These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

299 related articles for article (PubMed ID: 12508340)

  • 21. 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]  

  • 22. 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]  

  • 23. Hereditary pancreatitis caused by a novel PRSS1 mutation (Arg-122 --> Cys) that alters autoactivation and autodegradation of cationic trypsinogen.
    Simon P; Weiss FU; Sahin-Toth M; Parry M; Nayler O; Lenfers B; Schnekenburger J; Mayerle J; Domschke W; Lerch MM
    J Biol Chem; 2002 Feb; 277(7):5404-10. PubMed ID: 11719509
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A mouse model of hereditary pancreatitis generated by transgenic expression of R122H trypsinogen.
    Archer H; Jura N; Keller J; Jacobson M; Bar-Sagi D
    Gastroenterology; 2006 Dec; 131(6):1844-55. PubMed ID: 17087933
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Motion--genetic testing is useful in the diagnosis of nonhereditary pancreatic conditions: arguments for the motion.
    Whitcomb DC
    Can J Gastroenterol; 2003 Jan; 17(1):47-52. PubMed ID: 12560855
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A new polymorphism for the RI22H mutation in hereditary pancreatitis.
    Howes N; Greenhalf W; Rutherford S; O'Donnell M; Mountford R; Ellis I; Whitcomb D; Imrie C; Drumm B; Neoptolemos JP
    Gut; 2001 Feb; 48(2):247-50. PubMed ID: 11156648
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations.
    Chen JM; Montier T; Férec C
    Hum Genet; 2001 Sep; 109(3):245-52. PubMed ID: 11702203
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Role of genetic disorders in acute recurrent pancreatitis.
    Keim V
    World J Gastroenterol; 2008 Feb; 14(7):1011-5. PubMed ID: 18286680
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Hereditary pancreatitis caused by mutation-induced misfolding of human cationic trypsinogen: a novel disease mechanism.
    Kereszturi E; Szmola R; Kukor Z; Simon P; Weiss FU; Lerch MM; Sahin-Tóth M
    Hum Mutat; 2009 Apr; 30(4):575-82. PubMed ID: 19191323
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography.
    Le Maréchal C; Chen JM; Quéré I; Raguénès O; Férec C; Auroux J
    BMC Genet; 2001; 2():19. PubMed ID: 11734061
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Transgenic Expression of PRSS1
    Huang H; Swidnicka-Siergiejko AK; Daniluk J; Gaiser S; Yao Y; Peng L; Zhang Y; Liu Y; Dong M; Zhan X; Wang H; Bi Y; Li Z; Ji B; Logsdon CD
    Gastroenterology; 2020 Mar; 158(4):1072-1082.e7. PubMed ID: 31419436
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Mutations of SPINK1 and PRSS1 gene in Korean patients with chronic pancreatitis].
    Lee KH; Yoon WJ; Ryu JK; Kim YT; Yoon YB; Kim CY
    Korean J Gastroenterol; 2004 Aug; 44(2):93-8. PubMed ID: 15329520
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Trypsinogen mutations in pancreatic disorders.
    Vitone LJ; Greenhalf W; Howes NR; Raraty MG; Neoptolemos JP
    Endocrinol Metab Clin North Am; 2006 Jun; 35(2):271-87, viii. PubMed ID: 16632092
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Increased activation of hereditary pancreatitis-associated human cationic trypsinogen mutants in presence of chymotrypsin C.
    Szabó A; Sahin-Tóth M
    J Biol Chem; 2012 Jun; 287(24):20701-10. PubMed ID: 22539344
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Chronic pancreatitis--pancreas cancer: influence of genetic factors].
    Keim V
    Praxis (Bern 1994); 2005 May; 94(20):811-7. PubMed ID: 15957615
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Molecular basis of hereditary pancreatitis.
    Chen JM; Ferec C
    Eur J Hum Genet; 2000 Jul; 8(7):473-9. PubMed ID: 10909845
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. [Hereditary pancreatitis caused by a new mutation in the trypsinogen gene. Report of a family].
    Carbonell P; Glover G; Fernández JA; Ramírez M; Marín C; Castellanos G; Parrilla P
    Cir Esp; 2006 Apr; 79(4):252-4. PubMed ID: 16753108
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Gene mutations in children with chronic pancreatitis.
    Witt H
    Pancreatology; 2001; 1(5):432-8. PubMed ID: 12120220
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.