Showing results (11-20 of 283) with videos related to
Sort By:
Pageof 29
Cellular and Molecular Life Sciences : CMLS|February 13, 2015
La FAM fatale: USP9X in development and diseaseMariyam Murtaza, Lachlan A Jolly, Jozef Gecz, et al.European Journal of Human Genetics : EJHG|May 23, 2013
Rare copy number variation in cerebral palsyGai McMichael, Santhosh Girirajan, Andres Moreno-De-Luca, et al.American Journal of Human Genetics|March 11, 2014
Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growthClaire C Homan, Raman Kumar, Lam Son Nguyen, et al.American Journal of Medical Genetics|October 12, 2002
Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutationGillian Turner, Michael Partington, Bronwyn Kerr, et al.Human Molecular Genetics|March 20, 2009
Lessons learnt from large-scale exon re-sequencing of the X chromosomeF Lucy Raymond, Annabel Whibley, Michael R Stratton, et al.Human Molecular Genetics|October 15, 2013
Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulationKristie Lee, Tessa Mattiske, Kunio Kitamura, et al.American Journal of Medical Genetics. Part A|July 17, 2009
A novel de novo 27 bp duplication of the ARX gene, resulting from postzygotic mosaicism and leading to three severely affected males in two generationsOrit Reish, Tod Fullston, Miriam Regev, et al.Current Opinion in Genetics & Development|July 12, 2025
Transcription-Export complex in neurodevelopmental disordersRudrarup Bhattacharjee, Shreya Agarwala, Danielle Mazurkiewicz, et al.Human Molecular Genetics|November 1, 2016
Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox geneTessa Mattiske, Kristie Lee, Jozef Gecz, et al.Biological Psychiatry|June 6, 2022
The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental DisordersLachlan A Jolly, Raman Kumar, Peter Penzes, et al.Pageof 29