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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. Among authors: Ehrlich GD. Nat Genet. 1996 Oct;14(2):141-5. doi: 10.1038/ng1096-141. Nat Genet. 1996. PMID: 8841182
The Tsk2/+ mouse fibrotic phenotype is due to a gain-of-function mutation in the PIIINP segment of the Col3a1 gene.
Long KB, Li Z, Burgwin CM, Choe SG, Martyanov V, Sassi-Gaha S, Earl JP, Eutsey RA, Ahmed A, Ehrlich GD, Artlett CM, Whitfield ML, Blankenhorn EP. Long KB, et al. Among authors: Ehrlich GD. J Invest Dermatol. 2015 Mar;135(3):718-27. doi: 10.1038/jid.2014.455. Epub 2014 Oct 20. J Invest Dermatol. 2015. PMID: 25330296 Free PMC article.
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14.
Hu FZ, Preston RA, Post JC, White GJ, Kikuchi LW, Wang X, Leal SM, Levenstien MA, Ott J, Self TW, Allen G, Stiffler RS, McGraw C, Pulsifer-Anderson EA, Ehrlich GD. Hu FZ, et al. Among authors: Ehrlich GD. JAMA. 2000 Jul 19;284(3):325-34. doi: 10.1001/jama.284.3.325. JAMA. 2000. PMID: 10891964 Free PMC article.
Linkage and association between inflammatory bowel disease and a locus on chromosome 12.
Duerr RH, Barmada MM, Zhang L, Davis S, Preston RA, Chensny LJ, Brown JL, Ehrlich GD, Weeks DE, Aston CE. Duerr RH, et al. Among authors: Ehrlich GD. Am J Hum Genet. 1998 Jul;63(1):95-100. doi: 10.1086/301929. Am J Hum Genet. 1998. PMID: 9634527 Free PMC article.
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. Among authors: Ehrlich GD. Gastroenterology. 1996 Jun;110(6):1975-80. doi: 10.1053/gast.1996.v110.pm8964426. Gastroenterology. 1996. PMID: 8964426 Clinical Trial.
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