Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: Inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting

Human Molecular Genetics

Volumn 8, Issue 7, 1999, Pages 1337-1352

  Dao, Diem ^a   Walsh, Colum P ^a   Yuan, Luwa ^a   Gorelov, Dmitri ^a   Feng, Lin ^a   Hensle, Terrence ^a   Nisen, Perry ^b   Yamashiro, Darrell J ^a   Bestor, Timothy H ^a   Tycko, Benjamin ^a  

^a Columbia Univ Coll Phys Surgs ^*  (United States)

^b ABBOTT LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARCINOGENESIS; CHROMOSOME 11P; CHROMOSOME 7; CPG ISLAND; DNA METHYLATION; GENE EXPRESSION; GENE SILENCING; HETEROZYGOSITY LOSS; INTRON; NEPHROBLASTOMA; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ANIMALS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; DNA METHYLATION; GENES, WILMS TUMOR; GENOMIC IMPRINTING; HUMANS; INSULIN-LIKE GROWTH FACTOR II; KIDNEY; LOSS OF HETEROZYGOSITY; MICE; MUSCLE PROTEINS; RNA, NEOPLASM; RNA, UNTRANSLATED; WILMS TUMOR;

EID: 0032797231     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.7.1337     Document Type: Article

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