Search Results - Thomas C. Hart

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  1. 1
    Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

    Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects by Thomas C. Hart

    Published 2003
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  2. 2
    Haim-Munk syndrome and Papillon-Lefevre syndrome are allelic mutations in cathepsin C

    Haim-Munk syndrome and Papillon-Lefevre syndrome are allelic mutations in cathepsin C by Thomas C. Hart

    Published 2000
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  3. 3
    Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation

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

    Published 2000
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  4. 4
    Disorders of Human Dentin

    Disorders of Human Dentin by P. Suzanne Hart, Thomas C. Hart

    Published 2007
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  5. 5
    Characterization of Fibroblasts with<i>Son of Sevenless-1</i>Mutation

    Characterization of Fibroblasts with<i>Son of Sevenless-1</i>Mutation by Eun Jin Lee, Shyh-Ing Jang, Débora Pallos, Jorge Kather, Thomas C. Hart

    Published 2006
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  6. 6
    A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families.

    A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families. by Jennifer A. Price, J. Timothy Wright, Katherine Kula, Donald W. Bowden, Thomas C. Hart

    Published 1998
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  7. 7
    Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein

    Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein by Anthony J. Bleyer, Thomas C. Hart, Zak K. Shihabi, Vicki Robins, John R. Hoyer

    Published 2004
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  8. 8
    Overlapping <i>DSPP</i> Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

    Overlapping <i>DSPP</i> Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta by Dianalee McKnight, James P. Simmer, P. Suzanne Hart, Thomas C. Hart, Larry W. Fisher

    Published 2008
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  9. 9
    Genetic Linkage of Hereditary Gingival Fibromatosis to Chromosome 2p21

    Genetic Linkage of Hereditary Gingival Fibromatosis to Chromosome 2p21 by Thomas C. Hart, Débora Pallos, Donald W. Bowden, Joey Bolyard, Mark J. Pettenati, José Roberto Cortelli

    Published 1998
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  10. 10
    Heritability of Oral Microbial Species in Caries-Active and Caries-Free Twins

    Heritability of Oral Microbial Species in Caries-Active and Caries-Free Twins by Patricia Corby, Walter A. Bretz, Thomas C. Hart, Nicholas J. Schork, Jennifer Wessel, James Lyons‐Weiler, Bruce J. Paster

    Published 2007
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  11. 11
    Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

    Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta by Maria Cristina Leme Godoy dos Santos, P. Suzanne Hart, Mukundhan Ramaswami, Cláudia Misue Kanno, Thomas C. Hart, Sergio RP Line

    Published 2007
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  12. 12
    A comprehensive analysis of normal variation and disease-causing mutations in the human<i>DSPP</i>gene

    A comprehensive analysis of normal variation and disease-causing mutations in the human<i>DSPP</i>gene by Dianalee McKnight, P. Suzanne Hart, Thomas C. Hart, James K. Hartsfield, Anne Wilson, J. Timothy Wright, Larry W. Fisher

    Published 2008
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  13. 13
    Mutant DLX 3 disrupts odontoblast polarization and dentin formation

    Mutant DLX 3 disrupts odontoblast polarization and dentin formation by S.J. Choi, Insun Song, J.Q. Feng, Tian Gao, Naoto Haruyama, Pawan Gautam, Pamela Gehron Robey, Thomas C. Hart

    Published 2010
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  14. 14
    Cellular Zinc Levels Are Modulated by <scp>TRPML1–TMEM163</scp> Interaction

    Cellular Zinc Levels Are Modulated by <scp>TRPML1–TMEM163</scp> Interaction by Math P. Cuajungco, Luigi C. Basilio, Joshua Silva, Thomas C. Hart, Jonathan Tringali, Cheng‐Chang Chen, Martin Biel, Christian Grimm

    Published 2014
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  15. 15
    Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome

    Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome by Thomas C. Hart, Patricia Hart, Donald W. Bowden, Michael Michalec, Scott A. Callison, Steve J. Walker, Yingze Zhang, Erhan Fıratlı

    Published 1999
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  16. 16
    <i>MMP20</i> Active-site Mutation in Hypomaturation Amelogenesis Imperfecta

    <i>MMP20</i> Active-site Mutation in Hypomaturation Amelogenesis Imperfecta by Didem Özdemır, P. Suzanne Hart, Ok Hee Ryu, S.J. Choi, Meltem Özdemir Karataş, Erhan Fıratlı, N. P. Piesco, Thomas C. Hart

    Published 2005
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  17. 17
    Phenotypic Variation in<i>FAM83H-</i>associated Amelogenesis Imperfecta

    Phenotypic Variation in<i>FAM83H-</i>associated Amelogenesis Imperfecta by J. Timothy Wright, Sylvia A. Frazier‐Bowers, Darrin Simmons, K. Alexander, P J Crawford, Sangwoo T. Han, P. Suzanne Hart, Thomas C. Hart

    Published 2009
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  18. 18
    A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1

    A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1 by Thomas C. Hart, Yingze Zhang, Michael Gorry, Patricia Hart, Margaret E. Cooper, Mary L. Marazita, Jared M. Marks, José Roberto Cortelli, Débora Pallos

    Published 2002
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  19. 19
    Identification of Microbial and Proteomic Biomarkers in Early Childhood Caries

    Identification of Microbial and Proteomic Biomarkers in Early Childhood Caries by Thomas C. Hart, Patricia Corby, Miloš Hauskrecht, Ok Hee Ryu, Richard Pelikan, Michal Vaľko, Maria Betânia Melo de Oliveira, Gerald T. Hoehn, Walter A. Bretz

    Published 2011
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  20. 20
    Inheritance of Occlusal Topography: A Twin Study

    Inheritance of Occlusal Topography: A Twin Study by Ching‐Hua Su, Patricia Corby, M. A. Elliot, Deborah Studen‐Pavlovich, Dennis N. Ranalli, Bruno T. Rosa, Jennifer Wessel, Nicholas J. Schork, Thomas C. Hart, Walter A. Bretz

    Published 2008
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