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Significance of chromosome 7 abnormalities in myeloid malignancies / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1739-1743, 2014.
Article Dans Chinois | WPRIM | ID: wpr-340426
ABSTRACT
Chromosome 7 abnormalities are the most common cytogenetic alterations found in myeloid malignancies. Myeloid malignancies exhibiting monosomy 7/del (7q) have been confirmed to associate with high susceptibility to infections, poor response to chemotherapy, and short survival time, so speculating that chromosome 7 has important tumor suppressor genes. Commonly deleted segments (such as 7q22) of chromosome 7 have been identified by FISH and other technologies. Genes (EZH2, MLL5, DOCK4, SAMD9L/SAMD9) located in commonly deleted segments of 7q have been cloned and characterized along with the advance of molecular biology.This review summaries the current advancement about myeloid malignancies associated with monosomy7/del(7q).
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Chromosomes humains de la paire 7 / Leucémie myéloïde / Délétion de segment de chromosome / Génétique / Syndromes myéloprolifératifs Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2014 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Chromosomes humains de la paire 7 / Leucémie myéloïde / Délétion de segment de chromosome / Génétique / Syndromes myéloprolifératifs Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2014 Type: Article