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The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiencyD Naville, L Barjhoux, C Jaillard, et al.Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.Cell Death and Differentiation|February 9, 2010
The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stressT Cronin, W Raffelsberger, I Lee-Rivera, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2005
Edg8/S1P5: an oligodendroglial receptor with dual function on process retraction and cell survivalC Jaillard, S Harrison, B Stankoff, et al.Neuropsychologia|February 18, 2005
Differing neuropsychological and neuroanatomical correlates of abnormal reading in early-stage semantic dementia and dementia of the Alzheimer typeBrian T Gold, Dave A Balota, Michael J Cortese, et al.Brain Research. Molecular Brain Research|February 20, 2003
Molecular cloning and characterisation of a novel GABAB-related G-protein coupled receptorA R Calver, D Michalovich, T T Testa, et al.Pageof 5