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Showing items 1-25 of 35  (2 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2022-06-14T23:24:19Z 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.
臺大學術典藏 2021-12-14T23:12:30Z Synergistic mutations of lrp6 and wnt10a in familial tooth agenesis Chu, Kuan Yu; YIN-LIN WANG; Chou, Yu Ren; JUNG-TSU CHEN; YI-PING WANG; Simmer, James P.; Hu, Jan C.C.; SHIH-KAI Wang
臺大學術典藏 2021-11-21T23:19:43Z Mouse Dspp frameshift model of human dentinogenesis imperfecta Liang, Tian; Hu, Yuanyuan; Zhang, Hong; Xu, Qian; Smith, Charles E.; Zhang, Chuhua; Kim, Jung Wook; SHIH-KAI Wang; Saunders, Thomas L.; Lu, Yongbo; Hu, Jan C.C.; Simmer, James P.
臺大學術典藏 2021-11-21T23:19:42Z 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.
臺大學術典藏 2021-07-06T10:00:04Z 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.
臺大學術典藏 2021-07-06T10:00:03Z Novel PAX9 and COL1A2 Missense Mutations Causing Tooth Agenesis and OI/DGI without Skeletal Abnormalities SHIH-KAI Wang; Chan H.-C.; Makovey I.; Simmer J.P.; Hu J.C.-C.
臺大學術典藏 2021-07-06T10:00:03Z 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.
臺大學術典藏 2021-07-06T10:00:03Z Potential contribution of neural crest cells to dental enamel formation SHIH-KAI Wang; Komatsu Y.; Mishina Y.
臺大學術典藏 2021-07-06T10:00:02Z FAM20C functions intracellularly within both ameloblasts and odontoblasts in vivo SHIH-KAI Wang; Samann A.C.; Hu J.C.-C.; Simmer J.P.
臺大學術典藏 2021-07-06T10:00:02Z Secreted protein kinases? SHIH-KAI Wang; Samann A.C.; Simmer J.P.
臺大學術典藏 2021-07-06T10:00:02Z Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing SHIH-KAI Wang; Hu Y.; Simmer J.P.; Seymen F.; Estrella N.M.R.P.; Pal S.; Reid B.M.; Yildirim M.; Bayram M.; Bartlett J.D.; Hu J.C.-C.
臺大學術典藏 2021-07-06T10:00:02Z 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.
臺大學術典藏 2021-07-06T10:00:01Z 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.
臺大學術典藏 2021-07-06T10:00:01Z STIM1 and SLC24A4 Are Critical for Enamel Maturation SHIH-KAI Wang; Choi M.; Richardson A.S.; Reid B.M.; Seymen F.; Yildirim M.; Tuna E.; Gen?ay K.; Simmer J.P.; Hu J.C.
臺大學術典藏 2021-07-06T10:00:01Z 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.
臺大學術典藏 2021-07-06T10:00:01Z 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.
臺大學術典藏 2021-07-06T10:00:00Z Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC) Vieira A.R.; Lee M.; Vairo F.; Loguercio Leite J.C.; Munerato M.C.; Visioli F.; D'?vila S.R.; SHIH-KAI Wang; Choi M.; Simmer J.P.; Hu J.C.-C.
臺大學術典藏 2021-07-06T10:00:00Z 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.
臺大學術典藏 2021-07-06T10:00:00Z Taurodontism, variations in tooth number, and misshapened crowns in wnt10a null mice and human kindreds Yang J.; SHIH-KAI Wang; Choi M.; Reid B.M.; Hu Y.; Lee Y.-L.; Herzog C.R.; Kim-Berman H.; Lee M.; Benke P.J.; Kent Lloyd K.C.; Simmer J.P.; Hu J.C.-C.
臺大學術典藏 2021-07-06T09:59:59Z 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.; 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.
臺大學術典藏 2021-07-06T09:59:59Z 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.; SHIH-KAI Wang; Hu Y.; Smith C.E.; Yang J.; Zeng C.; Kim J.-W.; Hu J.C.C.; Simmer J.P.
臺大學術典藏 2021-07-06T09:59:59Z 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.;Lee Y.-L.;Seymen F.;Koruyucu M.;Gencay K.;Lee M.;Choi M.;Kim J.-W.;Hu J.C.-C.;Simmer J.P.; SHIH-KAI Wang; Hu Y.; Yang J.; Smith C.E.; Richardson A.S.; Yamakoshi Y.; Lee Y.-L.; Seymen F.; Koruyucu M.; Gencay K.; Lee M.; Choi M.; Kim J.-W.; Hu J.C.-C.; Simmer J.P.
臺大學術典藏 2021-07-06T09:59:58Z Novel REST Truncation Mutations Causing Hereditary Gingival Fibromatosis Chen J.T.; Lin C.H.; Huang H.W.; Wang Y.P.; Kao P.C.; Yang T.P.; SHIH-KAI Wang
臺大學術典藏 2021-07-06T09:59:58Z 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.; Wang Y.-L.; Lu P.-Y.; Kim J.-W.; Foster B.L.; Bartlett J.D.; Simmer J.P.; Hu J.C.C.
臺大學術典藏 2021-07-06T09:59:58Z Transcriptome analysis of gingival tissues of enamel-renal syndrome Wang Y.-P.;Lin H.-Y.;Zhong W.-L.;Simmer J.P.;Shih-Kai Wang; Wang Y.-P.; Lin H.-Y.; Zhong W.-L.; Simmer J.P.; SHIH-KAI Wang

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