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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 19207109)

  • 1. 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]  

  • 2. 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]  

  • 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. Otosclerosis Associated with a De Novo Mutation -832G > A in the TGFB1 Gene Promoter Causing a Decreased Expression Level.
    Priyadarshi S; Hansdah K; Ray CS; Biswal NC; Ramchander PV
    Sci Rep; 2016 Jul; 6():29572. PubMed ID: 27404893
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Association of bone morphogenetic proteins with otosclerosis.
    Schrauwen I; Thys M; Vanderstraeten K; Fransen E; Dieltjens N; Huyghe JR; Ealy M; Claustres M; Cremers CR; Dhooge I; Declau F; Van de Heyning P; Vincent R; Somers T; Offeciers E; Smith RJ; Van Camp G
    J Bone Miner Res; 2008 Apr; 23(4):507-16. PubMed ID: 18021008
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transforming growth factor beta 1 polymorphisms and haplotypes associated with breast cancer susceptibility: A case-control study in Tunisian women.
    Hadj-Ahmed M; Ghali RM; Bouaziz H; Habel A; Stayoussef M; Ayedi M; Hachiche M; Rahal K; Yacoubi-Loueslati B; Almawi WY
    Tumour Biol; 2019 Aug; 41(8):1010428319869096. PubMed ID: 31405342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of TGFB1 in European and Japanese Moyamoya disease patients.
    Liu C; Roder C; Schulte C; Kasuya H; Akagawa H; Nishizawa T; Yoneyama T; Okada Y; Khan N; Tatagiba M; Berg D; Krischek B
    Eur J Med Genet; 2012 Oct; 55(10):531-4. PubMed ID: 22659181
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Insufficient evidence for a role of SERPINF1 in otosclerosis.
    Valgaeren H; Sommen M; Beyens M; Vandeweyer G; Schrauwen I; Schepers A; Schatteman I; Topsakal V; Dhooge I; Kunst H; Zanetti D; Huber AM; Hoischen A; Fransen E; Van Camp G
    Mol Genet Genomics; 2019 Aug; 294(4):1001-1006. PubMed ID: 30968248
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetics of otosclerosis.
    Thys M; Van Camp G
    Otol Neurotol; 2009 Dec; 30(8):1021-32. PubMed ID: 19546831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Resequencing of genes for transforming growth factor beta1 (TGFB1) type 1 and 2 receptors (TGFBR1, TGFBR2), and association analysis of variants with diabetic nephropathy.
    McKnight AJ; Savage DA; Patterson CC; Sadlier D; Maxwell AP
    BMC Med Genet; 2007 Feb; 8():5. PubMed ID: 17319955
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis.
    Højland AT; Tavernier LJM; Schrauwen I; Sommen M; Topsakal V; Schatteman I; Dhooge I; Huber A; Zanetti D; Kunst HPM; Hoischen A; Petersen MB; Van Camp G; Fransen E
    Hum Genet; 2022 Apr; 141(3-4):951-963. PubMed ID: 34410490
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes.
    Ichimura S; Sasaki S; Murata T; Fukumura R; Gondo Y; Ikegawa S; Furuichi T
    Exp Anim; 2017 May; 66(2):137-144. PubMed ID: 27928112
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transforming growth factor-β1 gene promoter -509C/T polymorphism in association with expression affects colorectal cancer development and depends on gender.
    Stanilova S; Stanilov N; Julianov A; Manolova I; Miteva L
    PLoS One; 2018; 13(8):e0201775. PubMed ID: 30071009
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. The c.29T>C polymorphism of the transforming growth factor beta-1 (TGFB1) gene, bone mineral density and the occurrence of low-energy fractures in patients with inflammatory bowel disease.
    Krela-Kaźmierczak I; Michalak M; Wawrzyniak A; Szymczak A; Eder P; Łykowska-Szuber L; Kaczmarek-Ryś M; Drwęska-Matelska N; Skrzypczak-Zielińska M; Linke K; Słomski R
    Mol Biol Rep; 2017 Dec; 44(6):455-461. PubMed ID: 28993955
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.