Neurodegenerative DiseasesDisease SusceptibilityGenetic Predisposition to DiseaseNerve DegenerationPolymorphism, Single NucleotideAlzheimer DiseaseGenotypeBrainAmyotrophic Lateral SclerosisAllelesNeuronsHaplotypestau ProteinsHuntington DiseaseParkinson Diseasealpha-SynucleinPolymorphism, GeneticDisease Models, AnimalMutationGenome-Wide Association StudyGene FrequencyNerve Tissue ProteinsPrionsTauopathiesNeuroprotective AgentsCase-Control StudiesPrion DiseasesMice, TransgenicPhenotypeGenetic VariationInclusion BodiesLinkage DisequilibriumHeredodegenerative Disorders, Nervous SystemProteostasis DeficienciesMice, Inbred C57BLGenetic LinkageChromosome MappingMicrogliaMicrobial Sensitivity TestsGenetic MarkersMolecular Sequence DataSynucleinsCell DeathOxidative StressAmyloid beta-PeptidesSpinocerebellar AtaxiasFrontotemporal Lobar DegenerationCells, CulturedGenome, HumanAgingTrinucleotide Repeat ExpansionMitochondriaGene Expression RegulationFrontotemporal DementiaFriedreich AtaxiaHLA-DQ AntigensSignal TransductionImmunity, InnateModels, GeneticGenetic Association StudiesNod2 Signaling Adaptor ProteinEpistasis, GeneticAutophagyCrohn DiseaseModels, BiologicalHLA-DRB1 ChainsAmino Acid SequenceGuamHLA-DR3 AntigenHLA-DQ beta-ChainsAmyloidNeuronal Ceroid-LipofuscinosesComplement C4aPlant DiseasesMice, KnockoutHLA-DR AntigensGenetic LociAnti-Bacterial AgentsProtein FoldingPeptidesPedigreeDementiaNeurofibrillary TanglesGenetic Diseases, InbornSuperoxide DismutaseAstrocytesNeurotoxinsLewy Body DiseaseAge of OnsetParkinsonian DisordersCell LineBahrainChromosomes, Human, Pair 6Salicylic AcidGenetic TestingDiseaseBase SequenceGenes, MHC Class IICentral Nervous SystemApoptosis