期刊文献+

产后抑郁与Foxp3基因位点924(rs2232365)多态性的相关性探讨 被引量:1

Discussion of the correlation between postpartum depression and Foxp3 Locus 924(rs2232365) polymorphism
下载PDF
导出
摘要 目的探讨Foxp3-924(rs2232365)基因位点多态性与产后抑郁的相关性。方法选取211例在越秀区光塔街社区卫生服务中心分娩的产妇进行回访研究,所有产妇均经PCR-SSP技术对Foxp3-924(rs2232365)基因位点分型。结果对比产后抑郁组与对照组产妇Foxp3-924各种基因型频率,结果显示均无差异(P>0.05)。结论产后抑郁和Foxp3-924(rs2232365)位点基因多态性无较大关联。 Objective To investigate the distribution of-924( rs2232365) genotypes and to explore the correlation between gene loci polymorphism and postpartum depression. Methods In puerpera in Yuexiu district Guangta street community health center, there were 211 cases of childbirth study visits, who were confirmed by PCR-SSP technique Foxp3-924( rs2232365) gene locus genotyping. Results Compared postpartum depression group and control group Foxp3-924 various genotypes,it showed no great difference( P 〉 0. 05). Conclusion It has no greater relevance between postpartum depression and Foxp3-924( rs2232365) polymorphism loci.
出处 《广州医药》 2016年第3期1-4,共4页 Guangzhou Medical Journal
基金 广东省人口和计划生育委员会科研项目(20132054)
关键词 产后抑郁 基因位点 多态性 Postpartum depression Gene locus Polymorphism
  • 相关文献

参考文献1

二级参考文献20

  • 1甘长清,王小毅.CD4^+CD25^+调节性T细胞和Foxp3在不同病理类型乳腺癌患者外周血和组织中表达水平及其临床意义[J].免疫学杂志,2009,25(3):322-325. 被引量:9
  • 2Zoller M, MeElwee KJ, Engel P, et al. Transient CD44 variant isoform expression and reduction in CD4 (+)/CD25 (+) regulatory T cells in C3H/HeJ mice with alopecia areata [J]. J Invest Dermatol, 2002, 118 (6): 983-992.
  • 3McElwee K J, Freyschmidt Paul P, Hoffmann R, et al. Transfer of CDS(+) cells induces localized hair loss whereas CD4(+) /CD25 (-) cells promote systemic alopecia areata and CD4(+) /CD25(-) cells blockade disease onset in the C3H/HeJ mouse model [J]. J Invest Dermatol, 2005, 124 (5): 947-957.
  • 4MorganME,Van Bilsen JH, Bakker AM, et aL Expression of FOXP3 mRNA is not confined to CD4(+) CD25(+) T regulatory cells in humans [J]. Hum I mmunol, 2005, 66 (1): 13 - 20.
  • 5Morgan ME, van Bilsen, Bakker AM, et al. Expression of FOXP3 mRNA is not confined to CD4+CD25+T regulatory cells in humans [J]. Hum Immunol, 2005, 66 (1): 13- 20.
  • 6ho T, Ito N, Bettermann A, et al. Collapse and restoration of MHC class-I-dependent immune privilege: exploiting the human hair follicle as a model [J]. Am J Pathol, 2004, 164 (2): 623-634.
  • 7Khattri R, Cox T, Yasayko SA, et al. An essential role for Scurfin in CD4+ CD25+ T regulatory cells [J]. Nat Immunol,2003, 4(4): 337 - 342.
  • 8Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4+ CD25+ regulatory T cells [J]. Nat Immunol, 2003, 4 (4): 330- 336.
  • 9Cosmi L, Liotta F, Lazzeri E, et al . Human CD8+ CD25+ thymocytes share phenotypic and functional features with CD4+ CD25+ regulatory thymocytes [J]. Blood, 2003,102 (12): 4107 - 4114.
  • 10Kasprowicz D J, Smallwood PS, Tyznik A J, et al. Scurfin (Foxp3) controls T-dependent immune responses in vivo through regulation of CD4+ T cell effector function [J]. J Immunol, 2003, 171(3): 1 216 - 1 223.

共引文献7

同被引文献4

引证文献1

二级引证文献10

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