Neurodegenerative DiseasesDisease SusceptibilityGenetic Predisposition to DiseaseNerve DegenerationPolymorphism, Single NucleotideGenotypeAlzheimer DiseaseBrainAmyotrophic Lateral SclerosisAllelesNeuronsHaplotypestau ProteinsHuntington DiseaseParkinson Diseasealpha-SynucleinDisease Models, AnimalPolymorphism, GeneticMutationGenome-Wide Association StudyGene FrequencyNerve Tissue ProteinsPrionsCase-Control StudiesNeuroprotective AgentsTauopathiesPrion DiseasesMice, TransgenicPhenotypeGenetic VariationInclusion BodiesLinkage DisequilibriumHeredodegenerative Disorders, Nervous SystemProteostasis DeficienciesMice, Inbred C57BLGenetic LinkageChromosome MappingMicrogliaMicrobial Sensitivity TestsGenetic MarkersMolecular Sequence DataSynucleinsCell DeathOxidative StressAmyloid beta-PeptidesSpinocerebellar AtaxiasGenome, HumanCells, CulturedFrontotemporal Lobar DegenerationAgingGene Expression RegulationMitochondriaTrinucleotide Repeat ExpansionSignal TransductionFrontotemporal DementiaModels, BiologicalFriedreich AtaxiaModels, GeneticImmunity, InnateHLA-DQ AntigensGenetic Association StudiesNod2 Signaling Adaptor ProteinEpistasis, GeneticAutophagyCrohn DiseaseAmino Acid SequenceHLA-DRB1 ChainsGuamAmyloidHLA-DR3 AntigenPlant DiseasesMice, KnockoutHLA-DQ beta-ChainsNeuronal Ceroid-LipofuscinosesComplement C4aHLA-DR AntigensAnti-Bacterial AgentsGenetic LociPedigreeProtein FoldingPeptidesDementiaGenetic Diseases, InbornAge of OnsetNeurofibrillary TanglesSuperoxide DismutaseAstrocytesNeurotoxinsLewy Body DiseaseCell LineParkinsonian DisordersGenetic TestingBahrainChromosomes, Human, Pair 6DiseaseSalicylic AcidTime FactorsBase SequenceApoptosisGenes, MHC Class II