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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 8, 2006
The role of RELN in lissencephaly and neuropsychiatric diseaseBernard S Chang, Fusun Duzcan, Seonhee Kim, et al.
Molecular Cell|August 4, 2012
Molecular basis for specific regulation of neuronal kinesin-3 motors by doublecortin family proteinsJudy S Liu, Christian R Schubert, Xiaoqin Fu, et al.
Annals of Neurology|September 22, 2020
Polymicrogyria is Associated With Pathogenic Variants in PTENDiane D Shao, Christelle M Achkar, Abbe Lai, et al.
Journal of the American Heart Association|July 3, 2024
Contributions of Germline and Somatic Mosaic Genetics to Thoracic Aortic Aneurysms in Nonsyndromic IndividualsMing Hui Chen, Ellen S Deng, Jessica M Yamada, et al.
Nature Structural Biology|April 15, 2003
The DCX-domain tandems of doublecortin and doublecortin-like kinaseMyung Hee Kim, Tomasz Cierpicki, Urszula Derewenda, et al.
European Journal of Medical Genetics|March 4, 2017
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophyShenela Lakhani, Ryan Doan, Mariam Almureikhi, et al.
American Journal of Human Genetics|February 15, 2002
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21Xianhua Piao, Lina Basel-Vanagaite, Rachel Straussberg, et al.
Brain : a Journal of Neurology|February 3, 2026
ARX mutation-associated interneuron defects provide insights into mechanisms underlying developmental epilepsiesYoungshin Lim, Shyam K Akula, Abigail K Myers, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|July 18, 2013
Effect of surfactant type and redox polymer type on single-walled carbon nanotube modified electrodesJie Chen, Tu O Tran, Michael T Ray, et al.
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