Sukyeong Lee
Overview
Explore the profile of Sukyeong Lee including associated specialties, affiliations and a list of published articles.
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Articles
43
Citations
1150
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Recent Articles
1.
Aceves-Ewing N, Lanza D, Marcogliese P, Lu D, Hsu C, Gonzalez M, et al.
medRxiv
. 2024 Dec;
PMID: 39677486
Heterozygous pathogenic variants in are associated with oligodontia-colorectal cancer syndrome (ODCRCS), a disorder characterized by oligodontia, colorectal cancer, and in some cases, sparse hair and eyebrows. We have identified four...
2.
Lee M, Bhattarai D, Jang H, Baek A, Yeo I, Lee S, et al.
J Med Chem
. 2024 Mar;
67(6):5109-5110.
PMID: 38471117
No abstract available.
3.
Brooks D, Burke E, Lee S, Eble T, OLeary M, Osei-Owusu I, et al.
Hum Genet
. 2024 Mar;
143(3):279-291.
PMID: 38451290
Biallelic pathogenic variants in MAP3K20, which encodes a mitogen-activated protein kinase, are a rare cause of split-hand foot malformation (SHFM), hearing loss, and nail abnormalities or congenital myopathy. However, heterozygous...
4.
Eisa N, Crowley V, Elahi A, Kommalapati V, Serwetnyk M, Llbiyi T, et al.
iScience
. 2023 Nov;
26(12):108308.
PMID: 38025772
Low response rates and immune-related adverse events limit the remarkable impact of cancer immunotherapy. To improve clinical outcomes, preclinical studies have shown that combining immunotherapies with N-terminal Hsp90 inhibitors resulted...
5.
Zhang H, Murphy P, Yu J, Lee S, Tsai F, van Hoof A, et al.
Nucleic Acids Res
. 2023 Sep;
51(19):10606-10618.
PMID: 37742077
Aminoacyl-tRNA synthetases (aaRSs) are essential enzymes that ligate amino acids to tRNAs, and often require editing to ensure accurate protein synthesis. Recessive mutations in aaRSs cause various neurological disorders in...
6.
Lee S, Lee S, Sung N, Xu W, Chang C, Kim H, et al.
Nat Commun
. 2023 Apr;
14(1):2028.
PMID: 37041140
Mitochondria are critical to cellular and organismal health. To prevent damage, mitochondria have evolved protein quality control machines to survey and maintain the mitochondrial proteome. SKD3, also known as CLPB,...
7.
Whittle E, Chilian M, Karimiani E, Progri H, Buhas D, Kose M, et al.
Genet Med
. 2022 Dec;
25(2):100332.
PMID: 36520152
Purpose: This study aimed to establish the genetic cause of a novel autosomal recessive neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities. Methods: We performed a...
8.
Lee G, Kim R, Lee S, Lee S, Tsai F
Biochem Soc Trans
. 2022 Dec;
50(6):1725-1736.
PMID: 36454589
Hsp100 chaperones, also known as Clp proteins, constitute a family of ring-forming ATPases that differ in 3D structure and cellular function from other stress-inducible molecular chaperones. While the vast majority...
9.
Mercado J, Lee S, Chang C, Sung N, Soong L, Catic A, et al.
Proteins
. 2022 Feb;
90(6):1242-1246.
PMID: 35122310
Hsp100 is an ATP-dependent unfoldase that promotes protein disaggregation or facilitates the unfolding of aggregation-prone polypeptides marked for degradation. Recently, new Hsp100 functions are emerging. In Plasmodium, an Hsp100 drives...
10.
Yap Z, Efthymiou S, Seiffert S, Vargas Parra K, Lee S, Nasca A, et al.
Am J Hum Genet
. 2021 Nov;
108(12):2368-2384.
PMID: 34800363
The 2-oxoglutarate dehydrogenase-like (OGDHL) protein is a rate-limiting enzyme in the Krebs cycle that plays a pivotal role in mitochondrial metabolism. OGDHL expression is restricted mainly to the brain in...