Home > PUBLICATIONS > 2017

Cheon CK, Lim SH, Kim YM, Kim D, Lee NY, Yoo TS, Kim NS, Kim E, and Lee JR. (2017).
Autosomal dominant transmission of complicated hereditary spastic paraplegia due to a dominant negative mutation of KIF1A, SPG30 gene.
Sci Rep in press. 
Bae YS, Yoon SH, Han JY, Woo J, Cho YS, Kwon SK, Bae YC, Kim D, Kim E, Kim MH. (2017).
Deficiency of aminopeptidase P1 causes behavioral hyperactivity, cognitive deficits, and hippocampal neurodegeneration.
Genes Brain Behav  in press. (abstract)
Lee Y, Kim SG, Lee B, Zhang Y, Kim Y, Kim S, Kim E, Kang H, and Han K. (2017).
Striatal transcritome and interactome analysis of Shank3-overexpressing mice reveals the connectivity between Shank3 and mTORC1 signaling.
Front Mol Neurosci 10:201. (abstract)
Kim JA*, Kim D*, Won SY, Han KA, Park D, Cho E, Yun N, An HJ, Um JW, Kim E, Lee JO, Ko J, and Kim HM. (2017).
Structural Insights into Modulation of Neurexin-Neuroligin Trans-synaptic Adhesion by MDGA1/Neuroligin-2 Complex.
Neuron 94:1121-1131. (abstract)
Jang S*, Lee H*, and Kim E. (2017).
Synaptic adhesion molecules and excitatory synaptic transmission.
Curr Opin Neurobiol 45:45-50. (abstract)
Roh JD*, Choi SY*, Cho YS, Choi TY, Park JS, Cutforth T, Chung W, Park H, Lee D, Kim MH, Lee Y, Mo S, Rhee JS, Kim H, Ko J, Choi SY, Bae YC, Shen K, Kim E#, and Han K#. (2017).
Increased excitatory synaptic transmission of dentate granule neurons in mice lacking PSD-95-interacting adhesion molecule Neph2/Kirrel3 during the early postnatal period.
Front Mol Neurosci
10:81. (abstract)
​Lim​ CS, Kim H, Yu NK, Kang SJ, Kim T, Ko HG, Lee J, Yang JE, Ryu HH, Park T, Gim J, Nam HJ, Baek SH, Wegener S, Schmitz D, Boeckers TM, Lee MG, Kim E, Lee J, Lee YS, Kaang BK. (2017).
Enhancing inhibitory synaptic function reverses spatial memory deficits in Shank2 mutant mice.
Neuropharmacology 112:104-112.