Hart TC - 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: hart ps. 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

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: hart tc. 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

3

Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosis.

Jang SI, Lee EJ, Hart PS, Ramaswami M, Pallos D, Hart TC. Jang SI, et al. Among authors: hart ps, hart tc. J Biol Chem. 2007 Jul 13;282(28):20245-55. doi: 10.1074/jbc.M701609200. Epub 2007 May 17. J Biol Chem. 2007. PMID: 17510059 Free article.

4

Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21.

Hart TC, Pallos D, Bowden DW, Bolyard J, Pettenati MJ, Cortelli JR. Hart TC, et al. Am J Hum Genet. 1998 Apr;62(4):876-83. doi: 10.1086/301797. Am J Hum Genet. 1998. PMID: 9529355 Free PMC article.

5

Genetic heterogeneity of gingival fibromatosis on chromosome 2p.

Shashi V, Pallos D, Pettenati MJ, Cortelli JR, Fryns JP, von Kap-Herr C, Hart TC. Shashi V, et al. Among authors: hart tc. J Med Genet. 1999 Sep;36(9):683-6. J Med Genet. 1999. PMID: 10507724 Free PMC article.

6

Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.

Hart TC, Hart PS, Michalec MD, Zhang Y, Marazita ML, Cooper M, Yassin OM, Nusier M, Walker S. Hart TC, et al. Among authors: hart ps. J Med Genet. 2000 Feb;37(2):95-101. doi: 10.1136/jmg.37.2.95. J Med Genet. 2000. PMID: 10662808 Free PMC article.

7

Evidence of genetic heterogeneity for hereditary gingival fibromatosis.

Hart TC, Pallos D, Bozzo L, Almeida OP, Marazita ML, O'Connell JR, Cortelli JR. Hart TC, et al. J Dent Res. 2000 Oct;79(10):1758-64. doi: 10.1177/00220345000790100501. J Dent Res. 2000. PMID: 11077991 Review.

8

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: hart ps, hart tc. Cytogenet Cell Genet. 2001;95(3-4):146-52. doi: 10.1159/000059337. Cytogenet Cell Genet. 2001. PMID: 12063391

9

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: hart ps. 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.

10

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: hart ps. 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.

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