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Neurogenetics|November 21, 2001
APOE and APOC1 genetic polymorphisms in age-associated memory impairmentD Bartrés-Faz, I C Clemente, C Junqué, et al.Neurogenetics|November 29, 2016
A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesiaAna L Kolicheski, Gary S Johnson, Tendai Mhlanga-Mutangadura, et al.Neurogenetics|February 26, 2014
Brain-derived neurotrophic factor: its impact upon neuroplasticity and neuroplasticity inducing transcranial brain stimulation protocolsL Chaieb, A Antal, G G Ambrus, et al.Neurogenetics|March 25, 2014
Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissueMelanie Vanessa Heck, Mekhman Azizov, Tanja Stehning, et al.Neurogenetics|January 27, 2017
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrumHuma Tariq, Sadaf NazNeurogenetics|March 22, 2019
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian familyEliana Marisa Ramos, Alessandro Roca, Noravit Chumchim, et al.Neurogenetics|March 29, 2019
Rs10230207 genotype confers changes in HDAC9 and TWIST1, but not FERD3L in lymphoblasts from patients with intracranial aneurysmTheresa A Lansdell, Courtney Fisher, Kent Simmonds, et al.Neurogenetics|March 30, 2019
Pathogenic variants in AIMP1 cause pontocerebellar hypoplasiaAndrea Accogli, Laura Russell, Guillaume Sébire, et al.Neurogenetics|August 28, 2025
Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 geneRobin A Pilz, Matthias Begemann, Surema Pfister, et al.Neurogenetics|May 11, 2020
Rare copy number variations of planar cell polarity genes are associated with human neural tube defectsTian Tian, Yunping Lei, Yongyan Chen, et al.Pageof 96