Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center

Journal of Biological Chemistry

Volumn 278, Issue 17, 2003, Pages 14996-15000

  Xin, Zhenghan ^a   Tachibana, Makoto ^c   Guggiari, Michele ^d   Heard, Edith ^d   Shinkai, Yoichi ^c   Wagstaff, Joseph ^a,b,e  

^a UNIVERSITY OF VIRGINIA   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

^c KYOTO UNIVERSITY   (Japan)

^d INSTITUT CURIE   (France)

^e UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENCE; GENES; RNA;

EMBRYONIC STEM (ES) CELLS;

BIOCHEMISTRY;

CIS ACTING ELEMENT; HISTONE; HISTONE H3; METHYLTRANSFERASE;

ALLELE; ANIMAL CELL; ARTICLE; CHROMOSOME 15; CHROMOSOME 7; CPG ISLAND; DNA METHYLATION; EMBRYO; FLUORESCENCE IN SITU HYBRIDIZATION; GENE CLUSTER; GENE EXPRESSION REGULATION; GENE LOCATION; GENOME IMPRINTING; MOUSE; NONHUMAN; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

ANIMALS; AUTOANTIGENS; CELL LINE; DINUCLEOSIDE PHOSPHATES; DNA METHYLATION; EMBRYO; GENOMIC IMPRINTING; HISTONE-LYSINE N-METHYLTRANSFERASE; HISTONES; IN SITU HYBRIDIZATION, FLUORESCENCE; METHYLTRANSFERASES; MICE; PRADER-WILLI SYNDROME; REPRESSOR PROTEINS; RIBONUCLEOPROTEINS, SMALL NUCLEAR; STEM CELLS; TRANSGENES;

ANIMALIA; MAMMALIA;

EID: 0038003140     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M211753200     Document Type: Article

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