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Results: 1-23 |
Results: 23
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefevre syndrome patients
Authors: Zhang, Y Lundgren, T Renvert, S Takakis, DN Firatli, E Uygur, C Hart, PS Gorry, MC Marks, JJ Hart, TC
Citation: Y. Zhang et al., Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefevre syndrome patients, J MED GENET, 38(2), 2001, pp. 96-101
Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfectaand dentinogenesis imperfecta
Authors: Pallos, D Hart, PS Cortelli, JR Vian, S Wright, JT Korkko, J Brunoni, D Hart, TC
Citation: D. Pallos et al., Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfectaand dentinogenesis imperfecta, ARCH ORAL B, 46(5), 2001, pp. 459-470
National Institutes of Health Consensus Development Conference statement -Diagnosis and management of dental caries throughout life, March 26-28, 2001
Authors: Alfano, MC Coulter, ID Gerety, MB Hart, TC Imrey, PB LeResche, L Levy, J Luepker, RV Lurie, AG Page, RC Rye, LA Smith, L Walker, CB
Citation: Mc. Alfano et al., National Institutes of Health Consensus Development Conference statement -Diagnosis and management of dental caries throughout life, March 26-28, 2001, J AM DENT A, 132(8), 2001, pp. 1153-1161
The impact of molecular genetics on oral health paradigms
Authors: Hart, TC Marazita, ML Wright, JT
Citation: Tc. Hart et al., The impact of molecular genetics on oral health paradigms, CR R ORAL B, 11(1), 2000, pp. 26-56
An integrated physical and genetic map of the PLS locus interval on Chromosome 11q14
Authors: Hart, TC Walker, SJ Bowden, DW Hart, PS Callison, SA Bobby, PL Firatli, E
Citation: Tc. Hart et al., An integrated physical and genetic map of the PLS locus interval on Chromosome 11q14, MAMM GENOME, 11(3), 2000, pp. 243-246
Assignment of PDZ domain-containing protein GIPC gene (C19orf3) to human chromosome band 19p13.1 by in situ hybridization and radiation hybrid mapping
Authors: Von Kap-Herr, C Kandala, G Mann, SS Hart, TC Pettenati, MJ Setaluri, V
Citation: C. Von Kap-herr et al., Assignment of PDZ domain-containing protein GIPC gene (C19orf3) to human chromosome band 19p13.1 by in situ hybridization and radiation hybrid mapping, CYTOG C GEN, 89(3-4), 2000, pp. 234-235
Genetic polymorphisms of the IL-1 alpha and IL-1 beta genes in African-American LJP patients and an African-American control population
Authors: Walker, SJ Van Dyke, HE Rich, S Kornman, KS di Giovine, FS Hart, TC
Citation: Sj. Walker et al., Genetic polymorphisms of the IL-1 alpha and IL-1 beta genes in African-American LJP patients and an African-American control population, J PERIODONT, 71(5), 2000, pp. 723-728
Haim-Munk syndrome and Papillon-Lefevre syndrome are allelic mutations in cathepsin C
Authors: Hart, TC Hart, PS Michalec, MD Zhang, Y Firatli, E Van Dyke, TE Stabholz, A Zlorogorski, A Shapira, L Soskolne, WA
Citation: Tc. Hart et al., Haim-Munk syndrome and Papillon-Lefevre syndrome are allelic mutations in cathepsin C, J MED GENET, 37(2), 2000, pp. 88-94
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation
Authors: Hart, TC Hart, PS Michalec, MD Zhang, Y Marazita, ML Cooper, M Yassin, OM Nusier, M Walker, S
Citation: Tc. Hart et al., Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation, J MED GENET, 37(2), 2000, pp. 95-101
Identification of cathepsin C mutations in ethnically diverse Papillon-Lefevre syndrome patients
Authors: Hart, PS Zhang, Y Firatli, E Uygur, C Lotfazar, M Michalec, MD Marks, JJ Lu, X Coates, BJ Seow, WK MarshaIl, R Williams, D Reed, JB Wright, JT Hart, TC
Citation: Ps. Hart et al., Identification of cathepsin C mutations in ethnically diverse Papillon-Lefevre syndrome patients, J MED GENET, 37(12), 2000, pp. 927-932
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation
Authors: Ravassipour, DB Hart, PS Hart, TC Ritter, AV Yamauchi, M Gibson, C Wright, JT
Citation: Db. Ravassipour et al., Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation, J DENT RES, 79(7), 2000, pp. 1476-1481
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth development
Authors: Hu, CC Hart, TC Dupont, BR Chen, JJ Sun, X Qian, Q Zhang, CH Jiang, H Mattern, VL Wright, JT Simmer, JP
Citation: Cc. Hu et al., Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth development, J DENT RES, 79(4), 2000, pp. 912-919
Evidence of genetic heterogeneity for hereditary gingival fibromatosis
Authors: Hart, TC Pallos, D Bozzo, L Almeida, OP Marazita, ML O'Connell, JR Cortelli, JR
Citation: Tc. Hart et al., Evidence of genetic heterogeneity for hereditary gingival fibromatosis, J DENT RES, 79(10), 2000, pp. 1758-1764
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27
Authors: Shashi, V Berry, MN Shoaf, S Sciote, JJ Goldstein, D Hart, TC
Citation: V. Shashi et al., A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27, AM J HU GEN, 66(2), 2000, pp. 469-479
Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22
Authors: Hart, TC Price, JA Bobby, PL Pettenati, MJ Shashi, V Herr, CV Van Dyke, TE
Citation: Tc. Hart et al., Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22, GENOMICS, 56(2), 1999, pp. 233-235
Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2alias NaDC-1) to human chromosome region 17p11.1 -> q11.1 by radiation hybrid mapping and fluorescence in situ hybridization
Authors: Mann, SS Hart, TC Pettenati, MJ von Kap-herr, C Holmes, RP
Citation: Ss. Mann et al., Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2alias NaDC-1) to human chromosome region 17p11.1 -> q11.1 by radiation hybrid mapping and fluorescence in situ hybridization, CYTOG C GEN, 84(1-2), 1999, pp. 89-90
Genetic heterogeneity of gingival fibromatosis on chromosome 2p
Authors: Shashi, V Pallos, D Pettenati, MJ Cortelli, JR Fryns, JP von Kap-Herr, C Hart, TC
Citation: V. Shashi et al., Genetic heterogeneity of gingival fibromatosis on chromosome 2p, J MED GENET, 36(9), 1999, pp. 683-686
Mutations of the cathepsin C gene are responsible for Papillon-Lefevre syndrome
Authors: Hart, TC Hart, PS Bowden, DW Michalec, MD Callison, SA Walker, SJ Zhang, YZ Firatli, E
Citation: Tc. Hart et al., Mutations of the cathepsin C gene are responsible for Papillon-Lefevre syndrome, J MED GENET, 36(12), 1999, pp. 881-887
Using geographic information to acquire wild crop germplasm for ex situ collections: I. Map development and field use
Authors: Greene, SL Hart, TC Afonin, A
Citation: Sl. Greene et al., Using geographic information to acquire wild crop germplasm for ex situ collections: I. Map development and field use, CROP SCI, 39(3), 1999, pp. 836-842
Using geographic information to acquire wild crop germplasm for ex situ collections: II. Post-collection analysis
Authors: Greene, SL Hart, TC Afonin, A
Citation: Sl. Greene et al., Using geographic information to acquire wild crop germplasm for ex situ collections: II. Post-collection analysis, CROP SCI, 39(3), 1999, pp. 843-849
Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions
Authors: Price, JA Wright, JT Walker, SJ Crawford, PJM Aldred, MJ Hart, TC
Citation: Ja. Price et al., Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions, CLIN GENET, 56(1), 1999, pp. 35-40
Reassignment of peptidyl prolyl isomerase-like 1 gene (PPIL1) to human chromosome region 6p21.1 by radiation hybrid mapping and fluorescence in situ hybridization
Authors: Mann, SS Pettenati, MJ von Kap-herr, C Hart, TC
Citation: Ss. Mann et al., Reassignment of peptidyl prolyl isomerase-like 1 gene (PPIL1) to human chromosome region 6p21.1 by radiation hybrid mapping and fluorescence in situ hybridization, CYTOG C GEN, 83(3-4), 1998, pp. 228-229
Enamel structure and composition in the tricho-dento-osseous syndrome
Authors: Spangler, GS Hall, KI Kula, K Hart, TC Wright, JT
Citation: Gs. Spangler et al., Enamel structure and composition in the tricho-dento-osseous syndrome, CONNECT TIS, 39(1-3), 1998, pp. 469-479
Risultati: 1-23 |