the presynaptic
receptor may be activated by as yet unidentified endogenous ligands released by
the GABAergic terminals or the postsynaptic dendrites.
author:
- first_name: Péter
full_name: Somogyi, Péter
last_name: Somogyi
- first_name: Yannis
full_name: Dalezios, Yannis
last_name: Dalezios
- first_name: Rafael
full_name: Luján, Rafael
last_name: Luján
- first_name: John
full_name: Roberts, John D
last_name: Roberts
- first_name: Masahiko
full_name: Watanabe, Masahiko
last_name: Watanabe
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
citation:
ama: Somogyi P, Dalezios Y, Luján R, Roberts J, Watanabe M, Shigemoto R. High level
of mGluR7 in the presynaptic active zones of select populations of GABAergic terminals
innervating interneurons in the rat hippocampus. European Journal of Neuroscience.
2003;17(12):2503-2520. doi:10.1046/j.1460-9568.2003.02697.x
apa: Somogyi, P., Dalezios, Y., Luján, R., Roberts, J., Watanabe, M., & Shigemoto,
R. (2003). High level of mGluR7 in the presynaptic active zones of select populations
of GABAergic terminals innervating interneurons in the rat hippocampus. European
Journal of Neuroscience. Wiley-Blackwell. https://doi.org/10.1046/j.1460-9568.2003.02697.x
chicago: Somogyi, Péter, Yannis Dalezios, Rafael Luján, John Roberts, Masahiko Watanabe,
and Ryuichi Shigemoto. “High Level of MGluR7 in the Presynaptic Active Zones of
Select Populations of GABAergic Terminals Innervating Interneurons in the Rat
Hippocampus.” European Journal of Neuroscience. Wiley-Blackwell, 2003.
https://doi.org/10.1046/j.1460-9568.2003.02697.x.
ieee: P. Somogyi, Y. Dalezios, R. Luján, J. Roberts, M. Watanabe, and R. Shigemoto,
“High level of mGluR7 in the presynaptic active zones of select populations of
GABAergic terminals innervating interneurons in the rat hippocampus,” European
Journal of Neuroscience, vol. 17, no. 12. Wiley-Blackwell, pp. 2503–2520,
2003.
ista: Somogyi P, Dalezios Y, Luján R, Roberts J, Watanabe M, Shigemoto R. 2003.
High level of mGluR7 in the presynaptic active zones of select populations of
GABAergic terminals innervating interneurons in the rat hippocampus. European
Journal of Neuroscience. 17(12), 2503–2520.
mla: Somogyi, Péter, et al. “High Level of MGluR7 in the Presynaptic Active Zones
of Select Populations of GABAergic Terminals Innervating Interneurons in the Rat
Hippocampus.” European Journal of Neuroscience, vol. 17, no. 12, Wiley-Blackwell,
2003, pp. 2503–20, doi:10.1046/j.1460-9568.2003.02697.x.
short: P. Somogyi, Y. Dalezios, R. Luján, J. Roberts, M. Watanabe, R. Shigemoto,
European Journal of Neuroscience 17 (2003) 2503–2520.
date_created: 2018-12-11T11:58:46Z
date_published: 2003-06-01T00:00:00Z
date_updated: 2021-01-12T06:58:41Z
day: '01'
doi: 10.1046/j.1460-9568.2003.02697.x
extern: 1
intvolume: ' 17'
issue: '12'
month: '06'
page: 2503 - 2520
publication: European Journal of Neuroscience
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4269'
quality_controlled: 0
status: public
title: High level of mGluR7 in the presynaptic active zones of select populations
of GABAergic terminals innervating interneurons in the rat hippocampus
type: journal_article
volume: 17
year: '2003'
...
---
_id: '2628'
abstract:
- lang: eng
text: We aimed to estimate the number of AMPA receptors (AMPARs) bound by the quantal
transmitter packet, their single-channel conductance and their density in the
postsynaptic membrane at cerebellar Purkinje cell synapses. The synaptic and extrasynaptic
AMPARs were examined in Purkinje cells in 2- to 4-day-old rats, when they receive
synaptic inputs solely from climbing fibres (CFs). Evoked CF EPSCs and whole-cell
AMPA currents displayed roughly linear current-voltage relationships, consistent
with the presence of GluR2 subunits in synaptic and extrasynaptic AMPARs. The
mean quantal size, estimated from the miniature EPSCs (MEPSCs), was ∼300 pS. Peak-scaled
non-stationary fluctuation analysis of spontaneous EPSCs and MEPSCs gave a weighted-mean
synaptic channel conductance of ∼5 pS (∼7 pS when corrected for filtering). By
applying non-stationary fluctuation analysis to extrasynaptic currents activated
by brief glutamate pulses (5 mM), we also obtained a small single-channel conductance
estimate for extrasynaptic AMPARs (∼11 pS). This approach allowed us to obtain
a maximum open probability (Po,max) value for the extrasynaptic receptors (Po,max
= 0.72). Directly resolved extrasynaptic channel openings in the continued presence
of glutamate exhibited clear multiple-conductance levels. The mean area of the
postsynaptic density (PSD) of these synapses was 0.074 μm2, measured by reconstructing
electron-microscopic (EM) serial sections. Postembedding immunogold labelling
by anti-GluR2/3 antibody revealed that AMPARs are localised in PSDs. From these
data and by simulating error factors, we estimate that at least 66 AMPARs are
bound by a quantal transmitter packet at CF-Purkinje cell synapses, and the receptors
are packed at a minimum density of ∼900 μm-2 in the postsynaptic membrane.
author:
- first_name: Akiko
full_name: Momiyama, Akiko
last_name: Momiyama
- first_name: Rachel
full_name: Silver, Rachel A
last_name: Silver
- first_name: Michael
full_name: Häusser, Michael A
last_name: Häusser
- first_name: Takuya
full_name: Notomi, Takuya
last_name: Notomi
- first_name: Yue
full_name: Wu, Yue
last_name: Wu
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Stuart
full_name: Cull-Candy, Stuart G
last_name: Cull Candy
citation:
ama: Momiyama A, Silver R, Häusser M, et al. The density of AMPA receptors activated
by a transmitter quantum at the climbing fibre - Purkinje cell synapse in immature
rats. Journal of Physiology. 2003;549(1):75-92. doi:10.1113/jphysiol.2002.033472
apa: Momiyama, A., Silver, R., Häusser, M., Notomi, T., Wu, Y., Shigemoto, R., &
Cull Candy, S. (2003). The density of AMPA receptors activated by a transmitter
quantum at the climbing fibre - Purkinje cell synapse in immature rats. Journal
of Physiology. Wiley-Blackwell. https://doi.org/10.1113/jphysiol.2002.033472
chicago: Momiyama, Akiko, Rachel Silver, Michael Häusser, Takuya Notomi, Yue Wu,
Ryuichi Shigemoto, and Stuart Cull Candy. “The Density of AMPA Receptors Activated
by a Transmitter Quantum at the Climbing Fibre - Purkinje Cell Synapse in Immature
Rats.” Journal of Physiology. Wiley-Blackwell, 2003. https://doi.org/10.1113/jphysiol.2002.033472.
ieee: A. Momiyama et al., “The density of AMPA receptors activated by a transmitter
quantum at the climbing fibre - Purkinje cell synapse in immature rats,” Journal
of Physiology, vol. 549, no. 1. Wiley-Blackwell, pp. 75–92, 2003.
ista: Momiyama A, Silver R, Häusser M, Notomi T, Wu Y, Shigemoto R, Cull Candy S.
2003. The density of AMPA receptors activated by a transmitter quantum at the
climbing fibre - Purkinje cell synapse in immature rats. Journal of Physiology.
549(1), 75–92.
mla: Momiyama, Akiko, et al. “The Density of AMPA Receptors Activated by a Transmitter
Quantum at the Climbing Fibre - Purkinje Cell Synapse in Immature Rats.” Journal
of Physiology, vol. 549, no. 1, Wiley-Blackwell, 2003, pp. 75–92, doi:10.1113/jphysiol.2002.033472.
short: A. Momiyama, R. Silver, M. Häusser, T. Notomi, Y. Wu, R. Shigemoto, S. Cull
Candy, Journal of Physiology 549 (2003) 75–92.
date_created: 2018-12-11T11:58:45Z
date_published: 2003-05-15T00:00:00Z
date_updated: 2021-01-12T06:58:40Z
day: '15'
doi: 10.1113/jphysiol.2002.033472
extern: 1
intvolume: ' 549'
issue: '1'
month: '05'
page: 75 - 92
publication: Journal of Physiology
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4270'
quality_controlled: 0
status: public
title: The density of AMPA receptors activated by a transmitter quantum at the climbing
fibre - Purkinje cell synapse in immature rats
type: journal_article
volume: 549
year: '2003'
...
---
_id: '2631'
abstract:
- lang: eng
text: Cyclic ADP-ribose (cADP-ribose) is a putative second messenger or modulator.
However, the role of cADP-ribose in the downstream signals of the metabotropic
glutamate receptors (mGluRs) is unclear. Here, we show that glutamate stimulates
ADP-ribosyl cyclase activity in rat or mouse crude membranes of retina via group
III mGluRs or in superior cervical ganglion via group I mGluRs. The retina of
mGluR6-deficient mice showed no increase in the ADP-ribosyl cyclase level in response
to glutamate. GTP enhanced the initial rate of basal and glutamate-stimulated
cyclase activity. GTP-γ-S also stimulated basal activity. To determine whether
the coupling mode of mGluRs to ADP-ribosyl cyclase is a feature common to individual
cloned mGluRs, we expressed each mGluR subtype in NG108-15 neuroblastoma x glioma
hybrid cells. The glutamate-induced stimulation of the cyclase occurs preferentially
in NG108-15 cells over-expressing mGluRs1, 3, 5, and 6. Cells expressing mGluR2
or mGluRs4 and 7 exhibit inhibition or no coupling, respectively. Glutamate-induced
activation or inhibition of the cyclase activity was eliminated after pre-treatment
with cholera or pertussis toxin, respectively. Thus, the subtype-specific coupling
of mGluRs to ADP-ribosyl cyclase via G proteins suggests that some glutamate-evoked
neuronal functions are mediated by cADP-ribose.
author:
- first_name: Haruhiro
full_name: Higashida, Haruhiro
last_name: Higashida
- first_name: Jia
full_name: Zhang, Jia-Sheng
last_name: Zhang
- first_name: Sumiko
full_name: Mochida, Sumiko
last_name: Mochida
- first_name: Xiao
full_name: Chen, Xiao-Liang
last_name: Chen
- first_name: Yeonsook
full_name: Shin, Yeonsook
last_name: Shin
- first_name: Mami
full_name: Noda, Mami
last_name: Noda
- first_name: Kazi
full_name: Hossain, Kazi Z
last_name: Hossain
- first_name: Naoto
full_name: Hoshi, Naoto
last_name: Hoshi
- first_name: Minako
full_name: Hashii, Minako
last_name: Hashii
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Shigetada
full_name: Nakanishi, Shigetada
last_name: Nakanishi
- first_name: Yutaka
full_name: Fukuda, Yutaka
last_name: Fukuda
- first_name: Shigeru
full_name: Yokoyama, Shigeru
last_name: Yokoyama
citation:
ama: Higashida H, Zhang J, Mochida S, et al. Subtype-specific coupling with ADP-ribosyl
cyclase of metabotropic glutamate receptors in retina, cervical superior ganglion
and NG108-15 cells. Journal of Neurochemistry. 2003;85(5):1148-1158. doi:10.1046/j.1471-4159.2003.01751.x
apa: Higashida, H., Zhang, J., Mochida, S., Chen, X., Shin, Y., Noda, M., … Yokoyama,
S. (2003). Subtype-specific coupling with ADP-ribosyl cyclase of metabotropic
glutamate receptors in retina, cervical superior ganglion and NG108-15 cells.
Journal of Neurochemistry. Wiley-Blackwell. https://doi.org/10.1046/j.1471-4159.2003.01751.x
chicago: Higashida, Haruhiro, Jia Zhang, Sumiko Mochida, Xiao Chen, Yeonsook Shin,
Mami Noda, Kazi Hossain, et al. “Subtype-Specific Coupling with ADP-Ribosyl Cyclase
of Metabotropic Glutamate Receptors in Retina, Cervical Superior Ganglion and
NG108-15 Cells.” Journal of Neurochemistry. Wiley-Blackwell, 2003. https://doi.org/10.1046/j.1471-4159.2003.01751.x.
ieee: H. Higashida et al., “Subtype-specific coupling with ADP-ribosyl cyclase
of metabotropic glutamate receptors in retina, cervical superior ganglion and
NG108-15 cells,” Journal of Neurochemistry, vol. 85, no. 5. Wiley-Blackwell,
pp. 1148–1158, 2003.
ista: Higashida H, Zhang J, Mochida S, Chen X, Shin Y, Noda M, Hossain K, Hoshi
N, Hashii M, Shigemoto R, Nakanishi S, Fukuda Y, Yokoyama S. 2003. Subtype-specific
coupling with ADP-ribosyl cyclase of metabotropic glutamate receptors in retina,
cervical superior ganglion and NG108-15 cells. Journal of Neurochemistry. 85(5),
1148–1158.
mla: Higashida, Haruhiro, et al. “Subtype-Specific Coupling with ADP-Ribosyl Cyclase
of Metabotropic Glutamate Receptors in Retina, Cervical Superior Ganglion and
NG108-15 Cells.” Journal of Neurochemistry, vol. 85, no. 5, Wiley-Blackwell,
2003, pp. 1148–58, doi:10.1046/j.1471-4159.2003.01751.x.
short: H. Higashida, J. Zhang, S. Mochida, X. Chen, Y. Shin, M. Noda, K. Hossain,
N. Hoshi, M. Hashii, R. Shigemoto, S. Nakanishi, Y. Fukuda, S. Yokoyama, Journal
of Neurochemistry 85 (2003) 1148–1158.
date_created: 2018-12-11T11:58:46Z
date_published: 2003-06-01T00:00:00Z
date_updated: 2021-01-12T06:58:42Z
day: '01'
doi: 10.1046/j.1471-4159.2003.01751.x
extern: 1
intvolume: ' 85'
issue: '5'
month: '06'
page: 1148 - 1158
publication: Journal of Neurochemistry
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4268'
quality_controlled: 0
status: public
title: Subtype-specific coupling with ADP-ribosyl cyclase of metabotropic glutamate
receptors in retina, cervical superior ganglion and NG108-15 cells
type: journal_article
volume: 85
year: '2003'
...
---
_id: '2633'
abstract:
- lang: eng
text: The modulation of calcium channels by metabotropic glutamate receptors (mGluRs)
is a key event in the fine-tuning of neurotransmitter release. Here we report
that, in cerebrocortical nerve terminals of adult rats, the inhibition of glutamate
release is mediated by mGluR7. In this preparation, the major component of glutamate
release is supported by P/Q-type Ca2+ channels (72.7%). However, mGluR7 selectively
reduced the release component that is associated with N-type Ca2+ channels (29.9%).
Inhibition of P/Q channels by mGluR7 is not masked by the higher efficiency of
these channels in driving glutamate release when compared with N-type channels.
Thus, activation of mGluR7 failed to reduce the release associated with P/Q channels
when the extracellular calcium concentration, ([Ca2+]o), was reduced from 1.3
to 0.5 mM. Through Ca2+ imaging, we show that Ca2+ channels are distributed in
a heterogeneous manner in individual nerve terminals. Indeed, in this preparation,
nerve terminals were observed that contain N-type (31.1%; conotoxin GVIA-sensitive)
or P/Q-type (64.3%; agatoxin IVA-sensitive) channels or that were insensitive
to these two toxins (4.6%). Interestingly, the great majority of the responses
to L-AP4 (95.4%) were observed in nerve terminals containing N-type channels.
This specific co-localization of mGluR7 and N-type Ca2+-channels could explain
the failure of the receptor to inhibit the P/Q channel-associated release component
and also reveal the existence of specific targeting mechanisms to localize the
two proteins in the same nerve terminal subset.
author:
- first_name: Carmelo
full_name: Millán, Carmelo
last_name: Millán
- first_name: Enrique
full_name: Castro, Enrique G
last_name: Castro
- first_name: Magdalena
full_name: Torres, Magdalena
last_name: Torres
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: José
full_name: Sánchez-Prieto, José
last_name: Sánchez Prieto
citation:
ama: Millán C, Castro E, Torres M, Shigemoto R, Sánchez Prieto J. Co-expression
of metabotropic glutamate receptor 7 and N-type Ca2+ channels in single cerebrocortical
nerve terminals of adult rats. Journal of Biological Chemistry. 2003;278(26):23955-23962.
doi:10.1074/jbc.M211471200
apa: Millán, C., Castro, E., Torres, M., Shigemoto, R., & Sánchez Prieto, J.
(2003). Co-expression of metabotropic glutamate receptor 7 and N-type Ca2+ channels
in single cerebrocortical nerve terminals of adult rats. Journal of Biological
Chemistry. American Society for Biochemistry and Molecular Biology. https://doi.org/10.1074/jbc.M211471200
chicago: Millán, Carmelo, Enrique Castro, Magdalena Torres, Ryuichi Shigemoto, and
José Sánchez Prieto. “Co-Expression of Metabotropic Glutamate Receptor 7 and N-Type
Ca2+ Channels in Single Cerebrocortical Nerve Terminals of Adult Rats.” Journal
of Biological Chemistry. American Society for Biochemistry and Molecular Biology,
2003. https://doi.org/10.1074/jbc.M211471200.
ieee: C. Millán, E. Castro, M. Torres, R. Shigemoto, and J. Sánchez Prieto, “Co-expression
of metabotropic glutamate receptor 7 and N-type Ca2+ channels in single cerebrocortical
nerve terminals of adult rats,” Journal of Biological Chemistry, vol. 278,
no. 26. American Society for Biochemistry and Molecular Biology, pp. 23955–23962,
2003.
ista: Millán C, Castro E, Torres M, Shigemoto R, Sánchez Prieto J. 2003. Co-expression
of metabotropic glutamate receptor 7 and N-type Ca2+ channels in single cerebrocortical
nerve terminals of adult rats. Journal of Biological Chemistry. 278(26), 23955–23962.
mla: Millán, Carmelo, et al. “Co-Expression of Metabotropic Glutamate Receptor 7
and N-Type Ca2+ Channels in Single Cerebrocortical Nerve Terminals of Adult Rats.”
Journal of Biological Chemistry, vol. 278, no. 26, American Society for
Biochemistry and Molecular Biology, 2003, pp. 23955–62, doi:10.1074/jbc.M211471200.
short: C. Millán, E. Castro, M. Torres, R. Shigemoto, J. Sánchez Prieto, Journal
of Biological Chemistry 278 (2003) 23955–23962.
date_created: 2018-12-11T11:58:47Z
date_published: 2003-07-27T00:00:00Z
date_updated: 2021-01-12T06:58:42Z
day: '27'
doi: 10.1074/jbc.M211471200
extern: 1
intvolume: ' 278'
issue: '26'
month: '07'
page: 23955 - 23962
publication: Journal of Biological Chemistry
publication_status: published
publisher: American Society for Biochemistry and Molecular Biology
publist_id: '4265'
quality_controlled: 0
status: public
title: Co-expression of metabotropic glutamate receptor 7 and N-type Ca2+ channels
in single cerebrocortical nerve terminals of adult rats
type: journal_article
volume: 278
year: '2003'
...
---
_id: '2632'
abstract:
- lang: eng
text: In many brain regions, hyperpolarization-activated cationic currents (Ih)
are involved in the generation of rhythmic activities, but the role of Ih in olfactory
oscillations remains unclear. Knowledge of the cellular and subcellular distributions
of hyperpolarization-activated and cyclic nucleotide-gated channel (HCN) subunits
is necessary for understanding the role of Ih in olfactory network activities.
Using light microscopic immunocytochemistry, we demonstrate strong HCN1 labelling
of the glomerular layer and moderate staining of granule cell, internal and external
plexiform layers of the rat main olfactory bulb. In the glomerular layer, among
many unlabelled neurons, two distinct subpopulations of juxtaglomerular cells
are labelled. Approximately 10% of the juxtaglomerular cells strongly express
HCN1. These small diameter cells are immunoreactive for GABA and comprise a subpopulation
of periglomerular cells. An additional subset of juxtaglomerular cells (≈ 1%)
expresses low levels of HCN1. They are large in diameter, GABA immunonegative
but immunopositive for vesicular glutamate transporter 2, characterizing them
as external tufted cells. Quantitative immunogold localization revealed that the
somatic plasma membranes of periglomerular cells contain approximately four times
more HCN1 labelling than those of external tufted cells. Unlike in cortical pyramidal
cells, immunogold density for HCN1 does not significantly differ in somatic and
dendritic plasma membranes of external tufted cells, indicating that post-synaptic
potentials arriving at proximal and distal dendrites are modulated by the same
density of I h. Our results demonstrate a cell type-dependent expression of HCN1
in the olfactory bulb and predict a differential contribution of distinct juxtaglomerular
cell types to network oscillations.
author:
- first_name: Noémi
full_name: Holderith, Noémi B
last_name: Holderith
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Zoltán
full_name: Nusser, Zoltán
last_name: Nusser
citation:
ama: Holderith N, Shigemoto R, Nusser Z. Cell type-dependent expression of HCN1
in the main olfactory bulb. European Journal of Neuroscience. 2003;18(2):344-354.
doi:10.1046/j.1460-9568.2003.02756.x
apa: Holderith, N., Shigemoto, R., & Nusser, Z. (2003). Cell type-dependent
expression of HCN1 in the main olfactory bulb. European Journal of Neuroscience.
Wiley-Blackwell. https://doi.org/10.1046/j.1460-9568.2003.02756.x
chicago: Holderith, Noémi, Ryuichi Shigemoto, and Zoltán Nusser. “Cell Type-Dependent
Expression of HCN1 in the Main Olfactory Bulb.” European Journal of Neuroscience.
Wiley-Blackwell, 2003. https://doi.org/10.1046/j.1460-9568.2003.02756.x.
ieee: N. Holderith, R. Shigemoto, and Z. Nusser, “Cell type-dependent expression
of HCN1 in the main olfactory bulb,” European Journal of Neuroscience,
vol. 18, no. 2. Wiley-Blackwell, pp. 344–354, 2003.
ista: Holderith N, Shigemoto R, Nusser Z. 2003. Cell type-dependent expression of
HCN1 in the main olfactory bulb. European Journal of Neuroscience. 18(2), 344–354.
mla: Holderith, Noémi, et al. “Cell Type-Dependent Expression of HCN1 in the Main
Olfactory Bulb.” European Journal of Neuroscience, vol. 18, no. 2, Wiley-Blackwell,
2003, pp. 344–54, doi:10.1046/j.1460-9568.2003.02756.x.
short: N. Holderith, R. Shigemoto, Z. Nusser, European Journal of Neuroscience 18
(2003) 344–354.
date_created: 2018-12-11T11:58:47Z
date_published: 2003-07-01T00:00:00Z
date_updated: 2021-01-12T06:58:42Z
day: '01'
doi: 10.1046/j.1460-9568.2003.02756.x
extern: 1
intvolume: ' 18'
issue: '2'
month: '07'
page: 344 - 354
publication: European Journal of Neuroscience
publication_status: published
publisher: Wiley-Blackwell
publist_id: '4266'
quality_controlled: 0
status: public
title: Cell type-dependent expression of HCN1 in the main olfactory bulb
type: journal_article
volume: 18
year: '2003'
...
---
_id: '2635'
abstract:
- lang: eng
text: Metabotropic GABAB receptors mediate slow inhibitory effects presynaptically
and postsynaptically. Using preembedding immunohistochemical methods combined
with quantitative analysis of GABAB receptor subunit immunoreactivity, this study
provides a detailed description of the cellular and subcellular localization of
GABAB1a/b and GABA B2 in the rat hippocampus. At the light microscopic level,
an overlapping distribution of GABAB1a/b and GABAB2 was revealed in the dendritic
layers of the hippocampus. In addition, expression of the GABAB1a/b subunit was
found in somata of CA1 pyramidal cells and of a subset of GABAergic interneurons.
At the electron microscopic level, immunoreactivity for both subunits was observed
on presynaptic and, more abundantly, on postsynaptic elements. Presynaptically,
subunits were mainly detected in the extrasynaptic membrane and occasionally over
the presynaptic membrane specialization of putative glutamatergic and, to a lesser
extent, GABAergic axon terminals. Postsynaptically, the majority of GABAB receptor
subunits were localized to the extrasynaptic plasma membrane of spines and dendritic
shafts of principal cells and shafts of interneuron dendrites. Quantitative analysis
revealed enrichment of GABAB1a/b around putative glutamatergic synapses on spines
and an even distribution on dendritic shafts of pyramidal cells contacted by GABAergic
boutons. The association of GABAB receptors with glutamatergic synapses at both
presynaptic and postsynaptic sides indicates their intimate involvement in the
modulation of glutamatergic neurotransmission. The dominant extrasynaptic localization
of GABAB receptor subunits suggests that their activation is dependent on spillover
of GABA requiring simultaneous activity of populations of GABAergic cells as it
occurs during population oscillations or epileptic seizures.
author:
- first_name: Ákos
full_name: Kulik, Ákos
last_name: Kulik
- first_name: Imre
full_name: Vida, Imre
last_name: Vida
- first_name: Rafael
full_name: Luján, Rafael
last_name: Luján
- first_name: Carola
full_name: Haas, Carola A
last_name: Haas
- first_name: Guillermina
full_name: López-Bendito, Guillermina
last_name: López Bendito
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Michael
full_name: Frotscher, Michael
last_name: Frotscher
citation:
ama: Kulik Á, Vida I, Luján R, et al. Subcellular Localization of Metabotropic GABAB
Receptor Subunits GABAB1a/b and GABAB2 in the Rat Hippocampus. Journal of Neuroscience.
2003;23(35):11026-11035.
apa: Kulik, Á., Vida, I., Luján, R., Haas, C., López Bendito, G., Shigemoto, R.,
& Frotscher, M. (2003). Subcellular Localization of Metabotropic GABAB Receptor
Subunits GABAB1a/b and GABAB2 in the Rat Hippocampus. Journal of Neuroscience.
Society for Neuroscience.
chicago: Kulik, Ákos, Imre Vida, Rafael Luján, Carola Haas, Guillermina López Bendito,
Ryuichi Shigemoto, and Michael Frotscher. “Subcellular Localization of Metabotropic
GABAB Receptor Subunits GABAB1a/b and GABAB2 in the Rat Hippocampus.” Journal
of Neuroscience. Society for Neuroscience, 2003.
ieee: Á. Kulik et al., “Subcellular Localization of Metabotropic GABAB Receptor
Subunits GABAB1a/b and GABAB2 in the Rat Hippocampus,” Journal of Neuroscience,
vol. 23, no. 35. Society for Neuroscience, pp. 11026–11035, 2003.
ista: Kulik Á, Vida I, Luján R, Haas C, López Bendito G, Shigemoto R, Frotscher
M. 2003. Subcellular Localization of Metabotropic GABAB Receptor Subunits GABAB1a/b
and GABAB2 in the Rat Hippocampus. Journal of Neuroscience. 23(35), 11026–11035.
mla: Kulik, Ákos, et al. “Subcellular Localization of Metabotropic GABAB Receptor
Subunits GABAB1a/b and GABAB2 in the Rat Hippocampus.” Journal of Neuroscience,
vol. 23, no. 35, Society for Neuroscience, 2003, pp. 11026–35.
short: Á. Kulik, I. Vida, R. Luján, C. Haas, G. López Bendito, R. Shigemoto, M.
Frotscher, Journal of Neuroscience 23 (2003) 11026–11035.
date_created: 2018-12-11T11:58:47Z
date_published: 2003-12-03T00:00:00Z
date_updated: 2021-01-12T06:58:43Z
day: '03'
extern: 1
intvolume: ' 23'
issue: '35'
month: '12'
page: 11026 - 11035
publication: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '4263'
quality_controlled: 0
status: public
title: Subcellular Localization of Metabotropic GABAB Receptor Subunits GABAB1a/b
and GABAB2 in the Rat Hippocampus
type: journal_article
volume: 23
year: '2003'
...
---
_id: '2634'
abstract:
- lang: eng
text: To better understand the role of neurotransmitter receptors in neuronal differentiation
and maturation a detailed knowledge of their identity, location and function in
the plasma membrane of specific neuronal populations during development is required.
Combining pre-embedding immunocytochemistry with cell tracking in embryonic brain
slice cultures we show that virtually all neurons (∼98%) migrating through the
lower intermediate zone (LIZ) on their way from the medial ganglionic eminence
to the cerebral cortex, express GABA BR1. Blockade of GABABRs with a specific
antagonist, CGP52432, resulted in a concentration-dependent accumulation of these
tangentially migrating neurons in the ventricular/subventricular zones (VZ/SVZ)
of the cortex and fewer cells were observed in the cortical plate/marginal zone
(CP/MZ) and LIZ. Moreover, they had significantly shorter leading processes compared
with similar migrating cells in control slices. Electrophysiological recording
in LIZ and CP cells revealed no direct effect of either CGP52432 or the GABABR
agonist, baclofen, on resting membrane properties suggesting that the effect of
CGP52432 on migration might be mediated through a metabotropic action or the regulation
of release of factors controlling migration. These results suggest that GABABRs
have an important modulatory role in the migration of cortical interneurons.
author:
- first_name: Guillermina
full_name: López-Bendito, Guillermina
last_name: López Bendito
- first_name: Rafael
full_name: Luján, Rafael
last_name: Luján
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Paul
full_name: Ganter, Paul
last_name: Ganter
- first_name: Ole
full_name: Paulsen, Ole
last_name: Paulsen
- first_name: Zoltán
full_name: Molnár, Zoltán
last_name: Molnár
citation:
ama: López Bendito G, Luján R, Shigemoto R, Ganter P, Paulsen O, Molnár Z. Blockade
of GABAB receptors alters the tangential migration of cortical neurons. Cerebral
Cortex. 2003;13(9):932-942. doi:10.1093/cercor/13.9.932
apa: López Bendito, G., Luján, R., Shigemoto, R., Ganter, P., Paulsen, O., &
Molnár, Z. (2003). Blockade of GABAB receptors alters the tangential migration
of cortical neurons. Cerebral Cortex. Oxford University Press. https://doi.org/10.1093/cercor/13.9.932
chicago: López Bendito, Guillermina, Rafael Luján, Ryuichi Shigemoto, Paul Ganter,
Ole Paulsen, and Zoltán Molnár. “Blockade of GABAB Receptors Alters the Tangential
Migration of Cortical Neurons.” Cerebral Cortex. Oxford University Press,
2003. https://doi.org/10.1093/cercor/13.9.932.
ieee: G. López Bendito, R. Luján, R. Shigemoto, P. Ganter, O. Paulsen, and Z. Molnár,
“Blockade of GABAB receptors alters the tangential migration of cortical neurons,”
Cerebral Cortex, vol. 13, no. 9. Oxford University Press, pp. 932–942,
2003.
ista: López Bendito G, Luján R, Shigemoto R, Ganter P, Paulsen O, Molnár Z. 2003.
Blockade of GABAB receptors alters the tangential migration of cortical neurons.
Cerebral Cortex. 13(9), 932–942.
mla: López Bendito, Guillermina, et al. “Blockade of GABAB Receptors Alters the
Tangential Migration of Cortical Neurons.” Cerebral Cortex, vol. 13, no.
9, Oxford University Press, 2003, pp. 932–42, doi:10.1093/cercor/13.9.932.
short: G. López Bendito, R. Luján, R. Shigemoto, P. Ganter, O. Paulsen, Z. Molnár,
Cerebral Cortex 13 (2003) 932–942.
date_created: 2018-12-11T11:58:47Z
date_published: 2003-09-01T00:00:00Z
date_updated: 2021-01-12T06:58:43Z
day: '01'
doi: 10.1093/cercor/13.9.932
extern: 1
intvolume: ' 13'
issue: '9'
month: '09'
page: 932 - 942
publication: Cerebral Cortex
publication_status: published
publisher: Oxford University Press
publist_id: '4264'
quality_controlled: 0
status: public
title: Blockade of GABAB receptors alters the tangential migration of cortical neurons
type: journal_article
volume: 13
year: '2003'
...
---
_id: '2630'
abstract:
- lang: eng
text: Taste-metabotropic glutamate receptor 4 (taste-mGluR4) and the heteromers
of T1R1 and T1R3 are candidate receptors involved in the sense of umami (monosodium
glutamate) taste. Although the expression of group III mGluRs (taste-mGluR4) has
been demonstrated in taste tissues, no mention has been made of the expression
of group I mGluRs (mGluR1 and mGluR5) in taste tissues. We examined the expression
of mGluR1 and mGluR5 in rat gustatory tissues by using reverse transcription-polymerase
chain reaction (RT-PCR), in situ hybridization, immunohistochemistry and immunoelectron
microscopy. RT-PCR assay showed that mGluR1α and mGluR1β mRNAs were expressed
in circumvallate papillae, but mGluR5 mRNA was not expressed. The positive signals
of mGluR1 mRNA were detected only in circumvallate taste buds by in situ hybridization
analysis. In cryosections of fungiform, foliate and circumvallate papillae, the
antibody against mGluRla gave intense labeling on the taste hairs in all taste
pores examined. In the developing taste buds, the positive signals of mGluR1α
in taste hairs gradually increased with the increase in number of taste bud cells.
These results show that, in addition to taste-mGluR4 and the heteromer of T1R1
and T1R3, mGluR1α may function as a receptor for glutamate (umami) taste sensation.
author:
- first_name: Takashi
full_name: Toyono, Takashi
last_name: Toyono
- first_name: Yuji
full_name: Seta, Yuji
last_name: Seta
- first_name: Shinji
full_name: Kataoka, Shinji
last_name: Kataoka
- first_name: Shintaro
full_name: Kawano, Shintaro
last_name: Kawano
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Kuniaki
full_name: Toyoshima, Kuniaki
last_name: Toyoshima
citation:
ama: Toyono T, Seta Y, Kataoka S, Kawano S, Shigemoto R, Toyoshima K. Expression
of metabotropic glutamate receptor group I in rat gustatory papillae. Cell
and Tissue Research. 2003;313(1):29-35. doi:10.1007/s00441-003-0740-2
apa: Toyono, T., Seta, Y., Kataoka, S., Kawano, S., Shigemoto, R., & Toyoshima,
K. (2003). Expression of metabotropic glutamate receptor group I in rat gustatory
papillae. Cell and Tissue Research. Springer. https://doi.org/10.1007/s00441-003-0740-2
chicago: Toyono, Takashi, Yuji Seta, Shinji Kataoka, Shintaro Kawano, Ryuichi Shigemoto,
and Kuniaki Toyoshima. “Expression of Metabotropic Glutamate Receptor Group I
in Rat Gustatory Papillae.” Cell and Tissue Research. Springer, 2003. https://doi.org/10.1007/s00441-003-0740-2.
ieee: T. Toyono, Y. Seta, S. Kataoka, S. Kawano, R. Shigemoto, and K. Toyoshima,
“Expression of metabotropic glutamate receptor group I in rat gustatory papillae,”
Cell and Tissue Research, vol. 313, no. 1. Springer, pp. 29–35, 2003.
ista: Toyono T, Seta Y, Kataoka S, Kawano S, Shigemoto R, Toyoshima K. 2003. Expression
of metabotropic glutamate receptor group I in rat gustatory papillae. Cell and
Tissue Research. 313(1), 29–35.
mla: Toyono, Takashi, et al. “Expression of Metabotropic Glutamate Receptor Group
I in Rat Gustatory Papillae.” Cell and Tissue Research, vol. 313, no. 1,
Springer, 2003, pp. 29–35, doi:10.1007/s00441-003-0740-2.
short: T. Toyono, Y. Seta, S. Kataoka, S. Kawano, R. Shigemoto, K. Toyoshima, Cell
and Tissue Research 313 (2003) 29–35.
date_created: 2018-12-11T11:58:46Z
date_published: 2003-07-01T00:00:00Z
date_updated: 2021-01-12T06:58:41Z
day: '01'
doi: 10.1007/s00441-003-0740-2
extern: 1
intvolume: ' 313'
issue: '1'
month: '07'
page: 29 - 35
publication: Cell and Tissue Research
publication_status: published
publisher: Springer
publist_id: '4267'
quality_controlled: 0
status: public
title: Expression of metabotropic glutamate receptor group I in rat gustatory papillae
type: journal_article
volume: 313
year: '2003'
...
---
_id: '2637'
abstract:
- lang: eng
text: While the cholinergic depletion in Alzheimer's disease (AD) has been known
for some time, a definitive involvement of other neurotransmitter systems has
been somewhat more elusive. Our study demonstrates a clear involvement of both
glutamatergic and, to a lesser extent, GABAergic neurons in an early onset transgenic
mouse model of AD-like amyloid pathology. Immunohistochemical staining and subsequent
quantification has revealed a statistically significant increased density of glutamatergic
and GABAergic presynaptic boutons in both the plaque free and plaque adjacent
cortical neuropile areas of transgenic mice as compared to non-transgenic controls.
Furthermore, amyloid plaque size was shown to have a statistically significant
effect on the relative area occupied by dystrophic glutamatergic neurites in the
peri-plaque neuropile. These findings support our hypothesis that the amyloid
pathology progresses in a time and neurotransmitter specific manner, first in
the cholinergic system which appears to be most vulnerable, followed by the glutamatergic
presynaptic boutons and finally the somewhat more resilient GABAergic terminals.
author:
- first_name: Karen
full_name: Bell, Karen F
last_name: Bell
- first_name: G J
full_name: De Kort, G J
last_name: De Kort
- first_name: S
full_name: Steggerda, S
last_name: Steggerda
- first_name: Ryuichi
full_name: Ryuichi Shigemoto
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Alfredo
full_name: Ribeiro-da-Silva, Alfredo
last_name: Ribeiro Da Silva
- first_name: Augusto
full_name: Cuello, Augusto C
last_name: Cuello
citation:
ama: Bell K, De Kort GJ, Steggerda S, Shigemoto R, Ribeiro Da Silva A, Cuello A.
Structural involvement of the glutamatergic presynaptic boutons in a transgenic
mouse model expressing early onset amyloid pathology. Neuroscience Letters.
2003;353(2):143-147. doi:10.1016/j.neulet.2003.09.027
apa: Bell, K., De Kort, G. J., Steggerda, S., Shigemoto, R., Ribeiro Da Silva, A.,
& Cuello, A. (2003). Structural involvement of the glutamatergic presynaptic
boutons in a transgenic mouse model expressing early onset amyloid pathology.
Neuroscience Letters. Elsevier. https://doi.org/10.1016/j.neulet.2003.09.027
chicago: Bell, Karen, G J De Kort, S Steggerda, Ryuichi Shigemoto, Alfredo Ribeiro
Da Silva, and Augusto Cuello. “Structural Involvement of the Glutamatergic Presynaptic
Boutons in a Transgenic Mouse Model Expressing Early Onset Amyloid Pathology.”
Neuroscience Letters. Elsevier, 2003. https://doi.org/10.1016/j.neulet.2003.09.027.
ieee: K. Bell, G. J. De Kort, S. Steggerda, R. Shigemoto, A. Ribeiro Da Silva, and
A. Cuello, “Structural involvement of the glutamatergic presynaptic boutons in
a transgenic mouse model expressing early onset amyloid pathology,” Neuroscience
Letters, vol. 353, no. 2. Elsevier, pp. 143–147, 2003.
ista: Bell K, De Kort GJ, Steggerda S, Shigemoto R, Ribeiro Da Silva A, Cuello A.
2003. Structural involvement of the glutamatergic presynaptic boutons in a transgenic
mouse model expressing early onset amyloid pathology. Neuroscience Letters. 353(2),
143–147.
mla: Bell, Karen, et al. “Structural Involvement of the Glutamatergic Presynaptic
Boutons in a Transgenic Mouse Model Expressing Early Onset Amyloid Pathology.”
Neuroscience Letters, vol. 353, no. 2, Elsevier, 2003, pp. 143–47, doi:10.1016/j.neulet.2003.09.027.
short: K. Bell, G.J. De Kort, S. Steggerda, R. Shigemoto, A. Ribeiro Da Silva, A.
Cuello, Neuroscience Letters 353 (2003) 143–147.
date_created: 2018-12-11T11:58:48Z
date_published: 2003-12-19T00:00:00Z
date_updated: 2021-01-12T06:58:44Z
day: '19'
doi: 10.1016/j.neulet.2003.09.027
extern: 1
intvolume: ' 353'
issue: '2'
month: '12'
page: 143 - 147
publication: Neuroscience Letters
publication_status: published
publisher: Elsevier
publist_id: '4262'
quality_controlled: 0
status: public
title: Structural involvement of the glutamatergic presynaptic boutons in a transgenic
mouse model expressing early onset amyloid pathology
type: journal_article
volume: 353
year: '2003'
...
---
_id: '2784'
abstract:
- lang: eng
text: We report the results of an experimental study of magnetohydrodynamic damping
of sidewall convection in a rectangular enclosure filled with gallium. In particular
we investigate the suppression of convection when a steady magnetic field is applied
separately in each of the three principal directions of the flow. The strongest
damping of the steady flow is found for a vertical magnetic field, which is in
agreement with theory. However, we observe that the application of a field transverse
to the flow provides greater damping than a longitudinal one, which seems to contradict
available theory. We provide a possible resolution of this apparent dichotomy
in terms of the length scale of the experiment.
author:
- first_name: Björn
full_name: Björn Hof
id: 3A374330-F248-11E8-B48F-1D18A9856A87
last_name: Hof
orcid: 0000-0003-2057-2754
- first_name: Anne
full_name: Juel, Anne
last_name: Juel
- first_name: Tom
full_name: Mullin, Tom P
last_name: Mullin
citation:
ama: Hof B, Juel A, Mullin T. Magnetohydrodynamic damping of convective flows in
molten gallium. Journal of Fluid Mechanics. 2003;482:163-179. doi:10.1017/S0022112003004014
apa: Hof, B., Juel, A., & Mullin, T. (2003). Magnetohydrodynamic damping of
convective flows in molten gallium. Journal of Fluid Mechanics. Cambridge
University Press. https://doi.org/10.1017/S0022112003004014
chicago: Hof, Björn, Anne Juel, and Tom Mullin. “Magnetohydrodynamic Damping of
Convective Flows in Molten Gallium.” Journal of Fluid Mechanics. Cambridge
University Press, 2003. https://doi.org/10.1017/S0022112003004014.
ieee: B. Hof, A. Juel, and T. Mullin, “Magnetohydrodynamic damping of convective
flows in molten gallium,” Journal of Fluid Mechanics, vol. 482. Cambridge
University Press, pp. 163–179, 2003.
ista: Hof B, Juel A, Mullin T. 2003. Magnetohydrodynamic damping of convective flows
in molten gallium. Journal of Fluid Mechanics. 482, 163–179.
mla: Hof, Björn, et al. “Magnetohydrodynamic Damping of Convective Flows in Molten
Gallium.” Journal of Fluid Mechanics, vol. 482, Cambridge University Press,
2003, pp. 163–79, doi:10.1017/S0022112003004014.
short: B. Hof, A. Juel, T. Mullin, Journal of Fluid Mechanics 482 (2003) 163–179.
date_created: 2018-12-11T11:59:35Z
date_published: 2003-05-13T00:00:00Z
date_updated: 2021-01-12T06:59:42Z
day: '13'
doi: 10.1017/S0022112003004014
extern: 1
intvolume: ' 482'
month: '05'
page: 163 - 179
publication: Journal of Fluid Mechanics
publication_status: published
publisher: Cambridge University Press
publist_id: '4105'
quality_controlled: 0
status: public
title: Magnetohydrodynamic damping of convective flows in molten gallium
type: journal_article
volume: 482
year: '2003'
...
---
_id: '2785'
abstract:
- lang: eng
text: Experimental evidence for the scaling of the finite amplitude of perturbation
theory required to promote transition in Poiseuille flow was found. The exponent
is -1 and was uncovered using considerable care in the design and execution of
the experiment. Interestingly, this exponent was also found in experiments on
transition in boundary layers.
author:
- first_name: Björn
full_name: Björn Hof
id: 3A374330-F248-11E8-B48F-1D18A9856A87
last_name: Hof
orcid: 0000-0003-2057-2754
- first_name: Anne
full_name: Juel, Anne
last_name: Juel
- first_name: Tom
full_name: Mullin, Tom P
last_name: Mullin
citation:
ama: Hof B, Juel A, Mullin T. Scaling of the turbulence transition threshold in
a pipe. Physical Review Letters. 2003;91(24):244502/1-244502/4. doi:10.1103/PhysRevLett.91.244502
apa: Hof, B., Juel, A., & Mullin, T. (2003). Scaling of the turbulence transition
threshold in a pipe. Physical Review Letters. American Physical Society.
https://doi.org/10.1103/PhysRevLett.91.244502
chicago: Hof, Björn, Anne Juel, and Tom Mullin. “Scaling of the Turbulence Transition
Threshold in a Pipe.” Physical Review Letters. American Physical Society,
2003. https://doi.org/10.1103/PhysRevLett.91.244502.
ieee: B. Hof, A. Juel, and T. Mullin, “Scaling of the turbulence transition threshold
in a pipe,” Physical Review Letters, vol. 91, no. 24. American Physical
Society, p. 244502/1-244502/4, 2003.
ista: Hof B, Juel A, Mullin T. 2003. Scaling of the turbulence transition threshold
in a pipe. Physical Review Letters. 91(24), 244502/1-244502/4.
mla: Hof, Björn, et al. “Scaling of the Turbulence Transition Threshold in a Pipe.”
Physical Review Letters, vol. 91, no. 24, American Physical Society, 2003,
p. 244502/1-244502/4, doi:10.1103/PhysRevLett.91.244502.
short: B. Hof, A. Juel, T. Mullin, Physical Review Letters 91 (2003) 244502/1-244502/4.
date_created: 2018-12-11T11:59:35Z
date_published: 2003-12-12T00:00:00Z
date_updated: 2021-01-12T06:59:42Z
day: '12'
doi: 10.1103/PhysRevLett.91.244502
extern: 1
intvolume: ' 91'
issue: '24'
month: '12'
page: 244502/1 - 244502/4
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '4104'
quality_controlled: 0
status: public
title: Scaling of the turbulence transition threshold in a pipe
type: journal_article
volume: 91
year: '2003'
...