If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Fingerprint is based on mining the text of the expert's scholarly documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 2 Similar Profiles
Nuclear Receptor Co-Repressor 1 Medicine & Life Sciences
Neurons Medicine & Life Sciences
Fragile X Mental Retardation Protein Medicine & Life Sciences
MEF2 Transcription Factors Medicine & Life Sciences
Messenger RNA Medicine & Life Sciences
Fragile X Syndrome Medicine & Life Sciences
Genes Chemical Compounds
Ubiquitination Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2005 2018

Dysregulation and restoration of homeostatic network plasticity in fragile X syndrome mice

Jewett, K. A., Lee, K. Y., Eagleman, D. E., Soriano, S. & Tsai, N-P., Aug 1 2018, In : Neuropharmacology. 138, p. 182-192 11 p.

Research output: Contribution to journalArticle

Fragile X Syndrome
Fragile X Mental Retardation Protein
Neurons
Ubiquitination
GABA-A Receptors

Loss of fragile X protein FMRP impairs homeostatic synaptic downscaling through tumor suppressor p53 and ubiquitin E3 ligase Nedd4-2

Lee, K. Y., Jewett, K. A., Chung, H. J. & Tsai, N-P., Jan 1 2018, In : Human molecular genetics. 27, 16, p. 2805-2816 12 p.

Research output: Contribution to journalArticle

Fragile X Mental Retardation Protein
Ubiquitin-Protein Ligases
Neurons
Fragile X Syndrome
Ubiquitination

Reduced axonal surface expression and phosphoinositide sensitivity in Kv7 channels disrupts their function to inhibit neuronal excitability in Kcnq2 epileptic encephalopathy

Kim, E. C., Zhang, J., Pang, W., Wang, S., Lee, K. Y., Cavaretta, J. P., Walters, J., Procko, E., Tsai, N-P. & Chung, H. J., Oct 1 2018, In : Neurobiology of Disease. 118, p. 76-93 18 p.

Research output: Contribution to journalArticle

Brain Diseases
Phosphatidylinositols
Calmodulin
Mutation
Voltage-Gated Potassium Channels

Epilepsy-associated gene Nedd4-2 mediates neuronal activity and seizure susceptibility through AMPA receptors

Zhu, J., Lee, K. Y., Jewett, K. A., Man, H. Y., Chung, H. J. & Tsai, N-P., Feb 1 2017, In : PLoS Genetics. 13, 2, e1006634.

Research output: Contribution to journalArticle

AMPA Receptors
epilepsy
seizures
Epilepsy
Seizures

FMRP-dependent Mdm2 dephosphorylation is required for MEF2-induced synapse elimination

Tsai, N-P., Wilkerson, J. R., Guo, W. & Huber, K. M., Jan 1 2017, In : Human molecular genetics. 26, 2, p. 293-304 12 p.

Research output: Contribution to journalArticle

MEF2 Transcription Factors
Synapses
Neurons
Proteolysis
Peptide Elongation Factor 1