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Oral Diseases
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May 24, 2021
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia
Yejin Lee, Hong Zhang, Figen Seymen, et al.
Human Mutation
|
May 20, 2008
Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification
Sook-Kyung Lee, Jan C-C Hu, John D Bartlett, et al.
Journal of Personalized Medicine
|
February 25, 2023
Novel <i>WDR72</i> Mutations Causing Hypomaturation Amelogenesis Imperfecta
Youn Jung Kim, Hong Zhang, Yejin Lee, et al.
Journal of Personalized Medicine
|
February 25, 2022
Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis Imperfecta
Yejin Lee, Hong Zhang, Figen Seymen, et al.
European Journal of Oral Sciences
|
January 17, 2012
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families
Shih-Kai Wang, Hui-Chen Chan, Sudha Rajderkar, et al.
International Journal of Molecular Sciences
|
July 29, 2025
Citrate Transporter Expression and Localization: The <i>Slc13a5</i><sup>Flag</sup> Mouse Model
Jan C-C Hu, Tian Liang, Hong Zhang, et al.
Scientific Reports
|
April 19, 2023
Dentin defects caused by a Dspp<sup>-1</sup> frameshift mutation are associated with the activation of autophagy
Tian Liang, Charles E Smith, Yuanyuan Hu, et al.
Plos One
|
January 28, 2014
Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus model
Masashi Shin, Yuanyuan Hu, Coralee E Tye, et al.
Journal of Dental Sciences
|
January 26, 2026
Novel <i>MMP20</i> (matrix metalloproteinase 20) mutations causing hypoplastic-hypomaturation amelogenesis imperfecta
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
International Journal of Molecular Sciences
|
June 19, 2024
<i>AMELX</i> Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
Oral Diseases
|
May 24, 2021
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia
Yejin Lee, Hong Zhang, Figen Seymen, et al.
Human Mutation
|
May 20, 2008
Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification
Sook-Kyung Lee, Jan C-C Hu, John D Bartlett, et al.
Journal of Personalized Medicine
|
February 25, 2023
Novel <i>WDR72</i> Mutations Causing Hypomaturation Amelogenesis Imperfecta
Youn Jung Kim, Hong Zhang, Yejin Lee, et al.
Journal of Personalized Medicine
|
February 25, 2022
Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis Imperfecta
Yejin Lee, Hong Zhang, Figen Seymen, et al.
European Journal of Oral Sciences
|
January 17, 2012
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families
Shih-Kai Wang, Hui-Chen Chan, Sudha Rajderkar, et al.
International Journal of Molecular Sciences
|
July 29, 2025
Citrate Transporter Expression and Localization: The <i>Slc13a5</i><sup>Flag</sup> Mouse Model
Jan C-C Hu, Tian Liang, Hong Zhang, et al.
Scientific Reports
|
April 19, 2023
Dentin defects caused by a Dspp<sup>-1</sup> frameshift mutation are associated with the activation of autophagy
Tian Liang, Charles E Smith, Yuanyuan Hu, et al.
Plos One
|
January 28, 2014
Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus model
Masashi Shin, Yuanyuan Hu, Coralee E Tye, et al.
Journal of Dental Sciences
|
January 26, 2026
Novel <i>MMP20</i> (matrix metalloproteinase 20) mutations causing hypoplastic-hypomaturation amelogenesis imperfecta
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
International Journal of Molecular Sciences
|
June 19, 2024
<i>AMELX</i> Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Page
of 14