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English
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總筆數 :2856753
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造訪人次 :
53853541
線上人數 :
1143
教育部委託研究計畫 計畫執行:國立臺灣大學圖書館
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"yanagawa y"的相關文件
顯示項目 1-6 / 6 (共1頁)
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| 臺大學術典藏 |
2020-11-04T01:59:21Z |
Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development
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Chang F.-C.; Hsiao J.H.; Khorkova O.; Liou H.-H.; Yanagawa Y.; Lee L.-J.; Lin S.-W.; Tsai M.-S.; Lee M.-L.; Chang C.-Y.; Fan H.-H.; Yu I.-S.; YOU-TZUNG CHEN; You J.-Y.; Chen C.-Y. |
| 臺大學術典藏 |
2020-11-03T09:53:23Z |
Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development
|
Tsai M.-S.;Lee M.-L.;Chang C.-Y.;Fan H.-H.;Yu I.-S.;Chen Y.-T.;You J.-Y.;Chen C.-Y.;Chang F.-C.;Hsiao J.H.;Khorkova O.;Horng-Huei Liou;Yanagawa Y.;Lee L.-J.;Lin S.-W.; Tsai M.-S.; Lee M.-L.; Chang C.-Y.; Fan H.-H.; Yu I.-S.; Chen Y.-T.; You J.-Y.; Chen C.-Y.; Chang F.-C.; Hsiao J.H.; Khorkova O.; HORNG-HUEI LIOU; Yanagawa Y.; Lee L.-J.; Lin S.-W. |
| 臺大學術典藏 |
2020-03-02T05:45:40Z |
Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development
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Tsai M.-S.; Lee M.-L.; Chang C.-Y.; Fan H.-H.; Yu I.-S.; Chen Y.-T.; You J.-Y.; Chen C.-Y.; Chang F.-C.; Hsiao J.H.; Khorkova O.; Liou H.-H.; Yanagawa Y.; LI-JEN LEE; Lin S.-W. |
| 臺大學術典藏 |
2020-02-26T07:30:11Z |
Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development
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Tsai M.-S; Lee M.-L; Chang C.-Y; Fan H.-H; Yu I.-S; Chen Y.-T; You J.-Y; Chen C.-Y; Chang F.-C; Hsiao J.H; Khorkova O; HORNG-HUEI LIOU; Yanagawa Y; Lee L.-J; Lin S.-W. |
| 中國醫藥大學 |
2001 |
ATP7A gene mutations in 16 patients with Menkes disease and a patient with occipital horn syndrome
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Gu, YH; Kodama, H; Murata, Y; Mochizuki, D; Yanagawa, Y; Ushijima, H; Shiba, T; Lee, CC |
| 中國醫藥大學 |
2001 |
ATP7A gene mutations in 16 patients with Menkes disease and a patient with occipital horn syndrome
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Gu, YH; Kodama, H; Murata, Y; Mochizuki, D; Yanagawa, Y; Ushijima, H; Shiba, T; Lee, CC |
顯示項目 1-6 / 6 (共1頁)
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