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Jan C C Hu

Showing results (91-100 of 112) with videos related to

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The Journal of Biological Chemistry|February 7, 2008
Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in miceJan C-C Hu, Yuanyuan Hu, Charles E Smith, et al.
Frontiers in Physiology|May 6, 2017
Analyses of <i>MMP20</i> Missense Mutations in Two Families with Hypomaturation Amelogenesis ImperfectaYoun Jung Kim, Jenny Kang, Figen Seymen, et al.
Molecular Genetics & Genomic Medicine|September 4, 2019
ENAM mutations and digenic inheritanceHong Zhang, Yuanyuan Hu, Figen Seymen, et al.
Scientific Reports|October 20, 2021
Mouse Dspp frameshift model of human dentinogenesis imperfectaTian Liang, Yuanyuan Hu, Hong Zhang, et al.
Human Genetics|December 14, 2004
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type IIJung-Wook Kim, Jan C-C Hu, Jae-Il Lee, et al.
American Journal of Human Genetics|February 7, 2008
FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfectaJung-Wook Kim, Sook-Kyung Lee, Zang Hee Lee, et al.
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.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
The Journal of Biological Chemistry|February 7, 2008
Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in miceJan C-C Hu, Yuanyuan Hu, Charles E Smith, et al.
Frontiers in Physiology|May 6, 2017
Analyses of <i>MMP20</i> Missense Mutations in Two Families with Hypomaturation Amelogenesis ImperfectaYoun Jung Kim, Jenny Kang, Figen Seymen, et al.
Molecular Genetics & Genomic Medicine|September 4, 2019
ENAM mutations and digenic inheritanceHong Zhang, Yuanyuan Hu, Figen Seymen, et al.
Scientific Reports|October 20, 2021
Mouse Dspp frameshift model of human dentinogenesis imperfectaTian Liang, Yuanyuan Hu, Hong Zhang, et al.
Human Genetics|December 14, 2004
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type IIJung-Wook Kim, Jan C-C Hu, Jae-Il Lee, et al.
American Journal of Human Genetics|February 7, 2008
FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfectaJung-Wook Kim, Sook-Kyung Lee, Zang Hee Lee, et al.
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.
Pageof 12