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European Journal of Neurology|February 23, 2008
Hyperhomocysteinaemia is a significant risk factor for white matter lesions in Japanese type 2 diabetic patientsT Shimomura, F Anan, Y Umeno, et al.Biochemical and Biophysical Research Communications|December 5, 1998
Anticancer activity of morphine and its synthetic derivative, KT-90, mediated through apoptosis and inhibition of NF-kappaB activationE Sueoka, N Sueoka, Y Kai, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 15, 2008
Neuroprotective and antiamnesic effect of donepezil, a nicotinic acetylcholine-receptor activator, on rats with concussive mild traumatic brain injuryMinoru Fujiki, Takeshi Kubo, Tohru Kamida, et al.Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 27, 2007
Alterations in the molecular species of plasmalogen phospholipids and glycolipids due to peroxisomal dysfunction in Chinese hamster ovary-mutant Z65 cells by FABMS methodMakiko Saito, Makoto Horikawa, Yuriko Iwamori, et al.Transplantation|November 29, 2022
Liver Paired Exchange: Programmatic Hopes and FearsAfshin A Khan, Koji Hashimoto, Choon H David Kwon, et al.Neuropsychiatric Disease and Treatment|May 23, 2013
Reduced prefrontal cortex activation using the Trail Making Test in schizophreniaRyo Fujiki, Kiichiro Morita, Mamoru Sato, et al.International Journal of Oncology|May 10, 2007
Flt3 ligand promotes myeloid dendritic cell differentiation of human hematopoietic progenitor cells: possible application for cancer immunotherapySachio Harada, Takafumi Kimura, Hiroshi Fujiki, et al.Internal Medicine (Tokyo, Japan)|September 21, 2022
Lymphoid Hyperplasia of the Gallbladder Extending to the Bile DuctKazuya Miyamoto, Kazuyuki Matsumoto, Koki Matsubara, et al.Iscience|March 23, 2020
Cul5-type Ubiquitin Ligase KLHDC1 Contributes to the Elimination of Truncated SELENOS Produced by Failed UGA/Sec DecodingFumihiko Okumura, Yuha Fujiki, Nodoka Oki, et al.Human Genome Variation|April 8, 2020
Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiencyMina Nakama, Hideo Sasai, Mitsuru Kubota, et al.Pageof 239