6 Publications

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[6]
2018 | Journal Article | IST-REx-ID: 547
T. Gstrein et al., “Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans,” Nature Neuroscience, vol. 21, no. 2, pp. 207–217, 2018.
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[5]
2017 | Journal Article | IST-REx-ID: 960   OA
A. H. Hansen, C. F. Düllberg, C. Mieck, M. Loose, and S. Hippenmeyer, “Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks,” Frontiers in Cellular Neuroscience, vol. 11, 2017.
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[4]
2017 | Journal Article | IST-REx-ID: 1016
M. Breuss et al., “Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability,” Human Molecular Genetics, vol. 26, no. 2, pp. 258–269, 2017.
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[3]
2017 | Journal Article | IST-REx-ID: 1017   OA
M. Breuss, I. Leca, T. Gstrein, A. H. Hansen, and D. Keays, “Tubulins and brain development: The origins of functional specification,” Molecular and Cellular Neuroscience, vol. 84, pp. 58–67, 2017.
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[2]
2017 | Journal Article | IST-REx-ID: 1107   OA
M. Breuss, A. H. Hansen, L. Landler, and D. Keays, “Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition,” Behavioural Brain Research, vol. 323, pp. 47–55, 2017.
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[1]
2015 | Journal Article | IST-REx-ID: 1106
M. Isrie et al., “Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type,” The American Journal of Human Genetics, vol. 97, no. 6, pp. 790–800, 2015.
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6 Publications

Mark all

[6]
2018 | Journal Article | IST-REx-ID: 547
T. Gstrein et al., “Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans,” Nature Neuroscience, vol. 21, no. 2, pp. 207–217, 2018.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960   OA
A. H. Hansen, C. F. Düllberg, C. Mieck, M. Loose, and S. Hippenmeyer, “Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks,” Frontiers in Cellular Neuroscience, vol. 11, 2017.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
M. Breuss et al., “Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability,” Human Molecular Genetics, vol. 26, no. 2, pp. 258–269, 2017.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017   OA
M. Breuss, I. Leca, T. Gstrein, A. H. Hansen, and D. Keays, “Tubulins and brain development: The origins of functional specification,” Molecular and Cellular Neuroscience, vol. 84, pp. 58–67, 2017.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107   OA
M. Breuss, A. H. Hansen, L. Landler, and D. Keays, “Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition,” Behavioural Brain Research, vol. 323, pp. 47–55, 2017.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
M. Isrie et al., “Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type,” The American Journal of Human Genetics, vol. 97, no. 6, pp. 790–800, 2015.
View | DOI
 

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Citation Style: IEEE

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