BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 19812525)

  • 1. Independent contribution of common CFTR variants to chronic pancreatitis.
    de Cid R; Ramos MD; Aparisi L; García C; Mora J; Estivill X; Farré A; Casals T
    Pancreas; 2010 Mar; 39(2):209-15. PubMed ID: 19812525
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.
    Weiss FU; Simon P; Bogdanova N; Mayerle J; Dworniczak B; Horst J; Lerch MM
    Gut; 2005 Oct; 54(10):1456-60. PubMed ID: 15987793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis.
    Tzetis M; Kaliakatsos M; Fotoulaki M; Papatheodorou A; Doudounakis S; Tsezou A; Makrythanasis P; Kanavakis E; Nousia-Arvanitakis S
    Clin Genet; 2007 May; 71(5):451-7. PubMed ID: 17489851
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR alleles.
    Steiner B; Truninger K; Sanz J; Schaller A; Gallati S
    Hum Mutat; 2004 Aug; 24(2):120-9. PubMed ID: 15241793
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis.
    Gallegos-Orozco JF; E Yurk C; Wang N; Rakela J; Charlton MR; Cutting GR; Balan V
    Am J Gastroenterol; 2005 Apr; 100(4):874-8. PubMed ID: 15784035
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations.
    Midha S; Khajuria R; Shastri S; Kabra M; Garg PK
    Gut; 2010 Jun; 59(6):800-7. PubMed ID: 20551465
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers.
    Cohn JA; Neoptolemos JP; Feng J; Yan J; Jiang Z; Greenhalf W; McFaul C; Mountford R; Sommer SS
    Hum Mutat; 2005 Oct; 26(4):303-7. PubMed ID: 16134171
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Frequency of CFTR gene mutations in idiopathic pancreatitis].
    Maire F; Bienvenu T; Ngukam A; Hammel P; Ruszniewski P; Lévy P
    Gastroenterol Clin Biol; 2003 Apr; 27(4):398-402. PubMed ID: 12759680
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis.
    Castellani C; Gomez Lira M; Frulloni L; Delmarco A; Marzari M; Bonizzato A; Cavallini G; Pignatti P; Mastella G
    Hum Mutat; 2001 Aug; 18(2):166. PubMed ID: 11462247
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M
    Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in Brazilian patients.
    Bernardino AL; Guarita DR; Mott CB; Pedroso MR; Machado MC; Laudanna AA; Tani CM; Almeida FL; Zatz M
    JOP; 2003 Sep; 4(5):169-77. PubMed ID: 14526128
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry.
    Alonso MJ; Heine-Suñer D; Calvo M; Rosell J; Giménez J; Ramos MD; Telleria JJ; Palacio A; Estivill X; Casals T
    Ann Hum Genet; 2007 Mar; 71(Pt 2):194-201. PubMed ID: 17331079
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of CFTR, SPINK1, PRSS1 and AAT mutations in children with acute or chronic pancreatitis.
    Sobczyńska-Tomaszewska A; Bak D; Oralewska B; Oracz G; Norek A; Czerska K; Mazurczak T; Teisseyre M; Socha J; Zagulski M; Bal J
    J Pediatr Gastroenterol Nutr; 2006 Sep; 43(3):299-306. PubMed ID: 16954950
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of SPINK1 gene mutation and CFTR gene polymorphisms in patients with pancreas divisum presenting with idiopathic pancreatitis.
    Garg PK; Khajuria R; Kabra M; Shastri SS
    J Clin Gastroenterol; 2009 Oct; 43(9):848-52. PubMed ID: 19593166
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CFTR, SPINK1, CTRC and PRSS1 variants in chronic pancreatitis: is the role of mutated CFTR overestimated?
    Rosendahl J; Landt O; Bernadova J; Kovacs P; Teich N; Bödeker H; Keim V; Ruffert C; Mössner J; Kage A; Stumvoll M; Groneberg D; Krüger R; Luck W; Treiber M; Becker M; Witt H
    Gut; 2013 Apr; 62(4):582-92. PubMed ID: 22427236
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K; Weren M; Proesmans M; Kerem E
    Pediatrics; 2005 Apr; 115(4):e463-9. PubMed ID: 15772171
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens.
    Steiner B; Rosendahl J; Witt H; Teich N; Keim V; Schulz HU; Pfützer R; Löhr M; Gress TM; Nickel R; Landt O; Koudova M; Macek M; Farre A; Casals T; Desax MC; Gallati S; Gomez-Lira M; Audrezet MP; Férec C; des Georges M; Claustres M; Truninger K
    Hum Mutat; 2011 Aug; 32(8):912-20. PubMed ID: 21520337
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Increased frequency of CFTR gene mutations in sarcoidosis: a case/control association study.
    Bombieri C; Luisetti M; Belpinati F; Zuliani E; Beretta A; Baccheschi J; Casali L; Pignatti PF
    Eur J Hum Genet; 2000 Sep; 8(9):717-20. PubMed ID: 10980579
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterisation of mutations and genotype-phenotype correlation in cystic fibrosis: experience from India.
    Shastri SS; Kabra M; Kabra SK; Pandey RM; Menon PS
    J Cyst Fibros; 2008 Mar; 7(2):110-5. PubMed ID: 17716958
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.