6 Publications

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[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, T., Edwards, A., Přistoupilová, A., Leca, I., Breuss, M., Pilat Carotta, S., … Keays, D. (2018). Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience, 21(2), 207–217. https://doi.org/10.1038/s41593-017-0053-5
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[5]
2017 | Journal Article | IST-REx-ID: 960   OA
Hansen, A. H., Düllberg, C. F., Mieck, C., Loose, M., & Hippenmeyer, S. (2017). Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience, 11. https://doi.org/10.3389/fncel.2017.00176
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[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, M., Nguyen, T., Srivatsan, A., Leca, I., Tian, G., Fritz, T., … Gleeson, J. (2017). Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics, 26(2), 258–269. https://doi.org/10.1093/hmg/ddw383
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[3]
2017 | Journal Article | IST-REx-ID: 1017   OA
Breuss, M., Leca, I., Gstrein, T., Hansen, A. H., & Keays, D. (2017). Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience, 84, 58–67. https://doi.org/10.1016/j.mcn.2017.03.002
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[2]
2017 | Journal Article | IST-REx-ID: 1107   OA
Breuss, M., Hansen, A. H., Landler, L., & Keays, D. (2017). Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research, 323, 47–55. https://doi.org/10.1016/j.bbr.2017.01.029
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[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, M., Breuss, M., Tian, G., Hansen, A. H., Cristofoli, F., Morandell, J., … Van Esch, H. (2015). Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics, 97(6), 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014
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6 Publications

Mark all

[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, T., Edwards, A., Přistoupilová, A., Leca, I., Breuss, M., Pilat Carotta, S., … Keays, D. (2018). Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience, 21(2), 207–217. https://doi.org/10.1038/s41593-017-0053-5
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960   OA
Hansen, A. H., Düllberg, C. F., Mieck, C., Loose, M., & Hippenmeyer, S. (2017). Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience, 11. https://doi.org/10.3389/fncel.2017.00176
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, M., Nguyen, T., Srivatsan, A., Leca, I., Tian, G., Fritz, T., … Gleeson, J. (2017). Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics, 26(2), 258–269. https://doi.org/10.1093/hmg/ddw383
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017   OA
Breuss, M., Leca, I., Gstrein, T., Hansen, A. H., & Keays, D. (2017). Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience, 84, 58–67. https://doi.org/10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107   OA
Breuss, M., Hansen, A. H., Landler, L., & Keays, D. (2017). Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research, 323, 47–55. https://doi.org/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., Hansen, A. H., Cristofoli, F., Morandell, J., … Van Esch, H. (2015). Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics, 97(6), 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014
View | DOI
 

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