|
English
|
正體中文
|
简体中文
|
总笔数 :0
|
|
造访人次 :
51027462
在线人数 :
920
教育部委托研究计画 计画执行:国立台湾大学图书馆
|
|
|
"ming jen lee"的相关文件
显示项目 1-10 / 123 (共13页)
1 2 3 4 5 6 7 8 9 10 > >>
每页显示[10|25|50]项目
| 臺大學術典藏 |
2022-06-14T23:24:17Z |
Kinetic Alterations in Resurgent Sodium Currents of Mutant Nav1.4 Channel in Two Patients Affected by Paramyotonia Congenita
|
MING-JEN LEE; Lin, Pi Chen; Lin, Ming Hong; Chiou, Hsin Ying Clair; Wang, Kai; Huang, Chiung Wei |
| 臺大學術典藏 |
2022-02-14T23:55:55Z |
Recent Advances in RNA Therapy and Its Carriers to Treat the Single-Gene Neurological Disorders
|
MING-JEN LEE; Lee, Inyoul; Wang, Kai |
| 臺大學術典藏 |
2021-09-14T23:19:07Z |
DNA hypermethylation involves in the down-regulation of chloride intracellular channel 4 (CLIC4) induced by photodynamic therapy
|
Chiang, Pei Chi; Li, Pei Tzu; MING-JEN LEE; CHIN-TIN CHEN |
| 臺大學術典藏 |
2021-03-02T14:00:28Z |
Changes in resurgent sodium current contribute to the hyperexcitability of muscles in patients with paramyotonia congenita
|
Huang, Chiung Wei; Lai, Hsing Jung; Lin, Pi Chen; MING-JEN LEE |
| 臺大學術典藏 |
2020-11-03T11:32:32Z |
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene
|
Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.; Davis M.B.; An S.-F.; Sweeney M.G.; Groves M.J.; Stephenson D.A.; MING-JEN LEE |
| 臺大學術典藏 |
2020-11-03T11:32:31Z |
Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C
|
Su Y.-N.; Chiou P.-C.; Yang C.-C.; Fietz M.J.; Yu C.-L.; Hwu W.-L.; MING-JEN LEE |
| 臺大學術典藏 |
2020-11-03T11:32:31Z |
Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
|
Yip P.-K.; Jeng J.-S.; MING-JEN LEE; Tang S.-C. |
| 臺大學術典藏 |
2020-11-03T11:32:30Z |
Recent developments in neurofibromatosis type 1
|
Stephenson D.A.; MING-JEN LEE |
| 臺大學術典藏 |
2020-11-03T11:32:28Z |
Notch signaling and CADASIL
|
Jeng J.-S.; Tang S.-C.; MING-JEN LEE; Yip P.-K. |
| 臺大學術典藏 |
2020-03-03T02:33:37Z |
Genetic aspects of hereditary motor and sensory neuropathy
|
MING-JEN LEE; Reilly M.M. |
显示项目 1-10 / 123 (共13页)
1 2 3 4 5 6 7 8 9 10 > >>
每页显示[10|25|50]项目
|
