Showing results (641-650 of 1,131) with videos related to
Sort By:
Pageof 114
Advances in Experimental Medicine and Biology|February 25, 2003
Guanylate cyclase activating proteins, guanylate cyclase and diseaseRichard J Newbold, Evelyne C Deery, Annette M Payne, et al.Health Care Financing Review|March 6, 1987
Factors affecting appropriateness of hospital use in MassachusettsJ D Restuccia, B E Kreger, S M Payne, et al.The Journal of Biological Chemistry|August 29, 1998
Octamer formation and coupling of cardiac sarcomeric mitochondrial creatine kinase are mediated by charged N-terminal residuesZ A Khuchua, W Qin, J Boero, et al.Circulation|May 1, 1992
Validation of a Doppler guide wire for intravascular measurement of coronary artery flow velocityJ W Doucette, P D Corl, H M Payne, et al.Journal of Neurophysiology|February 24, 2025
Excellent test-retest reliability of perturbation-evoked cortical responses supports feasibility of the balance N1 as a clinical biomarkerJasmine L Mirdamadi, Alex Poorman, Gaetan Munter, et al.Journal of the Academy of Nutrition and Dietetics|April 23, 2013
Effects of HIV and antiretroviral therapy on resting energy expenditure in adult HIV-infected women-a matched, prospective, cross-sectional studyAlison L Mittelsteadt, Corrilynn O Hileman, Stephanie R Harris, et al.Annals of Clinical and Translational Neurology|February 6, 2020
Visual spatial learning outcomes for clinical trials in neurofibromatosis type 1Nicole J Ullrich, Jonathan M Payne, Karin S Walsh, et al.Mutation Research|April 1, 1995
A comparison of the mutagenicity of mainstream cigarette smoke condensates from a representative sample of the U.S. cigarette market with a Kentucky reference cigarette (K1R4F)R H Steele, V M Payne, C W Fulp, et al.Experimental Neurology|August 1, 1997
The expression of creatine kinase isoenzymes in neocortex of patients with neurodegenerative disorders: Alzheimer's and Pick's diseaseM Y Aksenov, M V Aksenova, R M Payne, et al.Human Mutation|April 3, 1999
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. OnlineD A Bessant, S Khaliq, A Hameed, et al.Pageof 114