Ehrlich GD - Search Results

1

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. Among authors: ehrlich gd. Gastroenterology. 1997 Oct;113(4):1063-8. doi: 10.1053/gast.1997.v113.pm9322498. Gastroenterology. 1997. PMID: 9322498

2

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

3

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

4

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. Among authors: ehrlich gd. Am J Gastroenterol. 1997 Jul;92(7):1113-6. Am J Gastroenterol. 1997. PMID: 9219780

5

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. Among authors: ehrlich gd. Pancreas. 1998 Oct;17(3):278-80. doi: 10.1097/00006676-199810000-00009. Pancreas. 1998. PMID: 9788542

6

Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family.

Zhang Y, Gorry MC, Post JC, Ehrlich GD. Zhang Y, et al. Among authors: ehrlich gd. Gene. 1999 Apr 1;230(1):69-79. doi: 10.1016/s0378-1119(99)00047-5. Gene. 1999. PMID: 10196476

7

Refined localization of a gene for pediatric gastroesophageal reflux makes HTR2A an unlikely candidate gene.

Hu FZ, Post JC, Johnson S, Ehrlich GD, Preston RA. Hu FZ, et al. Among authors: ehrlich gd. Hum Genet. 2000 Nov;107(5):519-25. doi: 10.1007/s004390000405. Hum Genet. 2000. PMID: 11140952

8

Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome.

Gorry MC, Preston RA, White GJ, Zhang Y, Singhal VK, Losken HW, Parker MG, Nwokoro NA, Post JC, Ehrlich GD. Gorry MC, et al. Among authors: ehrlich gd. Hum Mol Genet. 1995 Aug;4(8):1387-90. doi: 10.1093/hmg/4.8.1387. Hum Mol Genet. 1995. PMID: 7581378

9

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.

10

Evidence of bacterial metabolic activity in culture-negative otitis media with effusion.

Rayner MG, Zhang Y, Gorry MC, Chen Y, Post JC, Ehrlich GD. Rayner MG, et al. Among authors: ehrlich gd. JAMA. 1998 Jan 28;279(4):296-9. doi: 10.1001/jama.279.4.296. JAMA. 1998. PMID: 9450714

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

Text availability

Article attribute

Article type

Publication date

259 results

Search Page