Tao Wang

Associate Professor

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Intellectual Disability Medicine & Life Sciences
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AMPA Receptors Medicine & Life Sciences
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Research Output 1994 2018

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

Piard, J., Hu, J. H., Campeau, P. M., Rzońca, S., Esch, H. V., Vincent, E., Han, M., Rossignol, E., Castaneda, J., Chelly, J., Skinner, C., Kalscheuer, V. M., Wang, R., Lemyre, E., Kosińska, J., Stawinski, P., Bal, J., Hoffman, D. A., Schwartz, C. E., Maldergem, L. V. & 2 othersWang, T. & Worley, P. F., Feb 15 2018, In : Human Molecular Genetics. 27, 4, p. 589-600 12 p., ddx426.

Research output: Contribution to journalArticle

PDZ Domains
Dendritic Spines
Intellectual Disability

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

Chiu, S-L., Diering, G. H., Ye, B., Takamiya, K., Chen, C. M., Jiang, Y., Niranjan, T., Schwartz, C. E., Wang, T. & Huganir, R. L., Mar 22 2017, In : Neuron. 93, 6, p. 1405-1419.e8

Research output: Contribution to journalArticle

Neuronal Plasticity
AMPA Receptors
Intellectual Disability

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

Vaidyanathan, K., Niranjan, T., Selvan, N., Teo, C. F., May, M., Patel, S., Weatherly, B., Skinner, C., Opitz, J., Carey, J., Viskochil, D., Gecz, J., Shaw, M., Peng, Y., Alexov, E., Wang, T., Schwartz, C. & Wells, L., May 26 2017, In : Journal of Biological Chemistry. 292, 21, p. 8948-8963 16 p.

Research output: Contribution to journalArticle

Missense Mutation
Intellectual Disability
Post Translational Protein Processing

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

Han, M., Mejias, R., Chiu, S-L., Rose, R., Adamczyk, A., Huganir, R. L. & Wang, T., Mar 15 2017, In : Behavioural Brain Research. 321, p. 176-184 9 p.

Research output: Contribution to journalArticle

Interpersonal Relations
Knockout Mice
Autistic Disorder
Social Behavior

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

Lah, M., Niranjan, T., Srikanth, S., Holloway, L., Schwartz, C. E., Wang, T. & Weaver, D. D., Apr 1 2016, In : American Journal of Medical Genetics, Part A. 170, 4, p. 881-890 10 p.

Research output: Contribution to journalArticle