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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 2 |
1997 | 2 |
1998 | 1 |
2000 | 1 |
2024 | 0 |
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6 results
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Page 1
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
Nat Genet. 1996 Oct;14(2):141-5. doi: 10.1038/ng1096-141.
Nat Genet. 1996.
PMID: 8841182
A gene for hereditary pancreatitis maps to chromosome 7q35.
Whitcomb DC, Preston RA, Aston CE, Sossenheimer MJ, Barua PS, Zhang Y, Wong-Chong A, White GJ, Wood PG, Gates LK Jr, Ulrich C, Martin SP, Post JC, Ehrlich GD.
Whitcomb DC, et al.
Gastroenterology. 1996 Jun;110(6):1975-80. doi: 10.1053/gast.1996.v110.pm8964426.
Gastroenterology. 1996.
PMID: 8964426
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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
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PYY regulates pancreatic exocrine secretion through multiple receptors in the awake rat.
Guarita DR, Deng X, Huh YB, Wood PG, Reeve JR Jr, Whitcomb DC.
Guarita DR, et al.
Dig Dis Sci. 2000 Sep;45(9):1696-702. doi: 10.1023/a:1005550732146.
Dig Dis Sci. 2000.
PMID: 11052307
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Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG).
Sossenheimer MJ, Aston CE, Preston RA, Gates LK Jr, Ulrich CD, Martin SP, Zhang Y, Gorry MC, Ehrlich GD, Whitcomb DC.
Sossenheimer MJ, et al.
Am J Gastroenterol. 1997 Jul;92(7):1113-6.
Am J Gastroenterol. 1997.
PMID: 9219780
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Lack of R117H mutation in the cationic trypsinogen gene in patients with tropical pancreatitis from Bangladesh.
Rossi L, Whitcomb DC, Ehrlich GD, Gorry MC, Parvin S, Sattar S, Ali L, Azad Khan AK, Gyr N.
Rossi L, et al.
Pancreas. 1998 Oct;17(3):278-80. doi: 10.1097/00006676-199810000-00009.
Pancreas. 1998.
PMID: 9788542
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