150 related articles for article (PubMed ID: 26358851)
1. Contribution of M470V variant to cystic fibrosis: First study in CF and normal Tunisian population.
Nefzi M; Hadj Fredj S; Tebib N; Barsaoui S; Boussetta K; Siala H; Messaoud T
Pathol Biol (Paris); 2015 Sep; 63(4-5):169-74. PubMed ID: 26358851
[TBL] [Abstract][Full Text] [Related]
2. Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis.
Nefzi M; Fredj SH; Dabboubi R; Hamouda S; Tebib N; Boussetta K; Messaoud T
Ann Biol Clin (Paris); 2021 Feb; 79(1):63-68. PubMed ID: 33589413
[TBL] [Abstract][Full Text] [Related]
3. Association of IVS6A GATT polymorphism of CFTR gene with cystic fibrosis: first study in CF and normal Tunisian population.
Chaima S; Sondess HF; Khedija B; Ahmed M; Taieb M
Ann Biol Clin (Paris); 2020 Jun; 78(3):314-318. PubMed ID: 32540817
[TBL] [Abstract][Full Text] [Related]
4. Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study.
Wahabi I; Hadj Fredj S; Nefzi M; Dabboubi R; Siala H; Khalsi F; Bousetta K; Messaoud T
Allergol Immunopathol (Madr); 2019; 47(2):159-165. PubMed ID: 30268379
[TBL] [Abstract][Full Text] [Related]
5. Highly preferential association of NonF508del CF mutations with the M470 allele.
Ciminelli BM; Bonizzato A; Bombieri C; Pompei F; Gabaldo M; Ciccacci C; Begnini A; Holubova A; Zorzi P; Piskackova T; Macek M; Castellani C; Modiano G; Pignatti PF
J Cyst Fibros; 2007 Jan; 6(1):15-22. PubMed ID: 16784904
[TBL] [Abstract][Full Text] [Related]
6. Comparative analysis of common CFTR polymorphisms poly-T, TG-repeats and M470V in a healthy Chinese population.
Huang Q; Ding W; Wei MX
World J Gastroenterol; 2008 Mar; 14(12):1925-30. PubMed ID: 18350634
[TBL] [Abstract][Full Text] [Related]
7. Analysis of common CFTR polymorphisms 5T, M470V and R75Q in healthy Serbian population.
Nikolic A; Divac A; Stankovic M; Dinic J; Tomic B; Ljujic M
Genetika; 2006 Jul; 42(7):996-8. PubMed ID: 16915933
[TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens.
Radpour R; Gilani MA; Gourabi H; Dizaj AV; Mollamohamadi S
Mol Hum Reprod; 2006 Jul; 12(7):469-73. PubMed ID: 16714368
[TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis transmembrane regulator haplotypes in households of patients with cystic fibrosis.
Furgeri DT; Marson FAL; Correia CAA; Ribeiro JD; Bertuzzo CS
Gene; 2018 Jan; 641():137-143. PubMed ID: 29054758
[TBL] [Abstract][Full Text] [Related]
10. Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.
Petrova NV; Kashirskaya NY; Saydaeva DK; Polyakov AV; Adyan TA; Simonova OI; Gorinova YV; Kondratyeva EI; Sherman VD; Novoselova OG; Vasilyeva TA; Marakhonov AV; Macek M; Ginter EK; Zinchenko RA
BMC Med Genet; 2019 Mar; 20(1):44. PubMed ID: 30898088
[TBL] [Abstract][Full Text] [Related]
11. Association of MP6d9 Polymorphism with Clinical Variability in Cystic Fibrosis Patients.
Sahli C; Hadj-Fredj S; Dabboubi R; Bousseta K; Mehrzi A; Messaoud T
Clin Lab; 2016 Nov; 62(11):2139-2143. PubMed ID: 28164663
[TBL] [Abstract][Full Text] [Related]
12. Identification of a cystic fibrosis mutation W19X in Tunisia.
Boudaya M; Fredj SH; Siala H; Bibi A; Messaoud T
Ann Biol Clin (Paris); 2013; 71(2):223-6. PubMed ID: 23587593
[TBL] [Abstract][Full Text] [Related]
13. CFTR allelic heterogeneity in Mexican patients with cystic fibrosis: implications for molecular screening.
Chávez-Saldaña M; Yokoyama E; Lezana JL; Carnevale A; Macías M; Vigueras RM; López M; Orozco L
Rev Invest Clin; 2010; 62(6):546-52. PubMed ID: 21416780
[TBL] [Abstract][Full Text] [Related]
14. Lung disease associated with the IVS8 5T allele of the CFTR gene.
Noone PG; Pue CA; Zhou Z; Friedman KJ; Wakeling EL; Ganeshananthan M; Simon RH; Silverman LM; Knowles MR
Am J Respir Crit Care Med; 2000 Nov; 162(5):1919-24. PubMed ID: 11069835
[TBL] [Abstract][Full Text] [Related]
15. Cystic fibrosis transmembrane conductance regulator mutation spectrum in patients with cystic fibrosis in Tunisia.
Fredj SH; Messaoud T; Templin C; des Georges M; Fattoum S; Claustres M
Genet Test Mol Biomarkers; 2009 Oct; 13(5):577-81. PubMed ID: 19715466
[TBL] [Abstract][Full Text] [Related]
16. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
[TBL] [Abstract][Full Text] [Related]
17. Analysis of CFTR gene mutations and cystic fibrosis incidence in the Ecuadorian population.
Valle EP; Burgos RI; Valle JR; Egas Béjar D; Ruiz-Cabezas JC
Invest Clin; 2007 Mar; 48(1):91-8. PubMed ID: 17432547
[TBL] [Abstract][Full Text] [Related]
18. Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations.
Pompei F; Ciminelli BM; Bombieri C; Ciccacci C; Koudova M; Giorgi S; Belpinati F; Begnini A; Cerny M; Des Georges M; Claustres M; Ferec C; Macek M; Modiano G; Pignatti PF
Eur J Hum Genet; 2006 Jan; 14(1):85-93. PubMed ID: 16251901
[TBL] [Abstract][Full Text] [Related]
19. Genotype patterns for mutations of the cystic fibrosis transmembrane conductance regulator gene: a retrospective descriptive study from Saudi Arabia.
Banjar HH; Tuleimat L; El Seoudi AAA; Mogarri I; Alhaider S; Nizami IY; AlMaghamsi T; Alkaf SA; Moghrabi N
Ann Saudi Med; 2020; 40(1):15-24. PubMed ID: 32026723
[TBL] [Abstract][Full Text] [Related]
20. Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation.
de Souza DA; Faucz FR; de Alexandre RB; Santana MA; de Souza EL; Reis FJ; Pereira-Ferrari L; Sotomaior VS; Culpi L; Phillips JA; Raskin S
Genetica; 2017 Feb; 145(1):19-25. PubMed ID: 28160168
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]