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Premature centromere division in patients with multiple endocrine neoplasia type 1.
Sakurai, A; Katai, M; Itakura, Y; Ikeo, Y; Hashizume, K.
Afiliação
  • Sakurai A; Department of Geriatrics, Endocrinology, and Metabolism, Shinshu University School of Medicine, Matsumoto, Japan.
Cancer Genet Cytogenet ; 109(2): 138-40, 1999 Mar.
Article em En | MEDLINE | ID: mdl-10087948
ABSTRACT
Frequency of mitoses with premature centromere division (PCD) was examined in lymphocytes from subjects with multiple endocrine neoplasia type 1 (MEN 1). An increase in PCD after exposure to an alkylating agent was observed in subjects with MEN 1 who carry a heterozygous MEN1 gene mutation but not in normal controls or in affected subjects without the MEN1 gene mutation. These findings support the inclusion of MEN 1 as a chromosome instability syndrome and recognition of PCD as a manifestation of chromosome instability. Furthermore, these results suggest that the MEN1 gene product may function to maintain the integrity of DNA.
Assuntos
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Base de dados: MEDLINE Assunto principal: Centrômero / Proteínas Proto-Oncogênicas / Neoplasia Endócrina Múltipla Tipo 1 Limite: Adult / Aged / Humans / Middle aged Idioma: En Revista: Cancer Genet Cytogenet Ano de publicação: 1999 Tipo de documento: Article País de afiliação: Japão
Buscar no Google
Base de dados: MEDLINE Assunto principal: Centrômero / Proteínas Proto-Oncogênicas / Neoplasia Endócrina Múltipla Tipo 1 Limite: Adult / Aged / Humans / Middle aged Idioma: En Revista: Cancer Genet Cytogenet Ano de publicação: 1999 Tipo de documento: Article País de afiliação: Japão