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Iscience|October 21, 2020
Lipid Droplets Maintain Energy Homeostasis and Glioblastoma Growth via Autophagic Release of Stored Fatty AcidsXiaoning Wu, Feng Geng, Xiang Cheng, et al.Plos One|September 9, 2010
Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPsDelphine Fradin, Keely Cheslack-Postava, Christine Ladd-Acosta, et al.Experimental Gerontology|April 12, 2005
IL-6 gene variation is not associated with increased serum levels of IL-6, muscle, weakness, or frailty in older womenJ Walston, D E Arking, D Fallin, et al.Journal of Neurological Surgery. Part B, Skull Base|March 19, 2025
Surgical Approaches to Resection of Olfactory Groove Meningiomas: Comparative Meta-analysis of the Endoscopic Endonasal versus Transcranial and Unilateral versus Bilateral ApproachesNolan J Brown, Zach Pennington, Saarang Patel, et al.Plos One|March 2, 2013
Identification of sensitive serum microRNA biomarkers for radiation biodosimetryNaduparambil Korah Jacob, James V Cooley, Tamara N Yee, et al.American Journal of Human Genetics|October 1, 1993
A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD)S T Winokur, B Schutte, B Weiffenbach, et al.Genome Research|February 5, 2003
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure programXiaofeng Zhu, Denise Yan, Richard S Cooper, et al.Cellular Immunology|February 28, 2007
Class II MHC antigen presentation defect in neonatal monocytes is not correlated with decreased MHC-II expressionDavid H Canaday, Soma Chakravarti, Tarun Srivastava, et al.European Journal of Pharmacology|March 8, 2011
A novel flavonoid isolated from the steam-bark of Ulmus wallichiana planchon stimulates osteoblast function and inhibits osteoclast and adipocyte differentiationGaurav Swarnkar, Kunal Sharan, Jawed A Siddiqui, et al.American Journal of Human Genetics|April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17P I Patel, B Franco, C Garcia, et al.Pageof 157