127 related articles for article (PubMed ID: 24581601)
1. WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis.
Tang R; Dang Y; Qin Y; Zou S; Li G; Wang Y; Chen ZJ
Reprod Biomed Online; 2014 Apr; 28(4):503-7. PubMed ID: 24581601
[TBL] [Abstract][Full Text] [Related]
2. Analysis of WNT9B mutations in Chinese women with Mayer-Rokitansky-Küster-Hauser syndrome.
Wang M; Li Y; Ma W; Li H; He F; Pu D; Su T; Wang S
Reprod Biomed Online; 2014 Jan; 28(1):80-5. PubMed ID: 24268733
[TBL] [Abstract][Full Text] [Related]
3. Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
Ma W; Li Y; Wang M; Li H; Su T; Li Y; Wang S
PLoS One; 2015; 10(6):e0130202. PubMed ID: 26075712
[TBL] [Abstract][Full Text] [Related]
4. Variants of the WNT7A gene in Chinese patients with müllerian duct abnormalities.
Dang Y; Qin Y; Tang R; Mu Y; Li G; Xia M; Chen ZJ
Fertil Steril; 2012 Feb; 97(2):391-4. PubMed ID: 22177312
[TBL] [Abstract][Full Text] [Related]
5. Lack of association of WNT5A mutations with Müllerian duct abnormalities.
Wu K; Chang X; Wei D; Xu C; Qin Y; Chen ZJ
Reprod Biomed Online; 2013 Feb; 26(2):164-7. PubMed ID: 23265959
[TBL] [Abstract][Full Text] [Related]
6. Mutation screening of HOXA7 and HOXA9 genes in Chinese women with Müllerian duct abnormalities.
Chen X; Mu Y; Li C; Li G; Zhao H; Qin Y; Chen ZJ
Reprod Biomed Online; 2014 Nov; 29(5):595-9. PubMed ID: 25246116
[TBL] [Abstract][Full Text] [Related]
7. Mutations in HOXA11 are not responsible for Müllerian duct anomalies in Chinese patients.
Chen X; Li G; Qin Y; Cui Y; You L; Chen ZJ
Reprod Biomed Online; 2014 Jun; 28(6):739-42. PubMed ID: 24745830
[TBL] [Abstract][Full Text] [Related]
8. Analysis of PBX1 mutations in 192 Chinese women with Müllerian duct abnormalities.
Ma J; Qin Y; Liu W; Duan H; Xia M; Chen ZJ
Fertil Steril; 2011 Jun; 95(8):2615-7. PubMed ID: 21575942
[TBL] [Abstract][Full Text] [Related]
9. PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis.
Wang P; Zhao H; Sun M; Li Y; Chen ZJ
Reprod Biomed Online; 2012 Aug; 25(2):219-22. PubMed ID: 22683154
[TBL] [Abstract][Full Text] [Related]
10. Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women.
Chang X; Qin Y; Xu C; Li G; Zhao X; Chen ZJ
Reprod Biomed Online; 2012 Jun; 24(6):630-3. PubMed ID: 22503279
[TBL] [Abstract][Full Text] [Related]
11. Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Waschk DE; Tewes AC; Römer T; Hucke J; Kapczuk K; Schippert C; Hillemanns P; Wieacker P; Ledig S
Clin Genet; 2016 May; 89(5):590-6. PubMed ID: 26610373
[TBL] [Abstract][Full Text] [Related]
12. Genetic analysis of DACT1 in 100 Chinese Han women with Müllerian duct anomalies.
Xing Q; Xu Z; Zhu Y; Wang X; Wang J; Chen D; Xu Y; He X; Xiang H; Wang B; Cao Y
Reprod Biomed Online; 2016 Apr; 32(4):420-6. PubMed ID: 26856455
[TBL] [Abstract][Full Text] [Related]
13. Mutational analysis of the WNT gene family in women with Mayer-Rokitansky-Kuster-Hauser syndrome.
Ravel C; Lorenço D; Dessolle L; Mandelbaum J; McElreavey K; Darai E; Siffroi JP
Fertil Steril; 2009 Apr; 91(4 Suppl):1604-7. PubMed ID: 19171330
[TBL] [Abstract][Full Text] [Related]
14. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
[TBL] [Abstract][Full Text] [Related]
15. Novel mutations in the TP63 gene are potentially associated with Müllerian duct anomalies.
Wang X; Zhang X; Liu S; Li G; Cui L; Qin Y; Chen ZJ
Hum Reprod; 2016 Dec; 31(12):2865-2871. PubMed ID: 27798044
[TBL] [Abstract][Full Text] [Related]
16. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.
Chen N; Zhao S; Jolly A; Wang L; Pan H; Yuan J; Chen S; Koch A; Ma C; Tian W; Jia Z; Kang J; Zhao L; Qin C; Fan X; Rall K; Coban-Akdemir Z; Chen Z; Jhangiani S; Liang Z; Niu Y; Li X; Yan Z; Wu Y; Dong S; Song C; Qiu G; Zhang S; Liu P; Posey JE; Zhang F; Luo G; Wu Z; ; Su J; Zhang J; Chen EY; Rouskas K; Glentis S; Bacopoulou F; Deligeoroglou E; Chrousos G; Lyonnet S; Polak M; Rosenberg C; Dingeldein I; Bonilla X; Borel C; Gibbs RA; Dietrich JE; Dimas AS; Antonarakis SE; Brucker SY; Lupski JR; Wu N; Zhu L
Am J Hum Genet; 2021 Feb; 108(2):337-345. PubMed ID: 33434492
[TBL] [Abstract][Full Text] [Related]
17. Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system.
Carroll TJ; Park JS; Hayashi S; Majumdar A; McMahon AP
Dev Cell; 2005 Aug; 9(2):283-92. PubMed ID: 16054034
[TBL] [Abstract][Full Text] [Related]
18. LHX1 mutation screening in 96 patients with müllerian duct abnormalities.
Xia M; Zhao H; Qin Y; Mu Y; Wang J; Bian Y; Ma J; Chen ZJ
Fertil Steril; 2012 Mar; 97(3):682-5. PubMed ID: 22217964
[TBL] [Abstract][Full Text] [Related]
19. Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study.
Philibert P; Biason-Lauber A; Rouzier R; Pienkowski C; Paris F; Konrad D; Schoenle E; Sultan C
J Clin Endocrinol Metab; 2008 Mar; 93(3):895-900. PubMed ID: 18182450
[TBL] [Abstract][Full Text] [Related]
20. WNT7A mutations in patients with Müllerian duct abnormalities.
Timmreck LS; Pan HA; Reindollar RH; Gray MR
J Pediatr Adolesc Gynecol; 2003 Aug; 16(4):217-21. PubMed ID: 14550385
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]