• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
An explanation of the mechanisms underlying fragile X-associated premature ovarian insufficiency.脆性 X 相关卵巢早衰发病机制的阐释。
J Assist Reprod Genet. 2020 Jun;37(6):1313-1322. doi: 10.1007/s10815-020-01774-x. Epub 2020 May 6.
2
Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.含有多聚甘氨酸的蛋白质FMRpolyG阳性的包涵体的存在表明,重复相关的非AUG翻译在脆性X相关的原发性卵巢功能不全中起作用。
Hum Reprod. 2016 Jan;31(1):158-68. doi: 10.1093/humrep/dev280. Epub 2015 Nov 3.
3
Granulosa cell and oocyte mitochondrial abnormalities in a mouse model of fragile X primary ovarian insufficiency.脆性X染色体相关原发性卵巢功能不全小鼠模型中的颗粒细胞和卵母细胞线粒体异常
Mol Hum Reprod. 2016 Jun;22(6):384-96. doi: 10.1093/molehr/gaw023. Epub 2016 Mar 9.
4
FMRpolyG accumulates in FMR1 premutation granulosa cells.脆性 X 综合征一号基因(FMR1)前突变的颗粒细胞中积累了 FMRpolyG。
J Ovarian Res. 2020 Feb 26;13(1):22. doi: 10.1186/s13048-020-00623-w.
5
Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).了解FMR1前突变女性携带者生育力下降的原因:脆性X相关原发性卵巢功能不全(FXPOI)的一种可能机制。
Reprod Health. 2014 Aug 19;11:67. doi: 10.1186/1742-4755-11-67.
6
Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.脆性 X 原发性卵巢功能不全小鼠模型中的卵巢异常。
J Histochem Cytochem. 2012 Jun;60(6):439-56. doi: 10.1369/0022155412441002. Epub 2012 Apr 2.
7
Fragile X syndrome: An overview and update of the FMR1 gene.脆性 X 综合征:FMR1 基因概述及最新研究进展。
Clin Genet. 2018 Feb;93(2):197-205. doi: 10.1111/cge.13075. Epub 2017 Oct 1.
8
[FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].[脆性X智力低下1号基因前突变携带者——他们真的没有症状吗?]
Harefuah. 2018 Apr;157(4):241-244.
9
Tremor-Ataxia syndrome and primary ovarian insufficiency in an premutation carrier.一名前突变携带者的震颤-共济失调综合征和原发性卵巢功能不全
Colomb Med (Cali). 2017 Sep 30;48(3):148-151. doi: 10.25100/cm.v48i3.3019.
10
[Fragile X syndrome and FMR1-dependent diseases - clinical presentation, epidemiology and molecular background].[脆性X综合征与FMR1相关疾病——临床表现、流行病学及分子背景]
Dev Period Med. 2018;22(1):14-21. doi: 10.34763/devperiodmed.20182201.1421.

引用本文的文献

1
Diminished Ovarian Reserve: A Narrative Review of Etiologies and Possible Therapeutic Approaches.卵巢储备功能减退:病因及可能治疗方法的叙述性综述
J Menopausal Med. 2025 Aug;31(2):85-94. doi: 10.6118/jmm.25109.
2
A matter of new life and cell death: programmed cell death in the mammalian ovary.新生命与细胞死亡的问题:哺乳动物卵巢中的细胞程序性死亡。
J Biomed Sci. 2024 Mar 20;31(1):31. doi: 10.1186/s12929-024-01017-6.
3
A systematic review and standardized clinical validity assessment of genes involved in female reproductive failure.系统性综述及女性生殖失败相关基因的标准化临床有效性评估
Reproduction. 2022 Apr 22;163(6):351-363. doi: 10.1530/REP-21-0486.
4
Molecular Pathogenesis and Peripheral Monitoring of Adult Fragile X-Associated Syndromes.成年脆性 X 相关综合征的分子发病机制和外周监测。
Int J Mol Sci. 2021 Aug 4;22(16):8368. doi: 10.3390/ijms22168368.

本文引用的文献

1
Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome.脆性 X 相关震颤共济失调综合征核内包涵体的组成。
Acta Neuropathol Commun. 2019 Sep 3;7(1):143. doi: 10.1186/s40478-019-0796-1.
2
Preantral follicular atresia occurs mainly through autophagy, while antral follicles degenerate mostly through apoptosis.原始卵泡闭锁主要通过自噬发生,而腔前卵泡退化主要通过细胞凋亡发生。
Biol Reprod. 2018 Oct 1;99(4):853-863. doi: 10.1093/biolre/ioy116.
3
Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update.卵巢卵泡膜细胞募集、分化及其对生育的影响:2017 年更新。
Endocr Rev. 2018 Feb 1;39(1):1-20. doi: 10.1210/er.2017-00164.
4
Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics.脆性X相关震颤/共济失调综合征:从分子发病机制到治疗方法的发展
Front Cell Neurosci. 2017 May 5;11:128. doi: 10.3389/fncel.2017.00128. eCollection 2017.
5
The ovarian response in fragile X patients and premutation carriers undergoing IVF-PGD: reappraisal.脆性 X 综合征患者和脆性 X 前突变携带者行 IVF-PGD 中的卵巢反应:再评估。
Hum Reprod. 2017 Jul 1;32(7):1508-1511. doi: 10.1093/humrep/dex090.
6
A putative role for anti-Müllerian hormone (AMH) in optimising ovarian reserve expenditure.抗苗勒管激素(AMH)在优化卵巢储备消耗中的假定作用。
J Endocrinol. 2017 Apr;233(1):R1-R13. doi: 10.1530/JOE-16-0522. Epub 2017 Jan 27.
7
Microsatellite Expansion Diseases: Repeat Toxicity Found in Translation.微卫星扩展疾病:翻译中发现重复毒性。
Neuron. 2017 Jan 18;93(2):249-251. doi: 10.1016/j.neuron.2017.01.001.
8
Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.含有多聚甘氨酸的蛋白质FMRpolyG阳性的包涵体的存在表明,重复相关的非AUG翻译在脆性X相关的原发性卵巢功能不全中起作用。
Hum Reprod. 2016 Jan;31(1):158-68. doi: 10.1093/humrep/dev280. Epub 2015 Nov 3.
9
Xenopus LAP2β protein knockdown affects location of lamin B and nucleoporins and has effect on assembly of cell nucleus and cell viability.非洲爪蟾LAP2β蛋白敲低会影响核纤层蛋白B和核孔蛋白的定位,并对细胞核组装和细胞活力产生影响。
Protoplasma. 2016 May;253(3):943-956. doi: 10.1007/s00709-015-0861-y. Epub 2015 Jul 25.
10
The Relationship Between Variation in Size of the Primordial Follicle Pool and Age at Natural Menopause.原始卵泡池大小变化与自然绝经年龄之间的关系。
J Clin Endocrinol Metab. 2015 Jun;100(6):E845-51. doi: 10.1210/jc.2015-1298. Epub 2015 Apr 27.

脆性 X 相关卵巢早衰发病机制的阐释。

An explanation of the mechanisms underlying fragile X-associated premature ovarian insufficiency.

机构信息

Brown Fertility, 8149 Point Meadows Way, Jacksonville, FL, 32256, USA.

Department of Obstetrics and Gynecology, University of Central Florida, Orlando, FL, 32816, USA.

出版信息

J Assist Reprod Genet. 2020 Jun;37(6):1313-1322. doi: 10.1007/s10815-020-01774-x. Epub 2020 May 6.

DOI:10.1007/s10815-020-01774-x
PMID:32377997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7311620/
Abstract

Fragile X and fragile X-associated tremor-ataxia syndrome (FXTAS) are caused by mutations of the FMR1 gene. The mutations causing FXTAS can expand in a generation to a "full mutation" causing fragile X syndrome. The mutations causing FXTAS and the phenotype, fragile X-associated premature ovarian insufficiency (FXPOI), are referred to as the FMR1 premutation (PM). The objective of this paper was to formulate a theory to explain the Mechanism for FXPOI.Recent research on fragile X syndrome and FXTAS has led to sophisticated theories about the mechanisms underlying these diseases. It has been proposed that similar mechanisms underlie FXPOI. Utilizing recent research on FXTAS, but a more detailed application of ovarian physiology, we present a more ovarian specific theory as to the primary mechanism explaining the development of FXPOI.The FXPOI phenotype may best be viewed as derivative of the observation that fragile X PM carriers experience menopause an average of 5 years earlier than non-carriers. Women carrying the PM experience an earlier menopause because of an accelerated activation of their primordial follicle pool. This acceleration of primordial follicle activation occurs, in part, because of diminished AMH production. AMH production is diminished because of accelerated atresia of early antral follicles. This accelerated atresia likely occurs because the fragile X PM leads to a slowing of the rate of granulosa cell mitosis in some follicles.

摘要

脆性 X 综合征和脆性 X 相关震颤共济失调综合征(FXTAS)由 FMR1 基因突变引起。导致 FXTAS 的突变可以在一代中扩展为导致脆性 X 综合征的“完全突变”。导致 FXTAS 和表型脆性 X 相关卵巢早衰(FXPOI)的突变被称为 FMR1 前突变(PM)。本文的目的是提出一个理论来解释 FXPOI 的机制。

脆性 X 综合征和 FXTAS 的最新研究导致了关于这些疾病潜在机制的复杂理论。有人提出,FXPOI 的发病机制类似。利用 FXTAS 的最新研究,但更详细地应用卵巢生理学,我们提出了一个更具卵巢特异性的理论,解释 FXPOI 发展的主要机制。

FXPOI 表型最好被视为这样一个观察结果的衍生,即脆性 X PM 携带者的绝经年龄比非携带者平均早 5 年。携带 PM 的女性出现更早的绝经,是因为其原始卵泡池的激活加速。原始卵泡激活的这种加速部分是由于 AMH 产生减少所致。AMH 产生减少是因为早期窦卵泡的闭锁加速。这种加速的闭锁可能是因为脆性 X PM 导致一些卵泡中颗粒细胞有丝分裂的速度减慢。