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Y染色体缺失在男性不育中的作用。

The role of Y chromosome deletions in male infertility.

作者信息

Ma K, Mallidis C, Bhasin S

机构信息

Division of Endocrinology, Metabolism and Molecular Medicine, Department of Internal Medicine, Charles R Drew University of Medicine and Science, 1731 East 120th Street, Los Angeles, California 90050, USA.

出版信息

Eur J Endocrinol. 2000 May;142(5):418-30. doi: 10.1530/eje.0.1420418.

Abstract

Male infertility affects approximately 2-7% of couples around the world. Over one in ten men who seek help at infertility clinics are diagnosed as severely oligospermic or azoospermic. Recent extensive molecular studies have revealed that deletions in the azoospermia factor region of the long arm of the Y chromosome are associated with severe spermatogenic impairment (absent or severely reduced germ cell development). Genetic research into male infertility, in the last 7 years, has resulted in the isolation of a great number of genes or gene families on the Y chromosome, some of which are believed to influence spermatogenesis.

摘要

男性不育影响着全球约2%至7%的夫妇。在不育诊所寻求帮助的男性中,超过十分之一被诊断为严重少精子症或无精子症。最近广泛的分子研究表明,Y染色体长臂无精子症因子区域的缺失与严重的生精障碍(生殖细胞发育缺失或严重减少)有关。在过去7年里,对男性不育的基因研究已导致在Y染色体上分离出大量基因或基因家族,其中一些被认为会影响精子发生。

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