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Hyeonho Kim

Showing results (21-30 of 25) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Autism-associated MDGA1 missense mutations impair distinct facets of central nervous system developmentSeungjoon Kim, Hyeonho Kim, Javier Pelayo, et al.
Biological Psychiatry|February 27, 2022
IQSEC3 Deletion Impairs Fear Memory Through Upregulation of Ribosomal S6K1 Signaling in the HippocampusDongwook Kim, Hyeji Jung, Yoshinori Shirai, et al.
EMBO Molecular Medicine|March 21, 2026
Bazedoxifene reverses sexually dimorphic autistic-like abnormalities in biallelic MDGA1-mutant miceSeungjoon Kim, Hyeonho Kim, Javier Porta Pelayo, et al.
Nature Communications|July 15, 2022
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in miceSalima El Chehadeh, Kyung Ah Han, Dongwook Kim, et al.
American Journal of Human Genetics|January 22, 2026
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathyHeba Morsy, Hyeonho Kim, Gyubin Jang, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Autism-associated MDGA1 missense mutations impair distinct facets of central nervous system developmentSeungjoon Kim, Hyeonho Kim, Javier Pelayo, et al.
Biological Psychiatry|February 27, 2022
IQSEC3 Deletion Impairs Fear Memory Through Upregulation of Ribosomal S6K1 Signaling in the HippocampusDongwook Kim, Hyeji Jung, Yoshinori Shirai, et al.
EMBO Molecular Medicine|March 21, 2026
Bazedoxifene reverses sexually dimorphic autistic-like abnormalities in biallelic MDGA1-mutant miceSeungjoon Kim, Hyeonho Kim, Javier Porta Pelayo, et al.
Nature Communications|July 15, 2022
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in miceSalima El Chehadeh, Kyung Ah Han, Dongwook Kim, et al.
American Journal of Human Genetics|January 22, 2026
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathyHeba Morsy, Hyeonho Kim, Gyubin Jang, et al.
Pageof 3