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Connective Tissue Research
|
December 20, 2002
MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21
Mary MacDougall, Darrin Simmons, Ting Ting Gu, et al.
Scientific Reports
|
September 9, 2017
BMP-2 induced Dspp transcription is mediated by Dlx3/Osx signaling pathway in odontoblasts
Guobin Yang, Guohua Yuan, Mary MacDougall, et al.
Dental Materials : Official Publication of the Academy of Dental Materials
|
August 10, 2005
In vitro cytotoxicity of a remineralizing resin-based calcium phosphate cement
Edward J Boland, Mary MacDougall, David L Carnes, et al.
Progress in Orthodontics
|
December 29, 2022
Non-syndromic hypodontia of maxillary lateral incisors and its association with other dental anomalies
Giana Maria Lupinetti, Peng Li, Kyle Feagin, et al.
Developmental Biology
|
August 13, 2013
Inactivation of Tgfbr2 in Osterix-Cre expressing dental mesenchyme disrupts molar root formation
Ying Wang, Megan K Cox, George Coricor, et al.
Orthodontics & Craniofacial Research
|
August 9, 2025
Utilising Next-Generation Sequencing to Explore the Molecular Etiology of Short Root Anomaly
Emily A Joy, David K Crossman, Mary MacDougall, et al.
Journal of Cellular Biochemistry
|
April 27, 2004
Binding of two nuclear factors to a novel silencer element in human dentin matrix protein 1 (DMP1) promoter regulates the cell type-specific DMP1 gene expression
Shuo Chen, Natalyia Inozentseva-Clayton, Juan Dong, et al.
Toxicology
|
May 31, 2008
Fluoride at non-toxic dose affects odontoblast gene expression in vitro
Tilmann Wurtz, Sophia Houari, Nicole Mauro, et al.
Frontiers in Genetics
|
June 8, 2018
Gene-Expression Analysis Identifies IGFBP2 Dysregulation in Dental Pulp Cells From Human Cleidocranial Dysplasia
Stephen L Greene, Olga Mamaeva, David K Crossman, et al.
American Journal of Medical Genetics. Part A
|
January 25, 2005
DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
Juan Dong, David Amor, Michael J Aldred, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 82) with videos related to
Sort By:
Page
of 9
Connective Tissue Research
|
December 20, 2002
MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21
Mary MacDougall, Darrin Simmons, Ting Ting Gu, et al.
Scientific Reports
|
September 9, 2017
BMP-2 induced Dspp transcription is mediated by Dlx3/Osx signaling pathway in odontoblasts
Guobin Yang, Guohua Yuan, Mary MacDougall, et al.
Dental Materials : Official Publication of the Academy of Dental Materials
|
August 10, 2005
In vitro cytotoxicity of a remineralizing resin-based calcium phosphate cement
Edward J Boland, Mary MacDougall, David L Carnes, et al.
Progress in Orthodontics
|
December 29, 2022
Non-syndromic hypodontia of maxillary lateral incisors and its association with other dental anomalies
Giana Maria Lupinetti, Peng Li, Kyle Feagin, et al.
Developmental Biology
|
August 13, 2013
Inactivation of Tgfbr2 in Osterix-Cre expressing dental mesenchyme disrupts molar root formation
Ying Wang, Megan K Cox, George Coricor, et al.
Orthodontics & Craniofacial Research
|
August 9, 2025
Utilising Next-Generation Sequencing to Explore the Molecular Etiology of Short Root Anomaly
Emily A Joy, David K Crossman, Mary MacDougall, et al.
Journal of Cellular Biochemistry
|
April 27, 2004
Binding of two nuclear factors to a novel silencer element in human dentin matrix protein 1 (DMP1) promoter regulates the cell type-specific DMP1 gene expression
Shuo Chen, Natalyia Inozentseva-Clayton, Juan Dong, et al.
Toxicology
|
May 31, 2008
Fluoride at non-toxic dose affects odontoblast gene expression in vitro
Tilmann Wurtz, Sophia Houari, Nicole Mauro, et al.
Frontiers in Genetics
|
June 8, 2018
Gene-Expression Analysis Identifies IGFBP2 Dysregulation in Dental Pulp Cells From Human Cleidocranial Dysplasia
Stephen L Greene, Olga Mamaeva, David K Crossman, et al.
American Journal of Medical Genetics. Part A
|
January 25, 2005
DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
Juan Dong, David Amor, Michael J Aldred, et al.
Page
of 9