SCOPUS 정보 검색 플랫폼

Volumn 61, Issue 12, 2001, Pages 4815-4819

VHL and FHIT locus loss of heterozygosity is common in all renal cancer morphotypes but differs in pattern and prognostic significance

(4) Velickovic, Marija a Delahunt, Brett a Störkel, Stephan b Grebe, Stefan K G a

a UNIVERSITY OF OTAGO (New Zealand)

b UNIVERSITY OF WITTEN HERDECKE (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ADULT; ARTICLE; CARCINOGENESIS; CHROMOSOME 3P; CHROMOSOME DELETION; CLINICAL ARTICLE; FEMALE; GENE INACTIVATION; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; KIDNEY CANCER; KIDNEY CARCINOMA; MALE; PRIORITY JOURNAL; PROGNOSIS; TUMOR SUPPRESSOR GENE;

ACID ANHYDRIDE HYDROLASES; ADENOCARCINOMA, CLEAR CELL; CARCINOMA, PAPILLARY; CARCINOMA, RENAL CELL; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; HUMANS; KIDNEY NEOPLASMS; LIGASES; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; NEOPLASM PROTEINS; PROGNOSIS; PROTEINS; TUMOR SUPPRESSOR PROTEINS; UBIQUITIN-PROTEIN LIGASES; VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN;

EID: 0035874947 PISSN: 00085472 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (60)

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