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Nihon Kokyuki Gakkai Zasshi = the Journal of the Japanese Respiratory Society|August 9, 2002
[A case of pulmonary sarcoidosis with pneumothorax and pleural effusion after improvement of pulmonary impairment]Hitoshi Nakamura, Osamu Kitada, Kazumi Aragane, et al.Bioscience of Microbiota, Food and Health|February 4, 2020
Associations of gut microbiota, dietary intake, and serum short-chain fatty acids with fecal short-chain fatty acidsRyodai Yamamura, Koshi Nakamura, Naoya Kitada, et al.Archives of Biochemistry and Biophysics|January 25, 2019
Human airway trypsin-like protease enhances interleukin-8 synthesis in bronchial epithelial cells by activating protease-activated receptor 2Mari Miki, Susumu Yasuoka, Rie Tsutsumi, et al.Clinical Rheumatology|August 8, 2022
Effect and safety profile of belimumab and tacrolimus combination therapy in thirty-three patients with systemic lupus erythematosusTakehiro Nakai, Sho Fukui, Genki Kidoguchi, et al.Microbiology Spectrum|March 16, 2022
Direct Attachment with Erythrocytes Augments Extracellular Growth of Pathogenic MycobacteriaYukiko Nishiuchi, Yoshitaka Tateishi, Hiroshi Hirano, et al.Journal of Neurochemistry|June 20, 2001
Developmental changes in the expression of parkin and UbcR7, a parkin-interacting and ubiquitin-conjugating enzyme, in rat brainM Wang, T Suzuki, T Kitada, et al.Journal of Neural Transmission. Supplementum|December 29, 2000
PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonismN Shimizu, S Asakawa, S Minoshima, et al.Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 22, 2011
Degradation of filamin induces contraction of vascular smooth muscle cells in type-I collagen matrix honeycombsMasashi Uchida, Itsuko Ishii, Kaori Hirata, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 9, 2011
Q172H replacement overcomes effects on the metabolism of cyclophosphamide and efavirenz caused by CYP2B6 variant with Arg262Noritaka Ariyoshi, Miyuki Ohara, Mayumi Kaneko, et al.Journal of Neurology|August 9, 2011
Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortexHidekazu Suzuki, Tomokatsu Yoshida, Mari Kitada, et al.Pageof 211