Shin Jeon
Overview
Explore the profile of Shin Jeon including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
175
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Lee J, Jung H, Pasqua B, Park Y, Tang Q, Jeon S, et al.
Front Cell Dev Biol
. 2025 Feb;
13:1466948.
PMID: 39925741
MLL4, also known as KMT2D, is a histone methyltransferase that acts as an important epigenetic regulator in various organogenesis programs. Mutations in the gene are the major cause of Kabuki...
2.
Jeon S, Park J, Moon J, Shin D, Li L, OShea H, et al.
bioRxiv
. 2025 Feb;
PMID: 39896554
Single allelic mutations in the forebrain-specific transcription factor gene lead to FOXG1 syndrome (FS). To decipher the disease mechanisms of FS, which vary depending on FOXG1 mutation types, patient-specific animal...
3.
Lee J, Jung H, Pasqua B, Park Y, Tang Q, Jeon S, et al.
bioRxiv
. 2024 Oct;
PMID: 39372750
MLL4, also known as KMT2D, is a histone methyltransferase that acts as an important epigenetic regulator in various organogenesis programs. Mutations in the gene are the major cause of Kabuki...
4.
Jeon S, Park J, Likhite S, Moon J, Shin D, Li L, et al.
Mol Ther Methods Clin Dev
. 2024 Jul;
32(3):101275.
PMID: 39022742
Heterozygous mutations in the gene manifest as FOXG1 syndrome, a severe neurodevelopmental disorder characterized by structural brain anomalies, including agenesis of the corpus callosum, hippocampal reduction, and myelination delays. Despite...
5.
Park J, Moon J, OShea H, Shin D, Hwang S, Li L, et al.
Res Sq
. 2023 Jul;
PMID: 37398410
Single allelic mutations in the gene encoding the forebrain-specific transcription factor FOXG1 lead to FOXG1 syndrome (FS). Patient-specific animal models are needed to understand the etiology of FS, as FS...
6.
Younger S, Boutros S, Cargnin F, Jeon S, Lee J, Lee S, et al.
Front Pharmacol
. 2022 Jun;
13:927296.
PMID: 35754477
FOXG1 syndrome (FS, aka a congenital variant of Rett syndrome) is a recently defined rare and devastating neurodevelopmental disorder characterized by various symptoms, including severe intellectual disability, autistic features, involuntary,...
7.
Kim J, Kang J, Yoo K, Jeong J, Park I, Park J, et al.
JCI Insight
. 2022 May;
7(10).
PMID: 35603786
The survival of motor neuron (SMN) protein is a major component of the pre-mRNA splicing machinery and is required for RNA metabolism. Although SMN has been considered a fundamental gene...
8.
Jeong J, Jung I, Kim J, Jeon S, Hyeon D, Min H, et al.
Cell Death Differ
. 2022 Apr;
29(11):2151-2162.
PMID: 35473985
Hematopoiesis occurs within a unique bone marrow (BM) microenvironment, which consists of various niche cells, cytokines, growth factors, and extracellular matrix components. These multiple components directly or indirectly regulate the...
9.
Huisman C, Kim Y, Jeon S, Shin B, Choi J, Lim S, et al.
Nat Commun
. 2021 Jan;
12(1):256.
PMID: 33431871
In humans, inactivating mutations in MLL4, which encodes a histone H3-lysine 4-methyltransferase, lead to Kabuki syndrome (KS). While dwarfism is a cardinal feature of KS, the underlying etiology remains unclear....
10.
Hwang S, Lee C, Park K, Oh S, Jeon S, Kang B, et al.
Cell Death Differ
. 2020 May;
27(11):3053-3064.
PMID: 32424141
CD4/CD8 T-cell lineage differentiation is a key process in immune system development; however, a defined regulator(s) that converts the signal from T-cell receptor and co-receptor complexes into lineage differentiation remains...