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机构 日期 题名 作者
臺大學術典藏 2021-10-18T05:41:11Z Dental malformations associated with biallelic MMP20 mutations Wang S.-K.; 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.
臺大學術典藏 2021-07-07T02:12:38Z Transcriptome analysis of gingival tissues of enamel-renal syndrome Yi-Ping Wang;Lin H.-Y.;Zhong W.-L.;Simmer J.P.;Wang S.-K.; YI-PING WANG; Lin H.-Y.; Zhong W.-L.; Simmer J.P.; Wang S.-K.
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 2021-07-06T10:00:02Z 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 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 2021-07-05T07:35:47Z Taurodontism, variations in tooth number, and misshapened crowns in wnt10a null mice and human kindreds Yang J.; Wang S.-K.; Choi M.; Reid B.M.; Hu Y.; YUAN-LING LEE; 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 2021-07-05T07:35:47Z Fam83h null mice support a neomorphic mechanism for human ADHCAI Wang S.-K.;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.; Wang S.-K.; 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.
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.

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