te Morsche R - Search Results

1

A common variant of PNPLA3 (p.I148M) is not associated with alcoholic chronic pancreatitis.

Rosendahl J, Tönjes A, Schleinitz D, Kovacs P, Wiegand J, Ruffert C, Jesinghaus M, Schober R, Herms M, Grützmann R, Schulz HU, Stickel F, Werner J, Bugert P, Blüher M, Stumvoll M, Böhm S, Berg T, Wittenburg H, Mössner J, te Morsche R, Derikx M, Keim V, Witt H, Drenth JP. Rosendahl J, et al. Among authors: te morsche r. PLoS One. 2012;7(1):e29433. doi: 10.1371/journal.pone.0029433. Epub 2012 Jan 20. PLoS One. 2012. PMID: 22276112 Free PMC article.

2

Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis.

Drenth JP, te Morsche R, Jansen JB. Drenth JP, et al. Among authors: te morsche r. Gut. 2002 May;50(5):687-92. doi: 10.1136/gut.50.5.687. Gut. 2002. PMID: 11950817 Free PMC article.

3

Genetic basis of chronic pancreatitis.

Jansen JB, te Morsche R, van Goor H, Drenth JP. Jansen JB, et al. Among authors: te morsche r. Scand J Gastroenterol Suppl. 2002;(236):91-4. doi: 10.1080/003655202320621535. Scand J Gastroenterol Suppl. 2002. PMID: 12408512 Review.

4

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease.

Drenth JP, te Morsche RH, Smink R, Bonifacino JS, Jansen JB. Drenth JP, et al. Among authors: te morsche rh. Nat Genet. 2003 Mar;33(3):345-7. doi: 10.1038/ng1104. Epub 2003 Feb 10. Nat Genet. 2003. PMID: 12577059

5

Glutathione S-transferase Mu null genotype affords protection against alcohol induced chronic pancreatitis.

Verlaan M, te Morsche RH, Roelofs HM, Laheij RJ, Jansen JB, Peters WH, Drenth JP. Verlaan M, et al. Am J Med Genet A. 2003 Jul 1;120A(1):34-9. doi: 10.1002/ajmg.a.20010. Am J Med Genet A. 2003. PMID: 12794689

6

Genetic polymorphisms in alcohol-metabolizing enzymes and chronic pancreatitis.

Verlaan M, Te Morsche RH, Roelofs HM, Laheij RJ, Jansen JB, Peters WH, Drenth JP. Verlaan M, et al. Alcohol Alcohol. 2004 Jan-Feb;39(1):20-4. doi: 10.1093/alcalc/agh001. Alcohol Alcohol. 2004. PMID: 14691069

7

Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease.

Drenth JP, Tahvanainen E, te Morsche RH, Tahvanainen P, Kääriäinen H, Höckerstedt K, van de Kamp JM, Breuning MH, Jansen JB. Drenth JP, et al. Hepatology. 2004 Apr;39(4):924-31. doi: 10.1002/hep.20141. Hepatology. 2004. PMID: 15057895

8

Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease.

Drenth JP, Martina JA, Te Morsche RH, Jansen JB, Bonifacino JS. Drenth JP, et al. Gastroenterology. 2004 Jun;126(7):1819-27. doi: 10.1053/j.gastro.2004.02.023. Gastroenterology. 2004. PMID: 15188177

9

Functional polymorphisms of UDP-glucuronosyltransferases 1A1, 1A6 and 1A8 are not involved in chronic pancreatitis.

Verlaan M, te Morsche RH, Pap A, Laheij RJ, Jansen JB, Peters WH, Drenth JP. Verlaan M, et al. Pharmacogenetics. 2004 Jun;14(6):351-7. doi: 10.1097/00008571-200406000-00004. Pharmacogenetics. 2004. PMID: 15247627 Free article.

10

SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.

Drenth JP, te Morsche RH, Guillet G, Taieb A, Kirby RL, Jansen JB. Drenth JP, et al. Among authors: te morsche rh. J Invest Dermatol. 2005 Jun;124(6):1333-8. doi: 10.1111/j.0022-202X.2005.23737.x. J Invest Dermatol. 2005. PMID: 15955112 Free article.

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