Gorry MC - Search Results

1

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: gorry mc. Pancreas. 1998 Oct;17(3):278-80. doi: 10.1097/00006676-199810000-00009. Pancreas. 1998. PMID: 9788542

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: gorry mc. Nat Genet. 1996 Oct;14(2):141-5. doi: 10.1038/ng1096-141. Nat Genet. 1996. PMID: 8841182

3

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

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: gorry mc. Am J Gastroenterol. 1997 Jul;92(7):1113-6. Am J Gastroenterol. 1997. PMID: 9219780

5

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: gorry mc. Gene. 1999 Apr 1;230(1):69-79. doi: 10.1016/s0378-1119(99)00047-5. Gene. 1999. PMID: 10196476

6

RNA differential display of scarless wound healing in fetal rabbit indicates downregulation of a CCT chaperonin subunit and upregulation of a glycophorin-like gene transcript.

Darden DL, Hu FZ, Ehrlich MD, Gorry MC, Dressman D, Li HS, Whitcomb DC, Hebda PA, Dohar JE, Ehrlich GD. Darden DL, et al. Among authors: gorry mc. J Pediatr Surg. 2000 Mar;35(3):406-19. doi: 10.1016/s0022-3468(00)90204-5. J Pediatr Surg. 2000. PMID: 10726679

7

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: gorry mc. JAMA. 1998 Jan 28;279(4):296-9. doi: 10.1001/jama.279.4.296. JAMA. 1998. PMID: 9450714

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. Hum Mol Genet. 1995 Aug;4(8):1387-90. doi: 10.1093/hmg/4.8.1387. Hum Mol Genet. 1995. PMID: 7581378

9

Structure and sequence of human FGF8.

Gemel J, Gorry M, Ehrlich GD, MacArthur CA. Gemel J, et al. Genomics. 1996 Jul 1;35(1):253-7. doi: 10.1006/geno.1996.0349. Genomics. 1996. PMID: 8661131

10

Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

Ozen RS, Baysal BE, Devlin B, Farr JE, Gorry M, Ehrlich GD, Richard CW. Ozen RS, et al. Am J Hum Genet. 1999 Jun;64(6):1646-54. doi: 10.1086/302403. Am J Hum Genet. 1999. PMID: 10330351 Free PMC article.

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