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着床期间子宫接受性的遗传控制。

Genetic control of uterine receptivity during implantation.

作者信息

Ma L, Yao M, Maas R L

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

Semin Reprod Endocrinol. 1999;17(3):205-16. doi: 10.1055/s-2007-1016228.

DOI:10.1055/s-2007-1016228
PMID:10797939
Abstract

Implantation involves complex molecular interactions between implanting blastocysts and the hormonally primed uterus. Gene targeting allows the generation of mice lacking a specific gene or genes and has proved to be of considerable value when combined with classical physiology in understanding many biological questions, such as the process of implantation. In this article, we review genes that have been demonstrated by gene targeting in mice to be required in the uterus for implantation. In particular, we focus on a specific class of developmental control genes, the mammalian Hox genes, and their role in this process. Lastly, we attempt to synthesize current knowledge about the genetic control of implantation and to build a working genetic model for the implantation pathway.

摘要

着床涉及植入的囊胚与经激素预处理的子宫之间复杂的分子相互作用。基因靶向技术可产生缺乏特定一个或多个基因的小鼠,并且在与经典生理学相结合以理解许多生物学问题(如着床过程)时已证明具有相当大的价值。在本文中,我们综述了通过小鼠基因靶向技术已证实在子宫着床过程中必需的基因。特别地,我们聚焦于一类特定的发育控制基因——哺乳动物Hox基因,及其在这一过程中的作用。最后,我们试图综合目前关于着床遗传控制的知识,并构建一个关于着床途径的有效遗传模型。

相似文献

1
Genetic control of uterine receptivity during implantation.着床期间子宫接受性的遗传控制。
Semin Reprod Endocrinol. 1999;17(3):205-16. doi: 10.1055/s-2007-1016228.
2
Implantation: molecular basis of embryo-uterine dialogue.着床:胚胎与子宫对话的分子基础。
Int J Dev Biol. 2001;45(3):597-605.
3
Implantation in the human: the role of HOX genes.人类着床过程中HOX基因的作用。
Semin Reprod Med. 2000;18(3):311-20. doi: 10.1055/s-2000-12568.
4
Maternal Hoxa10 is required for pinopod formation in the development of mouse uterine receptivity to embryo implantation.母体Hoxa10对于小鼠子宫对胚胎着床的接受性发育过程中的微绒毛形成是必需的。
Dev Dyn. 2001 Nov;222(3):538-44. doi: 10.1002/dvdy.1209.
5
Progesterone supplementation extends uterine receptivity for blastocyst implantation in mice.补充孕酮可延长小鼠子宫对囊胚着床的接受期。
Reproduction. 2007 Feb;133(2):487-93. doi: 10.1530/REP-06-0330.
6
Differential expression of ezrin/radixin/moesin (ERM) and ERM-associated adhesion molecules in the blastocyst and uterus suggests their functions during implantation.埃兹蛋白/根蛋白/膜突蛋白(ERM)及ERM相关黏附分子在囊胚和子宫中的差异表达表明它们在着床过程中的作用。
Biol Reprod. 2004 Mar;70(3):729-36. doi: 10.1095/biolreprod.103.022764. Epub 2003 Nov 12.
7
Mouse models of implantation.着床的小鼠模型。
Trends Endocrinol Metab. 2007 Aug;18(6):234-9. doi: 10.1016/j.tem.2007.06.002. Epub 2007 Jun 27.
8
Deciphering the cross-talk of implantation: advances and challenges.解读着床的相互作用:进展与挑战
Science. 2002 Jun 21;296(5576):2185-8. doi: 10.1126/science.1071601.
9
Abdominal B (AbdB) Hoxa genes: regulation in adult uterus by estrogen and progesterone and repression in müllerian duct by the synthetic estrogen diethylstilbestrol (DES).腹部B(AbdB)型Hoxa基因:在成年子宫中受雌激素和孕激素调控,在苗勒管中受合成雌激素己烯雌酚(DES)抑制。
Dev Biol. 1998 May 15;197(2):141-54. doi: 10.1006/dbio.1998.8907.
10
The role of HOX genes in human implantation.HOX基因在人类着床过程中的作用。
Ann N Y Acad Sci. 2004 Dec;1034:1-18. doi: 10.1196/annals.1335.001.

引用本文的文献

1
Signaling through retinoic acid receptors is essential for mammalian uterine receptivity and decidualization.视黄酸受体信号转导对于哺乳动物子宫容受性和蜕膜化至关重要。
JCI Insight. 2021 Sep 8;6(17):e150254. doi: 10.1172/jci.insight.150254.
2
HoxA-11 and FOXO1A cooperate to regulate decidual prolactin expression: towards inferring the core transcriptional regulators of decidual genes.HoxA-11 和 FOXO1A 合作调节蜕膜催乳素的表达:推断蜕膜基因的核心转录调控因子。
PLoS One. 2009 Sep 3;4(9):e6845. doi: 10.1371/journal.pone.0006845.
3
Use of transgenic mice model for understanding the placentation: towards clinical applications in human obstetrical pathologies?
利用转基因小鼠模型理解胎盘形成:迈向人类产科病理学的临床应用?
Transgenic Res. 2001 Oct;10(5):377-98. doi: 10.1023/a:1012085713898.
4
Cellular and molecular responses of the uterus to embryo implantation can be elicited by locally applied growth factors.子宫对胚胎着床的细胞和分子反应可由局部应用的生长因子引发。
Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):1047-52. doi: 10.1073/pnas.98.3.1047.