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Medrxiv : the Preprint Server for Health Sciences
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June 30, 2025
Autism-associated MDGA1 missense mutations impair distinct facets of central nervous system development
Seungjoon 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 Hippocampus
Dongwook Kim, Hyeji Jung, Yoshinori Shirai, et al.
EMBO Molecular Medicine
|
March 21, 2026
Bazedoxifene reverses sexually dimorphic autistic-like abnormalities in biallelic MDGA1-mutant mice
Seungjoon 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 mice
Salima 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 encephalopathy
Heba Morsy, Hyeonho Kim, Gyubin Jang, et al.
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Search research articles
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Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 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 development
Seungjoon 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 Hippocampus
Dongwook Kim, Hyeji Jung, Yoshinori Shirai, et al.
EMBO Molecular Medicine
|
March 21, 2026
Bazedoxifene reverses sexually dimorphic autistic-like abnormalities in biallelic MDGA1-mutant mice
Seungjoon 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 mice
Salima 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 encephalopathy
Heba Morsy, Hyeonho Kim, Gyubin Jang, et al.
Page
of 3