BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

340 related articles for article (PubMed ID: 16436643)

  • 21. 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]  

  • 22. 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]  

  • 23. Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I).
    Onay T; Topaloglu O; Zielenski J; Gokgoz N; Kayserili H; Camcioglu Y; Cokugras H; Akcakaya N; Apak M; Tsui LC; Kirdar B
    Hum Genet; 1998 Feb; 102(2):224-30. PubMed ID: 9521595
    [TBL] [Abstract][Full Text] [Related]  

  • 24. XV-2c/KM-19 haplotype analysis of cystic fibrosis mutations in Mexican patients.
    Orozco L; González L; Chávez M; Velázquez R; Lezana JL; Saldaña Y; Villarreal T; Carnevale A
    Am J Med Genet; 2001 Aug; 102(3):277-81. PubMed ID: 11484207
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
    Sharma H; Mavuduru RS; Singh SK; Prasad R
    Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Heterogeneous spectrum of CFTR gene mutations in Korean patients with cystic fibrosis.
    Jung H; Ki CS; Koh WJ; Ahn KM; Lee SI; Kim JH; Ko JS; Seo JK; Cha SI; Lee ES; Kim JW
    Korean J Lab Med; 2011 Jul; 31(3):219-24. PubMed ID: 21779199
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The molecular basis of cystic fibrosis in South Africa.
    Goldman A; Labrum R; Claustres M; Desgeorges M; Guittard C; Wallace A; Ramsay M
    Clin Genet; 2001 Jan; 59(1):37-41. PubMed ID: 11168023
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations.
    Kambouris M; Banjar H; Moggari I; Nazer H; Al-Hamed M; Meyer BF
    Eur J Pediatr; 2000 May; 159(5):303-9. PubMed ID: 10834512
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Complete screening of the CFTR gene in Argentine cystic fibrosis patients.
    Visich A; Zielenski J; Castaños C; Diez G; Grenoville M; Segal E; Barreiro C; Tsui LC; Chertkoff L
    Clin Genet; 2002 Mar; 61(3):207-13. PubMed ID: 12000363
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene mutations in North Egyptian population: implications for the genetic diagnosis in Egypt.
    El-Seedy A; Pasquet MC; Shafiek H; Morsi T; Kitzis A; Ladevèze V
    Cell Mol Biol (Noisy-le-grand); 2016 Nov; 62(13):21-28. PubMed ID: 28040058
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.
    Roqué M; Godoy CP; Castellanos M; Pusiol E; Mayorga LS
    Hum Mutat; 2001 Aug; 18(2):167. PubMed ID: 11462248
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocols.
    Giannattasio S; Bobba A; Jurgelevicius V; Vacca RA; Lattanzio P; Merafina RS; Utkus A; Kucinskas V; Marra E
    Genet Test; 2006; 10(3):169-73. PubMed ID: 17020467
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients.
    Lenarduzzi S; Morgutti M; Crovella S; Coiana A; Rosatelli MC
    Genet Mol Res; 2014 Nov; 13(4):9636-41. PubMed ID: 25501174
    [TBL] [Abstract][Full Text] [Related]  

  • 36. XV-2c/KM19 haplotypes analysis of cystic fibrosis patients from western Mexico.
    Flores-Martínez SE; Martínez JF; Machorro-Lazo MV; García-Zapién AG; Salgado-Goytia L; Cruz-Quevedo EG; Morán-Moguel MC; Sánchez-Corona J
    Acta Physiol Hung; 2008 Sep; 95(3):313-25. PubMed ID: 18788470
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes.
    Hughes D; Wallace A; Taylor J; Tassabehji M; McMahon R; Hill A; Nevin N; Graham C
    Hum Mutat; 1996; 8(3):229-35. PubMed ID: 8889582
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Analysis of the spectra of mutations and polymorphic loci of cystic fibrosis transmembrane conductance regulator in the population of Bashkortostan].
    Korytina GF; Viktorova TV; Baĭkova GV; Khusnutdinova EK
    Genetika; 2002 Sep; 38(9):1270-5. PubMed ID: 12391889
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cystic Fibrosis Gene Mutation Frequency Among a Group of Suspected Children in King Hussein Medical Center.
    Al-Abadi B; Al-Hiary M; Khasawneh R; Al-Momani A; Bani-Salameh A; Al-Saeidat S; Al-Khlaifat A; Aboalsondos O
    Med Arch; 2019 Apr; 73(2):118-120. PubMed ID: 31391700
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.