High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19

Oncogene

Volumn 12, Issue 2, 1996, Pages 423-430

  Douc Rasy, S ^a   Barrois, M ^a   Fogel, S ^a   Ahomadegbe, J C ^a   Stehelin D ^b   Coll, J ^b   Riou, G ^a  

^a INSTITUT GUSTAVE ROUSSY   (France)

^b INSTITUT PASTEUR DE LILLE   (France)

Author keywords

Allele switch; Cervical cancer; H19; IGF2; Loss of imprinting; Methylation

Indexed keywords

GROWTH FACTOR; SOMATOMEDIN B;

ALLELE; ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER STAGING; CHROMOSOME 11P; CLINICAL ARTICLE; CONTROLLED STUDY; DEMETHYLATION; DISEASE COURSE; DNA METHYLATION; FEMALE; FETUS; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENE FUNCTION; GENE LOCATION; GENOME IMPRINTING; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; NEPHROBLASTOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; UTERINE CERVIX CARCINOMA;

ALLELES; CHROMOSOME DELETION; FEMALE; GENOMIC IMPRINTING; HUMANS; INSULIN-LIKE GROWTH FACTOR II; METHYLATION; MUSCLE PROTEINS; RNA, UNTRANSLATED; UTERINE CERVICAL NEOPLASMS;

EID: 0030053512     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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