Roles for Dnmt3b in mammalian development: A mouse model for the ICF syndrome

Development

Volumn 133, Issue 6, 2006, Pages 1183-1192

  Ueda, Yoshihide ^a   Okano, Masaki ^a,b   Williams, Christine ^a   Chen, Taiping ^a,c   Georgopoulos, Katia ^a   Li, En ^a,c  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b RIKEN Center for Biosystems Dynamics Research   (Japan)

^c NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH   (United States)

Author keywords

Apoptosis; DNA methylation; Dnmt3b; ICF syndrome; T cell

Indexed keywords

DNA METHYLTRANSFERASE 3B;

AMINO ACID SEQUENCE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BLEEDING DISORDER; CLINICAL FEATURE; DNA METHYLATION; EMBRYO; EMBRYO DEVELOPMENT; ENZYME ACTIVE SITE; ENZYME ACTIVITY; GENE DELETION; GENE FUNCTION; GENE MUTATION; GENETIC CODE; GENETIC PREDISPOSITION; GENETIC RISK; HEART VENTRICLE SEPTUM DEFECT; HOMOZYGOSITY; HYPOTROPHY; ICF SYNDROME; LIVER DISEASE; MAMMAL; MISSENSE MUTATION; MOUSE; MUTATIONAL ANALYSIS; NONHUMAN; NULL ALLELE; PHENOTYPE; PRIORITY JOURNAL; RISK ASSESSMENT; T LYMPHOCYTE;

ANIMALS; ANIMALS, NEWBORN; APOPTOSIS; CENTROMERE; DISEASE MODELS, ANIMAL; DNA (CYTOSINE-5-)-METHYLTRANSFERASE; EMBRYO; EMBRYO LOSS; FACE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MICE; MUTATION; PROTEIN BINDING; SYNDROME; THYMUS GLAND;

ANIMALIA; MAMMALIA;

EID: 33645735015     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.02293     Document Type: Article

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