臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 11-20 of 35 (4 Page(s) Totally)
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Institution	Date	Title	Author
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.

Showing items 11-20 of 35 (4 Page(s) Totally)
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