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Biochemical and Biophysical Research Communications|June 15, 2013
Cleavage of the interchain disulfide bonds in rituximab increases its affinity for FcγRIIIAMami Suzuki, Ayaka Yamanoi, Yusuke Machino, et al.
European Journal of Pharmacology|September 18, 2012
Feasibility study of B16 melanoma therapy using oxidized ATP to target purinergic receptor P2X7Fumie Hattori, Yasuhiro Ohshima, Shizuka Seki, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 10, 2009
The activation of P2X7 receptor impairs lysosomal functions and stimulates the release of autophagolysosomes in microglial cellsTakato Takenouchi, Masaaki Nakai, Yoshifumi Iwamaru, et al.
Medicines (Basel, Switzerland)|April 3, 2021
A Unique Anti-Cancer 3-Styrylchromone Suppresses Inflammatory Response via HMGB1-RAGE SignalingHideaki Abe, Miwa Okazawa, Takahiro Oyama, et al.
Biological & Pharmaceutical Bulletin|December 22, 2024
Amodiaquine Analogs Are Potent Inhibitors of Interleukin-6 Production Induced by Activation of Toll-Like Receptors Recognizing Pathogen Nucleic AcidsYohei Takenaka, Tomohiro Tanaka, Shotaro Otaki, et al.
Anticancer Research|December 30, 2023
Luminal B Breast Cancer Coexpressing <i>p62</i> and <i>ALDH1A3</i> Is Less Susceptible to RadiotherapyAyaka Ozaki, Akari Matsuda, Yuki Maemura, et al.
Biochemical and Biophysical Research Communications|June 10, 2021
A 3-styrylchromone converted from trimebutine 3D pharmacophore possesses dual suppressive effects on RAGE and TLR4 signaling pathwaysMiwa Okazawa, Takahiro Oyama, Hideaki Abe, et al.
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