These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
134 related articles for article (PubMed ID: 19113055)
1. Otosclerosis and TGF-beta 1 gene in black South Africans. Tshifularo M; Joseph CA S Afr Med J; 2008 Sep; 98(9):720-3. PubMed ID: 19113055 [TBL] [Abstract][Full Text] [Related]
2. Otosclerosis among South African indigenous blacks. Tshifularo MI; Joseph CA East Afr Med J; 2005 May; 82(5):223-5. PubMed ID: 16119750 [TBL] [Abstract][Full Text] [Related]
3. The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations. Thys M; Schrauwen I; Vanderstraeten K; Janssens K; Dieltjens N; Van Den Bogaert K; Fransen E; Chen W; Ealy M; Claustres M; Cremers CR; Dhooge I; Declau F; Claes J; Van de Heyning P; Vincent R; Somers T; Offeciers E; Smith RJ; Van Camp G Hum Mol Genet; 2007 Sep; 16(17):2021-30. PubMed ID: 17588962 [TBL] [Abstract][Full Text] [Related]
4. Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients. Thys M; Schrauwen I; Vanderstraeten K; Dieltjens N; Fransen E; Ealy M; Cremers CW; van de Heyning P; Vincent R; Offeciers E; Smith RH; van Camp G Ann Hum Genet; 2009 Mar; 73(2):171-5. PubMed ID: 19207109 [TBL] [Abstract][Full Text] [Related]
5. Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. Khalfallah A; Schrauwen I; Mnejja M; HadjKacem H; Dhouib L; Mosrati MA; Hakim B; Lahmar I; Charfeddine I; Driss N; Ayadi H; Ghorbel A; Van Camp G; Masmoudi S Ann Hum Genet; 2011 Sep; 75(5):598-604. PubMed ID: 21777208 [TBL] [Abstract][Full Text] [Related]
6. Case-Control Genotyping of the c.788C>T Variant of Transforming Growth Factor-Beta 1 Gene in Otosclerosis in the South Indian Population. Kale D; Rekha S; Vinoth S; Ramalingam R; Parani M J Int Adv Otol; 2022 Mar; 18(2):112-117. PubMed ID: 35418358 [TBL] [Abstract][Full Text] [Related]
7. Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. Sommen M; Van Camp G; Liktor B; Csomor P; Fransen E; Sziklai I; Schrauwen I; Karosi T Otol Neurotol; 2014 Jul; 35(6):1058-64. PubMed ID: 24643032 [TBL] [Abstract][Full Text] [Related]
8. The contribution of the C-824T tyrosine hydroxylase polymorphism to the prevalence of hypertension in a South African cohort: the SABPA study. van Deventer CA; Louw R; van der Westhuizen FH; Vorster CB; Malan L Clin Exp Hypertens; 2013; 35(8):614-9. PubMed ID: 23489065 [TBL] [Abstract][Full Text] [Related]
9. Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India. Priyadarshi S; Panda KC; Panda AK; Ramchander PV Genet Mol Res; 2010 Sep; 9(3):1914-20. PubMed ID: 20882487 [TBL] [Abstract][Full Text] [Related]
10. The incidence of otosclerosis in the general population. Gapany-Gapanavicius B Isr J Med Sci; 1975 May; 11(5):465-8. PubMed ID: 1158659 [TBL] [Abstract][Full Text] [Related]
11. Genetic association and gene expression profiles of TGFB1 and the contribution of TGFB1 to otosclerosis susceptibility. Priyadarshi S; Ray CS; Panda KC; Desai A; Nayak SR; Biswal NC; Ramchander PV J Bone Miner Res; 2013 Dec; 28(12):2490-7. PubMed ID: 23703862 [TBL] [Abstract][Full Text] [Related]
12. Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. Mowat AJ; Crompton M; Ziff JL; Aldren CP; Lavy JA; Saeed SR; Dawson SJ Hum Genet; 2018 May; 137(5):357-363. PubMed ID: 29728750 [TBL] [Abstract][Full Text] [Related]
13. The genetics of otosclerosis: a review. Gordon MA Am J Otol; 1989 Nov; 10(6):426-38. PubMed ID: 2692453 [TBL] [Abstract][Full Text] [Related]
14. Two cases of otosclerosis in Kumasi, Ghana, case report. Brobby GW Trop Geogr Med; 1986 Sep; 38(3):292-5. PubMed ID: 3750398 [TBL] [Abstract][Full Text] [Related]
15. A genetic study of otosclerosis in a population living in the north of Tunisia. Ben Arab S; Bonaïti-Pellié C; Belkahia A Ann Genet; 1993; 36(2):111-6. PubMed ID: 8215216 [TBL] [Abstract][Full Text] [Related]
16. Otosclerosis and races. Tato JM; Tato JM Ann Otol Rhinol Laryngol; 1967 Dec; 76(5):1018-25. PubMed ID: 6074235 [No Abstract] [Full Text] [Related]
17. Genetics of otosclerosis. Thys M; Van Camp G Otol Neurotol; 2009 Dec; 30(8):1021-32. PubMed ID: 19546831 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel allele, HLA-DPB1*34:01:01:03, in Black South African individuals. Loubser S; Kwenda S; Sengupta D; Tiemessen CT HLA; 2019 Dec; 94(6):547-549. PubMed ID: 31464043 [TBL] [Abstract][Full Text] [Related]
19. The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population. Iossa S; Corvino V; Giannini P; Salvato R; Cavaliere M; Panetti M; Panetti G; Piantedosi B; Marciano E; Franzè A Acta Otorhinolaryngol Ital; 2013 Oct; 33(5):320-3. PubMed ID: 24227897 [TBL] [Abstract][Full Text] [Related]
20. Polymorphisms of the beta chain of the high-affinity immunoglobulin E receptor (Fcepsilon RI-beta) in South African black and white asthmatic and nonasthmatic individuals. Green SL; Gaillard MC; Song E; Dewar JB; Halkas A Am J Respir Crit Care Med; 1998 Nov; 158(5 Pt 1):1487-92. PubMed ID: 9817697 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]