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Journal Abstract Search

165 related items for PubMed ID: 20047061

  • 1. Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.
    Stanke F, Becker T, Hedtfeld S, Tamm S, Wienker TF, Tümmler B.
    Hum Genet; 2010 Apr; 127(4):383-94. PubMed ID: 20047061
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  • 2. An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion.
    Stanke F, Hedtfeld S, Becker T, Tümmler B.
    BMC Med Genet; 2011 May 06; 12():62. PubMed ID: 21548936
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  • 3. Genes in the vicinity of CFTR modulate the cystic fibrosis phenotype in highly concordant or discordant F508del homozygous sib pairs.
    Mekus F, Laabs U, Veeze H, Tümmler B.
    Hum Genet; 2003 Jan 06; 112(1):1-11. PubMed ID: 12483292
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  • 5. ATB(0)/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis.
    Larriba S, Sumoy L, Ramos MD, Giménez J, Estivill X, Casals T, Nunes V.
    Eur J Hum Genet; 2001 Nov 06; 9(11):860-6. PubMed ID: 11781704
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  • 8. Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B.
    Becker T, Pich A, Tamm S, Hedtfeld S, Ibrahim M, Altmüller J, Dalibor N, Toliat MR, Janciauskiene S, Tümmler B, Stanke F.
    Sci Rep; 2020 Dec 31; 10(1):22447. PubMed ID: 33384439
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  • 11. Immunotyping of clinically divergent p.Phe508del homozygous monozygous cystic fibrosis twins.
    Schamschula E, Hagmann W, Assenov Y, Hedtfeld S, Farag AK, Roesner LM, Wiehlmann L, Stanke F, Fischer S, Risch A, Tümmler B.
    J Cyst Fibros; 2021 Jan 31; 20(1):149-153. PubMed ID: 32540173
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  • 12. The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster is potentially implicated in Cystic Fibrosis pathogenesis.
    Endale Ahanda ML, Bienvenu T, Sermet-Gaudelus I, Mazzolini L, Edelman A, Zoorob R, Davezac N.
    J Cyst Fibros; 2015 Sep 31; 14(5):571-9. PubMed ID: 25800681
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  • 13. CEACAM3 decreases asthma exacerbations and modulates respiratory syncytial virus latent infection in children.
    Tsai CH, Wu AC, Chiang BL, Yang YH, Hung SP, Su MW, Chang YJ, Lee YL.
    Thorax; 2020 Sep 31; 75(9):725-734. PubMed ID: 32606071
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  • 15. Expression levels of FAS are regulated through an evolutionary conserved element in intron 2, which modulates cystic fibrosis disease severity.
    Kumar V, Becker T, Jansen S, van Barneveld A, Boztug K, Wölfl S, Tümmler B, Stanke F.
    Genes Immun; 2008 Dec 31; 9(8):689-96. PubMed ID: 18685642
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  • 18. TG15 T5 allele in clinically discordant monozygotic twins with cystic fibrosis.
    Picci L, Cameran M, Scarpa M, Pradal U, Melotti P, Assael BM, Castellani C.
    Am J Med Genet A; 2007 Aug 15; 143A(16):1936-7. PubMed ID: 17632788
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  • 19. Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosis.
    Choi EH, Ehrmantraut M, Foster CB, Moss J, Chanock SJ.
    Pediatr Pulmonol; 2006 Mar 15; 41(3):255-62. PubMed ID: 16429424
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  • 20. Loci of intestinal distress in cystic fibrosis knockout mice.
    Haston CK, Tsui LC.
    Physiol Genomics; 2003 Jan 15; 12(2):79-84. PubMed ID: 12441405
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