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相似文献

1
Do BRCA1/2 mutations and low FMR1 alleles interact or not?BRCA1/2基因突变与低FMR1等位基因是否相互作用？
Eur J Hum Genet. 2014 Feb;22(2):155-6. doi: 10.1038/ejhg.2013.213. Epub 2013 Sep 25.
2
Absence of BRCA/FMR1 correlations in women with ovarian cancers.卵巢癌女性中BRCA与FMR1不存在相关性。
PLoS One. 2014 Jul 18;9(7):e102370. doi: 10.1371/journal.pone.0102370. eCollection 2014.
3
BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study.BRCA1/2基因突变与FMR1等位基因呈随机分布：一项病例对照研究。
Eur J Hum Genet. 2014 Feb;22(2):277-9. doi: 10.1038/ejhg.2013.281. Epub 2013 Nov 27.
4
FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and the general population display distinct distribution patterns.以色列BRCA1/BRCA2突变携带者和普通人群中FMR1基因CGG等位基因长度呈现出不同的分布模式。
Genet Res (Camb). 2014 Oct 8;96:e11. doi: 10.1017/S0016672314000147.
5
The FMR1 CGG repeat test is not a candidate prescreening tool for identifying women with a high probability of being carriers of BRCA mutations.FMR1基因CGG重复序列检测并非用于识别携带BRCA突变高概率女性的候选预筛查工具。
Eur J Hum Genet. 2014 Feb;22(2):280-2. doi: 10.1038/ejhg.2013.193. Epub 2013 Sep 25.
6
BRCA1/2 mutations appear embryo-lethal unless rescued by low (CGG n<26) FMR1 sub-genotypes: explanation for the "BRCA paradox"?BRCA1/2 基因突变似乎会导致胚胎致死，除非被低（CGG n<26）FMR1 亚基因型拯救：这是否能解释“BRCA 悖论”？
PLoS One. 2012;7(9):e44753. doi: 10.1371/journal.pone.0044753. Epub 2012 Sep 12.
7
FMR1 low sub-genotype does not rescue BRCA1/2-mutated human embryos and does not explain primary ovarian insufficiency among BRCA1/2-carriers.FMR1 低亚基因型不能挽救 BRCA1/2 突变的人类胚胎，也不能解释 BRCA1/2 携带者中原发性卵巢功能不全的发生。
Hum Reprod. 2013 Aug;28(8):2308-11. doi: 10.1093/humrep/det254. Epub 2013 Jun 11.
8
Association of BRCA1/2 mutations with FMR1 genotypes: effects on menarcheal and menopausal age.BRCA1/2 基因突变与 FMR1 基因型的关联：对初潮和绝经年龄的影响。
Maturitas. 2013 Jun;75(2):148-51. doi: 10.1016/j.maturitas.2013.03.002. Epub 2013 Mar 23.
9
Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records.男性中低FMR1 CGG重复长度与BRCA相关癌症家族史相关吗？病历的探索性分析。
J Genet Couns. 2017 Dec;26(6):1401-1410. doi: 10.1007/s10897-017-0116-5. Epub 2017 Jun 30.
10
Assessment of the prevalence of de novo mutations in the BRCA1 and BRCA2 genes.评估BRCA1和BRCA2基因中新生突变的发生率。
Clin Genet. 2011 Jul;80(1):97-8. doi: 10.1111/j.1399-0004.2011.01691.x.

引用本文的文献

1
Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records.男性中低FMR1 CGG重复长度与BRCA相关癌症家族史相关吗？病历的探索性分析。
J Genet Couns. 2017 Dec;26(6):1401-1410. doi: 10.1007/s10897-017-0116-5. Epub 2017 Jun 30.
2
The impact of FMR1 gene mutations on human reproduction and development: a systematic review.FMR1基因突变对人类生殖与发育的影响：一项系统综述
J Assist Reprod Genet. 2016 Sep;33(9):1135-47. doi: 10.1007/s10815-016-0765-6. Epub 2016 Jul 18.
3
Absence of BRCA/FMR1 correlations in women with ovarian cancers.卵巢癌女性中BRCA与FMR1不存在相关性。
PLoS One. 2014 Jul 18;9(7):e102370. doi: 10.1371/journal.pone.0102370. eCollection 2014.

本文引用的文献

1
The FMR1 CGG repeat test is not a candidate prescreening tool for identifying women with a high probability of being carriers of BRCA mutations.FMR1基因CGG重复序列检测并非用于识别携带BRCA突变高概率女性的候选预筛查工具。
Eur J Hum Genet. 2014 Feb;22(2):280-2. doi: 10.1038/ejhg.2013.193. Epub 2013 Sep 25.
2
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.欧洲发现 BRCA1/2 基因突变：对遗传性乳腺癌-卵巢癌预防和控制的影响。
EPMA J. 2010 Sep;1(3):397-412. doi: 10.1007/s13167-010-0037-y. Epub 2010 Jun 27.
3
BRCA1/2 mutations appear embryo-lethal unless rescued by low (CGG n<26) FMR1 sub-genotypes: explanation for the "BRCA paradox"?BRCA1/2 基因突变似乎会导致胚胎致死，除非被低（CGG n<26）FMR1 亚基因型拯救：这是否能解释“BRCA 悖论”？
PLoS One. 2012;7(9):e44753. doi: 10.1371/journal.pone.0044753. Epub 2012 Sep 12.
4
Differences in ovarian aging patterns between races are associated with ovarian genotypes and sub-genotypes of the FMR1 gene.种族间卵巢衰老模式的差异与 FMR1 基因的卵巢基因型和亚基因型有关。
Reprod Biol Endocrinol. 2012 Sep 10;10:77. doi: 10.1186/1477-7827-10-77.
5
Association of FMR1 genotypes with in vitro fertilization (IVF) outcomes based on ethnicity/race.基于种族/民族的 FMR1 基因型与体外受精（IVF）结局的关联。
PLoS One. 2011 Apr 15;6(4):e18781. doi: 10.1371/journal.pone.0018781.
6
Ovarian reserve determinations suggest new function of FMR1 (fragile X gene) in regulating ovarian ageing.卵巢储备测定提示 FMR1（脆性 X 基因）在调节卵巢衰老中的新功能。
Reprod Biomed Online. 2010 Jun;20(6):768-75. doi: 10.1016/j.rbmo.2010.02.020. Epub 2010 Mar 1.
7
Effects of race/ethnicity on triple CGG counts in the FMR1 gene in infertile women and egg donors.种族/民族对 FMR1 基因中三 CGG 计数的影响在不孕妇女和卵子供体中。
Reprod Biomed Online. 2010 Apr;20(4):485-91. doi: 10.1016/j.rbmo.2009.12.017. Epub 2009 Dec 21.
8
Association of BRCA1 mutations with occult primary ovarian insufficiency: a possible explanation for the link between infertility and breast/ovarian cancer risks.BRCA1 突变与隐匿性卵巢功能不全的关联：不孕与乳腺癌/卵巢癌风险之间关联的一种可能解释。
J Clin Oncol. 2010 Jan 10;28(2):240-4. doi: 10.1200/JCO.2009.24.2057. Epub 2009 Dec 7.
9
Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families.517个荷兰乳腺癌和/或卵巢癌家族中不同BRCA1/BRCA2突变频率存在较大的地区差异。
Eur J Cancer. 2001 Nov;37(16):2082-90. doi: 10.1016/s0959-8049(01)00244-1.

Do BRCA1/2 mutations and low FMR1 alleles interact or not?

作者信息

Gleicher Norbert, Weghofer Andrea, Barad David H

机构信息

1] the Center for Human Reproduction, New York, NY, USA [2] the Foundation for Reproductive Medicine, New York, NY, USA.

Department of Obstetrics and Gynecology, Medical University of Vienna, Vienna, Austria.

出版信息

Eur J Hum Genet. 2014 Feb;22(2):155-6. doi: 10.1038/ejhg.2013.213. Epub 2013 Sep 25.

DOI:10.1038/ejhg.2013.213
PMID:24065113
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3895654/
Abstract
摘要