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骨髓纤维化伴髓外化生发病机制的批判性综述。

Critical review of pathogenetic mechanisms in myelofibrosis with myeloid metaplasia.

作者信息

Martyré Marie-Claire

机构信息

INSERM U365, Institut Curie, 26 Rue d'Ulm, 75248 Paris, France.

出版信息

Curr Hematol Rep. 2003 May;2(3):257-63.

Abstract

Myelofibrosis with myeloid metaplasia is an uncommon chronic myeloproliferative disorder characterized by extramedullary hematopoiesis associated with varying degrees of bone marrow fibrosis (hematopoiesis is clonal and fibrosis is a polyclonal reactive process). The primary defect in a pluripotent stem cell is still unknown. However, advances have been made during the past few years in the knowledge of the pathogenetic mechanisms in this disorder. This review focuses on current data on the cellular and molecular mechanisms possibly participating in the development of the disease.

摘要

伴有骨髓化生的骨髓纤维化是一种罕见的慢性骨髓增殖性疾病,其特征为髓外造血并伴有不同程度的骨髓纤维化(造血是克隆性的,而纤维化是多克隆反应性过程)。多能干细胞的原发性缺陷仍不清楚。然而,在过去几年中,对该疾病发病机制的认识有了进展。这篇综述聚焦于可能参与该疾病发展的细胞和分子机制的当前数据。

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