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原发无精症与少精症患者无精症缺失基因部分拷贝缺失的基因诊断研究 被引量：1

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作者 杨元 肖翠英 任洪进
机构地区 四川大学华西医院医学遗传室 成都市妇产科医院
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2004年第3期163-164,共2页 Chinese Journal of Laboratory Medicine
基金 四川省计划生育委员会基金课题 ( 2 0 0 14 9)
关键词 原发无精症 少精症 无精症缺失基因 拷贝缺失 基因诊断
分类号 R446.9 [医药卫生—诊断学]
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  • 1Kleiman SE, Yogev L, Paz G, et al. The prognostic value of the site and extent of Y chromosome microdeletions on spermatogenesis. Harefuah,2002,141 : 178-180.
  • 2Vogt PH. Human chromosome deletions in Yqll, AZF candidate genes and male infertility: history and update. Mol Hum Reprod, 1998,4: 739-744.
  • 3Foresta C, Moro E, Ferlin A. Y chromosome microdeletions and alterations of spermatogenesis. Endocr Rev, 2001,22: 226-239.
  • 4Simoni M, Bakker E, Eurlings MC, et al. Labortory guidelines for molecular diagnosis of Y-chromosomal microdeletions. Int J Androl, 1999,22: 292-299.
  • 5Liow SL, Yong EL, Ng SC. Prognostic value of Y deletion analysis: How reliable is the outcome of Y deletion analysis in providing a sound prognosis? Hum Reprod,2001,16: 9-12.
  • 6Pryor JL, Kent-First M, Muallem A, et al. Mierodeletions in the Y chromosome of infertile men. N Engl J Med,1997,336: 534-539.
  • 7Reijo R, Alagappan RK, Patrizio P, et al. Severe oligozoospermia resulting from deletions of azoospermla factor gene on Y chromosome. Lancet,1996,347 : 1290-1293.
  • 8Nakahori Y, Kurokl Y, Komaki R, et at. The Y chromosome region essential for spermatogenesls. Horm Res, 1996,46: 20-23.
  • 9Simonl M, Gromoll J, Dwornlczak B, et al. Screening for deletions of the Y chromosome involving the DAZ (deleted in AZoo spermia ) gene in azoospermia and severe oligzoospermia. Fertil Steril,1997,67 : 542-547.
  • 10Kleiman SE, Yogev L, Gamzu R, et al. Genetic evaluation of infertile men. Hum Reprod,1999,14: 33-38.

共引文献57

同被引文献14

  • 1阿周存,杨元,张思仲,林立.严重寡精症ICSI精子供体的DAZ基因拷贝缺失研究[J].遗传,2006,28(9):1057-1060. 被引量：6
  • 2Saxena R,De Vries JWA, Repping S,et al. Four genes in two dusters found in the AZFc region of the human Y chromosome. Genomic, 2000, 67:256 - 267.
  • 3Slee R, Grimes B, Speed RM, et al. A human DAZ transgene confers partial rescue of the mouse DAZ1 null phenotype. Natl Acad Sci, 1996, 8040 - 8045.
  • 4Fernandes AT, Fernandes S, Gonalves R, et al. DAZ gene copies: evidence of Y chromosome evolution. Mol Hum Reprod, 2002, 8 (3): 286 - 298.
  • 5Femandes S, Huellen K,Gonealves J,et al. High frequency of DAZ1/ DAZ2 gene deletions in patients with severe oligozoospermia. Mol Hum Rep, 2002,8(3) :286 -298.
  • 6Menke DB, Mutter GL, Page DC. Expression of DAZ, an azoospermia factor candidate, in human spermatogonia. Am J Hum Genet, 1997, 60 : 237 - 241.
  • 7Ferras C, Femandes S, Marques CJ, et al. AZF and DAZ gene copy - specific deletion analysis in maturation arrest and Sertoli cell - only syndrome. Mol Hum Reprod, 2004,10(10) :755-761.
  • 8Habermann B,Mi HF, Edelmann F, et al . DAZ gene encoding proteins located in human late spermatids and sperm tails. Hum Reprod, 1998,13:363-369.
  • 9Saxena R,Brown LG,Hawkins T,et al. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. Nature Genet, 1996 , 14: 292 - 299.
  • 10Xu EY, Frederick LM, Renee A. A gene family required for human germ cell development evolved from an ancient meiotic gene conserved in metazoans. Proc Natl Acad Sci U S A, 2001,98 (13):7414 - 7419.

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中华检验医学杂志
2004年 第3期

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