Department of Neural Sciences

  • Korea, Republic of

Fingerprint Dive into the research topics where Department of Neural Sciences is active. These topic labels come from the works of this organisation's members. Together they form a unique fingerprint.

Gene Expression Profiling Medicine & Life Sciences
Bipolar Disorder Medicine & Life Sciences
Synapses Medicine & Life Sciences
Post-Synaptic Density Medicine & Life Sciences
Transgenic Mice Medicine & Life Sciences
Brain Medicine & Life Sciences
Corpus Striatum Medicine & Life Sciences
Dendritic Spines Medicine & Life Sciences

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

Projects 2015 2019

Research Output 2015 2019

  • 122 Citations
  • 7 h-Index
  • 19 Article
  • 1 Comment/debate
  • 1 Review article

A kinome-wide RNAi screen identifies ERK2 as a druggable regulator of Shank3 stability

Wang, L., Adamski, C. J., Bondar, V. V., Craigen, E., Collette, J. R., Pang, K., Han, K., Jain, A., Y. Jung, S., Liu, Z., Sifers, R. N., Holder, J. L. & Zoghbi, H. Y., 2019 Jan 1, In : Molecular Psychiatry.

Research output: Contribution to journalArticle

Gene Dosage
RNA Interference
MAP Kinase Kinase Kinases
Haploinsufficiency
Gene Duplication
4 Citations (Scopus)

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

Wang, L., Pang, K., Han, K., Adamski, C. J., Wang, W., He, L., Lai, J. K., Bondar, V. V., Duman, J. G., Richman, R., Tolias, K. F., Barth, P., Palzkill, T., Liu, Z., Holder, J. L. & Zoghbi, H. Y., 2019 Jan 1, (Accepted/In press) In : Molecular Psychiatry.

Research output: Contribution to journalArticle

Missense Mutation
Autistic Disorder
Phosphorylation
Social Dominance
Phenotype

Neuronal function and dysfunction of CYFIP2: from actin dynamics to early infantile epileptic encephalopathy

Zhang, Y., Lee, Y. & Han, K., 2019 May 1, In : BMB reports. 52, 5, p. 304-311 8 p.

Research output: Contribution to journalComment/debate

Open Access
Brain Diseases
Actins
Fragile X Mental Retardation Protein
Exome
Fragile X Syndrome