PubMed (cited) for id: 276000

Year	Number of Results
1967	1
1981	1
1982	1
1984	3
1986	1
1990	1
1993	1
1996	2
1997	1
1999	2
2000	4
2001	1
2002	3
2003	1
2004	1
2005	1
2006	3
2008	2
2009	2
2010	1
2020	1
2024	0

1

Trypsin activity governs increased susceptibility to pancreatitis in mice expressing human PRSS1R122H.

Gui F, Zhang Y, Wan J, Zhan X, Yao Y, Li Y, Haddock AN, Shi J, Guo J, Chen J, Zhu X, Edenfield BH, Zhuang L, Hu C, Wang Y, Mukhopadhyay D, Radisky ES, Zhang L, Lugea A, Pandol SJ, Bi Y, Ji B. Gui F, et al. J Clin Invest. 2020 Jan 2;130(1):189-202. doi: 10.1172/JCI130172. J Clin Invest. 2020. PMID: 31550238 Free PMC article.

2

Uncertainties in the classification of human cationic trypsinogen (PRSS1) variants as hereditary pancreatitis-associated mutations.

Szmola R, Sahin-Tóth M. Szmola R, et al. J Med Genet. 2010 May;47(5):348-50. doi: 10.1136/jmg.2009.072751. J Med Genet. 2010. PMID: 20452997 Free PMC article.

3

Elucidation of the complex structure and origin of the human trypsinogen locus triplication.

Chauvin A, Chen JM, Quemener S, Masson E, Kehrer-Sawatzki H, Ohmle B, Cooper DN, Le Maréchal C, Férec C. Chauvin A, et al. Hum Mol Genet. 2009 Oct 1;18(19):3605-14. doi: 10.1093/hmg/ddp308. Epub 2009 Jul 7. Hum Mol Genet. 2009. PMID: 19584086

4

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. Kereszturi E, et al. Hum Mutat. 2009 Apr;30(4):575-82. doi: 10.1002/humu.20853. Hum Mutat. 2009. PMID: 19191323 Free PMC article.

5

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. Felderbauer P, et al. J Med Genet. 2008 Aug;45(8):507-12. doi: 10.1136/jmg.2007.056481. Epub 2008 May 29. J Med Genet. 2008. PMID: 18511571

6

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

Masson E, Le Maréchal C, Delcenserie R, Chen JM, Férec C. Masson E, et al. Hum Genet. 2008 Jun;123(5):521-9. doi: 10.1007/s00439-008-0508-6. Epub 2008 May 7. Hum Genet. 2008. PMID: 18461367

7

Hereditary pancreatitis caused by triplication of the trypsinogen locus.

Le Maréchal C, Masson E, Chen JM, Morel F, Ruszniewski P, Levy P, Férec C. Le Maréchal C, et al. Nat Genet. 2006 Dec;38(12):1372-4. doi: 10.1038/ng1904. Epub 2006 Oct 29. Nat Genet. 2006. PMID: 17072318

8

Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis.

Teich N, Rosendahl J, Tóth M, Mössner J, Sahin-Tóth M. Teich N, et al. Hum Mutat. 2006 Aug;27(8):721-30. doi: 10.1002/humu.20343. Hum Mutat. 2006. PMID: 16791840 Free PMC article. Review.

9

Biochemical models of hereditary pancreatitis.

Sahin-Tóth M. Sahin-Tóth M. Endocrinol Metab Clin North Am. 2006 Jun;35(2):303-12, ix. doi: 10.1016/j.ecl.2006.02.002. Endocrinol Metab Clin North Am. 2006. PMID: 16632094 Free PMC article. Review.

10

Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.

Teich N, Nemoda Z, Köhler H, Heinritz W, Mössner J, Keim V, Sahin-Tóth M. Teich N, et al. Hum Mutat. 2005 Apr;25(4):343-7. doi: 10.1002/humu.20148. Hum Mutat. 2005. PMID: 15776435 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

34 results

Results by year