130 related articles for article (PubMed ID: 25246116)
21. Lineage infidelity of epithelial ovarian cancers is controlled by HOX genes that specify regional identity in the reproductive tract.
Cheng W; Liu J; Yoshida H; Rosen D; Naora H
Nat Med; 2005 May; 11(5):531-7. PubMed ID: 15821746
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.
Wu ZY; Zhao GX; Chen WJ; Wang N; Wan B; Lin MT; Murong SX; Yu L
J Mol Med (Berl); 2006 May; 84(5):438-42. PubMed ID: 16649058
[TBL] [Abstract][Full Text] [Related]
24. A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman.
Biason-Lauber A; Konrad D; Navratil F; Schoenle EJ
N Engl J Med; 2004 Aug; 351(8):792-8. PubMed ID: 15317892
[TBL] [Abstract][Full Text] [Related]
25. Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.
Xu Z; Wu S; Xing Q; Wang X; Xiang H; Xu Y; Wang J; He X; Wang B; Cao Y
J Assist Reprod Genet; 2017 Jan; 34(1):125-129. PubMed ID: 27722936
[TBL] [Abstract][Full Text] [Related]
26. Genetic analysis of HOXA11 gene in Chinese patients with cryptorchidism.
Lu P; Wang Y; Wang F; Huang J; Zeng Y; He D; Huang H; Cheng Z
Andrologia; 2018 Feb; 50(1):. PubMed ID: 28261830
[TBL] [Abstract][Full Text] [Related]
27. HOXA10, EMX2 and TENM1 expression in the mid-secretory endometrium of infertile women with a Müllerian duct anomaly.
Zhu Y; Luo M; Huang H; Du X; Chen D; Xing Q; Wang B; Cao Y
Reprod Biomed Online; 2016 Apr; 32(4):388-93. PubMed ID: 26896429
[TBL] [Abstract][Full Text] [Related]
28. Analysis of LHX8 mutation in premature ovarian failure.
Qin Y; Zhao H; Kovanci E; Simpson JL; Chen ZJ; Rajkovic A
Fertil Steril; 2008 Apr; 89(4):1012-4. PubMed ID: 17624344
[TBL] [Abstract][Full Text] [Related]
29. Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure.
Qin Y; Shi Y; Zhao Y; Carson SA; Simpson JL; Chen ZJ
Fertil Steril; 2009 Apr; 91(4 Suppl):1507-9. PubMed ID: 18930203
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Transcription factor AP-2α regulates acute myeloid leukemia cell proliferation by influencing Hoxa gene expression.
Ding X; Yang Z; Zhou F; Wang F; Li X; Chen C; Li X; Hu X; Xiang S; Zhang J
Int J Biochem Cell Biol; 2013 Aug; 45(8):1647-56. PubMed ID: 23660297
[TBL] [Abstract][Full Text] [Related]
32. A novel mutation of HOXA11 in a patient with septate uterus.
Zhu Y; Cheng Z; Wang J; Liu B; Cheng L; Chen B; Cao Y; Wang B
Orphanet J Rare Dis; 2017 Dec; 12(1):178. PubMed ID: 29229001
[TBL] [Abstract][Full Text] [Related]
33. Analysis of the VSX1 gene in sporadic keratoconus patients from China.
Guan T; Wang X; Zheng LB; Wu HJ; Yao YF
BMC Ophthalmol; 2017 Sep; 17(1):173. PubMed ID: 28950846
[TBL] [Abstract][Full Text] [Related]
34. HOXA9 rs3801776 G>A polymorphism increases congenital talipes equinovarus risk in a Chinese population.
Li J; Wu J; Liu Y; Li Y; Xiao Z; Jiang X; Tang Y; Xu H
J Gene Med; 2019 Oct; 21(10):e3119. PubMed ID: 31424148
[TBL] [Abstract][Full Text] [Related]
35. MEIS1 and HOXA7 genes in human acute myeloid leukemia.
Afonja O; Smith JE; Cheng DM; Goldenberg AS; Amorosi E; Shimamoto T; Nakamura S; Ohyashiki K; Ohyashiki J; Toyama K; Takeshita K
Leuk Res; 2000 Oct; 24(10):849-55. PubMed ID: 10996203
[TBL] [Abstract][Full Text] [Related]
36. Mutation screening of BMP4, BMP7, HOXA4 and HOXB6 genes in Chinese patients with hypospadias.
Chen T; Li Q; Xu J; Ding K; Wang Y; Wang W; Li S; Shen Y
Eur J Hum Genet; 2007 Jan; 15(1):23-8. PubMed ID: 17003840
[TBL] [Abstract][Full Text] [Related]
37. Nup98-HoxA9 immortalizes myeloid progenitors, enforces expression of Hoxa9, Hoxa7 and Meis1, and alters cytokine-specific responses in a manner similar to that induced by retroviral co-expression of Hoxa9 and Meis1.
Calvo KR; Sykes DB; Pasillas MP; Kamps MP
Oncogene; 2002 Jun; 21(27):4247-56. PubMed ID: 12082612
[TBL] [Abstract][Full Text] [Related]
38. Sequence analysis and tissue specific expression of human HOXA7.
Kim MH; Jin H; Seol EY; Yoo M; Park HW
Mol Biotechnol; 2000 Jan; 14(1):19-24. PubMed ID: 10911612
[TBL] [Abstract][Full Text] [Related]
39. Detection of congenital müllerian duct anomalies using three-dimensional ultrasound.
Wu MH; Hsu CC; Huang KE
J Clin Ultrasound; 1997; 25(9):487-92. PubMed ID: 9350567
[TBL] [Abstract][Full Text] [Related]
40. SLC45A2 variations in Indian oculocutaneous albinism patients.
Sengupta M; Chaki M; Arti N; Ray K
Mol Vis; 2007 Aug; 13():1406-11. PubMed ID: 17768386
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]