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 *

110 related articles for article (PubMed ID: 8565216)

  • 21. Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene.
    Greil I; Wagner K; Eber E; Zach M; Rosenkranz W
    Wien Klin Wochenschr; 1995; 107(15):464-9. PubMed ID: 7545856
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [A molecular study of the delta-F508 mutation and genetic analysis of a sample of cystic fibrosis patients].
    Orozco L; Lezana JL; Chávez M; Valdez H; Moreno M; Carnevale A
    Bol Med Hosp Infant Mex; 1993 Jul; 50(7):457-62. PubMed ID: 7689846
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
    French PJ; van Doorninck JH; Peters RH; Verbeek E; Ameen NA; Marino CR; de Jonge HR; Bijman J; Scholte BJ
    J Clin Invest; 1996 Sep; 98(6):1304-12. PubMed ID: 8823295
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The cystic fibrosis delta F508 gene mutation and cancer.
    Padua RA; Warren N; Grimshaw D; Smith M; Lewis C; Whittaker J; Laidler P; Wright P; Douglas-Jones A; Fenaux P; Sharma A; Horgan K; West R
    Hum Mutat; 1997; 10(1):45-8. PubMed ID: 9222759
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosis.
    Gasparini P; Arbustini E; Restagno G; Zelante L; Stanziale P; Gatta L; Sbaiz L; Sedita AM; Banchieri N; Sapone L; Fiorucci GC; Brinson E; Shulse E; Rappaport E; Fortina P
    J Med Screen; 1999; 6(2):67-9. PubMed ID: 10444722
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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]  

  • 27. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations].
    Gimbovskaia SD; Kalinin VN; Ivashchenko TE; Baranov VS
    Genetika; 1994 Dec; 30(12):1616-20. PubMed ID: 7534245
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neonatal screening for the cystic fibrosis main mutation delta F508 in Estonia.
    Klaassen T; Teder M; Viikmaa M; Metspalu A
    J Med Screen; 1998; 5(1):16-9. PubMed ID: 9575453
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.
    Morral N; Nunes V; Casals T; Chillón M; Giménez J; Bertranpetit J; Estivill X
    Hum Mol Genet; 1993 Jul; 2(7):1015-22. PubMed ID: 7689896
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prevalence of delta F508 cystic fibrosis carriers in The Netherlands: logistic regression on sex, age, region of residence and number of offspring.
    de Vries HG; Collée JM; de Walle HE; van Veldhuizen MH; Smit Sibinga CT; Scheffer H; ten Kate LP
    Hum Genet; 1997 Jan; 99(1):74-9. PubMed ID: 9003498
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cystic fibrosis patients with mutation 1949del84 in exon 13 of the CFTR gene have a similar clinical severity as delta F508 homozygotes.
    Nunes V; Casals T; Gaona A; Antiñolo G; Ferrer-Calvete J; Pérez-Frias J; Tardío E; Molano J; Estivill X
    Hum Mutat; 1992; 1(5):375-9. PubMed ID: 1284539
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The incidence of different cystic fibrosis mutations in the Scottish population: effects on prenatal diagnosis and genetic counselling.
    Shrimpton AE; McIntosh I; Brock DJ
    J Med Genet; 1991 May; 28(5):317-21. PubMed ID: 1713973
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Phenotype and genotype of two Taiwanese cystic fibrosis siblings and a survey of delta F508 in East Asians.
    Lin CJ; Chang SP; Ke YY; Chiu HY; Tsao LY; Chen M
    Pediatr Neonatol; 2008 Dec; 49(6):240-4. PubMed ID: 19166122
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Delta F508 mutation of cystic fibrosis gene is not found in chronic bronchitis with severe obstruction in Japan.
    Akai S; Okayama H; Shimura S; Tanno Y; Sasaki H; Takishima T
    Am Rev Respir Dis; 1992 Sep; 146(3):781-3. PubMed ID: 1519863
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Mutation detection by mismatch binding protein, MutS, in amplified DNA: application to the cystic fibrosis gene.
    Lishanski A; Ostrander EA; Rine J
    Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2674-8. PubMed ID: 7511817
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center.
    Traystman MD; Schulte N; Colombo JL; Sammut PH; Reilly P; Patel C; Acquazzino D; Simanek B; Anderson R; Kimberling WJ
    Hum Mutat; 1993; 2(1):7-15. PubMed ID: 7682884
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic analysis of cystic fibrosis in Pakistan: a preliminary report.
    Bhutta ZA; Moattar T; Shah U
    J Pak Med Assoc; 2000 Jul; 50(7):217-9. PubMed ID: 10992696
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A single-tube multiplex system for the simultaneous detection of 10 common cystic fibrosis mutations.
    Axton RA; Brock DJ
    Hum Mutat; 1995; 5(3):260-2. PubMed ID: 7599637
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein.
    Brown CR; Hong-Brown LQ; Biwersi J; Verkman AS; Welch WJ
    Cell Stress Chaperones; 1996 Jun; 1(2):117-25. PubMed ID: 9222597
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.