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 *

118 related articles for article (PubMed ID: 15880249)

  • 1. Frequency of the deltaF508 mutation in 108 cystic fibrosis patients in Sao Paulo: comparison with reported Brazilian data.
    Okay TS; Oliveira WP; Raiz-Júnior R; Rodrigues JC; Del Negro GM
    Clinics (Sao Paulo); 2005 Apr; 60(2):131-4. PubMed ID: 15880249
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among cystic fibrosis patients from a Brazilian referral center.
    Bieger AM; Marson FA; Bertuzzo CS
    J Pediatr (Rio J); 2012; 88(6):531-4. PubMed ID: 23064458
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of deltaF508, G551D, G542X, and R553X mutations among cystic fibrosis patients in the North of Brazil.
    Araújo FG; Novaes FC; Santos NP; Martins VC; Souza SM; Santos SE; Ribeiro-dos-Santos AK
    Braz J Med Biol Res; 2005 Jan; 38(1):11-5. PubMed ID: 15665983
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A low prevalence of cystic fibrosis in Uruguayans of mainly European descent.
    Cardoso H; Crispino B; Mimbacas A; Cardoso ME
    Genet Mol Res; 2004 Jun; 3(2):258-63. PubMed ID: 15266396
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequency of the cystic fibrosis delta F 508 mutation in a population from São Paulo State, Brazil.
    Martins CS; Ribeiro F; Costa FF
    Braz J Med Biol Res; 1993 Oct; 26(10):1037-40. PubMed ID: 8312835
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cystic fibrosis Δf508 mutation screening in Brazilian women with altered fertility.
    Brunoro GV; Wolfgramm EV; Louro ID; Degasperi II; Busatto VC; Perrone AM; Batitucci MC
    Mol Biol Rep; 2011 Oct; 38(7):4343-6. PubMed ID: 21110105
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes.
    Raskin S; Petzl-Erler ML; Phillips JA; Pereira-Ferrari L; Probst CM; Faucz FR; Sotomaior V; Salzano FM; Culpi L
    Hum Biol; 2007 Feb; 79(1):79-91. PubMed ID: 17985657
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Protein kinase CK2, cystic fibrosis transmembrane conductance regulator, and the deltaF508 mutation: F508 deletion disrupts a kinase-binding site.
    Treharne KJ; Crawford RM; Xu Z; Chen JH; Best OG; Schulte EA; Gruenert DC; Wilson SM; Sheppard DN; Kunzelmann K; Mehta A
    J Biol Chem; 2007 Apr; 282(14):10804-13. PubMed ID: 17289674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Low frequency of the deltaAF508 mutation of the CFTR gene in a highly admixed population in Bahia, Brazil.
    Moura Costa FM; Santana MA; Lemos AC; Galvão-Castro B; Acosta AX
    Hum Biol; 2007 Jun; 79(3):293-7. PubMed ID: 18078202
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular temporal bone pathology: III. Genotyping of the deltaF508 deletion in the DNA of patients with cystic fibrosis.
    Wackym PA; Kerner MM; Grody WW
    Laryngoscope; 1998 Aug; 108(8 Pt 2 Suppl 88):1-3. PubMed ID: 9707259
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study.
    McKone EF; Emerson SS; Edwards KL; Aitken ML
    Lancet; 2003 May; 361(9370):1671-6. PubMed ID: 12767731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CFTR mutations in three Latin American countries.
    Restrepo CM; Pineda L; Rojas-Martínez A; Gutiérrez CA; Morales A; Gómez Y; Villalobos MC; Borjas L; Delgado W; Myers A; Barrera-Saldaña HA
    Am J Med Genet; 2000 Apr; 91(4):277-9. PubMed ID: 10766983
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Towards preimplantation diagnosis of cystic fibrosis using microarrays.
    Salvado CS; Trounson AO; Cram DS
    Reprod Biomed Online; 2004 Jan; 8(1):107-14. PubMed ID: 14759297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ΔF508 mutation screening of healthy individuals from two populations in Espírito Santo State, Brazil.
    Lanes AM; Louro LS; Ventorim DP; Stur E; Garcia FM; Agostini LP; Alves LN; Reis RS; Louro ID; Dettogni RS
    Genet Mol Res; 2016 Dec; 15(4):. PubMed ID: 28002612
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A defective flexible loop contributes to the processing and gating defects of the predominant cystic fibrosis-causing mutation.
    Chen X; Zhu S; Zhenin M; Xu W; Bose SJ; Wong MP; Leung GPH; Senderowitz H; Chen JH
    FASEB J; 2019 Apr; 33(4):5126-5142. PubMed ID: 30668920
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High morbidity and mortality in cystic fibrosis patients compound heterozygous for 3905insT and deltaF508.
    Schibler A; Bolt I; Gallati S; Schöni MH; Kraemer R
    Eur Respir J; 2001 Jun; 17(6):1181-6. PubMed ID: 11491162
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Potentiators (specific therapies for class III and IV mutations) for cystic fibrosis.
    Patel S; Sinha IP; Dwan K; Echevarria C; Schechter M; Southern KW
    Cochrane Database Syst Rev; 2015 Mar; (3):CD009841. PubMed ID: 25811419
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: study of 19 heterozygous and 2 homozygous patients.
    Casals T; Pacheco P; Barreto C; Giménez J; Ramos MD; Pereira S; Pinheiro JA; Cobos N; Curvelo A; Vázquez C; Rocha H; Séculi JL; Pérez E; Dapena J; Carrilho E; Duarte A; Palacio AM; Nunes V; Lavinha J; Estivill X
    Hum Mutat; 1997; 10(5):387-92. PubMed ID: 9375855
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.