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YRRM1基因检测在无精症病因分析中的应用 被引量:4

Analysis of YRRM gene in azoospermia
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摘要 YRRM(YchromosomeRNArecognitionmotif)为无精子因子(AZF)的重要候选成分,已证明YRRM的丢失可导致无精子或严重少精。应用PCR方法检测核型正常(46XY)的65例无精症男子和25例严重少精男子基因组DNA中的YRRM,发现6例无精症病人中有YRRM的丢失,严重少精病人中1例有YRRM的丢失。结果表明,应用该方法检测YRRM基因片段是切实可行的,对无精症和严重少精的病因诊断具有一定的应用价值。 YRRM is one of the important candidates for azoospermia factor(AZF). Ithas been proved that the deletion of AZF could cause azoospermia or severe oligozoospermia.In this paper, PCR was used to analyse YRRM gene in 65 azoospermic men and 25 oligozoospermia men with a cytologically normal Y chromosome. YRRM deletion was found in 6azoospermic men. In oligozoospermic men, no deletion was found. The results indicated that PCR assay can be used to analysis YRRM gene which is very useful for clinical diagnosis of azoospermia.
出处 《实用男科杂志》 CSCD 1997年第1期1-3,共3页
关键词 无精症 YRRM 病因 不育症 男性 azoospermia AZF YRRM PCR
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参考文献2

  • 1M. Andersson,D. C. Page,D. Pettay,I. Subrt,C. Turleau,J. Grouchy,A. Chapelle. Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11[J] 1988,Human Genetics(1):2~7
  • 2L. Tiepolo,Orsetta Zuffardi. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm[J] 1976,Human Genetics(2):119~124

同被引文献15

  • 1[6]Reijo R,Yilee T,Salo P,et al.Diverse spermatogenic defects in human caused by Y chromosome deletions encompassing a novel RNA-binging protein gene.Nature Genet,1995,10:383.
  • 2[7]Eberhart CG,Maines JZ,Wasserman SA.Meiotic cell cycle requirement for a fly homologue of human deleted in azoospermia.Nature,1996,38:783.
  • 3[8]Habermann B,Mi HF,Edelmann A,et al.DAZ genes encoding proteins located in human late spermatids and sperm tails.Hum Reprod,1998,13:363.
  • 4[9]Reijo R,Alagappan RK,Patrizio P,et al.Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome.Lancet,1996,347:1290.
  • 5[10]Nakahori Y,Kuroki Y,Komai R,et al.The Y chromosome region essential for spermatogenesis.Horm Res,1996,46:20.
  • 6[11]Najmabadi H,Huang V,Yen P,et al.Substantial prevalence of microdeletions of the Y chromosome in fertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy.J Clin Endocrinol Meteb,1996,81:1347.
  • 7[12]Kamischke A,Gromoln J,Simoni M,et al.Transmission of a Y chromosome deletion involving the deleted in azoospermia(DAZ) and chromodomain(CDY1) genes from father to son through ICSI.Hum Repord,1999,14:2320-2322.
  • 8[1]Tiepolo L,Zuffardi D.Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.Hum Genet,1976,34:19.
  • 9[2]Ma K,John D,Page DC,et al.A Ychromosome gene family with RNA-binding protein homology:Candidates for the azoospermia factor AZF controlling human spermatogenesis.Cell,1993,75:1287.
  • 10[3]Vollrath D,Foote S,Hilton A,et al.The human Y chromosome:a 43-interval map hased on naturally occurring deletions.Science,1992,258:52-59.

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