@article{4070,
abstract = {Let S be a set of n closed intervals on the x-axis. A ranking assigns to each interval, s, a distinct rank, p(s) [1, 2,…,n]. We say that s can see t if p(s)<p(t) and there is a point ps∩t so that pu for all u with p(s)<p(u)<p(t). It is shown that a ranking can be found in time O(n log n) such that each interval sees at most three other intervals. It is also shown that a ranking that minimizes the average number of endpoints visible from an interval can be computed in time O(n 5/2). The results have applications to intersection problems for intervals, as well as to channel routing problems which arise in layouts of VLSI circuits.},
author = {Herbert Edelsbrunner and Overmars, Mark H and Welzl, Emo and Hartman, Irith Ben-Arroyo and Feldman,Jack A},
journal = {International Journal of Computer Mathematics},
number = {3-4},
pages = {129 -- 144},
publisher = {Taylor & Francis},
title = {{Ranking intervals under visibility constraints}},
doi = {10.1080/00207169008803871},
volume = {34},
year = {1990},
}
@article{4075,
abstract = {A key problem in computational geometry is the identification of subsets of a point set having particular properties. We study this problem for the properties of convexity and emptiness. We show that finding empty triangles is related to the problem of determining pairs of vertices that see each other in a star-shaped polygon. A linear-time algorithm for this problem which is of independent interest yields an optimal algorithm for finding all empty triangles. This result is then extended to an algorithm for finding empty convex r-gons (r> 3) and for determining a largest empty convex subset. Finally, extensions to higher dimensions are mentioned.},
author = {Dobkin, David P and Herbert Edelsbrunner and Overmars, Mark H},
journal = {Algorithmica},
number = {4},
pages = {561 -- 571},
publisher = {Springer},
title = {{Searching for empty convex polygons}},
doi = {10.1007/BF01840404},
volume = {5},
year = {1990},
}
@inbook{4311,
author = {Nicholas Barton and Clark,A.},
booktitle = {Population biology: ecological and evolutionary viewpoints},
editor = {Wöhrmann, Klaus and Jain, Subodh K},
pages = {115 -- 174},
publisher = {Springer},
title = {{Population structure}},
year = {1990},
}
@article{2525,
abstract = {This paper describes the amino acid sequence of the rat substance P receptor and its comparison with that of the rat substance K receptor on the basis of molecular cloning and sequence analysis. From a rat brain cDNA library constructed with an RNA expression vector, we identified a cDNA mixture containing a functional substance P receptor cDNA by examining electrophysiologically a receptor expression following injection of the mRNAs synthesized in vitro into Xenopus oocytes. A receptor cDNA clone was then isolated by cross-hybridization with the bovine substance K receptor DNA. The clone was confirmed by selective binding of substance P to the cloned receptor expressed in mammalian COS cells. The deduced amino acid sequence (407 amino acid residues) possesses seven putative membrane spanning domains and shows a sequence similarity to the members of G-protein-coupled receptors. The rat substance P and substance K receptor are very similar in both size and amino acid sequences, particularly in the putative transmembrane similarity is in marked contrast to the sequence divergence in the amino- and carboxyl-terminal regions and the third cytoplasmic loop. The observed sequence similarytity and divergence would thus contribute to the expression of similar but pharmacological regions and the first and second cytoplasmic loops. This distinguishable activities of the two tachykinin receptors.},
author = {Yokota, Yoshifumi and Sasai, Yoshiki and Tanaka, Kohichi and Fujiwara, Tsutomu and Tsuchida, Kunihiro and Ryuichi Shigemoto and Kakizuka, Akira and Ohkubo, Hiroaki and Nakanishi, Shigetada},
journal = {Journal of Biological Chemistry},
number = {30},
pages = {17649 -- 17652},
publisher = {American Society for Biochemistry and Molecular Biology},
title = {{Molecular characterization of a functional cDNA for rat substance P receptor}},
volume = {264},
year = {1989},
}
@article{2479,
abstract = {Distribution of putative glutamatergic neurons in the lower brainstem and cerebellum of the rat was examined immunocytochemically by using a monoclonal antibody against phosphate-activated glutaminase, which has been proposed to be a major synthetic enzyme of transmitter glutamate and so may serve as a marker for glutamatergic neurons in the central nervous system. Intensely-immunolabeled neuronal cell bodies were densely distributed in the main precerebellar nuclei sending mossy fibers to the cerebellum; in the pontine nuclei, pontine tegmental reticular nucleus of Bechterew, external cuneate nucleus, and lateral reticular nucleus of the medulla oblongata. Phosphate-activated glutaminase-immunoreactive granular deposits were densely seen in the brachium pontis and restiform body, suggesting the immunolabeling of mossy fibers of passage. In the cerebellum, neuropil within the granule cell layer of the cerebellar cortex displayed intense phosphate-activated glutaminase-immunoreactivity, and that within the deep cerebellar nuclei showed moderate immunoreactivity. These results indicate that many mossy fiber terminals originate from phosphate-activated glutaminase-containing neurons and utilize phosphate-activated glutaminase for the synthesis of transmitter glutamate. Intensely-immunostained neuronal cell bodies were further observed in other regions which have been reported to contain neurons sending mossy fibers to the cerebellum; in the dorsal part of the principal sensory trigeminal nucleus, dorsomedial part of the oral subnucleus of the spinal trigeminal nucleus, interpolar subnucleus of the spinal trigeminal nucleus, paratrigeminal nucleus, supragenual nucleus, regions dorsal to the abducens nucleus and genu of the facial nerve, superior and medial vestibular nuclei, cell groups f, x and y, hypoglossal prepositus nucleus, intercalated nucleus, nucleus of Roller, reticular regions intercalated between the motor trigeminal and principal sensory trigeminal nuclei, linear nucleus, and gigantocellular and paramedian reticular formation. Neuronal cell bodies with intense phosphate-activated glutaminase-immunoreactivity were also found in other brainstem regions, such as the paracochlear glial substance, posterior ventral cochlear nucleus, and cell group e. Although it is still controversial whether all glutamatergic neurons use phosphate-activated glutaminase in a transmitter-related process and whether phosphate-activated glutaminase is involved in other metabolism-related processes, the neurons showing intense phosphate-activated glutaminase-immuno-reactivity in the present study were suggested to be putative glutamatergic neurons.},
author = {Kaneko, Takeshi and Itoh, Kazuo and Ryuichi Shigemoto and Mizuno, Noboru},
journal = {Neuroscience},
number = {1},
pages = {79 -- 98},
publisher = {Elsevier},
title = {{Glutaminase-like immunoreactivity in the lower brainstem and cerebellum of the adult rat}},
doi = {10.1016/0306-4522(89)90109-7},
volume = {32},
year = {1989},
}
@article{3465,
abstract = {Asymmetrical displacement currents and Na currents of single myelinated nerve fibers of Xenopus laevis were studied in the temperature range from 5 to 24 degrees C. The time constant of the on-response at E = 4 mV, tau on, was strongly temperature dependent, whereas the amount of displaced charge at E = 39 mV, Qon, was only slightly temperature dependent. The mean Q10 for tau on-1 was 2.54, the mean Q10 for Qon was 1.07. The time constant of charge immobilization, tau i, at E = 4 mV varied significantly (alpha = 0.001) with temperature. The mean Q10 for tau i-1 was 2.71 +/- 0.38. The time constants of immobilization of gating charge and of fast inactivation of Na permeability were similar in the temperature range from 6 to 22 degrees C. The Qoff/Qon ratio for E = 4 mV pulses of 0.5 msec duration decreased with increasing temperature. The temperature dependence of the time constant of the off-response could not be described by a single Q10 value, since the Q10 depended on the duration of the test pulse. Increasing temperature shifted Qon (E) curves to more negative potentials by 0.51 mV K-1, but shifted PNa (E) curves and h infinity (E) curves to more positive potentials by 0.43 and 0.57 mV K-1, respectively. h infinity (E = -70 mV) increased monotonously with increasing temperature. The present data indicate that considerable entropy changes may occur when the Na channel molecule passes from closed through open to inactivated states.},
author = {Peter Jonas},
journal = {Journal of Membrane Biology},
number = {3},
pages = {277 -- 289},
publisher = {Springer},
title = {{Temperature dependence of gating current in myelinated nerve fibers}},
doi = {10.1007/BF01870958},
volume = {112},
year = {1989},
}
@article{4083,
abstract = {It is shown that, given a set S of n points in $R^3 $, one can always find three planes that form an eight-partition of S, that is, a partition where at most ${n / 8}$ points of S lie in each of the eight open regions. This theorem is used to define a data structure, called an octant tree, for representing any point set in $R^3 $. An octant tree for n points occupies $O(n)$ space and can be constructed in polynomial time. With this data structure and its refinements, efficient solutions to various range query problems in two and three dimensions can be obtained, including (1) half-space queries: find all points of S that lie to one side of any given plane; (2) polyhedron queries: find all points that lie inside (outside) any given polyhedron; and (3) circle queries in $R^2 $: for a planar set S, find all points that lie inside (outside) any given circle. The retrieval time for all these queries is $T(n) = O(n^\alpha + m)$, where $\alpha = 0.8988$ (or 0.8471 in case (3)), and m is the size of the output. This performance is the best currently known for linear-space data structures that can be deterministically constructed in polynomial time.},
author = {Yao, F. Frances and Dobkin, David P and Herbert Edelsbrunner and Paterson,Michael S},
journal = {SIAM Journal on Computing},
number = {2},
pages = {371 -- 384},
publisher = {SIAM},
title = {{Partitioning space for range queries}},
doi = {10.1137/0218025},
volume = {18},
year = {1989},
}
@article{4088,
abstract = {Anarrangement ofn lines (or line segments) in the plane is the partition of the plane defined by these objects. Such an arrangement consists ofO(n 2) regions, calledfaces. In this paper we study the problem of calculating and storing arrangementsimplicitly, using subquadratic space and preprocessing, so that, given any query pointp, we can calculate efficiently the face containingp. First, we consider the case of lines and show that with (n) space1 and (n 3/2) preprocessing time, we can answer face queries in (n)+O(K) time, whereK is the output size. (The query time is achieved with high probability.) In the process, we solve three interesting subproblems: (1) given a set ofn points, find a straight-edge spanning tree of these points such that any line intersects only a few edges of the tree, (2) given a simple polygonal path , form a data structure from which we can find the convex hull of any subpath of quickly, and (3) given a set of points, organize them so that the convex hull of their subset lying above a query line can be found quickly. Second, using random sampling, we give a tradeoff between increasing space and decreasing query time. Third, we extend our structure to report faces in an arrangement of line segments in (n 1/3)+O(K) time, given(n 4/3) space and (n 5/3) preprocessing time. Lastly, we note that our techniques allow us to computem faces in an arrangement ofn lines in time (m 2/3 n 2/3+n), which is nearly optimal.},
author = {Herbert Edelsbrunner and Guibas, Leonidas and Hershberger, John and Seidel, Raimund and Sharir, Micha and Snoeyink, Jack and Welzl, Emo},
journal = {Discrete & Computational Geometry},
number = {1},
pages = {433 -- 466},
publisher = {Springer},
title = {{Implicitly representing arrangements of lines or segments}},
doi = {10.1007/BF02187742},
volume = {4},
year = {1989},
}
@article{4312,
author = {Nicholas Barton and Turelli, Michael},
journal = {Annual Review of Genetics},
pages = {337 -- 370},
publisher = {Annual Reviews},
title = {{Evolutionary quantitative genetics: how little do we know ?}},
doi = {10.1146/annurev.ge.23.120189.002005},
volume = {23},
year = {1989},
}
@article{2526,
abstract = {When WGA-HRP (wheat germ agglutinin-horseradish peroxidase conjugate) or HRP was injected into the regions around the superior central and/or the dorsal raphe nuclei in the cat, cell bodies of a number of non-pyramidal neurons were labeled in Ammon's horn. Thus the existence of direct projections from non-pyramidal neurons in Ammon's horn to the rostral raphe regions in the brainstem was suggested in the cat.},
author = {Ino, Tadashi and Itoh, Kazuo and Kamiya, Hiroto and Kaneko, Takeshi and Ryuichi Shigemoto and Akiguchi, Ichiro and Mizuno, Noboru},
journal = {Brain Research},
number = {1},
pages = {157 -- 161},
publisher = {Elsevier},
title = {{Direct projections from Ammon's horn to the rostral raphe regions in the brainstem of the cat}},
doi = {10.1016/0006-8993(89)91346-2},
volume = {479},
year = {1989},
}
@article{3466,
abstract = {Amphibian myelinated nerve fibers were treated with collagenase and protease. Axons with retraction of the myelin sheath were patch-clamped in the nodal and paranodal region. One type of Na channel was found. It has a single-channel conductance of 11 pS (15 degrees C) and is blocked by tetrodotoxin. Averaged events show the typical activation and inactivation kinetics of macroscopic Na current. Three potential-dependent K channels were identified (I, F, and S channel). The I channel, being the most frequent type, has a single-channel conductance of 23 pS (inward current, 105 mM K on both sides of the membrane), activates between -60 and -30 mV, deactivates with intermediate kinetics, and is sensitive to dendrotoxin. The F channel has a conductance of 30 pS, activates between -40 and 60 mV, and deactivates with fast kinetics. The former inactivates within tens of seconds; the latter inactivates within seconds. The third type, the S channel, has a conductance of 7 pS and deactivates slowly. All three channels can be blocked by external tetraethylammonium chloride. We suggest that these distinct K channel types form the basis for the different components of macroscopic K current described previously.},
author = {Peter Jonas and Bräu, Michael E and Hermsteiner, Markus and Vogel, Werner},
journal = {PNAS},
number = {18},
pages = {7238 -- 7242},
publisher = {National Academy of Sciences},
title = {{Single-channel recording in myelinated nerve fibers reveals one type of Na channel but different K channels}},
volume = {86},
year = {1989},
}
@article{4084,
abstract = {A tour of a finite set P of points is a necklace-tour if there are disks with the points in P as centers such that two disks intersect if and only if their centers are adjacent in . It has been observed by Sanders that a necklace-tour is an optimal traveling salesman tour.
In this paper, we present an algorithm that either reports that no necklace-tour exists or outputs a necklace-tour of a given set of n points in O(n2 log n) time. If a tour is given, then we can test in O(n2) time whether or not this tour is a necklace-tour. Both algorithms can be generalized to ƒ-factors of point sets in the plane. The complexity results rely on a combinatorial analysis of certain intersection graphs of disks defined for finite sets of points in the plane.},
author = {Herbert Edelsbrunner and Rote,Günter and Welzl, Emo},
journal = {Theoretical Computer Science},
number = {2},
pages = {157 -- 180},
publisher = {Elsevier},
title = {{Testing the necklace condition for shortest tours and optimal factors in the plane}},
doi = {10.1016/0304-3975(89)90133-3},
volume = {66},
year = {1989},
}
@article{4089,
abstract = {Motivated by a number of motion-planning questions, we investigate in this paper some general topological and combinatorial properties of the boundary of the union ofn regions bounded by Jordan curves in the plane. We show that, under some fairly weak conditions, a simply connected surface can be constructed that exactly covers this union and whose boundary has combinatorial complexity that is nearly linear, even though the covered region can have quadratic complexity. In the case where our regions are delimited by Jordan acrs in the upper halfplane starting and ending on thex-axis such that any pair of arcs intersect in at most three points, we prove that the total number of subarcs that appear on the boundary of the union is only (n(n)), where(n) is the extremely slowly growing functional inverse of Ackermann's function.},
author = {Herbert Edelsbrunner and Guibas, Leonidas and Hershberger, John and Pach, János and Pollack, Richard and Seidel, Raimund and Sharir, Micha and Snoeyink, Jack},
journal = {Discrete & Computational Geometry},
number = {1},
pages = {523 -- 539},
publisher = {Springer},
title = {{On arrangements of Jordan arcs with three intersections per pair}},
doi = {10.1007/BF02187745},
volume = {4},
year = {1989},
}
@inbook{4313,
author = {Nicholas Barton},
booktitle = {Speciation and its consequences},
editor = {Otte, Daniel and Endler, John A},
publisher = {Sinauer Press},
title = {{Founder effect speciation}},
year = {1989},
}
@inproceedings{4596,
abstract = {A real-time temporal logic for the specification of reactive systems is introduced. The novel feature of the logic, TPTL, is the adoption of temporal operators as quantifiers over time variables; every modality binds a variable to the time(s) it refers to. TPTL is demonstrated to be both a natural specification language and a suitable formalism for verification and synthesis. A tableau-based decision procedure and model-checking algorithm for TPTL are presented. Several generalizations of TPTL are shown to be highly undecidable.},
author = {Alur, Rajeev and Thomas Henzinger},
pages = {164 -- 169},
publisher = {IEEE},
title = {{A really temporal logic}},
doi = {10.1109/SFCS.1989.63473},
year = {1989},
}
@article{2527,
author = {Akimoto, Masumi and Ryuichi Shigemoto and Kawamura, Makiko and Yamagata, Hideharu and Kurihara, Takeshi and Takata, S and Miwa, Yoko and Akagami, N and Katsu, Kenichi and Yamauchi, D},
journal = {Japanese Journal of Gastroenterology},
number = {11},
publisher = {Japanese Society of Gastroenterology},
title = {{Effect of endothelin on gastric mucosal blood flow in rat}},
doi = {10.11405/nisshoshi1964.86.2627},
volume = {86},
year = {1989},
}
@inproceedings{3549,
author = {Herbert Edelsbrunner},
pages = {83 -- 89},
publisher = {Institute of the Electronics, Information and Communication Enginneers},
title = {{Spatial triangulations with dihedral angle conditions}},
year = {1989},
}
@article{3652,
abstract = {Frequency-dependent selection against rare forms can maintain clines. For weak selection, s, in simple linear models of frequency-dependence, single locus clines are stabilized with a maximum slope of between {complex}s/{complex}8 {sigma} and {complex}s/{complex}12 {delta}, where {sigma} is the dispersal distance. These clines are similar to those maintained by heterozygote disadvantage. Using computer simulations, the weak-selection analytical results are extended to higher selection pressures with up to three unlinked genes. Graphs are used to display the effect of selection, migration, dominance, and number of loci on cline widths, speeds of cline movements, two-way gametic correlations (``linkage disequilibria''), and heterozygote deficits. The effects of changing the order of reproduction, migration, and selection, are also briefly explored. Epistasis can also maintain tension zones. We show that epistatic selection is similar in its effects to frequency-dependent selection, except that the disequilibria produced in the zone will be higher for a given level of selection. If selection consists of a mixture of frequency-dependence and epistasis, as is likely in nature, the error made in estimating selection is usually less than twofold. From the graphs, selection and migration can be estimated using knowledge of the dominance and number of genes, of gene frequences and of gametic correlations from a hybrid zone.},
author = {Mallet, James L and Nicholas Barton},
journal = {Genetics},
number = {4},
pages = {967 -- 976},
publisher = {Genetics Society of America},
title = {{Inference from clines stabilized by frequency-dependent selection}},
volume = {122},
year = {1989},
}
@article{4080,
abstract = {This paper proves that any set of n points in the plane contains two points such that any circle through those two points encloses at least n12−112+O(1)n47 points of the set. The main ingredients used in the proof of this result are edge counting formulas for k-order Voronoi diagrams and a lower bound on the minimum number of semispaces of size at most k.},
author = {Herbert Edelsbrunner and Hasan, Nany and Seidel, Raimund and Shen, Xiao-Jun},
journal = {Geometriae Dedicata},
number = {1},
pages = {1 -- 12},
publisher = {Kluwer},
title = {{Circles through two points that always enclose many points}},
doi = {10.1007/BF00181432},
volume = {32},
year = {1989},
}
@inproceedings{4085,
abstract = {Let C be a cell complex in d-dimensional Euclidean space whose faces are obtained by orthogonal projection of the faces of a convex polytope in d + 1 dimensions. For example, the Delaunay triangulation of a finite point set is such a cell complex. This paper shows that the in_front/behind relation defined for the faces of C with respect to any fixed viewpoint x is acyclic. This result has applications to hidden line/surface removal and other problems in computational geometry.},
author = {Herbert Edelsbrunner},
pages = {145 -- 151},
publisher = {ACM},
title = {{An acyclicity theorem for cell complexes in d dimension}},
doi = {10.1145/73833.73850},
year = {1989},
}