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人类卵母细胞及植入前胚胎中印迹基因Snrpn mRNA的表达 被引量：2

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作者 马玲 李蓉 周亮 钟凯
机构地区 北京大学深圳医院生殖医学中心
出处 《生殖医学杂志》 CAS 2007年第2期111-114,共4页 Journal of Reproductive Medicine
基金 国家自然科学基金资助项目(30440057) 深圳市科技计划资助项目(200204102)
关键词 印迹基因 Snrpn基因 人类卵母细胞 植入前胚胎 单细胞
分类号 R715 [医药卫生—妇产科学]
  • 相关文献

参考文献7

  • 1Leff SE,Brannan CI,Reed ML,et al.Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region[J].Nature Genet,1992,2(4):259-264.
  • 2Cattanach BM,Barr JA,Evans EP,et al.A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression[J].Nature Genet,1992,2(4):270-274.
  • 3Ashreena S,John H,Virginia B,et al.The use of amplified cDNA to investigate the expression of seven imprinted genes in human oocytes and preimplantation embryos[J].Mol Hum Reprod,2001,7(9):839-844.
  • 4Reed ML,Leff SE.Maternal imprinting of human SNRPN,a gene deleted in Prader-Willi syndrome[J].Nature Gene,1994,6(2):163-167.
  • 5McAllister G,Amara SG,Lerner MR.Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypeptide N[J].Proc Nat Acad Sci,1988,85(14):5296-5300.
  • 6Kuslich CD,Kobori JA,Mohapatra G,et al.Prader-Willi syndrome is caused by disruption of the SNRPN gene[J].Am J Hum Genet,1999,64(1):70-76.
  • 7Elke G,Martine DR,André VS,et al.Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos[J].Hum Mol Genet,2003,12(22):2873-2879.

同被引文献28

  • 1沈文洁,孔令红,陈士岭,李红,邢福祺.印迹基因生长因子-受体结合蛋白10在人类卵子及种植前胚胎的表达[J].第一军医大学学报,2005,25(3):305-307. 被引量：4
  • 2B. Albrecht,Dr. K. Buiting.Prader-Willi-Syndrom und Angelman-Syndrom[J]. medizinische genetik . 2010 (4)
  • 3Xingrong Yan,Shumin Yu,Anmin Lei,Jinlian Hua,Fulin Chen,Liwen Li,Xin Xie,Xueyi Yang,Wenxin Geng,Zhongying Dou.Cellular Reprogramming(Formerly " Cloning and Stem Cells" ). . 2010
  • 4Korucuoglu U,Biri A.A,Konac E,Alp E,Onen I.H,Ilhan M.N,Turkyilrnaz E,Erdem A,Erdem M,Menevse S.Expression of the imprinted IGF2 and H19 genes in the endometrium of cases with unexplained infertility. European Journal of Obstetrics Gynecology and Reproductive Biology . 2010
  • 5John Huntriss,Ph.D,Joanna E.Huddleston, Ph.D.Quantitative analysis of DNA methylation of imprinted genes in single humanblastocysts by pyrosequencing. Fertility and Sterility . 2011
  • 6Marmens M,Aiders M.Ge nomic imprinting,concept an d clinical con-sequences. Annals of Internal Medicine . 1999
  • 7Rachmilewitz,J,Elkin,M,Looijenga, LHJ,Verkerk,AJMH,Gonik, B,Lustig,G,Werner,D,deGroot,N,Hochberg,A.Characterization of the imprinted IPW gene:Allelic expression in normal and tumorigenic human tissues. Oncegene . 1996
  • 8Yamazawa K,Nakabayashi K,Matsuoka K,Masubara K,Hata K,Horikawa R,Ogata T.Androgenetic/biparental mosaicism in a girl with Beckwith - Wiedemann syndrome - like and upd (14) pat - like phenotypes. Journal of Human Genetics . 2011
  • 9Ariel I,Weinstein D,Voutilainen B,et al.Genomic imprinting and the endometrial cycle:The expression of the imprinted gene H19 in the human female reproductive organs. Diagnostic Molecular Pathology . 1997
  • 10Rossignol S,Steunou V,Chalas C,Kerjean A,Rigolet M,Viegas-Pequignot E,Jouannet P,Le Bouc Y,Gicquel C.The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. Journal of Medical Genetics . 2006

引证文献2

生殖医学杂志
2007年 第2期

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