Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Top Cited Papers
- 1 August 2015
- journal article
- research article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 97 (2) , 343-352
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome SequencingThe American Journal of Human Genetics, 2013
- Transcription factor–mediated reprogramming of fibroblasts to expandable, myelinogenic oligodendrocyte progenitor cellsNature Biotechnology, 2013
- Determination of the Role of DDX3 a Factor Involved in Mammalian RNAi Pathway Using an shRNA-Expression LibraryPLOS ONE, 2013
- HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrainDevelopment, 2011
- A Motif Unique to the Human Dead-Box Protein DDX3 Is Important for Nucleic Acid Binding, ATP Hydrolysis, RNA/DNA Unwinding and HIV-1 ReplicationPLOS ONE, 2011
- Dosage compensation of the mammalian X chromosome influences the phenotypic variability of X-linked dominant male-lethal disordersJournal of Medical Genetics, 2008
- Dickkopf-1 regulates gastrulation movements by coordinated modulation of Wnt/βcatenin and Wnt/PCP activities, through interaction with the Dally-like homolog KnypekGenes & Development, 2007
- X-inactivation profile reveals extensive variability in X-linked gene expression in femalesNature, 2005
- Human DDX3Y, the Y-encoded isoform of RNA helicase DDX3, rescues a hamster temperature-sensitive ET24 mutant cell line with a DDX3X mutationExperimental Cell Research, 2004
- Inheritance of most X‐linked traits is not dominant or recessive, just X‐linkedAmerican Journal of Medical Genetics Part A, 2004