Tao Wang

发表

Targeted deletion of Nmnat1 in mouse retina leads to early severe retinal dystrophy

Xiaoling Wang, Yuanyuan Fang, Rong-Feng Liao, 2017, bioRxiv.

Mice lacking ornithine–δ–amino–transferase have paradoxical neonatal hypoornithinaemia and retinal degeneration

D. Valle, A. Milam, G. Steel, 1995, Nature Genetics.

Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans

Tao Wang, Gavin Rumbaugh, Lilei Zhang, 2007, Proceedings of the National Academy of Sciences.

Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders

J. Gécz, P. Tarpey, C. Skinner, 2019, Molecular genetics & genomic medicine.

Affected Sib-Pair Analyses Identify Signaling Networks Associated With Social Behavioral Deficits in Autism

J. Potash, P. Zandi, R. Huganir, 2019, Front. Genet..

ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons

Shannon K. Stefl, Cheol‐Hee Kim, P. Tarpey, 2015, Human molecular genetics.

Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability

Tao Wang, Emil Alexov, Brent Weatherly, 2017, The Journal of Biological Chemistry.

Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism

R. Huganir, C. Skinner, R. Stevenson, 2011, Proceedings of the National Academy of Sciences.

SynaptomeDB: an ontology-based knowledgebase for synaptic genes

Tao Wang, Mehdi Pirooznia, Dimitrios Avramopoulos, 2012, Bioinform..

X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation.

C. Obie, R. Stevenson, C. Schwartz, 2007, Genome research.

Affected Kindred Analysis of Human X Chromosome Exomes to Identify Novel X-Linked Intellectual Disability Genes

C. Skinner, R. Stevenson, C. Schwartz, 2015, PloS one.

GluA3-deficiency in mice is associated with increased social and aggressive behavior and elevated dopamine in striatum

R. Huganir, J. Cadet, K. Takamiya, 2012, Behavioural Brain Research.

GRASP1 Regulates Synaptic Plasticity and Learning through Endosomal Recycling of AMPA Receptors

R. Huganir, C. Schwartz, K. Takamiya, 2017, Neuron.

Purkinje cell-specific Grip1/2 knockout mice show increased repetitive self-grooming and enhanced mGluR5 signaling in cerebellum

R. Huganir, S. Chiu, Yifan Zhao, 2019, Neurobiology of Disease.

A distinct X‐linked syndrome involving joint contractures, keloids, large optic cup‐to‐disc ratio, and renal stones results from a filamin A (FLNA) mutation

C. Schwartz, D. Weaver, S. Srikanth, 2016, American journal of medical genetics. Part A.

Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice

Zheng-Xiong Xi, Tao Wang, Richard L. Huganir, 2021, Translational Psychiatry.

Mice lacking GRIP1/2 show increased social interactions and enhanced phosphorylation at GluA2-S880

R. Huganir, S. Chiu, Tao Wang, 2017, Behavioural Brain Research.

A microdeletion in Xp11.3 accounts for co‐segregation of retinitis pigmentosa and mental retardation in a large kindred

R. Stevenson, C. Schwartz, A. Wright, 2006, American journal of medical genetics. Part A.

FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis

D. Hoffman, P. Worley, C. Skinner, 2018, Human molecular genetics.

Bioinformatics Applications Note Databases and Ontologies Synaptomedb: an Ontology-based Knowledgebase for Synaptic Genes

J. Potash, P. Zandi, R. Huganir, 2022 .

GRASP1 Regulates Synaptic Plasticity and Learning through Endosomal Recycling of AMPA Receptors

R. Huganir, C. Schwartz, K. Takamiya, 2017, Neuron.