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 *

135 related articles for article (PubMed ID: 9972102)

  • 21. CFTR mutations in the Algerian population.
    Loumi O; Ferec C; Mercier B; Creff J; Fercot B; Denine R; Grangaud JP
    J Cyst Fibros; 2008 Jan; 7(1):54-9. PubMed ID: 17572159
    [TBL] [Abstract][Full Text] [Related]  

  • 22. G542X as a probable Phoenician cystic fibrosis mutation.
    Loirat F; Hazout S; Lucotte G
    Hum Biol; 1997 Jun; 69(3):419-25. PubMed ID: 9164051
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spectrum of CFTR mutations in the Middle North of Spain and identification of a novel mutation (1341G-->A). Mutation in brief no. 252. Online.
    Tellería JJ; Alonso MJ; Calvo C; Alonso M; Blanco A
    Hum Mutat; 1999; 14(1):89. PubMed ID: 10447267
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].
    Radivojević D; Guć-Sćekić M; Djurisić M; Lalić T; Minić P; Kanavakis E
    Srp Arh Celok Lek; 2001; 129 Suppl 1():6-9. PubMed ID: 15637983
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations.
    Jalalirad M; Houshmand M; Mirfakhraie R; Goharbari MH; Mirzajani F
    J Trop Pediatr; 2004 Dec; 50(6):359-61. PubMed ID: 15537723
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960.
    Scotet V; Gillet D; Duguépéroux I; Audrézet MP; Bellis G; Garnier B; Roussey M; Rault G; Parent P; De Braekeleer M; Férec C;
    Hum Genet; 2002 Sep; 111(3):247-54. PubMed ID: 12215837
    [TBL] [Abstract][Full Text] [Related]  

  • 28. CFTR gene analysis in Latin American CF patients: heterogeneous origin and distribution of mutations across the continent.
    Pérez MM; Luna MC; Pivetta OH; Keyeux G
    J Cyst Fibros; 2007 May; 6(3):194-208. PubMed ID: 16963320
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Complete map of cystic fibrosis mutation DF508 frequencies in Western Europe and correlation between mutation frequencies and incidence of disease.
    Lucotte G; Hazout S; De Braekeleer M
    Hum Biol; 1995 Oct; 67(5):797-803. PubMed ID: 8543293
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
    Casals T; Gimenez J; Ramos MD; Nunes V; Estivill X
    Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genotype-phenotype relationship for five CFTR mutations frequently identified in western France.
    Duguépéroux I; De Braekeleer M;
    J Cyst Fibros; 2004 Dec; 3(4):259-63. PubMed ID: 15698945
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular analysis of northwestern Mexican patients with cystic fibrosis: screening of 10 known mutations. Mutations in brief no. 185. Online.
    Flores-Martínez SE; Dean M; Saiki RK; Gallegos-Arreola MP; Morán-Moguel MC; Sánchez-Corona J
    Hum Mutat; 1998; 12(3):217-8. PubMed ID: 10660336
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular genetic analysis of Turkish cystic fibrosis patients.
    Köprübasi FF; Malik N; Bösch-al-Jadooa N; Alkan M; Tanac R; Bühler E
    Ann Genet; 1993; 36(3):144-9. PubMed ID: 8117058
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Cystic fibrosis transmembrane conductance regulator gene mutations and glutathione S-transferase null genotypes in cystic fibrosis patients in Brazil.
    Lima CS; Ortega MM; Marson FA; Zulli R; Ribeiro AF; Bertuzzo CS
    J Bras Pneumol; 2012; 38(1):50-6. PubMed ID: 22407040
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.
    Hamosh A; Trapnell BC; Zeitlin PL; Montrose-Rafizadeh C; Rosenstein BJ; Crystal RG; Cutting GR
    J Clin Invest; 1991 Dec; 88(6):1880-5. PubMed ID: 1721624
    [TBL] [Abstract][Full Text] [Related]  

  • 37. CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from São Paulo State, Brazil.
    Goloni-Bertollo EM; Rossit AR; Junior JB; Fett-Conte AC; Raskin S
    Hum Biol; 2003 Jun; 75(3):393-8. PubMed ID: 14527202
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution.
    Rendine S; Calafell F; Cappello N; Gagliardini R; Caramia G; Rigillo N; Silvetti M; Zanda M; Miano A; Battistini F; Marianelli L; Taccetti G; Diana MC; Romano L; Romano C; Giunta A; Padoan R; Pianaroli A; Raia V; De Ritis G; Battistini A; Grzincich G; Japichino L; Pardo F; Piazza A
    Ann Hum Genet; 1997 Sep; 61(Pt 5):411-24. PubMed ID: 9459003
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutational analysis of 30 Slovenian cystic fibrosis patients compared to known Slovenian and European CF mutation spectra.
    Vouk K; Strmecki L; Liovic M; Kopriva S; Micetic-Turk D; Komel R
    Pflugers Arch; 2000; 439(3 Suppl):R63-5. PubMed ID: 10653145
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population.
    Castaldo G; Polizzi A; Tomaiuolo R; Cazeneuve C; Girodon E; Santostasi T; Salvatore D; Raia V; Rigillo N; Goossens M; Salvatore F
    Ann Hum Genet; 2005 Jan; 69(Pt 1):15-24. PubMed ID: 15638824
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.