BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 9853929)

  • 1. Identification of a hereditary pancreatitis mutation in four West Virginia families.
    Elitsur Y; Chertow BC; Jewell RD; Finver SN; Primerano DA
    Pediatr Res; 1998 Dec; 44(6):927-30. PubMed ID: 9853929
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
    Férec C; Raguénès O; Salomon R; Roche C; Bernard JP; Guillot M; Quéré I; Faure C; Mercier B; Audrézet MP; Guillausseau PJ; Dupont C; Munnich A; Bignon JD; Le Bodic L
    J Med Genet; 1999 Mar; 36(3):228-32. PubMed ID: 10204851
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterogeneity in hereditary pancreatitis.
    Dasouki MJ; Cogan J; Summar ML; Neblitt W; Foroud T; Koller D; Phillips JA
    Am J Med Genet; 1998 Apr; 77(1):47-53. PubMed ID: 9557894
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening for human cationic trypsinogen (PRSS1) and trypsinogen inhibitor gene (SPINK1) mutations in a Finnish family with hereditary pancreatitis.
    Räty S; Piironen A; Babu M; Pelli H; Sand J; Uotila S; Nordback I; Herzig KH
    Scand J Gastroenterol; 2007 Aug; 42(8):1000-5. PubMed ID: 17613931
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis.
    Creighton JE; Lyall R; Wilson DI; Curtis A; Charnley RM
    Br J Surg; 2000 Feb; 87(2):170-5. PubMed ID: 10671922
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
    Teich N; Bauer N; Mössner J; Keim V
    Am J Gastroenterol; 2002 Feb; 97(2):341-6. PubMed ID: 11866271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
    Whitcomb DC; Gorry MC; Preston RA; Furey W; Sossenheimer MJ; Ulrich CD; Martin SP; Gates LK; Amann ST; Toskes PP; Liddle R; McGrath K; Uomo G; Post JC; Ehrlich GD
    Nat Genet; 1996 Oct; 14(2):141-5. PubMed ID: 8841182
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence that hereditary pancreatitis is genetically heterogeneous disorder.
    Ravnik-Glavac M; Dean M; di Sant'Agnese P; Chernick M; Kozelj M; Krizman I; Glavac D
    Pflugers Arch; 2000; 439(3 Suppl):R50-2. PubMed ID: 10653140
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG).
    Sossenheimer MJ; Aston CE; Preston RA; Gates LK; Ulrich CD; Martin SP; Zhang Y; Gorry MC; Ehrlich GD; Whitcomb DC
    Am J Gastroenterol; 1997 Jul; 92(7):1113-6. PubMed ID: 9219780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Implications of molecular diagnostic testing in families with hereditary pancreatitis.
    Pandya A; Xia XJ; Blanton SH; Landa B; Markello T; Nance WE
    Genet Test; 1997-1998; 1(3):207-11. PubMed ID: 10464647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [From gene to disease; hereditary pancreatitis].
    Drenth JP; Jansen JB
    Ned Tijdschr Geneeskd; 2000 Nov; 144(48):2301-2. PubMed ID: 11143296
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel mutation and polymorphism of PRSS1 gene in the Chinese patients with hereditary pancreatitis and chronic pancreatitis.
    Liu QC; Gao F; Ou QS; Zhuang ZH; Lin SR; Yang B; Cheng ZJ
    Chin Med J (Engl); 2008 Jan; 121(2):108-11. PubMed ID: 18272034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The variable phenotype of the p.A16V mutation of cationic trypsinogen (PRSS1) in pancreatitis families.
    Grocock CJ; Rebours V; Delhaye MN; Andrén-Sandberg A; Weiss FU; Mountford R; Harcus MJ; Niemczyck E; Vitone LJ; Dodd S; Jørgensen MT; Ammann RW; Schaffalitzky de Muckadell O; Butler JV; Burgess P; Kerr B; Charnley R; Sutton R; Raraty MG; Devière J; Whitcomb DC; Neoptolemos JP; Lévy P; Lerch MM; Greenhalf W;
    Gut; 2010 Mar; 59(3):357-63. PubMed ID: 19951905
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary pancreatitis caused by triplication of the trypsinogen locus.
    Le Maréchal C; Masson E; Chen JM; Morel F; Ruszniewski P; Levy P; Férec C
    Nat Genet; 2006 Dec; 38(12):1372-4. PubMed ID: 17072318
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations of the cationic trypsinogen in hereditary pancreatitis.
    Teich N; Mössner J; Keim V
    Hum Mutat; 1998; 12(1):39-43. PubMed ID: 9633818
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern Germany.
    Weiss FU; Zenker M; Ekici AB; Simon P; Mayerle J; Lerch MM
    Am J Gastroenterol; 2008 Oct; 103(10):2585-8. PubMed ID: 18702646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
    Teich N; Le Maréchal C; Kukor Z; Caca K; Witzigmann H; Chen JM; Tóth M; Mössner J; Keim V; Férec C; Sahin-Tóth M
    Hum Mutat; 2004 Jan; 23(1):22-31. PubMed ID: 14695529
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary pancreatitis and mutations of the cationic trypsinogen gene.
    O'Reilly DA; Kingsnorth AN
    Br J Surg; 2000 Jun; 87(6):708-17. PubMed ID: 10928807
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary pancreatitis in North America: the Pittsburgh-Midwest Multi-Center Pancreatic Study Group Study.
    Applebaum-Shapiro SE; Finch R; Pfützer RH; Hepp LA; Gates L; Amann S; Martin S; Ulrich CD; Whitcomb DC
    Pancreatology; 2001; 1(5):439-43. PubMed ID: 12120221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary pancreatitis: clinical features and inheritance characteristics of the R122C mutation in the cationic trypsinogen gene (PRSS1) in six Spanish families.
    de las Heras-Castaño G; Castro-Senosiaín B; Fontalba A; López-Hoyos M; Sánchez-Juán P
    JOP; 2009 May; 10(3):249-55. PubMed ID: 19454815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.