Wenlin Liao

发表

Hippocampal circuit abnormalities in MeCP2+/− mouse model of Rett syndrome

G. Carlson, Rachel E White, Julia Chartove, 2015, bioRxiv.

MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome

G. Carlson, Wenlin Liao, San-Hua Su, 2013, Brain Structure and Function.

Dopaminergic loss of cyclin-dependent kinase-like 5 recapitulates methylphenidate-remediable hyperlocomotion in mouse model of CDKL5 deficiency disorder.

Jin-Chung Chen, Wenlin Liao, Hom-Yi Lee, 2020, Human molecular genetics.

Deficiency of cyclin-dependent kinase-like 5 causes spontaneous epileptic seizures in neonatal mice

Wenlin Liao, Kun-Ze Lee, Yuju Luo, 2020, bioRxiv.

Mice lacking cyclin‐dependent kinase‐like 5 manifest autistic and ADHD‐like behaviors

Wenlin Liao, Y. Hsueh, Tzyy‐Nan Huang, 2017, Human molecular genetics.

MeCP2 in the Rostral Striatum Maintains Local Dopamine Content Critical for Psychomotor Control

Wenlin Liao, Yi-Bo Huang, San-Hua Su, 2015, The Journal of Neuroscience.

Psychomotor Dysfunction in Rett Syndrome: Insights into the Neurochemical and Circuit Roots

Wenlin Liao, 2018, Developmental neurobiology.

MeCP2+/− mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder

S. Siegel, M. Gandal, G. Carlson, 2012, Neurobiology of Disease.

Loss of CDKL5 disrupts respiratory function in mice

Wenlin Liao, Kun-Ze Lee, 2018, Respiratory Physiology & Neurobiology.