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Journal of Personalized Medicine
|
June 24, 2022
Translated Mutant <i>DSPP</i> mRNA Expression Level Impacts the Severity of Dentin Defects
Youn 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 syndrome
Mine 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 syndrome
Shih-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 Imperfecta
Youn Jung Kim, Jenny Kang, Figen Seymen, et al.
Archives of Oral Biology
|
December 15, 2010
MMP1 and MMP20 contribute to tooth agenesis in humans
Erika C Küchler, Renato Menezes, Nicholas Callahan, et al.
Molecular Genetics & Genomic Medicine
|
September 4, 2019
ENAM mutations and digenic inheritance
Hong Zhang, Yuanyuan Hu, Figen Seymen, et al.
Scientific Reports
|
October 1, 2022
Enamel defects in Acp4<sup>R110C/R110C</sup> mice and human ACP4 mutations
Tian Liang, Shih-Kai Wang, Charles Smith, et al.
Molecular Genetics & Genomic Medicine
|
January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentin
Jie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Human Mutation
|
October 13, 2011
Novel FAM20A mutations in hypoplastic amelogenesis imperfecta
Sang Hyun Cho, Figen Seymen, Kyung-Eun Lee, et al.
Plos One
|
December 20, 2012
Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6
Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 82) with videos related to
Sort By:
Page
of 9
Journal of Personalized Medicine
|
June 24, 2022
Translated Mutant <i>DSPP</i> mRNA Expression Level Impacts the Severity of Dentin Defects
Youn 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 syndrome
Mine 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 syndrome
Shih-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 Imperfecta
Youn Jung Kim, Jenny Kang, Figen Seymen, et al.
Archives of Oral Biology
|
December 15, 2010
MMP1 and MMP20 contribute to tooth agenesis in humans
Erika C Küchler, Renato Menezes, Nicholas Callahan, et al.
Molecular Genetics & Genomic Medicine
|
September 4, 2019
ENAM mutations and digenic inheritance
Hong Zhang, Yuanyuan Hu, Figen Seymen, et al.
Scientific Reports
|
October 1, 2022
Enamel defects in Acp4<sup>R110C/R110C</sup> mice and human ACP4 mutations
Tian Liang, Shih-Kai Wang, Charles Smith, et al.
Molecular Genetics & Genomic Medicine
|
January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentin
Jie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Human Mutation
|
October 13, 2011
Novel FAM20A mutations in hypoplastic amelogenesis imperfecta
Sang Hyun Cho, Figen Seymen, Kyung-Eun Lee, et al.
Plos One
|
December 20, 2012
Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6
Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, et al.
Page
of 9