Gorry MC - Search Results

1

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. Hart TC, et al. Among authors: gorry mc. Am J Hum Genet. 2002 Apr;70(4):943-54. doi: 10.1086/339689. Epub 2002 Feb 26. Am J Hum Genet. 2002. PMID: 11868160 Free PMC article.

2

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. Zhang Y, et al. Among authors: gorry mc. Cytogenet Cell Genet. 2001;95(3-4):146-52. doi: 10.1159/000059337. Cytogenet Cell Genet. 2001. PMID: 12063391

3

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. Hart TC, et al. Among authors: gorry mc. J Med Genet. 2002 Dec;39(12):882-92. doi: 10.1136/jmg.39.12.882. J Med Genet. 2002. PMID: 12471200 Free PMC article.

4

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. Hart PS, et al. Among authors: gorry mc. Eur J Oral Sci. 2003 Aug;111(4):326-31. doi: 10.1034/j.1600-0722.2003.00046.x. Eur J Oral Sci. 2003. PMID: 12887398

5

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. Zhang Y, et al. Among authors: gorry mc. J Med Genet. 2001 Feb;38(2):96-101. doi: 10.1136/jmg.38.2.96. J Med Genet. 2001. PMID: 11158173 Free PMC article.

6

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. Zhang Y, et al. Among authors: gorry mc. Genes Immun. 2003 Jan;4(1):22-9. doi: 10.1038/sj.gene.6363900. Genes Immun. 2003. PMID: 12595898

7

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. Hart TC, et al. Among authors: gorry mc. J Med Genet. 2003 Dec;40(12):900-6. doi: 10.1136/jmg.40.12.900. J Med Genet. 2003. PMID: 14684688 Free PMC article.

8

Aquaporin expression in developing human teeth and selected orofacial tissues.

Wang W, Hart PS, Piesco NP, Lu X, Gorry MC, Hart TC. Wang W, et al. Among authors: gorry mc. Calcif Tissue Int. 2003 Mar;72(3):222-7. doi: 10.1007/s00223-002-1014-9. Epub 2003 Jan 15. Calcif Tissue Int. 2003. PMID: 12522663

9

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

Bleyer AJ, Trachtman H, Sandhu J, Gorry MC, Hart TC. Bleyer AJ, et al. Among authors: gorry mc. Am J Kidney Dis. 2003 Aug;42(2):E20-6. doi: 10.1016/s0272-6386(03)00670-x. Am J Kidney Dis. 2003. PMID: 12900848

10

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

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