| 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 |
2021-07-06T10:00:01Z |
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 |
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 |
2021-07-05T07:35:47Z |
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 |
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 |
