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Items: 23

1.

A rationally designed A34R mutant oncolytic poxvirus: improved efficacy in peritoneal carcinomatosis.

Thirunavukarasu P, Sathaiah M, Gorry MC, O'Malley ME, Ravindranathan R, Austin F, Thorne SH, Guo ZS, Bartlett DL.

Mol Ther. 2013 May;21(5):1024-33. doi: 10.1038/mt.2013.27. Epub 2013 Feb 26.

2.

Three epigenetic drugs up-regulate homeobox gene Rhox5 in cancer cells through overlapping and distinct molecular mechanisms.

Li Q, Bartlett DL, Gorry MC, O'Malley ME, Guo ZS.

Mol Pharmacol. 2009 Nov;76(5):1072-81. doi: 10.1124/mol.109.056291. Epub 2009 Aug 13.

PMID:
19679824
3.

Oncolytic virotherapy for ovarian carcinomatosis using a replication-selective vaccinia virus armed with a yeast cytosine deaminase gene.

Chalikonda S, Kivlen MH, O'Malley ME, Eric Dong XD, McCart JA, Gorry MC, Yin XY, Brown CK, Zeh HJ 3rd, Guo ZS, Bartlett DL.

Cancer Gene Ther. 2008 Feb;15(2):115-25. Epub 2007 Dec 14.

4.

Clinico-pathologic findings in medullary cystic kidney disease type 2.

Bleyer AJ, Hart TC, Willingham MC, Iskandar SS, Gorry MC, Trachtman H.

Pediatr Nephrol. 2005 Jun;20(6):824-7. Epub 2005 Apr 21.

PMID:
15844001
5.

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.

Hart TC, Hart PS, Gorry MC, Michalec MD, Ryu OH, Uygur C, Ozdemir D, Firatli S, Aren G, Firatli E.

J Med Genet. 2003 Dec;40(12):900-6.

6.

Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) gene.

Bleyer AJ, Trachtman H, Sandhu J, Gorry MC, Hart TC.

Am J Kidney Dis. 2003 Aug;42(2):E20-6.

PMID:
12900848
7.

Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.

Hart PS, Wright JT, Savage M, Kang G, Bensen JT, Gorry MC, Hart TC.

Eur J Oral Sci. 2003 Aug;111(4):326-31.

PMID:
12887398
8.

Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene.

Bleyer AJ, Woodard AS, Shihabi Z, Sandhu J, Zhu H, Satko SG, Weller N, Deterding E, McBride D, Gorry MC, Xu L, Ganier D, Hart TC.

Kidney Int. 2003 Jul;64(1):36-42.

9.

Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients.

Zhang Y, Syed R, Uygar C, Pallos D, Gorry MC, Firatli E, Cortelli JR, VanDyke TE, Hart PS, Feingold E, Hart TC.

Genes Immun. 2003 Jan;4(1):22-9.

PMID:
12595898
10.

Aquaporin expression in developing human teeth and selected orofacial tissues.

Wang W, Hart PS, Piesco NP, Lu X, Gorry MC, Hart TC.

Calcif Tissue Int. 2003 Mar;72(3):222-7. Epub 2003 Jan 15.

PMID:
12522663
11.

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.

Hart TC, Gorry MC, Hart PS, Woodard AS, Shihabi Z, Sandhu J, Shirts B, Xu L, Zhu H, Barmada MM, Bleyer AJ.

J Med Genet. 2002 Dec;39(12):882-92.

12.

Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21.

Zhang Y, Gorry MC, Hart PS, Pettenati MJ, Wang L, Marks JJ, Lu X, Hart TC.

Cytogenet Cell Genet. 2001;95(3-4):146-52.

PMID:
12063391
13.

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1.

Hart TC, Zhang Y, Gorry MC, Hart PS, Cooper M, Marazita ML, Marks JM, Cortelli JR, Pallos D.

Am J Hum Genet. 2002 Apr;70(4):943-54. Epub 2002 Feb 26.

14.

Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients.

Zhang Y, Lundgren T, Renvert S, Tatakis DN, Firatli E, Uygur C, Hart PS, Gorry MC, Marks JJ, Hart TC.

J Med Genet. 2001 Feb;38(2):96-101.

15.

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.

J Pediatr Surg. 2000 Mar;35(3):406-19.

PMID:
10726679
16.
17.

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.

Pancreas. 1998 Oct;17(3):278-80.

PMID:
9788542
18.

Evolution of human immunodeficiency virus type 1 envelope sequences in infected individuals with differing disease progression profiles.

Shankarappa R, Gupta P, Learn GH Jr, Rodrigo AG, Rinaldo CR Jr, Gorry MC, Mullins JI, Nara PL, Ehrlich GD.

Virology. 1998 Feb 15;241(2):251-9.

19.

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

Rayner MG, Zhang Y, Gorry MC, Chen Y, Post JC, Ehrlich GD.

JAMA. 1998 Jan 28;279(4):296-9.

PMID:
9450714
20.

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.

Gastroenterology. 1997 Oct;113(4):1063-8.

PMID:
9322498
21.

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.

Am J Gastroenterol. 1997 Jul;92(7):1113-6.

PMID:
9219780
22.

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.

Nat Genet. 1996 Oct;14(2):141-5.

PMID:
8841182
23.

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.

Hum Mol Genet. 1995 Aug;4(8):1387-90.

PMID:
7581378

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