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Similar articles for PubMed (Select 14695529)

1.

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.

PMID:
14695529
2.

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 15;277(7):5404-10. Epub 2001 Nov 21.

3.

Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis.

Chen JM, Piepoli Bis A, Le Bodic L, Ruszniewski P, Robaszkiewicz M, Deprez PH, Raguenes O, Quere I, Andriulli A, Ferec C.

Clin Genet. 2001 Mar;59(3):189-93.

PMID:
11260229
4.

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. doi: 10.1136/jmg.2007.056481. Epub 2008 May 29.

PMID:
18511571
5.

Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.

Teich N, Ockenga J, Hoffmeister A, Manns M, Mössner J, Keim V.

Gastroenterology. 2000 Aug;119(2):461-5.

PMID:
10930381
6.
7.

[Significance of trypsinogen gene mutations in the etiology of hereditary pancreatitis].

Sahin-Tóth M, Tóth M.

Orv Hetil. 2001 Mar 25;142(12):603-6. Hungarian.

PMID:
11324217
8.

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.

9.
10.

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.

PMID:
17613931
11.

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. doi: 10.1002/humu.20853.

12.
13.

Presence of cathepsin B in the human pancreatic secretory pathway and its role in trypsinogen activation during hereditary pancreatitis.

Kukor Z, Mayerle J, Krüger B, Tóth M, Steed PM, Halangk W, Lerch MM, Sahin-Tóth M.

J Biol Chem. 2002 Jun 14;277(24):21389-96. Epub 2002 Apr 3.

14.

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.

PMID:
11866271
15.

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.

16.

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 8;287(24):20701-10. doi: 10.1074/jbc.M112.360065. Epub 2012 Apr 26.

17.

A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis.

Witt H, Sahin-Tóth M, Landt O, Chen JM, Kähne T, Drenth JP, Kukor Z, Szepessy E, Halangk W, Dahm S, Rohde K, Schulz HU, Le Maréchal C, Akar N, Ammann RW, Truninger K, Bargetzi M, Bhatia E, Castellani C, Cavestro GM, Cerny M, Destro-Bisol G, Spedini G, Eiberg H, Jansen JB, Koudova M, Rausova E, Macek M Jr, Malats N, Real FX, Menzel HJ, Moral P, Galavotti R, Pignatti PF, Rickards O, Spicak J, Zarnescu NO, Böck W, Gress TM, Friess H, Ockenga J, Schmidt H, Pfützer R, Löhr M, Simon P, Weiss FU, Lerch MM, Teich N, Keim V, Berg T, Wiedenmann B, Luck W, Groneberg DA, Becker M, Keil T, Kage A, Bernardova J, Braun M, Güldner C, Halangk J, Rosendahl J, Witt U, Treiber M, Nickel R, Férec C.

Nat Genet. 2006 Jun;38(6):668-73. Epub 2006 May 14.

19.
20.

Hereditary chronic pancreatitis.

Teich N, Mössner J.

Best Pract Res Clin Gastroenterol. 2008;22(1):115-30. doi: 10.1016/j.bpg.2007.10.019. Review.

PMID:
18206817
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