National Chengchi University, Social Science Center,Research & Development (Social network graph considers only
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WEN-LIN LIAO (29)
2023-12
CDKL5-mediated developmental tuning of neuronal excitability and concomitant regulation of transcriptome
2023-11
Developmental tuning of neuronal excitability and concomitant regulation of transcriptome by cyclin-dependent kinase-like 5
2023-09
CDKL5-mediated developmental tuning of neuronal excitability and concomitant regulation of transcriptome
2023-04
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
2022-09
Deciphering age-dependent neuronal hyperexcitability caused by CDKL5 deficiency
2020-06
Dopaminergic loss of cyclin-dependent kinase-like 5 recapitulates methylphenidate-remediable hyperlocomotion in mouse model of CDKL5 deficiency disorder
2020-03
Deficiency of cyclin-dependent kinase-like 5 causes spontaneous epileptic seizures in neonatal mice
2019-09
Dissecting psychomotor dysfunction in mouse models of CDKL5 deficiency disorder
2019-03
Aberrant protein phosphorylation of dopamine signaling molecules in mouse model of CDKL5 deficiency disorder
2019-01
Psychomotor dysfunction in Rett syndrome: insights into the neurochemical and circuit roots
2019-01
Methylphenidate ameliorates hyperlocomotion in CDKL5 deficiency mice
2018-01
Loss of CDKL5 disrupts respiratory function in mice
2017
Mice lacking cyclin-dependent kinase-like 5 manifest autistic and ADHD-like behaviors
2016-12
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
2015-04
MeCP2 in the rostral striatum maintains local dopamine content critical for psychomotor control
2013.10
MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome.
2012-04
MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder
2012
以瑞特氏症模式小鼠研究運動障礙之療癒
2011
瑞特氏症新穎模式小鼠之研究
2010
探索瑞特氏症心理運動失調之神經基礎---發育中紋狀體的角色
2009
Auditory evoked event related potentials and in vitro evoked circuit activity from adult MeCP2+/‐ mice indicate a shared autism phenotype and disrupted inhibitory cortical circuitry
2009
Aberrant neurochemical expression in striosomal compartments of the striatum in RXRγ null mutant mice
2009
Aberrant striatal gene expression and psychomotor impairments in a mouse model of Rett Syndrome
2008-05
Modular patterning of structure and function of the striatum by retinoid receptor signaling
2005.04
Retinoid signaling competence and RARbeta-mediated gene regulation in the developing mammalian telencephalon.
2005.01
RARbeta isoform-specific regulation of DARPP-32 gene expression: An ectopic expression study in the developing telencephalon
2005.01
Differential expression of RARbeta isoforms in the mouse striatum during development: a gradient of RARbeta2 expression along the rostrocaudal axis.
2003.10
Characterization of the rat A2A adenosine receptor gene: a 4.8-kb promoter-proximal DNA fragment confers selective expression in the central nervous system.
1994.12
Involvement of hippocampal NMDA and AMPA receptors in acquisition, formation and retrieval of spatial memory in the Morris water maze.
WEN-LIN LIAO
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