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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. Among authors: schnekenburger j. 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
Vascular smooth muscle and nitric oxide synthase.
Buchwalow IB, Podzuweit T, Bocker W, Samoilova VE, Thomas S, Wellner M, Baba HA, Robenek H, Schnekenburger J, Lerch MM. Buchwalow IB, et al. Among authors: schnekenburger j. FASEB J. 2002 Apr;16(6):500-8. doi: 10.1096/fj.01-0842com. FASEB J. 2002. PMID: 11919152
103 results