Wenlin Liao, Ph.D. - Publications

2009- NCCU, Taiwan 
Developmental disorders

8 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
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  1
2020 Luan H, Liao W, Song Y, Niu H, Hu T, Zhi H. Transgenic plant generated by RNAi-mediated knocking down of soybean Vma12 and soybean mosaic virus resistance evaluation. Amb Express. 10: 62. PMID 32253532 DOI: 10.1186/s13568-020-00997-6  0.4
2018 Liao W. Psychomotor dysfunction in Rett syndrome: insights into the neurochemical and circuit roots. Developmental Neurobiology. PMID 30430747 DOI: 10.1002/dneu.22651  0.01
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  0.08
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  0.24
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  1
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  1
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  1
Show low-probability matches.