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Items: 1 to 20 of 149

1.

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.

2.

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.

3.

Molecular basis of hereditary pancreatitis.

Chen JM, Ferec C.

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

4.

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
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.

Hereditary pancreatitis caused by a double gain-of-function trypsinogen mutation.

Masson E, Le Maréchal C, Delcenserie R, Chen JM, Férec C.

Hum Genet. 2008 Jun;123(5):521-9. doi: 10.1007/s00439-008-0508-6.

PMID:
18461367
7.

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
8.

Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.

Whitcomb DC, Gorry MC, Preston RA, Furey W, Sossenheimer MJ, Ulrich CD, Martin SP, Gates LK Jr, Amann ST, Toskes PP, Liddle R, McGrath K, Uomo G, Post JC, Ehrlich GD.

Nat Genet. 1996 Oct;14(2):141-5.

PMID:
8841182
9.

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
10.

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd.

Am J Med Genet. 1998 Apr 28;77(1):47-53.

PMID:
9557894
11.

Mutations of the cationic trypsinogen in hereditary pancreatitis.

Teich N, Mössner J, Keim V.

Hum Mutat. 1998;12(1):39-43.

PMID:
9633818
12.

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.

PMID:
11138965
13.

Identification of a hereditary pancreatitis mutation in four West Virginia families.

Elitsur Y, Chertow BC, Jewell RD, Finver SN, Primerano DA.

Pediatr Res. 1998 Dec;44(6):927-30.

PMID:
9853929
15.

Pancreatitis in fibrocalculous pancreatic diabetes mellitus is not associated with common mutations in the trypsinogen gene.

Hassan Z, Mohan V, McDermott MF, Ali L, Ogunkolade WB, Aganna E, Cassell PG, Deepa R, Khan AK, Hitman GA.

Diabetes Metab Res Rev. 2000 Nov-Dec;16(6):454-57.

PMID:
11114105
16.

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
17.

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.

Gorry MC, Gabbaizedeh D, Furey W, Gates LK Jr, Preston RA, Aston CE, Zhang Y, Ulrich C, Ehrlich GD, Whitcomb DC.

Gastroenterology. 1997 Oct;113(4):1063-8.

PMID:
9322498
18.

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 18;10(3):249-55.

19.
20.

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.

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