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 *

168 related articles for article (PubMed ID: 14731137)

  • 1. CFTR gene and cystic fibrosis.
    Gaskin KJ
    J Gastroenterol Hepatol; 2004 Feb; 19(2):228. PubMed ID: 14731137
    [No Abstract]   [Full Text] [Related]  

  • 2. Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D.
    Parad RB
    J Med Genet; 1996 Aug; 33(8):711-3. PubMed ID: 8863168
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Probing the basic defect in cystic fibrosis.
    Tsui LC
    Curr Opin Genet Dev; 1991 Jun; 1(1):4-10. PubMed ID: 1726721
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refining the continuum of CFTR-associated disorders in the era of newborn screening.
    Levy H; Nugent M; Schneck K; Stachiw-Hietpas D; Laxova A; Lakser O; Rock M; Dahmer MK; Biller J; Nasr SZ; Baker M; McColley SA; Simpson P; Farrell PM
    Clin Genet; 2016 May; 89(5):539-49. PubMed ID: 26671754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular Genetics of Cystic Fibrosis Transmembrane Conductance Regulator: Genotype and Phenotype.
    Sosnay PR; Raraigh KS; Gibson RL
    Pediatr Clin North Am; 2016 Aug; 63(4):585-98. PubMed ID: 27469177
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype.
    Kerem E; Nissim-Rafinia M; Argaman Z; Augarten A; Bentur L; Klar A; Yahav Y; Szeinberg A; Hiba O; Branski D; Corey M; Kerem B
    Pediatrics; 1997 Sep; 100(3):E5. PubMed ID: 9271620
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in pancreatitis.
    Ooi CY; Durie PR
    J Cyst Fibros; 2012 Sep; 11(5):355-62. PubMed ID: 22658665
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variant cystic fibrosis phenotypes in the absence of CFTR mutations.
    Couper RT
    N Engl J Med; 2002 Dec; 347(23):1892-3; author reply 1892-3. PubMed ID: 12466520
    [No Abstract]   [Full Text] [Related]  

  • 9. Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations.
    Geborek A; Hjelte L
    J Cyst Fibros; 2011 May; 10(3):187-92. PubMed ID: 21354377
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Modifier genes and cystic fibrosis].
    Corvol H; Flamant C; Vallet C; Clement A; Brouard J
    Arch Pediatr; 2006 Jan; 13(1):57-63. PubMed ID: 16274977
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M
    Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Protein repair therapy in cystic fibrosis].
    Clément A; Tamalet A; Fauroux B; Epaud R
    Rev Prat; 2003 Jan; 53(2):163-6. PubMed ID: 12664848
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetics of Cystic Fibrosis: Clinical Implications.
    Egan ME
    Clin Chest Med; 2016 Mar; 37(1):9-16. PubMed ID: 26857764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cystic fibrosis: basic science.
    McAuley DF; Elborn JS
    Paediatr Respir Rev; 2000 Jun; 1(2):93-100. PubMed ID: 12531100
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The "Goldilocks effect" in cystic fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse.
    Cohen JC; Lundblad LK; Bates JH; Levitzky M; Larson JE
    BMC Genet; 2004 Jul; 5():21. PubMed ID: 15279681
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.
    Wilschanski M; Zielenski J; Markiewicz D; Tsui LC; Corey M; Levison H; Durie PR
    J Pediatr; 1995 Nov; 127(5):705-10. PubMed ID: 7472820
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CFTR Genotype and Maximal Exercise Capacity in Cystic Fibrosis: A Cross-sectional Study.
    Radtke T; Hebestreit H; Gallati S; Schneiderman JE; Braun J; Stevens D; Hulzebos EH; Takken T; Boas SR; Urquhart DS; Lands LC; Tejero S; Sovtic A; Dwyer T; Petrovic M; Harris RA; Karila C; Savi D; Usemann J; Mei-Zahav M; Hatziagorou E; Ratjen F; Kriemler S;
    Ann Am Thorac Soc; 2018 Feb; 15(2):209-216. PubMed ID: 29140739
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recommendations for the classification of diseases as CFTR-related disorders.
    Bombieri C; Claustres M; De Boeck K; Derichs N; Dodge J; Girodon E; Sermet I; Schwarz M; Tzetis M; Wilschanski M; Bareil C; Bilton D; Castellani C; Cuppens H; Cutting GR; Drevínek P; Farrell P; Elborn JS; Jarvi K; Kerem B; Kerem E; Knowles M; Macek M; Munck A; Radojkovic D; Seia M; Sheppard DN; Southern KW; Stuhrmann M; Tullis E; Zielenski J; Pignatti PF; Ferec C
    J Cyst Fibros; 2011 Jun; 10 Suppl 2():S86-102. PubMed ID: 21658649
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Modifier genetics: cystic fibrosis.
    Cutting GR
    Annu Rev Genomics Hum Genet; 2005; 6():237-60. PubMed ID: 16124861
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations.
    Dean M; Santis G
    Hum Genet; 1994 Apr; 93(4):364-8. PubMed ID: 7513291
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.