Wenlin Liao, Ph.D. - Publications

Affiliations: 
2009- NCCU, Taiwan 
Area:
Developmental disorders

14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Liao W, Lee KZ. CDKL5-mediated developmental tuning of neuronal excitability and concomitant regulation of transcriptome. Human Molecular Genetics. PMID 37688574 DOI: 10.1093/hmg/ddad149  0.362
2020 Jhang CL, Lee HY, Chen J, Liao W. Dopaminergic loss of cyclin-dependent kinase-like 5 recapitulates methylphenidate-remediable hyperlocomotion in mouse model of CDKL5 deficiency disorder. Human Molecular Genetics. PMID 32588892 DOI: 10.1093/hmg/ddaa122  0.624
2018 Liao W. Psychomotor dysfunction in Rett syndrome: insights into the neurochemical and circuit roots. Developmental Neurobiology. PMID 30430747 DOI: 10.1002/dneu.22651  0.318
2017 Lee KZ, Liao W. Loss of CDKL5 disrupts respiratory function in mice. Respiratory Physiology & Neurobiology. 248: 48-54. PMID 29208534 DOI: 10.1016/J.Resp.2017.11.010  0.306
2017 Jhang CL, Huang TN, Hsueh YP, Liao W. Mice lacking cyclin-dependent kinase-like 5 manifest autistic and ADHD-like behaviors. Human Molecular Genetics. 26: 3922-3934. PMID 29016850 DOI: 10.1093/hmg/ddx279  0.357
2016 Liao W. Local striatal dopamine governs psychomotor behavior in mice Intrinsic Activity. 4: A18.2. DOI: 10.25006/IA.4.S2-A18.2  0.472
2015 Su SH, Kao FC, Huang YB, Liao W. MeCP2 in the rostral striatum maintains local dopamine content critical for psychomotor control. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 6209-20. PMID 25878291 DOI: 10.1523/Jneurosci.4624-14.2015  0.57
2015 Kao FC, Su SH, Carlson GC, Liao W. MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome. Brain Structure & Function. 220: 419-34. PMID 24218106 DOI: 10.1007/S00429-013-0664-X  0.513
2012 Liao W, Gandal MJ, Ehrlichman RS, Siegel SJ, Carlson GC. MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder. Neurobiology of Disease. 46: 88-92. PMID 22249109 DOI: 10.1016/J.Nbd.2011.12.048  0.632
2008 Liao WL, Tsai HC, Wang HF, Chang J, Lu KM, Wu HL, Lee YC, Tsai TF, Takahashi H, Wagner M, Ghyselinck NB, Chambon P, Liu FC. Modular patterning of structure and function of the striatum by retinoid receptor signaling. Proceedings of the National Academy of Sciences of the United States of America. 105: 6765-70. PMID 18443282 DOI: 10.1073/Pnas.0802109105  0.643
2005 Liao WL, Liu FC. RARbeta isoform-specific regulation of DARPP-32 gene expression: an ectopic expression study in the developing rat telencephalon. The European Journal of Neuroscience. 21: 3262-8. PMID 16026464 DOI: 10.1111/J.1460-9568.2005.04178.X  0.574
2005 Liao WL, Tsai HC, Wu CY, Liu FC. Differential expression of RARbeta isoforms in the mouse striatum during development: a gradient of RARbeta2 expression along the rostrocaudal axis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 233: 584-94. PMID 15778968 DOI: 10.1002/Dvdy.20344  0.514
2005 Liao WL, Wang HF, Tsai HC, Chambon P, Wagner M, Kakizuka A, Liu FC. Retinoid signaling competence and RARbeta-mediated gene regulation in the developing mammalian telencephalon. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 232: 887-900. PMID 15736225 DOI: 10.1002/Dvdy.20281  0.543
2003 Lee YC, Chien CL, Sun CN, Huang CL, Huang NK, Chiang MC, Lai HL, Lin YS, Chou SY, Wang CK, Tai MH, Liao WL, Lin TN, Liu FC, Chern Y. Characterization of the rat A2A adenosine receptor gene: a 4.8-kb promoter-proximal DNA fragment confers selective expression in the central nervous system. The European Journal of Neuroscience. 18: 1786-96. PMID 14622213 DOI: 10.1046/j.1460-9568.2003.02907.x  0.477
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