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Items: 1 to 20 of 210

1.

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.

2.

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
3.

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 20;121(2):108-11.

PMID:
18272034
4.

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; European Registry of Hereditary Pancreatitis and Pancreatic Cancer.

Gut. 2010 Mar;59(3):357-63. doi: 10.1136/gut.2009.186817. Epub 2009 Dec 1.

PMID:
19951905
5.

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
6.
7.

Hereditary pancreatitis: clinical characteristics and diagnostic criteria in Japan.

Otsuki M, Nishimori I, Hayakawa T, Hirota M, Ogawa M, Shimosegawa T; Research Committee on Intractable Disease of the Pancreas.

Pancreas. 2004 Mar;28(2):200-6.

PMID:
15028953
8.

Trypsinogen gene mutations in patients with chronic or recurrent acute pancreatitis.

Truninger K, Köck J, Wirth HP, Muellhaupt B, Arnold C, von Weizsäcker F, Seifert B, Ammann RW, Blum HE.

Pancreas. 2001 Jan;22(1):18-23.

9.

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.

11.

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.

PMID:
10653140
12.

Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene.

Keim V, Bauer N, Teich N, Simon P, Lerch MM, Mössner J.

Am J Med. 2001 Dec 1;111(8):622-6.

PMID:
11755505
13.

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
14.

Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis.

Nishimori I, Kamakura M, Fujikawa-Adachi K, Morita M, Onishi S, Yokoyama K, Makino I, Ishida H, Yamamoto M, Watanabe S, Ogawa M.

Gut. 1999 Feb;44(2):259-63.

15.

Molecular basis of hereditary pancreatitis.

Chen JM, Ferec C.

Eur J Hum Genet. 2000 Jul;8(7):473-9. Review.

16.

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.

PMID:
10671922
18.

Clinical and genetic characteristics of hereditary pancreatitis in Europe.

Howes N, Lerch MM, Greenhalf W, Stocken DD, Ellis I, Simon P, Truninger K, Ammann R, Cavallini G, Charnley RM, Uomo G, Delhaye M, Spicak J, Drumm B, Jansen J, Mountford R, Whitcomb DC, Neoptolemos JP; European Registry of Hereditary Pancreatitis and Pancreatic Cancer (EUROPAC).

Clin Gastroenterol Hepatol. 2004 Mar;2(3):252-61.

PMID:
15017610
19.

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
20.

Genetic analysis of the glutathione s-transferase genes MGST1, GSTM3, GSTT1, and GSTM1 in patients with hereditary pancreatitis.

Schneider A, Tögel S, Barmada MM, Whitcomb DC.

J Gastroenterol. 2004 Aug;39(8):783-7.

PMID:
15338373

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