136 related articles for article (PubMed ID: 28756021)
1. Association of clinical severity of cystic fibrosis with variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1 and SLC9A3).
Pereira SV; Ribeiro JD; Bertuzzo CS; Marson FAL
Gene; 2017 Sep; 629():117-126. PubMed ID: 28756021
[TBL] [Abstract][Full Text] [Related]
2. Interaction among variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1, and SLC9A3) and CFTR mutations with clinical markers of cystic fibrosis.
Pereira SVN; Ribeiro JD; Bertuzzo CS; Marson FAL
Pediatr Pulmonol; 2018 Jul; 53(7):888-900. PubMed ID: 29635781
[TBL] [Abstract][Full Text] [Related]
3. Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities.
Li W; Soave D; Miller MR; Keenan K; Lin F; Gong J; Chiang T; Stephenson AL; Durie P; Rommens J; Sun L; Strug LJ
Hum Genet; 2014 Feb; 133(2):151-61. PubMed ID: 24057835
[TBL] [Abstract][Full Text] [Related]
4. Extent of rescue of F508del-CFTR function by VX-809 and VX-770 in human nasal epithelial cells correlates with SNP rs7512462 in SLC26A9 gene in F508del/F508del Cystic Fibrosis patients.
Kmit A; Marson FAL; Pereira SV; Vinagre AM; Leite GS; Servidoni MF; Ribeiro JD; Ribeiro AF; Bertuzzo CS; Amaral MD
Biochim Biophys Acta Mol Basis Dis; 2019 Jun; 1865(6):1323-1331. PubMed ID: 30716472
[TBL] [Abstract][Full Text] [Related]
5. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
Bonadia LC; de Lima Marson FA; Ribeiro JD; Paschoal IA; Pereira MC; Ribeiro AF; Bertuzzo CS
Gene; 2014 May; 540(2):183-90. PubMed ID: 24583165
[TBL] [Abstract][Full Text] [Related]
6. Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis.
Miller MR; Soave D; Li W; Gong J; Pace RG; Boëlle PY; Cutting GR; Drumm ML; Knowles MR; Sun L; Rommens JM; Accurso F; Durie PR; Corvol H; Levy H; Sontag MK; Strug LJ
J Pediatr; 2015 May; 166(5):1152-1157.e6. PubMed ID: 25771386
[TBL] [Abstract][Full Text] [Related]
7. Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis.
Furlan LL; Ribeiro JD; Bertuzzo CS; Salomão Junior JB; Souza DRS; Marson FAL
J Pediatr (Rio J); 2017; 93(6):639-648. PubMed ID: 28719800
[TBL] [Abstract][Full Text] [Related]
8. Influence of pancreatic status, CFTR mutations, Staphylococcus aureus and/or Pseudomonas aeruginosa infection/colonization on lung function in cystic fibrosis during a 2-year follow-up period.
Pascoal MA; Marson FAL; Paschoal IA; Levy CE
Wien Klin Wochenschr; 2020 Oct; 132(19-20):572-580. PubMed ID: 32356101
[TBL] [Abstract][Full Text] [Related]
9. Polymorphisms in ADRB2 gene can modulate the response to bronchodilators and the severity of cystic fibrosis.
Marson FA; Bertuzzo CS; Ribeiro AF; Ribeiro JD
BMC Pulm Med; 2012 Sep; 12():50. PubMed ID: 22950544
[TBL] [Abstract][Full Text] [Related]
10. 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; 41(3):255-62. PubMed ID: 16429424
[TBL] [Abstract][Full Text] [Related]
11. Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study.
Marson FA; Bertuzzo CS; Ribeiro AF; Ribeiro JD
BMC Med Genet; 2014 Mar; 15():27. PubMed ID: 24593045
[TBL] [Abstract][Full Text] [Related]
12. Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.
Sun L; Rommens JM; Corvol H; Li W; Li X; Chiang TA; Lin F; Dorfman R; Busson PF; Parekh RV; Zelenika D; Blackman SM; Corey M; Doshi VK; Henderson L; Naughton KM; O'Neal WK; Pace RG; Stonebraker JR; Wood SD; Wright FA; Zielenski J; Clement A; Drumm ML; Boëlle PY; Cutting GR; Knowles MR; Durie PR; Strug LJ
Nat Genet; 2012 May; 44(5):562-9. PubMed ID: 22466613
[TBL] [Abstract][Full Text] [Related]
13. IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability.
Furlan LL; Marson FA; Ribeiro JD; Bertuzzo CS; Salomão Junior JB; Souza DR
Hum Genet; 2016 Aug; 135(8):881-94. PubMed ID: 27209008
[TBL] [Abstract][Full Text] [Related]
14. Familial concordance of phenotype and microbial variation among siblings with CF.
Picard E; Aviram M; Yahav Y; Rivlin J; Blau H; Bentur L; Avital A; Villa Y; Schwartz S; Kerem B; Kerem E
Pediatr Pulmonol; 2004 Oct; 38(4):292-7. PubMed ID: 15334505
[TBL] [Abstract][Full Text] [Related]
15. Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis.
Dorfman R; Taylor C; Lin F; Sun L; Sandford A; Paré P; Berthiaume Y; Corey M; Durie P; Zielenski J;
Pediatr Pulmonol; 2011 Apr; 46(4):385-92. PubMed ID: 20967843
[TBL] [Abstract][Full Text] [Related]
16. Mannose-binding lectin gene as a modifier of the cystic fibrosis phenotype in Argentinean pediatric patients.
Gravina LP; Crespo C; Giugno H; Sen L; Chertkoff L; Mangano A; Castaños C
J Cyst Fibros; 2015 Jan; 14(1):78-83. PubMed ID: 25178872
[TBL] [Abstract][Full Text] [Related]
17. Association of improved pulmonary phenotype in Irish cystic fibrosis patients with a 3' enhancer polymorphism in alpha-1-antitrypsin.
Courtney JM; Plant BJ; Morgan K; Rendall J; Gallagher C; Ennis M; Kalsheker N; Elborn S; O'Connor CM
Pediatr Pulmonol; 2006 Jun; 41(6):584-91. PubMed ID: 16617455
[TBL] [Abstract][Full Text] [Related]
18. Genetic modifiers of lung disease in cystic fibrosis.
Drumm ML; Konstan MW; Schluchter MD; Handler A; Pace R; Zou F; Zariwala M; Fargo D; Xu A; Dunn JM; Darrah RJ; Dorfman R; Sandford AJ; Corey M; Zielenski J; Durie P; Goddard K; Yankaskas JR; Wright FA; Knowles MR;
N Engl J Med; 2005 Oct; 353(14):1443-53. PubMed ID: 16207846
[TBL] [Abstract][Full Text] [Related]
19. SLC6A14 Impacts Cystic Fibrosis Lung Disease Severity
Mercier J; Calmel C; Mésinèle J; Sutanto E; Merabtene F; Longchampt E; Sage E; Kicic A; Boëlle PY; Corvol H; Ruffin M; Guillot L
Front Mol Biosci; 2022; 9():850261. PubMed ID: 35372502
[TBL] [Abstract][Full Text] [Related]
20. The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes.
Castellani C; Malerba G; Sangalli A; Delmarco A; Petrelli E; Rossini M; Assael BM; Mottes M
J Cyst Fibros; 2006 Dec; 5(4):229-35. PubMed ID: 16713399
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
