Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Saeyoung Park"'
Autor:
Shixia Wang, Kun-Wei Chan, Danlan Wei, Xiuwen Ma, Shuying Liu, Guangnan Hu, Saeyoung Park, Ruimin Pan, Ying Gu, Alexandra F. Nazzari, Adam S. Olia, Kai Xu, Bob C. Lin, Mark K. Louder, Krisha McKee, Nicole A. Doria-Rose, David Montefiori, Michael S. Seaman, Tongqing Zhou, Peter D. Kwong, James Arthos, Xiang-Peng Kong, Shan Lu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract The vaccine elicitation of HIV tier-2-neutralization antibodies has been a challenge. Here, we report the isolation and characterization of a CD4-binding site (CD4bs) specific monoclonal antibody, HmAb64, from a human volunteer immunized wit
Externí odkaz:
https://doaj.org/article/d4067003b45c4b2ab1dab731384dc0c2
Autor:
Na-Kyoung Yang, Yoo-Kyum Shin, Saeyoung Park, Sang-Min Kim, Bon-Jae Koo, Joonsoo Jeong, Min-Ho Seo
Publikováno v:
Micro and Nano Systems Letters, Vol 12, Iss 1, Pp 1-8 (2024)
Abstract Laser-induced graphene (LIG) is a three-dimensional graphene structure fabricated through the irradiation of a polymer substrate with laser energy (or fluence, equivalently). This methodology offers a cost-effective and facile means of produ
Externí odkaz:
https://doaj.org/article/77bf781e957b4c4f9b2675ec25f02081
Autor:
Yu Hwa Nam, Saeyoung Park, Yoonji Yum, Soyeon Jeong, Hyo Eun Park, Ho Jin Kim, Jaeseung Lim, Byung-Ok Choi, Sung-Chul Jung
Publikováno v:
Biomedicines, Vol 11, Iss 12, p 3334 (2023)
Charcot–Marie–Tooth disease (CMT) is a hereditary disease with heterogeneous phenotypes and genetic causes. CMT type 1A (CMT1A) is a type of disease affecting the peripheral nerves and is caused by the duplication of the peripheral myelin protein
Externí odkaz:
https://doaj.org/article/c9fe0194592845558a5d74cb717cd5b4
Autor:
Sung-Chul Jung, Saeyoung Park
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 4, p 3938 (2023)
For the clinical application of mesenchymal stem cells (MSCs), the optimization of biological products (e [...]
Externí odkaz:
https://doaj.org/article/5643c70c3ad344609a134477eea184f5
Autor:
Ji Yeon Kim, Saeyoung Park, Se-Young Oh, Yu Hwa Nam, Young Min Choi, Yeonzi Choi, Ha Yeong Kim, Soo Yeon Jung, Han Su Kim, Inho Jo, Sung-Chul Jung
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 2, p 715 (2022)
Mesenchymal stem cells (MSCs) can differentiate into endoderm lineages, especially parathyroid-hormone (PTH)-releasing cells. We have previously reported that tonsil-derived MSC (T-MSC) can differentiate into PTH-releasing cells (T-MSC-PTHCs), which
Externí odkaz:
https://doaj.org/article/59ddaa9e936340e2b12591702e80864b
Autor:
Saeyoung Park, Sung-Chul Jung
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10, p 5288 (2021)
Mesenchymal stem cells (MSCs) are multipotent cells derived from various tissues including bone marrow and adipose tissues [...]
Externí odkaz:
https://doaj.org/article/445a8e041ad446ffb7a547618dcc6aec
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 11, p 2702 (2019)
Human tonsil-derived mesenchymal stem cells (T-MSCs) are newly identified MSCs and present typical features of MSCs, including having the differentiation capacity into the three germ layers and excellent proliferation capacity. They are easily source
Externí odkaz:
https://doaj.org/article/f81661ac5b4748f2b47f1b36597061ce
Publikováno v:
mBio, Vol 7, Iss 1 (2016)
ABSTRACT Treatment of Staphylococcus aureus infections has become increasingly difficult because of the emergence of multidrug-resistant isolates. Development of a vaccine to prevent staphylococcal infections remains a priority. To determine whether
Externí odkaz:
https://doaj.org/article/9f730ade2b46441fb54402e484788f3a
Autor:
Saeyoung Park, Namhee Jung, Seoha Myung, Yoonyoung Choi, Ki Wha Chung, Byung-Ok Choi, Sung-Chul Jung
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 8, p 2393 (2018)
Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited motor and sensory neuropathy, and is caused by duplication of PMP22, alterations of which are a characteristic feature of demyelination. The clinical phenotype of CMT1A is deter
Externí odkaz:
https://doaj.org/article/2eac39ed45c24254a8dad433badf02b5
Autor:
Saeyoung Park, Moon H. Nahm
Publikováno v:
PLoS ONE, Vol 9, Iss 1 (2014)
Externí odkaz:
https://doaj.org/article/cb976dffe9d2443d98977c00a17d64e9