61 related articles for article (PubMed ID: 24114442)
21. Components of the transforming growth factor-beta family and the pathogenesis of human Achilles tendon pathology--a genetic association study.
Posthumus M; Collins M; Cook J; Handley CJ; Ribbans WJ; Smith RK; Schwellnus MP; Raleigh SM
Rheumatology (Oxford); 2010 Nov; 49(11):2090-7. PubMed ID: 20360039
[TBL] [Abstract][Full Text] [Related]
22. Association of TIRAP (MAL) gene polymorhisms with susceptibility to tuberculosis in a Chinese population.
Zhang YX; Xue Y; Liu JY; Zhao MY; Li FJ; Zhou JM; Wang HJ; Li JC
Genet Mol Res; 2011 Jan; 10(1):7-15. PubMed ID: 21218381
[TBL] [Abstract][Full Text] [Related]
23. The role of Gdf5 regulatory regions in development of hip morphology.
Kiapour AM; Cao J; Young M; Capellini TD
PLoS One; 2018; 13(11):e0202785. PubMed ID: 30388100
[TBL] [Abstract][Full Text] [Related]
24. Single-nucleotide polymorphism of the pri-miR-34b/c gene is not associated with susceptibility to congenital heart disease in the Han Chinese population.
Liu YM; Wang Y; Peng W; Wu Z; Wang XH; Wang ML; Wang W; Sun J; Zhang ZD; Mo XM
Genet Mol Res; 2013 Aug; 12(3):2937-44. PubMed ID: 24065649
[TBL] [Abstract][Full Text] [Related]
25. The GDF5 rs143383 polymorphism is associated with osteoarthritis of the knee with genome-wide statistical significance.
Valdes AM; Evangelou E; Kerkhof HJ; Tamm A; Doherty SA; Kisand K; Tamm A; Kerna I; Uitterlinden A; Hofman A; Rivadeneira F; Cooper C; Dennison EM; Zhang W; Muir KR; Ioannidis JP; Wheeler M; Maciewicz RA; van Meurs JB; Arden NK; Spector TD; Doherty M
Ann Rheum Dis; 2011 May; 70(5):873-5. PubMed ID: 20870806
[No Abstract] [Full Text] [Related]
26. Association of heparanase gene (HPSE-1) single nucleotide polymorphisms with gastric cancer.
Yue Z; Song Y; Wang Z; Luo Y; Jiang L; Xing L; Xu H; Zhang X
J Surg Oncol; 2010 Jul; 102(1):68-72. PubMed ID: 20578081
[TBL] [Abstract][Full Text] [Related]
27. The genetics of common degenerative skeletal disorders: osteoarthritis and degenerative disc disease.
Ikegawa S
Annu Rev Genomics Hum Genet; 2013; 14():245-56. PubMed ID: 24003854
[TBL] [Abstract][Full Text] [Related]
28. [Single nucleotide polymorphisms of three candidate genes in essential hypertension].
Hu BC; Chu SL; Wang JG; Wang GL; Gao PJ; Zhu DL
Zhonghua Nei Ke Za Zhi; 2006 Apr; 45(4):281-4. PubMed ID: 16780672
[TBL] [Abstract][Full Text] [Related]
29. CRISPLD2 polymorphisms are associated with non-syndromic cleft lip with or without cleft palate in a northern Chinese population.
Shi J; Jiao X; Song T; Zhang B; Qin C; Cao F
Eur J Oral Sci; 2010 Aug; 118(4):430-3. PubMed ID: 20662919
[TBL] [Abstract][Full Text] [Related]
30. Congenital hip dysplasia in the light of early and very early diagnosis.
Ortolani M
Clin Orthop Relat Res; 1976 Sep; (119):6-10. PubMed ID: 954324
[TBL] [Abstract][Full Text] [Related]
31. Association of Wnt3A gene variants with non-syndromic cleft lip with or without cleft palate in Chinese population.
Yao T; Yang L; Li PQ; Wu H; Xie HB; Shen X; Xie XD
Arch Oral Biol; 2011 Jan; 56(1):73-8. PubMed ID: 20932509
[TBL] [Abstract][Full Text] [Related]
32. Association of transforming growth factor-beta1 gene polymorphisms with genetic susceptibility to nasopharyngeal carcinoma.
Wei YS; Zhu YH; Du B; Yang ZH; Liang WB; Lv ML; Kuang XH; Tai SH; Zhao Y; Zhang L
Clin Chim Acta; 2007 May; 380(1-2):165-9. PubMed ID: 17368597
[TBL] [Abstract][Full Text] [Related]
33. [Inheritance of congenital hip dislocation and dysplasia of the hip joint].
Lordkipanidze EF
Ortop Travmatol Protez; 1975 May; (5):21-6. PubMed ID: 126402
[No Abstract] [Full Text] [Related]
34. Polymorphisms of human vascular endothelial growth factor gene are associated with acute cerebral infarction in the Chinese population.
Fu Y; Ni P; Ma J; Ying Y; Zhao J; Liu J; Chen S
Eur Neurol; 2011; 66(1):47-52. PubMed ID: 21757917
[TBL] [Abstract][Full Text] [Related]
35. [Gene mapping of developmental dysplasia of the hip in chromosome 17q21 region].
Li LY; Sun XK; Zhao Q; Zhang LJ; Li QW; Wang LL; Gao H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):620-5. PubMed ID: 21154319
[TBL] [Abstract][Full Text] [Related]
36. [Etiopathogenesis of congenital hip dislocation (hip dysplasia)].
Dogonadse MA
Beitr Orthop Traumatol; 1973 Mar; 20(3):151-9. PubMed ID: 4267481
[No Abstract] [Full Text] [Related]
37. Family studies of relation between Perthes disease and congenital dislocation of the hip.
Niclasen SD
J Med Genet; 1978 Aug; 15(4):296-9. PubMed ID: 712763
[TBL] [Abstract][Full Text] [Related]
38. Lack of association of hypogonadotropic genes with age at menarche: prospects for the future.
Seminara SB
J Clin Endocrinol Metab; 2008 Nov; 93(11):4224-5. PubMed ID: 18987281
[No Abstract] [Full Text] [Related]
39. [Brachydactyly type C due to a nonsense mutation in the GDF5 gene].
Travieso-Suárez L; Pereda A; Pozo-Román J; Pérez de Nanclares G; Argente J
An Pediatr (Engl Ed); 2018 Feb; 88(2):107-109. PubMed ID: 28391997
[No Abstract] [Full Text] [Related]
40. Mechanical osteoarthritis of the hip in a one medicine concept: a narrative review.
Tomé I; Alves-Pimenta S; Sargo R; Pereira J; Colaço B; Brancal H; Costa L; Ginja M
BMC Vet Res; 2023 Oct; 19(1):222. PubMed ID: 37875898
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
