BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 11143296)

  • 1. [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]  

  • 2. Cationic trypsinogen mutations and pancreatitis.
    Howes N; Greenhalf W; Stocken DD; Neoptolemos JP
    Gastroenterol Clin North Am; 2004 Dec; 33(4):767-87. PubMed ID: 15528017
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Significance of trypsinogen gene mutations in the etiology of hereditary pancreatitis].
    Sahin-Tóth M; Tóth M
    Orv Hetil; 2001 Mar; 142(12):603-6. PubMed ID: 11324217
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cationic trypsinogen mutations and pancreatitis.
    Howes N; Greenhalf W; Stocken DD; Neoptolemos JP
    Clin Lab Med; 2005 Mar; 25(1):39-59. PubMed ID: 15749231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Hereditary pancreatitis].
    Jørgensen MT; Schaffalitzky de Muckadell OB
    Ugeskr Laeger; 2003 Jan; 165(5):447-51. PubMed ID: 12599840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Hereditary chronic pancreatitis.
    Teich N; Mössner J
    Best Pract Res Clin Gastroenterol; 2008; 22(1):115-30. PubMed ID: 18206817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. [Hereditary pancreatitis is due to a mutation of the cationic trypsinogen gene].
    Niederau C; Lüthen R
    Z Gastroenterol; 1997 May; 35(5):363-5. PubMed ID: 9265397
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Hereditary pancreatitis and secondary screening for early pancreatic cancer.
    Vitone LJ; Greenhalf W; Howes NR; Neoptolemos JP
    Rocz Akad Med Bialymst; 2005; 50():73-84. PubMed ID: 16358943
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. A novel A121T mutation in human cationic trypsinogen associated with hereditary pancreatitis: functional data indicating a loss-of-function mutation influencing the R122 trypsin cleavage site.
    Felderbauer P; Schnekenburger J; Lebert R; Bulut K; Parry M; Meister T; Schick V; Schmitz F; Domschke W; Schmidt WE
    J Med Genet; 2008 Aug; 45(8):507-12. PubMed ID: 18511571
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The course of genetically determined chronic pancreatitis.
    Keim V; Witt H; Bauer N; Bodeker H; Rosendahl J; Teich N; Mossner J
    JOP; 2003 Jul; 4(4):146-54. PubMed ID: 12853682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.