11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments (JoVE). 2020;(159). doi:10.3791/61147
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, et al. Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum. bioRxiv. doi:10.1101/2020.03.18.997205
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras X, Davaatseren A, Amberg N, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. bioRxiv. 2020. doi:10.1101/2020.06.05.136192
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, Hippenmeyer S. Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology. 2020;8(9). doi:10.3389/fcell.2020.574382
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, et al. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 2020;107(6):1160-1179.e9. doi:10.1016/j.neuron.2020.06.031
View | Files available | DOI
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein T, Edwards A, Přistoupilová A, et al. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience. 2018;21(2):207-217. doi:10.1038/s41593-017-0053-5
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 2017;11. doi:10.3389/fncel.2017.00176
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, et al. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 2017;26(2):258-269. doi:10.1093/hmg/ddw383
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 2017;84:58-67. doi:10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, Landler L, Keays D. Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. 2017;323:47-55. doi:10.1016/j.bbr.2017.01.029
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie M, Breuss M, Tian G, et al. Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics. 2015;97(6):790-800. doi:10.1016/j.ajhg.2015.10.014
View | DOI
 

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11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments (JoVE). 2020;(159). doi:10.3791/61147
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, et al. Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum. bioRxiv. doi:10.1101/2020.03.18.997205
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras X, Davaatseren A, Amberg N, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. bioRxiv. 2020. doi:10.1101/2020.06.05.136192
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, Hippenmeyer S. Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology. 2020;8(9). doi:10.3389/fcell.2020.574382
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, et al. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 2020;107(6):1160-1179.e9. doi:10.1016/j.neuron.2020.06.031
View | Files available | DOI
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein T, Edwards A, Přistoupilová A, et al. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience. 2018;21(2):207-217. doi:10.1038/s41593-017-0053-5
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 2017;11. doi:10.3389/fncel.2017.00176
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, et al. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 2017;26(2):258-269. doi:10.1093/hmg/ddw383
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 2017;84:58-67. doi:10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, Landler L, Keays D. Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. 2017;323:47-55. doi:10.1016/j.bbr.2017.01.029
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie M, Breuss M, Tian G, et al. Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics. 2015;97(6):790-800. doi:10.1016/j.ajhg.2015.10.014
View | DOI
 

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