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 *

108 related articles for article (PubMed ID: 7606851)

  • 1. Mild cystic fibrosis disease in three Mexican delta-F508/G551S compound heterozygous siblings.
    Orozco L; Lezana JL; Villarreal MT; Chávez M; Carnevale A
    Clin Genet; 1995 Feb; 47(2):96-8. PubMed ID: 7606851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of the I507 deletion by site-directed mutagenesis.
    Orozco L; Friedman K; Chávez M; Lezana JL; Villarreal MT; Carnevale A
    Am J Med Genet; 1994 Jun; 51(2):137-9. PubMed ID: 8092189
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.
    Dörk T; Wulbrand U; Richter T; Neumann T; Wolfes H; Wulf B; Maass G; Tümmler B
    Hum Genet; 1991 Aug; 87(4):441-6. PubMed ID: 1715308
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Application in the identification of a cystic fibrosis patient with atypical clinical course.
    Poller W; Faber JP; Scholz S; Olek K; Müller KM
    Klin Wochenschr; 1991 Sep; 69(14):657-63. PubMed ID: 1749205
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A mouse model for the cystic fibrosis delta F508 mutation.
    van Doorninck JH; French PJ; Verbeek E; Peters RH; Morreau H; Bijman J; Scholte BJ
    EMBO J; 1995 Sep; 14(18):4403-11. PubMed ID: 7556083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis.
    Farrell PM; Koscik RE
    Pediatrics; 1996 Apr; 97(4):524-8. PubMed ID: 8632940
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The CFTR 3849+10kbC->T and 2789+5G->A alleles are associated with a mild CF phenotype.
    Duguépéroux I; De Braekeleer M
    Eur Respir J; 2005 Mar; 25(3):468-73. PubMed ID: 15738290
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency of delta F508 in a Mexican sample of cystic fibrosis patients.
    Orozco L; Salcedo M; Lezana JL; Chávez M; Valdez H; Moreno M; Carnevale A
    J Med Genet; 1993 Jun; 30(6):501-2. PubMed ID: 8326494
    [TBL] [Abstract][Full Text] [Related]  

  • 10. beta-adrenergic sweat responses in cystic fibrosis heterozygotes with and without the delta F508 allele.
    Johnson JP; Louie E; Lewiston NJ; Wine JJ
    Pediatr Res; 1991 Jun; 29(6):525-8. PubMed ID: 1650939
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (delta F508).
    Cui KH; Haan EA; Wang LJ; Matthews CD
    BMJ; 1995 Aug; 311(7004):536-40. PubMed ID: 7545043
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].
    Morales-Machin A; Borjas-Fajardo L; Pineda L; González S; Delgado W; Zabala W; Fernández E
    Invest Clin; 2004 Jun; 45(2):121-30. PubMed ID: 15211979
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of the cystic fibrosis delta-F508 mutation at autopsy by site-directed mutagenesis.
    Salcedo M; Chávez M; Ridaura C; Moreno M; Lezana JL; Orozco L
    Am J Med Genet; 1993 May; 46(3):268-70. PubMed ID: 8488869
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).
    Kerem E; Corey M; Kerem BS; Rommens J; Markiewicz D; Levison H; Tsui LC; Durie P
    N Engl J Med; 1990 Nov; 323(22):1517-22. PubMed ID: 2233932
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patients.
    Plieth J; Rininsland F; Schlösser M; Cooper DN; Reiss J
    Hum Genet; 1992 Jan; 88(3):283-7. PubMed ID: 1370807
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation.
    De Braekeleer M; Allard C; Leblanc JP; Simard F; Aubin G
    Hum Genet; 1997 Dec; 101(2):208-11. PubMed ID: 9402971
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype/phenotype association in cystic fibrosis: analyses of the delta F508, R553X, and 3905insT mutations.
    Liechti-Gallati S; Bonsall I; Malik N; Schneider V; Kraemer LG; Ruedeberg A; Moser H; Kraemer R
    Pediatr Res; 1992 Aug; 32(2):175-8. PubMed ID: 1380689
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 6.