公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2010 | Altered enamelin phosphorylation site causes amelogenesis imperfecta | Chan H.-C.; Mai L.; Oikonomopoulou A.; Chan H.L.; Richardson A.S.; SHIH-KAI WANG ; Simmer J.P.; Hu J.C.-C. | Journal of Dental Research | 43 | 39 | |
2019 | AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout-NLS-lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue-specificity | Liang T.; Hu Y.; Smith C.E.; Richardson A.S.; Zhang H.; Yang J.; Lin B.; SHIH-KAI WANG ; Kim J.-W.; Chun Y.-H.; Simmer J.P.; Hu J.C.C. | Molecular Genetics and Genomic Medicine | 21 | 20 | |
2014 | Ameloblast transcriptome changes from secretory to maturation stages | Simmer J.P.; Richardson A.S.; SHIH-KAI WANG ; Reid B.M.; Bai Y.; Hu Y.; Hu J.C.-C. | Connective Tissue Research | 16 | 14 | |
2024 | Craniofacial and olfactory sensory changes after long-term unilateral nasal obstruction-an animal study using MMP-3-LUC transgenic rats | Hsu, Li-Fang; Ratanasereeprasert, Nutthakarn; SHIH-KAI WANG ; JUNG-TSU CHEN ; YI-JANE CHEN ; TE-HUEI YEH ; Sung, Hsiang-Hsuan; JANE CHUNG-CHEN YAO | Scientific reports | | | |
2015 | Critical roles for wdr72 in calcium transport and matrix protein removal during enamel maturation | SHIH-KAI WANG ; Hu Y.; Yang J.; Smith C.E.; Nunez S.M.; Richardson A.S.; Pal S.; Samann A.C.; Hu J.C.-C.; Simmer J.P. | Molecular Genetics and Genomic Medicine | 40 | 39 | |
2020 | Dental malformations associated with biallelic MMP20 mutations | SHIH-KAI WANG ; Zhang H.; Chavez M.B.; Hu Y.; Seymen F.; Koruyucu M.; Kasimoglu Y.; Colvin C.D.; Kolli T.N.; Tan M.H.; YIN-LIN WANG ; Lu P.-Y.; Kim J.-W.; Foster B.L.; Bartlett J.D.; Simmer J.P.; Hu J.C.C. | Molecular Genetics and Genomic Medicine | 10 | 11 | |
2019 | ENAM mutations and digenic inheritance | Zhang H.; Hu Y.; Seymen F.; Koruyucu M.; Kasimoglu Y.; SHIH-KAI WANG ; Wright J.T.; Havel M.W.; Zhang C.; Kim J.-W.; Simmer J.P.; Hu J.C.C. | Molecular Genetics and Genomic Medicine | 10 | 8 | |
2022 | Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations | Liang, Tian; SHIH-KAI WANG ; Smith, Charles; Zhang, Hong; Hu, Yuanyuan; Seymen, Figen; Koruyucu, Mine; Kasimoglu, Yelda; Kim, Jung-Wook; Zhang, Chuhua; Saunders, Thomas L; Simmer, James P; Hu, Jan C-C | Scientific reports | 4 | 3 | |
2011 | Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families | SHIH-KAI WANG ; Chan H.-C.; Rajderkar S.; Milkovich R.N.; Uston K.A.; Kim J.-W.; Simmer J.P.; Hu J.C.-C. | European Journal of Oral Sciences | 25 | 23 | |
2019 | The Enamel Phenotype in Homozygous Fam83h Truncation Mice | SHIH-KAI WANG ; Hu Y.; Smith C.E.; Yang J.; Zeng C.; Kim J.-W.; Hu J.C.C.; Simmer J.P. | Molecular Genetics and Genomic Medicine | 15 | 17 | |
2023 | FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome | SHIH-KAI WANG ; Zhang, Hong; YIN-LIN WANG ; Lin, Hung-Ying; Seymen, Figen; Koruyucu, Mine; Wright, J Timothy; Kim, Jung-Wook; Simmer, James P; Hu, Jan C-C | International endodontic journal | 5 | | |
2014 | FAM20A mutations associated with enamel renal syndrome | SHIH-KAI WANG ; Reid B.M.; Dugan S.L.; Roggenbuck J.A.; Read L.; Aref P.; Taheri A.P.H.; Yeganeh M.Z.; Simmer J.P.; Hu J.C.-C. | Journal of Dental Research | 50 | 50 | |
2013 | FAM20A Mutations Can Cause Enamel-Renal Syndrome (ERS) | SHIH-KAI WANG ; Aref P.; Hu Y.; Milkovich R.N.; Simmer J.P.; El-Khateeb M.; Daggag H.; Baqain Z.H.; Hu J.C.-C. | PLoS Genetics | 76 | 78 | |
2013 | FAM20C functions intracellularly within both ameloblasts and odontoblasts in vivo | SHIH-KAI WANG ; Samann A.C.; Hu J.C.-C.; Simmer J.P. | Journal of Bone and Mineral Research | 17 | 15 | |
2021 | FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta | SHIH-KAI WANG ; Zhang H.; Hu C.Y.; Liu J.F.; Chadha S.; Kim J.W.; Simmer J.P.; Hu J.C.C. | Journal of Dental Research | 18 | 17 | |
2016 | Fam83h null mice support a neomorphic mechanism for human ADHCAI | SHIH-KAI WANG ; Hu Y.; Yang J.; Smith C.E.; Richardson A.S.; Yamakoshi Y.; YUAN-LING LEE ; Seymen F.; Koruyucu M.; Gencay K.; Lee M.; Choi M.; Kim J.-W.; Hu J.C.-C.; Simmer J.P. | Molecular Genetics and Genomic Medicine | 33 | 36 | |
2021 | A genetic model for the secretory stage of dental enamel formation | Simmer, James P; Hu, Jan C-C; Hu, Yuanyuan; Zhang, Shelly; Liang, Tian; SHIH-KAI WANG ; Kim, Jung-Wook; Yamakoshi, Yasuo; Chun, Yong-Hee; Bartlett, John D; Smith, Charles E | Journal of structural biology | 17 | 14 | |
2023 | The implication of integrating pediatric education into a pediatric dentistry course for undergraduate dental students | Cheng, Feng-Chou; Huang, Guay-Fen; YIN-LIN WANG ; HSIAO-HUA CHANG ; SHIH-KAI WANG ; Guo, Ming-Kuang; CHUN-PIN CHIANG | Journal of dental sciences | | | |
2014 | ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta | SHIH-KAI WANG ; Choi M.; Richardson A.S.; Reid B.M.; Lin B.P.; Wang S.J.; Kim J.; Simmer J.P.; Hu J.C.-C. | Human Molecular Genetics | 45 | 41 | |
2022 | The Modified Shields Classification and 12 Families with Defined DSPP Mutations | Simmer, James P; Zhang, Hong; Moon, Sophie J H; Donnelly, Lori A-J; YUAN-LING LEE ; Seymen, Figen; Koruyucu, Mine; Chan, Hui-Chen; Lee, Kevin Y; Wu, Suwei; Hsiang, Chia-Lan; Tsai, Anthony T P; Slayton, Rebecca L; Morrow, Melissa; SHIH-KAI WANG ; Shields, Edward D; Hu, Jan C-C | Genes | 9 | 8 | |