The methyl-CpG binding domain and the evolving role of DNA methylation in animalsHENDRICH, Brian; TWEEDIE, Susan.Trends in genetics (Regular ed.). 2003, Vol 19, Num 5, pp 269-277, issn 0168-9525, 9 p.Article

Human diseases with underlying defects in chromatin structure and modificationHENDRICH, Brian; BICKMORE, Wendy.Human molecular genetics (Print). 2001, Vol 10, Num 20, pp 2233-2242, issn 0964-6906Article

Methyl-CpG binding proteins and cancer: are MeCpGs more important than MBDs?PROKHORTCHOUK, Egor; HENDRICH, Brian.Oncogene (Basingstoke). 2002, Vol 21, Num 35, pp 5394-5399, issn 0950-9232, 6 p.Article

MeCP2 in neurons : closing in on the causes of Rett syndromeCABALLERO, Isabel Martin; HENDRICH, Brian.Human molecular genetics (Print). 2005, Vol 14, Num 1, pp R19-R26, issn 0964-6906, NSArticle

NuRD Suppresses Pluripotency Gene Expression to Promote Transcriptional Heterogeneity and Lineage CommitmentREYNOLDS, Nicola; LATOS, Paulina; COSTELLO, Ita et al.Cell stem cell. 2012, Vol 10, Num 5, pp 583-594, issn 1934-5909, 12 p.Article

c-Jun N-terminal phosphorylation antagonises recruitment of the Mbd3/NuRD repressor complexAGUILERA, Cristina; NAKAGAWA, Kentaro; SANCHO, Rocio et al.Nature (London). 2011, Vol 469, Num 7329, pp 231-235, issn 0028-0836, 5 p.Article

Deficiency of Mbd2 suppresses intestinal tumorigenesisSANSOM, Owen J; BERGER, Jennifer; BISHOP, Stefan M et al.Nature genetics. 2003, Vol 34, Num 2, pp 145-147, issn 1061-4036, 3 p.Article

Enhanced CpG mutability and tumorigenesis in MBD4-deficient miceMILLAR, Catherine B; GUY, Jacky; SANSOM, Owen J et al.Science (Washington, D.C.). 2002, Vol 297, Num 5580, pp 403-405, issn 0036-8075Article

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndromeGUY, Jacky; HENDRICH, Brian; HOLMES, Megan et al.Nature genetics. 2001, Vol 27, Num 3, pp 322-326, issn 1061-4036Article