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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 7, 2001
Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cellsJ Barclay, N Balaguero, M Mione, et al.Physical Chemistry Chemical Physics : PCCP|September 5, 2017
Analyses of sizable ZFS and magnetic tensors of high spin metallocomplexesTakeshi Yamane, Kenji Sugisaki, Tomoki Nakagawa, et al.Proceedings of the National Academy of Sciences of the United States of America|December 13, 2019
IgGs from patients with amyotrophic lateral sclerosis and diabetes target CaVα2δ1 subunits impairing islet cell function and survivalYue Shi, Kyoung Sun Park, Seung Hyun Kim, et al.The EMBO Journal|January 17, 2018
Mapping protein interactions of sodium channel NaV1.7 using epitope-tagged gene-targeted miceAlexandros H Kanellopoulos, Jennifer Koenig, Honglei Huang, et al.Pharmaceutical Research|December 11, 2023
Integrated Exposure-Response of Dupilumab in Children, Adolescents, and Adults With Atopic Dermatitis Using Categorical and Continuous Efficacy Assessments: A Population AnalysisEmily Briggs, Mohamed A Kamal, Matthew P Kosloski, et al.Journal of Medicinal Chemistry|November 7, 2000
Rational design, synthesis, and biological activity of benzoxazinones as novel factor Xa inhibitorsD A Dudley, A M Bunker, L Chi, et al.BMJ Open|December 9, 2023
Protocol for the Tallaght University Hospital Institute for Memory and Cognition-Biobank for Research in Ageing and NeurodegenerationAdam H Dyer, Helena Dolphin, Antoinette O'Connor, et al.Alzheimer'S Research & Therapy|August 19, 2024
Performance of plasma p-tau217 for the detection of amyloid-β positivity in a memory clinic cohort using an electrochemiluminescence immunoassayAdam H Dyer, Helena Dolphin, Antoinette O'Connor, et al.JBMR Plus|March 20, 2024
Loss of the auxiliary α2δ1 voltage-sensitive calcium channel subunit impairs bone formation and anabolic responses to mechanical loadingMadison M Kelly, Karan Sharma, Christian S Wright, et al.Nature Genetics|August 6, 2013
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertensionElena A B Azizan, Hanne Poulsen, Petronel Tuluc, et al.Pageof 52