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Showing results 1 to 4 of 4

1
De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy

Lee, Jae-Ran; Srour, Myriam; Kim, Doyoun; Hamdan, Fadi. F.; Lim, So-Hee; Brunel-Guitton, Catherine; Decarie, Jean-Claude; et al, HUMAN MUTATION, v.36, no.1, pp.69 - 78, 2015-01

2
Mice lacking the synaptic adhesion molecule Neph2/Kirrel3 display moderate hyperactivity and defective novel object preference

Choi, Su-Yeon; Han, Kihoon; Cutforth, Tyler; Chung, Woosuk; Park, Harem; Lee, Dongsoo; Kim, Ryunhee; et al, FRONTIERS IN CELLULAR NEUROSCIENCE, v.9, 2015-07

3
Postnatal age-differential ASD-like transcriptomic, synaptic, and behavioral deficits in Myt1l-mutant mice

Kim, Seongbin; Oh, Hyoseon; Choi, Sang Han; Yoo, Ye-Eun; Noh, Young Woo; Cho, Yisul; Im, Geun Ho; et al, CELL REPORTS, v.40, no.12, 2022-09

4
Scn2a Haploinsufficiency in Mice Suppresses Hippocampal Neuronal Excitability, Excitatory Synaptic Drive, and Long-Term Potentiation, and Spatial Learning and Memory

Shin, Wangyong; Kweon, Hanseul; Kang, Ryeonghwa; Kim, Doyoun; Kim, Kyungdeok; Kang, Muwon; Kim, Seo Yeong; et al, FRONTIERS IN MOLECULAR NEUROSCIENCE, v.12, 2019-06

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