Your browser doesn't support javascript.
loading
A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix.
Lee, J Y; Dong, S M; Kim, H S; Kim, S Y; Na, E Y; Shin, M S; Lee, S H; Park, W S; Kim, K M; Lee, Y S; Jang, J J; Yoo, N J.
Afiliação
  • Lee JY; Department of Pathology and Cancer Research Institute, Catholic University Medical College, Seoul, Korea.
Cancer Res ; 58(6): 1140-3, 1998 Mar 15.
Article em En | MEDLINE | ID: mdl-9515797
ABSTRACT
Adenoma malignum (AM) is known to be one of the malignant tumors that is commonly associated with Peutz-Jeghers syndrome. Recently, the genetic locus of Peutz-Jeghers syndrome was mapped to the telomeric region of chromosome 19p. We analyzed nine sporadic cases of AM with high-density loss of heterozygosity to study the region of chromosome 19p13.2-13.3 using eight microsatellite markers. Our deletion mapping data revealed a distinct region with 100% loss of heterozygosity frequency at marker D19S216. This result indicates that a putative tumor suppressor gene for AM is located at D19S216 on chromosomal band 19p13.3 and plays an important role in AM tumorigenesis.
Assuntos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 19 / Síndrome de Peutz-Jeghers / Adenoma / Neoplasias do Colo do Útero / Genes Supressores de Tumor Tipo de estudo: Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 1998 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 19 / Síndrome de Peutz-Jeghers / Adenoma / Neoplasias do Colo do Útero / Genes Supressores de Tumor Tipo de estudo: Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 1998 Tipo de documento: Article