Seung Hyun Jang
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Explore the profile of Seung Hyun Jang including associated specialties, affiliations and a list of published articles.
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12
Citations
25
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Recent Articles
1.
Joo S, Min H, Kim J, Kim S, Jang S, Lee H, et al.
Mol Cells
. 2025 Feb;
48(3):100190.
PMID: 39909336
It is crucial to manage hearing loss and its associated public health impacts. In this study, we aimed to understand the role of Sema3f in the development and maintenance of...
2.
Lee C, Jang S, Lim J, Park H, Ahn S, Park S, et al.
Exp Mol Med
. 2025 Jan;
57(1):235-248.
PMID: 39833561
Neuroinflammation, a significant contributor to various neurodegenerative diseases, is strongly associated with the aging process; however, to date, no efficacious treatments for neuroinflammation have been developed. In aged mouse brains,...
3.
Jang S, Yoon K, Gee H
Genomics Inform
. 2024 Nov;
22(1):27.
PMID: 39609929
Hearing loss is the most common sensory disorder. Genetic factors contribute substantially to this condition, although allelic heterogeneity and variable expressivity make a definite molecular diagnosis challenging. To provide a...
4.
Jung J, Joo S, Min H, Roh J, Kim K, Ma J, et al.
Exp Mol Med
. 2024 Nov;
56(11):2423-2435.
PMID: 39482536
Myh1 is a mouse deafness gene with an unknown function in the auditory system. Hearing loss in Myh1-knockout mice is characterized by an elevated threshold for the auditory brainstem response...
5.
Jung J, Jang S, Won D, Gee H, Choi J, Jung J
J Clin Med
. 2024 Aug;
13(16).
PMID: 39200993
Mutations in Wolfram syndrome 1 () cause Wolfram syndrome and autosomal dominant non-syndromic hearing loss DFNA6/14/38. To date, more than 300 pathogenic variants of have been identified. Generally, the audiological...
6.
Han J, Bae S, Joo S, Kim J, Kim S, Jang S, et al.
J Clin Med
. 2024 Apr;
13(7).
PMID: 38610765
The vestibular phenotypes of patients with genetic hearing loss are poorly understood. we performed genetic testing including exome sequencing and vestibular function tests to investigate vestibular phenotypes and functions in...
7.
Joo S, Jang S, Kim J, Kim S, Kim B, Kim H, et al.
J Korean Med Sci
. 2023 Dec;
38(48):e355.
PMID: 38084023
Background: Mutations in mitochondrial DNA (mtDNA) are associated with several genetic disorders, including sensorineural hearing loss. However, the prevalence of mtDNA mutations in a large cohort of Korean patients with...
8.
Kang M, Kim J, Song M, Joo S, Kim S, Jang S, et al.
Cells
. 2023 Sep;
12(18).
PMID: 37759551
Genetic hearing loss is the most common hereditary sensorial disorder. Though more than 120 genes associated with deafness have been identified, unveiled causative genes and variants of diverse types of...
9.
Oh K, Roh J, Joo S, Ryu K, Kim J, Kim S, et al.
Exp Mol Med
. 2023 Apr;
55(4):844-859.
PMID: 37009795
Pathogenic variants of KCNQ4 cause symmetrical, late-onset, progressive, high-frequency-affected hearing loss, which eventually involves all frequencies with age. To understand the contribution of KCNQ4 variants to hearing loss, we analyzed...
10.
Mohammed S, Jang S, Moon I
Indian J Otolaryngol Head Neck Surg
. 2023 Feb;
74(Suppl 3):4350-4355.
PMID: 36742801
Fibrous dysplasia of temporal bone is a rare benign bone disease. With the advance in imaging, more cases are likely to get reported and present with less disease severity. Temporal...