Results 251 to 260 of about 33,901 (278)

Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies

Lancet Neurology, The, 2020
Huda Y Zoghbi
exaly  

MECP2 Gene

2020
openaire   +1 more source

Rett syndrome-causing mutations compromise MeCP2-mediated liquid–liquid phase separation of chromatin

Cell Research, 2020
Liang Wang, Di Wu, Ping Chen
exaly  

MeCP2

2008
openaire   +1 more source

MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

Science, 2008
Maria H Chahrour, Huda Y Zoghbi
exaly  

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

Nature Genetics, 2001
Jacky Guy, Brian Hendrich, Megan Holmes
exaly  

Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition

Cell Research, 2013
Alika K Maunakea, Iouri Chepelev, Kairong Cui   +2 more
exaly  

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

Nature Genetics, 2004
Hannes Lohi, Stephen Scherer, John B Vincent   +2 more
exaly  

Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing

Nature Genetics, 2005
Said Sif
exaly  

MECP2 Gene

2018
openaire   +1 more source