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Journal of Inherited Metabolic Disease|January 27, 2009
Mitochondrial cytochrome c release: a factor to consider in mitochondrial disease?M L S Oppenheim, I P Hargreaves, S Pope, et al.
Molecular Genetics and Metabolism|January 4, 2001
Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemiaY P Conley, D N Finegold, D G Peters, et al.
Neurosurgery|August 1, 1995
Symptomatic cavernous malformations affecting the spine and spinal cordM J Harrison, M B Eisenberg, J S Ullman, et al.
Journal of Medicinal Chemistry|January 1, 1977
Synthesis of mono- and bifunctional alpha-methylene lactone systems as potential tumor inhibitorsP A Grieco, J A Noguez, Y Masaki, et al.
Archives of General Psychiatry|August 2, 2000
A serotonin transporter gene promoter polymorphism (5-HTTLPR) and prefrontal cortical binding in major depression and suicideJ J Mann, Y Y Huang, M D Underwood, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Assessment of growth hormone (GH) secretion in men with adult-onset GH deficiency compared with that in normal men--a clinical research center studyH B Baum, B M Biller, L Katznelson, et al.
Journal of Dairy Science|September 21, 2004
Hot topic: using a stearoyl-CoA desaturase transgene to alter milk fatty acid compositionW A Reh, E A Maga, N M B Collette, et al.
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