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Journal of Cell Science|January 1, 1994
Selective modulation of the interaction of alpha 7 beta 1 integrin with fibronectin and laminin by L-14 lectin during skeletal muscle differentiationM Gu, W Wang, W K Song, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.The Journal of Experimental Biology|January 26, 2013
Regulation of succinate-fuelled mitochondrial respiration in liver and skeletal muscle of hibernating thirteen-lined ground squirrelsJason C L Brown, Dillon J Chung, Alex N Cooper, et al.Human Genetics|July 4, 2013
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited diseaseDavid N Cooper, Michael Krawczak, Constantin Polychronakos, et al.Dose-Response : a Publication of International Hormesis Society|January 2, 2015
Drosophila melanogaster show a threshold effect in response to radiationMichael Antosh, David Fox, Thomas Hasselbacher, et al.Human Genetics|September 1, 1991
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqID S Millar, B Zoll, U Martinowitz, et al.Current Protocols in Molecular Biology|February 12, 2008
Preparation of cell cultures and vaccinia virus stocksP L Earl, N Cooper, L S Wyatt, et al.Human Brain Mapping|February 19, 2019
Cognitive regulation of ventromedial prefrontal activity evokes lasting change in the perceived self-relevance of persuasive messagingBruce P Doré, N Cooper, C Scholz, et al.Depression and Anxiety|August 27, 2020
Consumption of energy drinks is associated with depression, anxiety, and stress in young adult males: Evidence from a longitudinal cohort studySimrat Kaur, Hayley Christian, Matthew N Cooper, et al.Human Mutation|July 19, 2012
Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) geneLaura Thomas, Mark Richards, Matthew Mort, et al.Pageof 124