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核糖体功能障碍与遗传性骨髓衰竭。

Ribosomal dysfunction and inherited marrow failure.

作者信息

Ganapathi Karthik A, Shimamura Akiko

机构信息

Department of Haematology/Oncology, Children's Hospital/Dana Farber Cancer Institute, Boston, MA, USA.

出版信息

Br J Haematol. 2008 May;141(3):376-87. doi: 10.1111/j.1365-2141.2008.07095.x.

Abstract

Impairment of ribosome biogenesis or function characterizes several of the inherited bone marrow failure syndromes: Diamond-Blackfan anaemia, dyskeratosis congenita (DC), Shwachman-Diamond syndrome and cartilage-hair hypoplasia. These syndromes exhibit overlapping but distinct clinical phenotypes and each disorder involves different aspects of ribosomal biogenesis. The clinical characteristics of each syndrome are briefly reviewed. Molecular studies of ribosome biogenesis and function in each of these syndromes are discussed. Models of how impairment of ribosomal pathways might affect haematopoiesis and tumorigenesis are explored.

摘要

核糖体生物合成或功能受损是几种遗传性骨髓衰竭综合征的特征

钻石-黑范贫血、先天性角化不良(DC)、施-戴综合征和软骨毛发发育不全。这些综合征表现出重叠但不同的临床表型,每种疾病涉及核糖体生物合成的不同方面。本文简要回顾了每种综合征的临床特征。讨论了这些综合征中核糖体生物合成和功能的分子研究。探讨了核糖体途径受损可能影响造血和肿瘤发生的模型。

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