期刊文献+

人类Rh血型系统研究进展 被引量:38

在线阅读 下载PDF
导出
出处 《中国输血杂志》 CAS CSCD 2004年第3期211-214,共4页 Chinese Journal of Blood Transfusion
  • 相关文献

参考文献38

  • 1兰炯采,陈强,孙倩,武大林,丁红,张志梅,彭道波.RhD基因外显子多态性观察[J].中国免疫学杂志,2000,16(5):284-285. 被引量:14
  • 2徐群,张世训,张建业,司桂玲,宋永红,王玫,李京,王潍,聂向民.中国汉族群体RhD(-)个体D基因和CE基因外显子多态性研究[J].中国输血杂志,2001,14(1):16-18. 被引量:7
  • 3邵超鹏.RHD研究进展和中国人RHD研究现状分析[J].中国输血杂志,2003,16(5):354-358. 被引量:30
  • 4Okuda H, Suganuma H, Kamesaki T, et al. The analysis of nucleotide substitutions, gaps, and recombination events between RHD and RHCE genes through complete sequencing. Biochem Biophys Res Commun,2000,11;274(3):670
  • 5Avent ND, Martin PG, Armstrong-Fisher SS, et al.Evidence of genetic diversity underlying RhD-,weak D(Du),and partial D phenotypes as determined by mutiplex polymerase chain reaction using sequence-specific primer.Blood,1997,89(7):2568
  • 6Okuda H, Suganuma H, Kamesaki T, et al. The analysis of nucleotide substitutions, gaps, and recombination events between RHD and RHCE genes through complete sequencing. Biochem Biophys Res Commun,2000,11;274(3):670
  • 7Beckers EA, Faas BH, Ligthart P, et al. Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene. Transfusion,1997,37(6):616
  • 8Huang CH, Chen Y, Reid M, et al. Genetic recombination at the human RH locus:a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene. Am J Hum Genet,1996,59(4):825
  • 9Chiu RWK, Murphy MF, Fidler C, et al. Determination of RhD Zygosity:comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem,2001,47(4):667
  • 10Avent ND, LIu W, Jones JW, et al. Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DⅣvariant phenotype:an RHD gene deletion event does not generate all DⅣ ccEe phenotypes. Blood,1997,89(5):1779

二级参考文献57

  • 1邵超鹏,苏宇清,孔生生.Rh血型D抗原检测方法讨论[J].华南国防医学杂志,2001,15(1):50-51. 被引量:6
  • 2徐群,张世训,张建业,司桂玲,宋永红,王玫,李京,王潍,聂向民.中国汉族人群RHCE和RHD基因结构研究[J].临床输血与检验,2000,2(1):1-4. 被引量:5
  • 3Shao CP, Maas JH, Su YQ, et al. Molecular background of Rh Dpositive, D-negative, E# and weak D^el phenotypes in Chinese. Vox Sang,2002,83(2) : 156.
  • 4Flegel WA, Wagner FF. Molecular genetics of RH. Vox Sang,2000,78(Suppl 2) : 109.
  • 5Legler TJ,Maas JH,Kohler M,et al. RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis. Transfus Med,2001,11(5) :383.
  • 6Wagner FF,Gassner C, Muller TH, et al. Molecular basis of weak D phenotypes. Blood, 1999,93( 1 ) ~ 385.
  • 7Legler TJ, Wiemann V, Ohto H, et al. D(Va) category phenotype and genotype in Japanese families. Vox Sang,2000,78(3) : 194.
  • 8Chang JG,Wang JC, Yang TY,et al. Human RhD^el is caused by a deletion of 1,013 bp between introns 8 and 9 including exon 9 of RHD gene.Blood, 1998,92(7) :2602.
  • 9Perco P,Shao CP,Mayr WR,et al. Three different methods to test for RhD zygosity: description of altered downstream Rhesus Boxes and a new weak D type.Transfusion,2003,43(3) :335-339.
  • 10Chiu RW, Murphy MF, Fidler C, et al. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clln Cham,2001,47(4) :667.

共引文献42

同被引文献241

引证文献38

二级引证文献180

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部