Ling-jie He

发表

An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function

H. Zoghbi, Zhandong Liu, Carolyn J. Adamski, 2019, Molecular Psychiatry.

Reversal of Social Recognition Deficit in Adult Mice with MECP2 Duplication via Normalization of MeCP2 in the Medial Prefrontal Cortex

Huatai Xu, Z. Qiu, Tianlin Cheng, 2020, Neuroscience Bulletin.

Loss and Gain of MeCP2 Cause Similar Hippocampal Circuit Dysfunction that Is Rescued by Deep Brain Stimulation in a Rett Syndrome Mouse Model

Benjamin R. Arenkiel, H. Zoghbi, S. Smirnakis, 2016, Neuron.

Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders

H. Zoghbi, Jianrong Tang, M. Fiorotto, 2016, eLife.

Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice

H. Zoghbi, J. Medina, Shogo Ohmae, 2021, eLife.

Deleting Mecp2 from the entire cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice

H. Zoghbi, J. Medina, Shogo Ohmae, 2020, bioRxiv.

Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome

H. Zoghbi, Aya Ito-Ishida, Y. Sztainberg, 2016, eLife.

Conditional deletion of Mecp2 in parvalbumin-expressing GABAergic cells results in the absence of critical period plasticity

Tianlin Cheng, Nan Liu, Ling-jie He, 2014, Nature Communications.

Postinduction Requirement of NMDA Receptor Activation for Late-Phase Long-Term Potentiation of Developing Retinotectal Synapses In Vivo

M. Poo, Xiaohui Zhang, Xiaona Lu, 2011, The Journal of Neuroscience.

A weakened recurrent circuit in the hippocampus of Rett syndrome mice disrupts long-term memory representations

H. Zoghbi, Jianrong Tang, Wei Wang, 2022, Neuron.

Author response: Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome

H. Zoghbi, Aya Ito-Ishida, Y. Sztainberg, 2016 .