Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Yechan Lee"'
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 6032 (2024)
Anoctamin1 (ANO1), a calcium-activated chloride channel, is overexpressed in a variety of cancer cells, including prostate cancer, and is involved in cancer cell proliferation, migration, and invasion. Inhibition of ANO1 in these cancer cells exhibit
Externí odkaz:
https://doaj.org/article/b32502270a3e4698bafb56a2bc55bedd
Autor:
Yechan Lee, Hyung-Soon Park
Publikováno v:
Biomimetics, Vol 9, Iss 3, p 172 (2024)
The finger workspace is crucial for performing various grasping tasks. Thus, various soft rehabilitation gloves have been developed to assist individuals with paralyzed hands in activities of daily living (ADLs) or rehabilitation training. However, m
Externí odkaz:
https://doaj.org/article/cab8db7993eb4ac3acf27459ec622c46
Autor:
Yechan Lee, Sunhee Lee, Younho Lee, Doona Song, So-Hyeon Park, Jieun Kim, Wan Namkung, Ikyon Kim
Publikováno v:
Pharmaceuticals, Vol 17, Iss 2, p 231 (2024)
The epidermal growth factor receptor (EGFR), also known as ErbB1 and HER1, belongs to the receptor tyrosine kinase family. EGFR serves as the primary driver in non-small-cell lung cancer (NSCLC) and is a promising therapeutic target for NSCLC. In thi
Externí odkaz:
https://doaj.org/article/25afb50b92b64f0a88bdb9c7b8689080
Publikováno v:
Frontiers in Marine Science, Vol 10 (2023)
Five previously undescribed pentacyclic triterpenoid saponins, pannoside A–E (1–5), were discovered from the whole plant of seashore aster, Tripolium pannonicum, collected from the Songdo tidal flat, Incheon, Korea. The planar structures of panno
Externí odkaz:
https://doaj.org/article/c4364c26a6454224b1bb9b6c0493b8ed
Autor:
Sung Baek Jeong, Raju Das, Dong-Hyun Kim, Sion Lee, Hye In Oh, Sungwoo Jo, Yechan Lee, Jeongdong Kim, SeonJu Park, Dong Kyu Choi, Uk Yeol Moon, Oh-bin Kwon, Wan Namkung, Sungwoo Lee, Byoung Chul Cho, Joohan Woo, Yohan Seo
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 153, Iss , Pp 113373- (2022)
Anoctamin 1 (ANO1) is a calcium-activated chloride channel found in various cell types and is overexpressed in non-small cell lung cancer (NSCLC), a major cause of cancer-related mortality. With the rising interest in development of druggable compoun
Externí odkaz:
https://doaj.org/article/0d7d8a2863c942b9a4c38ca89e6a8cbc
Autor:
Yechan Lee, Hae-Deok Song
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
Managing learning continuity is critical for successful MOOC learning. Thus, enabling learners to have learning persistence needs to be integrated into the MOOC learning design. Motivation effort is a critical component enabling students to maintain
Externí odkaz:
https://doaj.org/article/c36882e06fb6476cbfa5a67831a20788
Autor:
Dongkyu Jeon, Minjae Jo, Yechan Lee, So-Hyeon Park, Hong Thi Lam Phan, Joo Hyun Nam, Wan Namkung
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1186 (2023)
Anoctamin1 (ANO1), a calcium-activated chloride channel, is involved in the proliferation, migration, and invasion of various cancer cells including head and neck squamous cell carcinoma, lung cancer, and prostate cancer. Inhibition of ANO1 activity
Externí odkaz:
https://doaj.org/article/f0a313988d214207bc69b5036f348fc1
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 22, p 14321 (2022)
Chloroquine (CQ) is an antimalaria drug that has been widely used for decades. However, CQ-induced pruritus remains one of the major obstacles in CQ treatment for uncomplicated malaria. Recent studies have revealed that MrgprX1 plays an essential rol
Externí odkaz:
https://doaj.org/article/ad8a619689e34ea7bcc94a6fb87d0fb4
Publikováno v:
Pharmaceuticals, Vol 15, Iss 11, p 1395 (2022)
A highly efficient approach to a new indolizine scaffold fused with pyrrolo[1,2-c]pyrimidine was achieved via one-pot three-component coupling followed by an oxidative cyclization reaction. The simple two-step sequence allowed rapid access to various
Externí odkaz:
https://doaj.org/article/6a127f732f9f46eb93e52b37b12145f4
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 18, p 10631 (2022)
Protease-activated receptor 2 (PAR2) is a G-protein-coupled receptor (GPCR) activated by proteolytic cleavage of its N-terminal domain. Once activated, PAR2 is rapidly desensitized and internalized by phosphorylation and β-arrestin recruitment. Due
Externí odkaz:
https://doaj.org/article/fee2f39d6aea4947b11a53ec5595c296