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Figen Seymen

Showing results (51-60 of 82) with videos related to

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Journal of Personalized Medicine|June 24, 2022
Translated Mutant <i>DSPP</i> mRNA Expression Level Impacts the Severity of Dentin DefectsYoun Jung Kim, Yejin Lee, Hong Zhang, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|March 4, 2018
Rethinking isolated cleft lip and palate as a syndromeMine Koruyucu, Yelda Kasimoğlu, Figen Seymen, et al.
International Endodontic Journal|May 9, 2023
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndromeShih-Kai Wang, Hong Zhang, Yin-Lin Wang, 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.
Archives of Oral Biology|December 15, 2010
MMP1 and MMP20 contribute to tooth agenesis in humansErika C Küchler, Renato Menezes, Nicholas Callahan, et al.
Molecular Genetics & Genomic Medicine|September 4, 2019
ENAM mutations and digenic inheritanceHong Zhang, Yuanyuan Hu, Figen Seymen, 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.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Human Mutation|October 13, 2011
Novel FAM20A mutations in hypoplastic amelogenesis imperfectaSang Hyun Cho, Figen Seymen, Kyung-Eun 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.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Journal of Personalized Medicine|June 24, 2022
Translated Mutant <i>DSPP</i> mRNA Expression Level Impacts the Severity of Dentin DefectsYoun Jung Kim, Yejin Lee, Hong Zhang, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|March 4, 2018
Rethinking isolated cleft lip and palate as a syndromeMine Koruyucu, Yelda Kasimoğlu, Figen Seymen, et al.
International Endodontic Journal|May 9, 2023
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndromeShih-Kai Wang, Hong Zhang, Yin-Lin Wang, 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.
Archives of Oral Biology|December 15, 2010
MMP1 and MMP20 contribute to tooth agenesis in humansErika C Küchler, Renato Menezes, Nicholas Callahan, et al.
Molecular Genetics & Genomic Medicine|September 4, 2019
ENAM mutations and digenic inheritanceHong Zhang, Yuanyuan Hu, Figen Seymen, 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.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Human Mutation|October 13, 2011
Novel FAM20A mutations in hypoplastic amelogenesis imperfectaSang Hyun Cho, Figen Seymen, Kyung-Eun 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.
Pageof 9