Min Jeong Kye
Overview
Explore the profile of Min Jeong Kye including associated specialties, affiliations and a list of published articles.
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24
Citations
988
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Recent Articles
1.
Lee D, Kwon Y, Um K, Yoo J, Ha W, Kim K, et al.
Theranostics
. 2025 Jan;
15(4):1221-1237.
PMID: 39816694
Adenovirus-based therapies have encountered significant challenges due to host immunity, particularly from pre-existing antibodies. Many trials have struggled to evade antibody response; however, the efficiency of these efforts was limited...
2.
Lee D, Yoo J, Um K, Ha W, Lee S, Park J, et al.
J Exp Clin Cancer Res
. 2024 Jun;
43(1):170.
PMID: 38886756
Background: Recent intravesical administration of adenoviral vectors, either as a single injection or in combination with immune checkpoint inhibitors, exemplified by cretostimogene grenadenorepvec and nadofaragene firadenovec, has demonstrated remarkable efficacy...
3.
Thelen M, Wirth B, Kye M
Acta Neuropathol Commun
. 2020 Dec;
8(1):223.
PMID: 33353564
Spinal muscular atrophy (SMA) is a neuromuscular disease characterized by loss of lower motor neurons, which leads to proximal muscle weakness and atrophy. SMA is caused by reduced survival motor...
4.
Goncalves I, Brecht J, Thelen M, Rehorst W, Peters M, Lee H, et al.
Sci Rep
. 2020 May;
10(1):8206.
PMID: 32398663
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
5.
Thelen M, Kye M
Front Mol Biosci
. 2020 Feb;
6:161.
PMID: 32010708
As neurons are one of the most highly polarized cells in our body, they require sophisticated cellular mechanisms to maintain protein homeostasis in their subcellular compartments such as axons and...
6.
Wirth B, Karakaya M, Kye M, Mendoza-Ferreira N
Annu Rev Genomics Hum Genet
. 2020 Feb;
21:231-261.
PMID: 32004094
Twenty-five years ago, the underlying genetic cause for one of the most common and devastating inherited diseases in humans, spinal muscular atrophy (SMA), was identified. Homozygous deletions or, rarely, subtle...
7.
Rehorst W, Thelen M, Nolte H, Turk C, Cirak S, Peterson J, et al.
Acta Neuropathol Commun
. 2019 Oct;
7(1):154.
PMID: 31615574
Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder, which causes dysfunction/loss of lower motor neurons and muscle weakness as well as atrophy. While SMA is primarily considered as a...
8.
Janzen E, Wolff L, Mendoza-Ferreira N, Hupperich K, Delle Vedove A, Hosseinibarkooie S, et al.
Front Neurosci
. 2019 Oct;
13:993.
PMID: 31607845
Many neurodegenerative disorders share common pathogenic pathways such as endocytic defects, Ca misregulation and defects in actin dynamics. Factors acting on these shared pathways are highly interesting as a therapeutic...
9.
Lindner A, Marbach F, Tschernitz S, Ortner C, Berneburg M, Felthaus O, et al.
Sci Rep
. 2019 Jun;
9(1):8444.
PMID: 31186450
Little is known on the causes and pathogenesis of the adipose tissue disorder (familial) Multiple Symmetric Lipomatosis (MSL). In a four-generation MSL-family, we performed whole exome sequencing (WES) in 3...
10.
Upadhyay A, Hosseinibarkooie S, Schneider S, Kaczmarek A, Torres-Benito L, Mendoza-Ferreira N, et al.
Front Mol Neurosci
. 2019 Mar;
12:19.
PMID: 30853885
Neurocalcin delta (NCALD) is a brain-enriched neuronal calcium sensor and its reduction acts protective against spinal muscular atrophy (SMA). However, the physiological function of NCALD and implications of NCALD reduction...