Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Seung Yeop Han"'
Autor:
Ashutosh Pandey, Antonio Galeone, Seung Yeop Han, Benjamin A. Story, Gaia Consonni, William F. Mueller, Lars M. Steinmetz, Thomas Vaccari, Hamed Jafar-Nejad
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Intestinal barrier dysfunction leads to inflammation and associated metabolic changes. However, the relative impact of gut bacteria versus non-bacterial insults on animal health in the context of barrier dysfunction is not well understood. H
Externí odkaz:
https://doaj.org/article/fc75a5d2d921427790e61a8613dba176
Publikováno v:
Bioengineering & Translational Medicine, Vol 8, Iss 3, Pp n/a-n/a (2023)
Abstract Esophageal stricture after extensive endoscopic submucosal dissection impairs the quality of life of patients with superficial esophageal carcinoma. Beyond the limitations of conventional treatments including endoscopic balloon dilatation an
Externí odkaz:
https://doaj.org/article/7860be462a474f83ad2d07cfbefcb266
Publikováno v:
Journal of Marine Science and Engineering, Vol 11, Iss 8, p 1486 (2023)
This study examined the seasonal and spatial changes in the marine algal community structure in the outer and inner areas of the intertidal zone of Yeongil Bay. A seasonal survey was conducted at 13 intertidal sites in Yeongil Bay between August 2021
Externí odkaz:
https://doaj.org/article/036eb6a03b5846d79da4fac74cab6819
Autor:
Seung Yeop Han, Ashutosh Pandey, Tereza Moore, Antonio Galeone, Lita Duraine, Tina M Cowan, Hamed Jafar-Nejad
Publikováno v:
PLoS Genetics, Vol 16, Iss 12, p e1009258 (2020)
Mutations in human N-glycanase 1 (NGLY1) cause the first known congenital disorder of deglycosylation (CDDG). Patients with this rare disease, which is also known as NGLY1 deficiency, exhibit global developmental delay and other phenotypes including
Externí odkaz:
https://doaj.org/article/38ad2190625241eaa6c24799b3b7819a
Publikováno v:
Cells, Vol 11, Iss 7, p 1155 (2022)
N-Glycanase 1 (NGLY1) is a cytosolic enzyme involved in removing N-linked glycans of misfolded N-glycoproteins and is considered to be a component of endoplasmic reticulum-associated degradation (ERAD). The 2012 identification of recessive NGLY1 muta
Externí odkaz:
https://doaj.org/article/1c12886607cd423a959955b0c22fd2df
Autor:
Antonio Galeone, Joshua M Adams, Shinya Matsuda, Maximiliano F Presa, Ashutosh Pandey, Seung Yeop Han, Yuriko Tachida, Hiroto Hirayama, Thomas Vaccari, Tadashi Suzuki, Cathleen M Lutz, Markus Affolter, Aamir Zuberi, Hamed Jafar-Nejad
Publikováno v:
eLife, Vol 9 (2020)
During endoplasmic reticulum-associated degradation (ERAD), the cytoplasmic enzyme N-glycanase 1 (NGLY1) is proposed to remove N-glycans from misfolded N-glycoproteins after their retrotranslocation from the ER to the cytosol. We previously reported
Externí odkaz:
https://doaj.org/article/7f96a57cf41d4be982d6c1682f81ca7d
Autor:
Antonio Galeone, Seung Yeop Han, Chengcheng Huang, Akira Hosomi, Tadashi Suzuki, Hamed Jafar-Nejad
Publikováno v:
eLife, Vol 6 (2017)
Mutations in the human N-glycanase 1 (NGLY1) cause a rare, multisystem congenital disorder with global developmental delay. However, the mechanisms by which NGLY1 and its homologs regulate embryonic development are not known. Here we show that Drosop
Externí odkaz:
https://doaj.org/article/81b9d527a212456abb63a49412940fed
Autor:
Soojin Hwang, Saera Song, Yoon Ki Hong, Gahee Choi, Yoon Seok Suh, Seung Yeop Han, Minjung Lee, Seung Hwan Park, Jang Ho Lee, Soojin Lee, Se Min Bang, Yuji Jeong, Won-Ju Chung, Im-Soon Lee, Gilsang Jeong, Jongkyeong Chung, Kyoung Sang Cho
Publikováno v:
PLoS Genetics, Vol 9, Iss 4, p e1003412 (2013)
DJ-1, a Parkinson's disease (PD)-associated gene, has been shown to protect against oxidative stress in Drosophila. However, the molecular mechanism underlying oxidative stress-induced phenotypes, including apoptosis, locomotive defects, and lethalit
Externí odkaz:
https://doaj.org/article/39c6aaec5ab441b69aa85342772f5b76
Publikováno v:
Advanced Therapeutics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2eb4b4171d462e9bc9fe7dfa3b2018e
https://doi.org/10.1002/adtp.202300125
https://doi.org/10.1002/adtp.202300125
Autor:
Jae Chul Hwang, Moohyun Kim, Sumin Kim, Hunkyu Seo, Soohwan An, Eui Hwa Jang, Seung Yeop Han, Mi Jung Kim, Nam Kyun Kim, Seung-Woo Cho, Sak Lee, Jang-Ung Park
Publikováno v:
Science Advances. 8
The in situ diagnosis of cardiac activities with simultaneous therapeutic electrical stimulation of the heart is key to preventing cardiac arrhythmia. Here, we present an unconventional single-device platform that enables in situ monitoring even in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8566f5037b1887ee08a1a4ab1e667361
https://doi.org/10.1126/sciadv.abq0897
https://doi.org/10.1126/sciadv.abq0897