Showing results 6 to 25 of 29
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Date | Title | Author(s) |
16-Jun-2023 | Deciphering age-dependent neuronal hyperexcitability caused by CDKL5 deficiency | 廖文霖; Liao, Wenlin |
13-Nov-2020 | Deficiency of cyclin-dependent kinase-like 5 causes spontaneous epileptic seizures in neonatal mice | 廖文霖; Liao, Wenlin; Kun-Ze Lee; Jinchung Chen; San-Hua Su; Yuju Luo |
23-Sep-2014 | Differential expression of RARbeta isoforms in the mouse striatum during development: a gradient of RARbeta2 expression along the rostrocaudal axis. | 廖文霖; Liao, Wen-Lin ;Tsai,HC;Wu,CY;Liu,FC |
5-Oct-2020 | Dissecting psychomotor dysfunction in mouse models of CDKL5 deficiency disorder | 廖文霖; Liao, Wenlin |
13-Nov-2020 | Dopaminergic loss of cyclin-dependent kinase-like 5 recapitulates methylphenidate-remediable hyperlocomotion in mouse model of CDKL5 deficiency disorder | 廖文霖; Liao, Wenlin; Jhang, Cian-Ling; Lee, Hom-Yi; Chen, Jin-Chung |
23-Sep-2014 | Involvement of hippocampal NMDA and AMPA receptors in acquisition, formation and retrieval of spatial memory in the Morris water maze. | 廖文霖; Liang, K. C. ; Hon, Wai ; Tyan, Yih-Min ; Liao, Wen-Lin |
29-Jan-2018 | Loss of CDKL5 disrupts respiratory function in mice | 廖文霖; Lee, Kun-Ze; Liao, Wenlin |
14-Jan-2016 | MeCP2 in the rostral striatum maintains local dopamine content critical for psychomotor control | Su, San-Hua;Kao, Fang-Chi;Huang, Yi-Bo;Liao, Wenlin; 廖文霖 |
27-May-2014 | MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder | 廖文霖; Liao, Wen-Lin |
17-Jan-2014 | MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome. | 廖文霖; Kao, Fang-Chi ;Su, San-Hua ; Carlson, Gregory C. ; Liao, Wenlin |
24-Jun-2020 | Methylphenidate ameliorates hyperlocomotion in CDKL5 deficiency mice | 廖文霖; Liao, Wen-Lin; Luo, Y; CL, Jhang |
28-Sep-2017 | Mice lacking cyclin-dependent kinase-like 5 manifest autistic and ADHD-like behaviors | 廖文霖; Jhang, Cian-Ling; Huang, Tzyy-Nan; Hsueh, Yi-Ping; Liao, Wenlin |
21-May-2018 | Modular patterning of structure and function of the striatum by retinoid receptor signaling | 廖文霖; Liao, Wen-Lin; Tsai, Hsiu-Chao; Wang, Hsiao-Fang; Chang, Josephine; Lu, Kuan-Ming; Wu, Hsiao-Lin; Lee, Yi-Chao |
17-Sep-2018 | Neurotensin-Conjugated Reduced Graphene Oxide with Multi-Stage Near-Infrared-Triggered Synergic Targeted Neuron Gene Transfection In Vitro and In Vivo for Neurodegenerative Disease Therapy | Hsieh, Tsung‐Ying;Huang, Wei‐Chen;Kang, Yi‐Da;Chu, Chao‐Yi;Liao, Wen‐Lin;Chen, You‐Yin; 廖文霖; Liao, Wen‐Lin |
2-Aug-2023 | Perinatal blockade of neuronal glutamine transport sex-differentially alters glutamatergic synaptic transmission and organization of neurons in the ventrolateral ventral media hypothalamus of adult rats | 廖文霖; Liao, Wen-Lin;Liang, Shu-Ling;Chen, Rou-Shayn |
12-Dec-2018 | Psychomotor dysfunction in Rett syndrome: insights into the neurochemical and circuit roots | 廖文霖; Liao, Wenlin |
23-Sep-2014 | RARbeta isoform-specific regulation of DARPP-32 gene expression: An ectopic expression study in the developing telencephalon | 廖文霖; Liao, Wen-Lin ; Liu, Fu-Chin |
23-Sep-2014 | Retinoid signaling competence and RARbeta-mediated gene regulation in the developing mammalian telencephalon. | 廖文霖; Liao, Wen-Lin ;Wang,HF;Tsai,HC;Chambon P;Wagner M;Kakizuka A;Liu,FC |
1-Apr-2015 | 以典型瑞特氏症模式小鼠研究運動障礙之療癒 | 黃弈博; Huang, Yi Bo |
15-Nov-2012 | 以瑞特氏症模式小鼠研究運動障礙之療癒 | 廖文霖; LIAO, WEN-LIN |