Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Shih‐Kai Wang"'
Autor:
Nutthakarn Ratanasereeprasert, Li-Fang Hsu, Shih-Kai Wang, Yi-Jane Chen, Jui-Heng Chang, Chung-Chen Jane Yao
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 4, Pp 442-451 (2024)
Background: The study aimed to observe molecular signaling, including reactive oxygen species (ROS) and mitochondrial membrane potential (ΔΨm), to evaluate the alteration of gene expression by low-level laser therapy (LLLT) and the correlation betw
Externí odkaz:
https://doaj.org/article/b6e3be2c5da64e4e9ce6cebb7619bbc4
Autor:
Li-Fang Hsu, Nutthakarn Ratanasereeprasert, Shih-Kai Wang, Jung-Tsu Chen, Yi-Jane Chen, Te-Huei Yeh, Hsiang-Hsuan Sung, Chung-Chen Jane Yao
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Nasal obstruction exerts considerable physiological effects on the respiratory system and craniofacial morphology during the developmental stage. This study used MMP-3-LUC transgenic rats for in vivo tracking of long-term expression in the r
Externí odkaz:
https://doaj.org/article/4582f8cba1ee4142b4601ad8df2601b1
Autor:
Feng-Chou Cheng, Guay-Fen Huang, Yin-Lin Wang, Hsiao-Hua Chang, Shih-Kai Wang, Ming-Kuang Guo, Chun-Pin Chiang
Publikováno v:
Journal of Dental Sciences, Vol 18, Iss 4, Pp 1794-1803 (2023)
Background/purpose: The separation of dentistry and medicine was initiated as a historical root. The purpose of this study was to evaluate the implication of integrating pediatric education into a pediatric dentistry course (so-called the integrated
Externí odkaz:
https://doaj.org/article/9ea8def03b904340815a61827e28788e
Autor:
Tian Liang, Shih-Kai Wang, Charles Smith, Hong Zhang, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Chuhua Zhang, Thomas L. Saunders, James P. Simmer, Jan C.-C. Hu
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-20 (2022)
Abstract Human ACP4 (OMIM*606362) encodes a transmembrane protein that belongs to histidine acid phosphatase (ACP) family. Recessive mutations in ACP4 cause non-syndromic hypoplastic amelogenesis imperfecta (AI1J, OMIM#617297). While ACP activity has
Externí odkaz:
https://doaj.org/article/b1ed9c32d099421cbc3e834f910de5b2
Autor:
Tian Liang, Yuanyuan Hu, Hong Zhang, Qian Xu, Charles E. Smith, Chuhua Zhang, Jung-Wook Kim, Shih-Kai Wang, Thomas L. Saunders, Yongbo Lu, Jan C.-C. Hu, James P. Simmer
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Non-syndromic inherited defects of tooth dentin are caused by two classes of dominant negative/gain-of-function mutations in dentin sialophosphoprotein (DSPP): 5′ mutations affecting an N-terminal targeting sequence and 3′ mutations that
Externí odkaz:
https://doaj.org/article/8cc6c2e7bcd84aac8371c3b57be3059c
Autor:
Shih‐Kai Wang, Hong Zhang, Michael B. Chavez, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Connor D. Colvin, Tamara N. Kolli, Michelle H. Tan, Yin‐Lin Wang, Pei‐Ying Lu, Jung‐Wook Kim, Brian L. Foster, John D. Bartlett, James P. Simmer, Jan C.‐C. Hu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background Matrix metallopeptidase 20 (MMP20) is an evolutionarily conserved protease that is essential for processing enamel matrix proteins during dental enamel formation. MMP20 mutations cause human autosomal recessive pigmented hypomatur
Externí odkaz:
https://doaj.org/article/89d3f87d0001415bb348c887bd7e7fc1
Autor:
Hong Zhang, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Shih‐Kai Wang, John Timothy Wright, Michael W. Havel, Chuhua Zhang, Jung‐Wook Kim, James P. Simmer, Jan C.‐C. Hu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background ENAM mutations cause autosomal dominant or recessive amelogenesis imperfecta (AI) and show a dose effect: enamel malformations are more severe or only penetrant when both ENAM alleles are defective. Methods Whole exome sequences o
Externí odkaz:
https://doaj.org/article/7b61b9235588451f9c86615f3eaad46c
Autor:
Tian Liang, Yuanyuan Hu, Charles E. Smith, Amelia S Richardson, Hong Zhang, Jie Yang, Brent Lin, Shih‐Kai Wang, Jung‐Wook Kim, Yong‐Hee Chun, James P. Simmer, Jan C.‐C. Hu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Abstract Background Ameloblastin (AMBN) is a secreted matrix protein that is critical for the formation of dental enamel and is enamel‐specific with respect to its essential functions. Biallelic AMBN defects cause non‐syndromic autosomal recessiv
Externí odkaz:
https://doaj.org/article/90502c4fc4e94899b48b326a4e03bb28
Autor:
Shih‐Kai Wang, Yuanyuan Hu, Charles E. Smith, Jie Yang, Chunhua Zeng, Jung‐Wook Kim, Jan C‐C. Hu, James P. Simmer
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background Truncation FAM83H mutations cause human autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI), an inherited disorder characterized by severe hardness defects in dental enamel. No enamel defects were observed in Fam83h
Externí odkaz:
https://doaj.org/article/6b4f5eeb5f434b398802d89035dd84e0
Autor:
Shih‐Kai Wang, Hong Zhang, Yin‐Lin Wang, Hung‐Ying Lin, Figen Seymen, Mine Koruyucu, J. Timothy Wright, Jung‐Wook Kim, James P. Simmer, Jan C.‐C. Hu
Publikováno v:
International Endodontic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15551525e4ba51b94d62bdd44e21df82
https://doi.org/10.1111/iej.13928
https://doi.org/10.1111/iej.13928