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机构 日期 题名 作者
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
臺大學術典藏 2021-07-06T09:59:58Z 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.; 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.
臺大學術典藏 2021-07-06T09:59:57Z 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.
臺大學術典藏 2018-09-10T15:00:53Z STIM1 and SLC24A4 Are Critical for Enamel Maturation Wang, S.;Choi, M.;Richardson, A.S.;Reid, B.M.;Seymen, F.;Yildirim, M.;Tuna, E.;Gen?Ay, K.;Simmer, J.P.;Hu, J.C.; SHIH-KAI Wang
臺大學術典藏 2018-09-10T15:00:52Z Ameloblast transcriptome changes from secretory to maturation stages Simmer, J.P.;Richardson, A.S.;Wang, S.-K.;Reid, B.M.;Bai, Y.;Hu, Y.;Hu, J.C.-C.; SHIH-KAI Wang
臺大學術典藏 2018-09-10T15:00:52Z FAM20A mutations associated with enamel renal syndrome Wang, S.K.;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.; SHIH-KAI Wang
臺大學術典藏 2018-09-10T15:00:52Z ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta Wang, S.;Choi, M.;Richardson, A.S.;Reid, B.M.;Lin, B.P.;Wang, S.J.;Kim, J.;Simmer, J.P.;Hu, J.C.-C.; SHIH-KAI Wang
臺大學術典藏 2018-09-10T08:47:44Z Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families SHIH-KAI Wang; Wang, S.-K.;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 2018-09-10T08:47:44Z Potential contribution of neural crest cells to dental enamel formation Wang, S.-K.;Komatsu, Y.;Mishina, Y.; SHIH-KAI Wang
國立交通大學 2014-12-12T02:26:11Z 利用Ni-based/MAO觸媒系統進行甲基丙烯酸三丁酯和原冰烯單聚合和共聚合反應的探討 王世凱; Shih-Kai Wang; 張豐志; Feng-Chih Chang
國立臺灣海洋大學 2012 修補砂漿基本性質之研究 Shih-Kai Wang; 王詩凱

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