Rezultati - Muhammad Mahajnah
- Showing 1 - 4 results of 4
-
1
A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly od Ganeshwaran H. Mochida, Muhammad Mahajnah, Anthony D. Hill, Lina Basel‐Vanagaite, Danielle Gleason, Robert Hill, Adria Bodell, Moira Crosier, Rachel Straussberg, Christopher A. Walsh
Izdano 2009Artigo -
2
-
3
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation od Martial Mallaret, Matthis Synofzik, Jae‐Ho Lee, Cari A. Sagum, Muhammad Mahajnah, Rajech Sharkia, Nathalie Drouot, M. Renaud, Fabrice Klein, Mathieu Anheim, Christine Tranchant, Cyril Mignot, Jean‐Louis Mandel, Mark T. Bedford, Peter Bauer, Mustafa A. Salih, Rebecca Schüle, Lüdger Schöls, C. Marcelo Aldaz, Michel Kœnig
Izdano 2013Artigo -
4
Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation od Yawei J. Yang, Andrew E. Baltus, Rebecca S. Mathew, Elisabeth A. Murphy, Gilad D. Evrony, Dilenny M. Gonzalez, Estee P. Wang, Christine A. Marshall-Walker, Brenda J. Barry, Jernej Murn, Antonis Tatarakis, MaryAnn Mahajan, Herbert H. Samuels, Yang Shi, Jeffrey A. Golden, Muhammad Mahajnah, Ruthie Shenhav, Christopher A. Walsh
Izdano 2012Artigo
Iskalna orodja:
Sorodne teme
Biology
Gene
Genetics
Neuroscience
Epilepsy
Microcephaly
Missense mutation
Phenotype
Suppressor
WWOX
Ataxia
Cancer
Cell
Cell biology
Cell fate determination
Cellular differentiation
Disease gene identification
Environmental health
Exome sequencing
Intellectual disability
Locus (genetics)
Medicine
Mutant
Mutation
Neural cell
Neural development
Neural stem cell
Neurogenesis
Nonsense mutation
Organoid