Showing results (2411-2420 of 2,951) with videos related to

Sort By:
Pageof 296
European Review for Medical and Pharmacological Sciences|June 25, 2016
Evidence for a role of GPRC6A in prostate cancer metastasis based on case-control and in vitro analysesM Liu, Y-Y Zhao, F Yang, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|November 24, 2021
[Evaluation of demand of resources for laboratory testing and prevention and control of COVID-19 in the context of global pandemic]Q Wang, T Zhang, Y Yang, et al.
Brain : a Journal of Neurology|January 21, 2009
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA)F Mochel, F Sedel, A Vanderver, et al.
Bioorganic & Medicinal Chemistry Letters|January 16, 2014
Diphenylpyridylethanamine (DPPE)-based aminoheterocycles as cholesteryl ester transfer protein inhibitorsYufeng Wang, Wu Yang, Heather J Finlay, et al.
Nature Genetics|January 4, 2001
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophyK Zhang, M Kniazeva, M Han, et al.
Journal of Animal Science|April 23, 2022
Nitrogen excretion from beef cattle fed a wide range of diets compiled in an intercontinental dataset: a meta-analysisAdeline Bougouin, Alexander Hristov, Diego Zanetti, et al.
Journal of Neurosurgery|September 1, 2023
Successful magnetic resonance-guided focused ultrasound treatment of tremor in patients with a skull density ratio of 0.4 or lessArtur Vetkas, Alexandre Boutet, Can Sarica, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|September 27, 2024
[Short-term results of a multicenter study based on a modified N7 induction regimen combined with arsenic trioxide in the treatment of children with high-risk neuroblastoma]S Yang, K L Chen, Y Y He, et al.
Circulation|December 23, 2009
Endothelial-specific deletion of connexin40 promotes atherosclerosis by increasing CD73-dependent leukocyte adhesionC E Chadjichristos, K E L Scheckenbach, T A B van Veen, et al.
Clinical Genetics|September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese familyJ Cheng, D Y Han, P Dai, et al.
Pageof 296