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 *

92 related articles for article (PubMed ID: 21036675)

  • 21. The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania.
    Frenţescu L; Brownsell E; Hinks J; Malone G; Shaw H; Budişan L; Bulman M; Schwarz M; Pop L; Filip M; Tomescu E; Moşescu S; Popa I; Benga G
    J Cyst Fibros; 2008 Sep; 7(5):423-8. PubMed ID: 18467194
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutations of the cystic fibrosis gene in patients with chronic pancreatitis.
    Sharer N; Schwarz M; Malone G; Howarth A; Painter J; Super M; Braganza J
    N Engl J Med; 1998 Sep; 339(10):645-52. PubMed ID: 9725921
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.
    Weiss FU; Simon P; Bogdanova N; Mayerle J; Dworniczak B; Horst J; Lerch MM
    Gut; 2005 Oct; 54(10):1456-60. PubMed ID: 15987793
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Correlation between phenotype and genotype in a group of patients with cystic fibrosis].
    Navarro H; Kolbach M; Repetto G; Guiraldes E; Harris P; Foradori A; Poggi H; Sánchez I
    Rev Med Chil; 2002 May; 130(5):475-81. PubMed ID: 12143267
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Frequency of common CFTR gene mutations in Venezuelan patients with cystic fibrosis.
    Sánchez K; Arcia O; Matute X; Mindiola L; Chaustre I; Takiff H
    Invest Clin; 2014 Mar; 55(1):44-54. PubMed ID: 24758101
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Increased frequency of CFTR gene mutations in sarcoidosis: a case/control association study.
    Bombieri C; Luisetti M; Belpinati F; Zuliani E; Beretta A; Baccheschi J; Casali L; Pignatti PF
    Eur J Hum Genet; 2000 Sep; 8(9):717-20. PubMed ID: 10980579
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Segregation analysis in cystic fibrosis at-risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism.
    D'Apice MR; Gambardella S; Russo S; Lucidi V; Nardone AM; Pietropolli A; Novelli G
    Prenat Diagn; 2004 Dec; 24(12):981-3. PubMed ID: 15614862
    [TBL] [Abstract][Full Text] [Related]  

  • 28. CFTR (TG)m(T)n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis.
    Chiang HS; Lu JF; Liu CH; Wu YN; Wu CC
    Clin Genet; 2009 Sep; 76(3):282-6. PubMed ID: 19737283
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Epidemiologic study of the cystic fibrosis gene in the Champagne-Ardenne region].
    Clavel C; Pennaforte F; Pigeon F; Mozelle M; Boutterin MC; Duval-Binninger I; F-erec C; Birembaut P
    Ann Biol Clin (Paris); 1996; 54(2):67-74. PubMed ID: 8763629
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis.
    Ooi CY; Dorfman R; Cipolli M; Gonska T; Castellani C; Keenan K; Freedman SD; Zielenski J; Berthiaume Y; Corey M; Schibli S; Tullis E; Durie PR
    Gastroenterology; 2011 Jan; 140(1):153-61. PubMed ID: 20923678
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis.
    Ko JM; Kim GH; Kim KM; Hong SJ; Yoo HW
    J Korean Med Sci; 2008 Oct; 23(5):912-5. PubMed ID: 18955805
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry.
    Alonso MJ; Heine-Suñer D; Calvo M; Rosell J; Giménez J; Ramos MD; Telleria JJ; Palacio A; Estivill X; Casals T
    Ann Hum Genet; 2007 Mar; 71(Pt 2):194-201. PubMed ID: 17331079
    [TBL] [Abstract][Full Text] [Related]  

  • 33. CFTR gene analysis in cystic fibrosis patients: detection of 91% of molecular defects and identification of the novel mutation D979V.
    Plouvier E; Cougoureux E; Sardet A; Tournier G; Aymard P; Feldmann D
    Ann Genet; 1997; 40(3):185-8. PubMed ID: 9401110
    [TBL] [Abstract][Full Text] [Related]  

  • 34. CFTR H609R mutation in Ecuadorian patients with cystic fibrosis.
    Moya-Quiles MR; Glover G; Mondéjar-López P; Pastor-Vivero MD; Fernández-Sánchez A; Sánchez-Solís M
    J Cyst Fibros; 2009 Jul; 8(4):280-1. PubMed ID: 19457724
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Cystic fibrosis modifying genes].
    Knauer N; Ratjen F; Grasemann H
    Pneumologie; 2005 Jun; 59(6):395-404. PubMed ID: 15991075
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High heterogeneity of CFTR mutations and unexpected low incidence of cystic fibrosis in the Mediterranean France.
    des Georges M; Guittard C; Altiéri JP; Templin C; Sarles J; Sarda P; Claustres M
    J Cyst Fibros; 2004 Dec; 3(4):265-72. PubMed ID: 15698946
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 3120+1 G-->A: a rare variant in Emirati CF patients.
    Saleheen D; Frossard PM
    J Coll Physicians Surg Pak; 2006 Feb; 16(2):139-40. PubMed ID: 16499810
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotypic variability in a family with pancreatitis and cystic fibrosis sharing common mild CFTR mutation: report on CFTR mutations and their phenotypic variability.
    Alghisi F; Bella S; Lucidi V; Angioni A; Tomaiuolo AC; D'Apice MR; Gambardella S; Novelli G
    Pancreas; 2009 Jan; 38(1):109-10. PubMed ID: 19106752
    [No Abstract]   [Full Text] [Related]  

  • 39. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K; Weren M; Proesmans M; Kerem E
    Pediatrics; 2005 Apr; 115(4):e463-9. PubMed ID: 15772171
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characterisation of mutations and genotype-phenotype correlation in cystic fibrosis: experience from India.
    Shastri SS; Kabra M; Kabra SK; Pandey RM; Menon PS
    J Cyst Fibros; 2008 Mar; 7(2):110-5. PubMed ID: 17716958
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.