Similar articles for PMID: 9322498

Year	Number of Results
1996	3
1997	4
1998	7
1999	19
2000	18
2001	20
2002	10
2003	7
2004	10
2005	6
2006	4
2007	4
2008	3
2009	2
2011	3
2014	1
2016	1
2017	1
2019	5
2020	2
2021	1
2022	2
2023	2
2024	0

1

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. Gorry MC, et al. Gastroenterology. 1997 Oct;113(4):1063-8. doi: 10.1053/gast.1997.v113.pm9322498. Gastroenterology. 1997. PMID: 9322498

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. Nishimori I, et al. Gut. 1999 Feb;44(2):259-63. doi: 10.1136/gut.44.2.259. Gut. 1999. PMID: 9895387 Free PMC article.

3

Analysis of the hereditary pancreatitis-associated cationic trypsinogen gene mutations in exons 2 and 3 by enzymatic mutation detection from a single 2.2-kb polymerase chain reaction product.

Ford ME, Whitcomb DC. Ford ME, et al. Mol Diagn. 1999 Sep;4(3):211-8. doi: 10.1016/s1084-8592(99)80024-1. Mol Diagn. 1999. PMID: 10553021

4

Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis.

Creighton JE, Lyall R, Wilson DI, Curtis A, Charnley RM. Creighton JE, et al. Br J Surg. 2000 Feb;87(2):170-5. doi: 10.1046/j.1365-2168.2000.01326.x. Br J Surg. 2000. PMID: 10671922

5

[From gene to disease; hereditary pancreatitis].

Drenth JP, Jansen JB. Drenth JP, et al. Ned Tijdschr Geneeskd. 2000 Nov 25;144(48):2301-2. Ned Tijdschr Geneeskd. 2000. PMID: 11143296 Review. Dutch.

6

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. Truninger K, et al. Pancreas. 2001 Jan;22(1):18-23. doi: 10.1097/00006676-200101000-00003. Pancreas. 2001. PMID: 11138965 Free article.

7

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

Sahin-Tóth M, Tóth M. Sahin-Tóth M, et al. Orv Hetil. 2001 Mar 25;142(12):603-6. Orv Hetil. 2001. PMID: 11324217 Hungarian.

8

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. Teich N, et al. Hum Mutat. 2004 Jan;23(1):22-31. doi: 10.1002/humu.10285. Hum Mutat. 2004. PMID: 14695529

9

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd. Dasouki MJ, et al. Am J Med Genet. 1998 Apr 28;77(1):47-53. Am J Med Genet. 1998. PMID: 9557894

10

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. Whitcomb DC, et al. Nat Genet. 1996 Oct;14(2):141-5. doi: 10.1038/ng1096-141. Nat Genet. 1996. PMID: 8841182

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