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Neurobiology of Aging|February 6, 2018
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's diseaseCornelis Blauwendraat, Demis A Kia, Lasse Pihlstrøm, et al.Molecular Biology Reports|March 20, 2021
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial diseaseAlejandro Horga, Andreea Manole, Alice L Mitchell, et al.Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.Journal of the American Heart Association|November 29, 2022
Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and MiceEnrico Bugiardini, Andreia M Nunes, Ariany Oliveira-Santos, et al.Neurology. Genetics|May 17, 2017
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial diseaseEnrico Bugiardini, Olivia V Poole, Andreea Manole, et al.Nature Genetics|October 16, 2007
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer riskPeter Broderick, Luis Carvajal-Carmona, Alan M Pittman, et al.Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.Journal of Fish Biology|May 20, 2022
Delineation of blacktip shark (Carcharhinus limbatus) nursery habitats in the north-western Gulf of MexicoPhilip Matich, Camryn L Bigelow, Barrett Chambers, et al.Neurobiology of Aging|September 6, 2016
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositisQiang Gang, Conceição Bettencourt, Pedro M Machado, et al.Pageof 19