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先天性髋脱位HOXA9、HOXB9和HOXD9基因同源盒突变研究 被引量:2

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出处 《中华小儿外科杂志》 CSCD 北大核心 2005年第8期447-448,共2页 Chinese Journal of Pediatric Surgery
基金 国家自然科学基金(39970762) 辽宁省自然科学基金(972248)
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参考文献6

  • 1麻宏伟,李祁伟,卢瑶,姜俊,王岳平,王旸,马瑞雪,吉士俊.先天性髋脱位与Hox基因传递不平衡研究[J].中国医科大学学报,2004,33(1):6-8. 被引量:7
  • 2Kosaki K, Kosaki R, Suzuki T, et al.Complete mutation analysis panel of the 39human HOX genes. Teratology, 2002,65: 50-62.
  • 3Krumlanf R. Hox genes in vertebrate development. Cell, 1994, 78: 191-201.
  • 4Mark M, Rijli FM, Chambon P. Homeobox genes in embryogenesis and pathogenesis. Pediatr Res, 1997, 42: 421-429.
  • 5Castelli-Gair J. Implications of the spatial and temporal regulation of Hox genes on development and evolution. Int J Dev Biol, 1998, 42: 437-444.
  • 6姜俊,麻宏伟,卢瑶,王岳平,王阳,李祁伟,吉士俊.先天性髋脱位与HOXB9基因或COL1A1基因传递不平衡研究[J].中华医学遗传学杂志,2003,20(3):193-195. 被引量:11

二级参考文献13

  • 1彭明惺,刘利君,周锡华,周素华.先天性髋关节脱位病因探讨(附706例遗传流行病学调查)[J].华西医学,1996,11(1):91-91. 被引量:14
  • 2Zakany J, Duboule D. Synpolydactyly in mice with a targeted deficency in the HoxD complex. Nature, 1996, 384: 69-71.
  • 3Davis AP, Capechi MR. A mutational analysis of the 5'HoxD genes : dissection of genetics interactions during limb development in mouse. Development, 1996,122: 1175-1185.
  • 4Pollock RA, Sreenath T, Ngo L, et al. Gain of function mutations for paralogous Hox genes: implications for the evolution of Hox gene function. Proc Natl Acad Sci U S A, 1995,92 : 4492-4496.
  • 5Mortlock DP, Innis JW. Mutation of HoxA13 in hand-foot-genital syndrome. Nat Genet, 1997, 15 : 179-180.
  • 6Goodman FR, Mundlos S, Muragaki Y, et al. Synpolydactyly phenotypes correlate with size of expansions in HoxD13 polyalanine tract. Proc Natl Acad Sci U S A, 1997, 94: 7458-7463.
  • 7Davis AP, Witte DP, Hsieh-Li HM, et al. Absence of radius and ulna in mice lacking Hoxa-11 and Hoxd-11. Nature, 1995, 375 :791-795.
  • 8Favier B, Rijli FM, Fromental-Ramain C, et al. Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton. Development,1996, 122: 449-460.
  • 9Krumlanf R. Hox genes in vertebrate development. Cell, 1994,78 : 191-201.
  • 10Giunta C, Superti-Furga A, Spranger S, et al. Ehlers-Danlos syndrome type Ⅵ :clinical features and molecular defects. J Bone Joint Surg Am, 1999, 81: 225-238.

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