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Jan C C Hu

Showing results (71-80 of 112) with videos related to

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Journal of Personalized Medicine|February 25, 2023
Novel <i>WDR72</i> Mutations Causing Hypomaturation Amelogenesis ImperfectaYoun Jung Kim, Hong Zhang, Yejin Lee, et al.
Journal of Personalized Medicine|February 25, 2022
Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis ImperfectaYejin Lee, Hong Zhang, Figen Seymen, et al.
Scientific Reports|April 19, 2023
Dentin defects caused by a Dspp<sup>-1</sup> frameshift mutation are associated with the activation of autophagyTian Liang, Charles E Smith, Yuanyuan Hu, et al.
European Journal of Oral Sciences|January 17, 2012
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two familiesShih-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 ModelJan C-C Hu, Tian Liang, Hong Zhang, et al.
Journal of Dental Sciences|January 26, 2026
Novel <i>MMP20</i> (matrix metalloproteinase 20) mutations causing hypoplastic-hypomaturation amelogenesis imperfectaShih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Journal of Personalized Medicine|November 27, 2021
Synergistic Mutations of <i>LRP6</i> and <i>WNT10A</i> in Familial Tooth AgenesisKuan-Yu Chu, Yin-Lin Wang, Yu-Ren Chou, et al.
Calcified Tissue International|July 3, 2026
ODAPH (p.Arg77*) Phenotype and Onset of Ameloblast Pathology During Postsecretory Transition Demonstrated by FIB-SEM Analyses of Odaph<sup>C41*/C41*</sup> MiceJan C-C Hu, Charles E Smith, Hong Zhang, et al.
International Journal of Molecular Sciences|June 19, 2024
<i>AMELX</i> Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis ImperfectaShih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Plos Genetics|March 8, 2013
FAM20A mutations can cause enamel-renal syndrome (ERS)Shih-Kai Wang, Parissa Aref, Yuanyuan Hu, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
Journal of Personalized Medicine|February 25, 2023
Novel <i>WDR72</i> Mutations Causing Hypomaturation Amelogenesis ImperfectaYoun Jung Kim, Hong Zhang, Yejin Lee, et al.
Journal of Personalized Medicine|February 25, 2022
Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis ImperfectaYejin Lee, Hong Zhang, Figen Seymen, et al.
Scientific Reports|April 19, 2023
Dentin defects caused by a Dspp<sup>-1</sup> frameshift mutation are associated with the activation of autophagyTian Liang, Charles E Smith, Yuanyuan Hu, et al.
European Journal of Oral Sciences|January 17, 2012
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two familiesShih-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 ModelJan C-C Hu, Tian Liang, Hong Zhang, et al.
Journal of Dental Sciences|January 26, 2026
Novel <i>MMP20</i> (matrix metalloproteinase 20) mutations causing hypoplastic-hypomaturation amelogenesis imperfectaShih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Journal of Personalized Medicine|November 27, 2021
Synergistic Mutations of <i>LRP6</i> and <i>WNT10A</i> in Familial Tooth AgenesisKuan-Yu Chu, Yin-Lin Wang, Yu-Ren Chou, et al.
Calcified Tissue International|July 3, 2026
ODAPH (p.Arg77*) Phenotype and Onset of Ameloblast Pathology During Postsecretory Transition Demonstrated by FIB-SEM Analyses of Odaph<sup>C41*/C41*</sup> MiceJan C-C Hu, Charles E Smith, Hong Zhang, et al.
International Journal of Molecular Sciences|June 19, 2024
<i>AMELX</i> Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis ImperfectaShih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Plos Genetics|March 8, 2013
FAM20A mutations can cause enamel-renal syndrome (ERS)Shih-Kai Wang, Parissa Aref, Yuanyuan Hu, et al.
Pageof 12