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James P Simmer

Showing results (121-130 of 138) with videos related to

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Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|September 5, 2015
Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC)Alexandre R Vieira, Moses Lee, Filippo Vairo, et al.
Molecular Genetics & Genomic Medicine|August 13, 2019
AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout-NLS-lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue-specificityTian Liang, Yuanyuan Hu, Charles E Smith, et al.
Scientific Reports|October 1, 2022
Enamel defects in Acp4<sup>R110C/R110C</sup> mice and human ACP4 mutationsTian Liang, Shih-Kai Wang, Charles Smith, et al.
Annals of the New York Academy of Sciences|April 3, 2023
PAX9 mutations and genetic synergism in familial tooth agenesisKuan-Yu Chu, Yin-Lin Wang, Jung-Tsu Chen, et al.
Scientific Reports|May 20, 2021
MMP20-generated amelogenin cleavage products prevent formation of fan-shaped enamel malformationsJohn D Bartlett, Charles E Smith, Yuanyuan Hu, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Plos One|December 20, 2012
Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.
International Journal of Oral Science|November 23, 2017
Meeting report: a hard look at the state of enamel researchOphir D Klein, Olivier Duverger, Wendy Shaw, et al.
International Journal of Oral Science|November 13, 2021
Correction: Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.
Pageof 14

Showing results (121-130 of 138) with videos related to

Sort By:
Pageof 14
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|September 5, 2015
Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC)Alexandre R Vieira, Moses Lee, Filippo Vairo, et al.
Molecular Genetics & Genomic Medicine|August 13, 2019
AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout-NLS-lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue-specificityTian Liang, Yuanyuan Hu, Charles E Smith, et al.
Scientific Reports|October 1, 2022
Enamel defects in Acp4<sup>R110C/R110C</sup> mice and human ACP4 mutationsTian Liang, Shih-Kai Wang, Charles Smith, et al.
Annals of the New York Academy of Sciences|April 3, 2023
PAX9 mutations and genetic synergism in familial tooth agenesisKuan-Yu Chu, Yin-Lin Wang, Jung-Tsu Chen, et al.
Scientific Reports|May 20, 2021
MMP20-generated amelogenin cleavage products prevent formation of fan-shaped enamel malformationsJohn D Bartlett, Charles E Smith, Yuanyuan Hu, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Plos One|December 20, 2012
Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.
International Journal of Oral Science|November 23, 2017
Meeting report: a hard look at the state of enamel researchOphir D Klein, Olivier Duverger, Wendy Shaw, et al.
International Journal of Oral Science|November 13, 2021
Correction: Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.
Pageof 14