246 related articles for article (PubMed ID: 25546417)
1. Gene conversion between cationic trypsinogen (PRSS1) and the pseudogene trypsinogen 6 (PRSS3P2) in patients with chronic pancreatitis.
Rygiel AM; Beer S; Simon P; Wertheim-Tysarowska K; Oracz G; Kucharzik T; Tysarowski A; Niepokój K; Kierkus J; Jurek M; Gawliński P; Poznański J; Bal J; Lerch MM; Sahin-Tóth M; Weiss FU
Hum Mutat; 2015 Mar; 36(3):350-6. PubMed ID: 25546417
[TBL] [Abstract][Full Text] [Related]
2. Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
Teich N; Nemoda Z; Köhler H; Heinritz W; Mössner J; Keim V; Sahin-Tóth M
Hum Mutat; 2005 Apr; 25(4):343-7. PubMed ID: 15776435
[TBL] [Abstract][Full Text] [Related]
3. Pathogenic cellular role of the p.L104P human cationic trypsinogen variant in chronic pancreatitis.
Balázs A; Hegyi P; Sahin-Tóth M
Am J Physiol Gastrointest Liver Physiol; 2016 Apr; 310(7):G477-86. PubMed ID: 26822915
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [Three cases of hereditary pancreatitis in two households in the same family associated with R122H mutation in cationic trypsinogen gene].
Lee TY; Oh HC; Kim MH; Kwon S; Lee SS; Seo DW; Lee SK
Korean J Gastroenterol; 2007 Jun; 49(6):395-9. PubMed ID: 17641559
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Gene conversion-like missense mutations in the human cationic trypsinogen gene and insights into the molecular evolution of the human trypsinogen family.
Chen JM; Ferec C
Mol Genet Metab; 2000 Nov; 71(3):463-9. PubMed ID: 11073713
[TBL] [Abstract][Full Text] [Related]
9. Functional effects of 13 rare PRSS1 variants presumed to cause chronic pancreatitis.
Schnúr A; Beer S; Witt H; Hegyi P; Sahin-Tóth M
Gut; 2014 Feb; 63(2):337-43. PubMed ID: 23455445
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Intragenic duplication: a novel mutational mechanism in hereditary pancreatitis.
Joergensen MT; Geisz A; Brusgaard K; Schaffalitzky de Muckadell OB; Hegyi P; Gerdes AM; Sahin-Tóth M
Pancreas; 2011 May; 40(4):540-6. PubMed ID: 21499207
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Human cationic trypsinogen (PRSS1) variants and chronic pancreatitis.
Németh BC; Sahin-Tóth M
Am J Physiol Gastrointest Liver Physiol; 2014 Mar; 306(6):G466-73. PubMed ID: 24458023
[TBL] [Abstract][Full Text] [Related]
14. Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis.
Teich N; Rosendahl J; Tóth M; Mössner J; Sahin-Tóth M
Hum Mutat; 2006 Aug; 27(8):721-30. PubMed ID: 16791840
[TBL] [Abstract][Full Text] [Related]
15. Uncertainties in the classification of human cationic trypsinogen (PRSS1) variants as hereditary pancreatitis-associated mutations.
Szmola R; Sahin-Tóth M
J Med Genet; 2010 May; 47(5):348-50. PubMed ID: 20452997
[TBL] [Abstract][Full Text] [Related]
16. The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis.
Masson E; Ewers M; Paliwal S; Kume K; Scotet V; Cooper DN; Rebours V; Buscail L; Rouault K; ; Abrantes A; Aguilera Munoz L; Albouys J; Alric L; Amiot X; Archambeaud I; Audiau S; Bastide L; Baudon J; Bellaiche G; Bellon S; Bertrand V; Bideau K; Billiemaz K; Billioud C; Bonnefoy S; Borderon C; Bournet B; Breton E; Brugel M; Buscail L; Cadiot G; Camus M; Carpentier-Pourquier M; Chamouard P; Chaput U; Chen JM; Cholet F; Ciocan DM; Clavel C; Coffin B; Coimet-Berger L; Cosconea S; Creveaux I; Culetto A; Daboussi O; De Mestier L; Degand T; D'engremont C; Denis B; Dermine S; Desgrippes ; Drouet D'Aubigny A; Enaud R; Fabre A; Férec C; Gargot D; Gelsi E; Gentilcore E; Gincul R; Ginglinger-Favre E; Giovannini M; Gomercic C; Gondran H; Grainville T; Grandval P; Grasset D; Grimaldi S; Grimbert S; Hagege H; Heissat S; Hentic O; Herber-Mayne A; Hervouet M; Hoibian S; Jacques J; Jais B; Kaassis M; Koch S; Lacaze E; Lacroute J; Lamireau T; Laurent L; Le Guillou X; Le Rhun M; Leblanc S; Levy P; Lievre A; Lorenzo D; Maire F; Marcel K; Masson E; Mauillon J; Morgant S; Moussata D; Muller N; Nambot S; Napoleon B; Olivier A; Pagenault M; Pelletier AL; Pennec O; Pinard F; Pioche M; Prost B; Queneherve L; Rebours V; Reboux N; Rekik S; Riachi G; Rohmer B; Roquelaure B; Rosa Hezode I; Rostain F; Saurin JC; Servais L; Stan-Iuga R; Subtil C; Tanneche J; Texier C; Thomassin L; Tougeron D; Vuitton L; Wallenhorst T; Wangerme M; Zanaldi H; Zerbib F; Bhaskar S; Kikuta K; Rao GV; Hamada S; Reddy DN; Masamune A; Chandak GR; Witt H; Férec C; Chen JM
Pancreatology; 2023 Jan; 23(1):48-56. PubMed ID: 36517351
[TBL] [Abstract][Full Text] [Related]
17. A 93 year old man with the PRSS1 R122H mutation, low SPINK1 expression, and no pancreatitis: insights into phenotypic non-penetrance.
Khalid A; Finkelstein S; Thompson B; Kelly L; Hanck C; Godfrey TE; Whitcomb DC
Gut; 2006 May; 55(5):728-31. PubMed ID: 16354799
[TBL] [Abstract][Full Text] [Related]
18. Multisite mutations of the PRSS1 gene in a Chinese patient with chronic pancreatitis.
Liu QC; Gao F; Cheng ZJ; Ou QS
Hepatobiliary Pancreat Dis Int; 2008 Jun; 7(3):331-2. PubMed ID: 18522894
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mouse model of PRSS1 p.R122H-related hereditary pancreatitis highlights context-dependent effect of autolysis-site mutation.
Jancsó Z; Morales Granda NC; Demcsák A; Sahin-Tóth M
Pancreatology; 2023 Mar; 23(2):131-142. PubMed ID: 36797199
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
