Zobrazeno 1 - 10
of 172
pro vyhledávání: '"matrix protein 2"'
Autor:
Yinjie Liang, Junjia Guo, Zhen Li, Shiyuan Liu, Ting Zhang, Shucai Sun, Funa Lu, Yuqian Zhai, Wenling Wang, Chuanyi Ning, Wenjie Tan
Publikováno v:
Biosafety and Health, Vol 6, Iss 3, Pp 178-185 (2024)
The matrix protein 2 (M2) is a preferred target for developing a universal vaccine against the influenza A virus (IAV). This study aimed to develop a method for assessing antibody-dependent cell-mediated cytotoxicity (ADCC) associated with M2-based i
Externí odkaz:
https://doaj.org/article/11ff126d9fd04d37aeafc2ce2f986a51
Autor:
Risa Konishi, Yuki Ichimura, Ryota Tanaka, Hanako Miyahara, Mari Okune, Masahide Miyamoto, Monami Hara, Atsushi Iwabuchi, Hidetoshi Takada, Yasuo Nakagishi, Mao Mizuta, Shuya Kaneko, Masaki Shimizu, Tomohiro Morio, Ichizo Nishino, Toshifumi Nomura, Naoko Okiyama
Publikováno v:
Immunological Medicine, Vol 47, Iss 2, Pp 100-105 (2024)
AbstractAnti-nuclear matrix protein 2 (NXP2) antibody-positive dermatomyositis (DM) is characterized by extensive and severe myositis. In this study, we evaluated which cytokines/chemokines involved with the activity of the myositis. We performed qua
Externí odkaz:
https://doaj.org/article/2b1791d436b1447aa8520e6fcdc13476
Autor:
TIAN Yuying, DENG Zhuoya
Publikováno v:
陆军军医大学学报, Vol 46, Iss 7, Pp 725-731 (2024)
Objective To construct a universal influenza mRNA vaccine and evaluate its immunogenicity. Methods The antigen sequence of hemagglutinin (HA), nucleoprotein (NP) and matrix protein 2 ectodomain (M2e) in influenza A/California/04/2009 was optimized.HA
Externí odkaz:
https://doaj.org/article/d86a2ea112a74ecfb38ed90fb8323645
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Juvenile dermatomyositis (JDM) is a rare autoimmune disorder with multi-system involvement, often presenting with a heliotrope rash, Gottron's papules, and proximal muscle weakness. JDM patients with anti-nuclear matrix protein 2 (anti-NXP2) positivi
Externí odkaz:
https://doaj.org/article/2dd8662dca714b27bbcf747ce20641d8
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Background Macrophage activation syndrome (MAS) is a severe and life-threatening syndrome associated with autoimmune diseases. The coexistence of MAS and juvenile dermatomyositis (JDM) is not well reported. This report describes a case of JD
Externí odkaz:
https://doaj.org/article/4aa0b1dfd2f54c16b1190b4b7eedbfd4
Autor:
Michelle Toker, BS, Roya S. Nazarian, MD, Pooja Srivastava, MD, Bijal Amin, MD, Benedict Wu, DO, PhD
Publikováno v:
JAAD Case Reports, Vol 33, Iss , Pp 77-80 (2023)
Externí odkaz:
https://doaj.org/article/a6d06d4b91e04e2d85103604c98968ec
Autor:
Jini Joseph, Sujith Janardhanan
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 7, Pp 03-05 (2023)
An eight-month-old male baby was brought to the hospital by his parents due to poor weight gain, lower respiratory tract infection, and exertional dyspnoea (noticed by the parents) for one month. During the clinical examination, a grade-III ejecti
Externí odkaz:
https://doaj.org/article/d0d4e9cf870640dab9171a842602f630
Autor:
Hsiao‐Han Tsai, Ping‐Han Huang, Leon CW Lin, Bing‐Yu Yao, Wan‐Ting Liao, Chen‐Hsueh Pai, Yu‐Han Liu, Hui‐Wen Chen, Che‐Ming J. Hu
Publikováno v:
Advanced Science, Vol 10, Iss 17, Pp n/a-n/a (2023)
Abstract The highly conserved matrix protein 2 ectodomain (M2e) of influenza viruses presents a compelling vaccine antigen candidate for stemming the pandemic threat of the mutation‐prone pathogen, yet the low immunogenicity of the diminutive M2e p
Externí odkaz:
https://doaj.org/article/661e6199182c4f3e9a670334efe34de2
Autor:
Bina Kassamali, BA, Daniel R. Mazori, MD, Avery H. LaChance, MD, MPH, Lisa Christopher-Stine, MD, MPH
Publikováno v:
International Journal of Women's Dermatology, Vol 7, Iss 5, Pp 576-582 (2021)
Externí odkaz:
https://doaj.org/article/a6ba3c23654a426aa80d3eccd7743711
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-9 (2021)
Abstract Background Juvenile dermatomyositis (JDM) is a rare and sometimes fatal disease in children. The anti-NXP2 antibody is one of the most common antibodies and muscle ischaemia associated with NXP2 autoantibodies was a severe subtype of JDM. Fu
Externí odkaz:
https://doaj.org/article/696361b33dc749988c57268f5b292654