Brian Hendrich

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

Jacky Guy, Brian Hendrich, Megan C. Holmes et al. · Nature Genetics · 2001 · 1.6K citations

Knockout Mouse, Molecular Neuroscience, Mendelian Disorder +12

Identification and Characterization of a Family of Mammalian Methyl-CpG Binding Proteins

Brian Hendrich, Adrian Bird · Molecular and Cellular Biology · 1998 · 1.3K citations · Full text

The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

Carolyn J. Brown, Brian Hendrich, Jim L. Rupert et al. · Cell · 1992 · 1.3K citations

Chromatin, Systems Biology, Engineering +8

Dynamic Reprogramming of DNA Methylation in the Early Mouse Embryo

Fátima Santos, Brian Hendrich, Wolf Reik et al. · Developmental Biology · 2002 · 1.2K citations

Chromatin, Developmental Biology, Epigenetic Change +9

MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex

Huck‐Hui Ng, Yi Zhang, Brian Hendrich et al. · Nature Genetics · 1999 · 922 citations · Full text

Chromatin, Transcriptional Regulation, Chromatin Structure +12