Neurodegenerative DiseasesDisease SusceptibilityGenetic Predisposition to DiseaseNerve DegenerationPolymorphism, Single NucleotideAlzheimer DiseaseGenotypeBrainNeuronsAmyotrophic Lateral SclerosisAllelestau ProteinsHaplotypesHuntington DiseaseDisease Models, AnimalParkinson Diseasealpha-SynucleinPolymorphism, GeneticMutationGenome-Wide Association StudyNerve Tissue ProteinsGene FrequencyMice, TransgenicPrionsTauopathiesCase-Control StudiesNeuroprotective AgentsPhenotypePrion DiseasesInclusion BodiesMice, Inbred C57BLGenetic VariationLinkage DisequilibriumProteostasis DeficienciesHeredodegenerative Disorders, Nervous SystemMicrogliaGenetic LinkageChromosome MappingMolecular Sequence DataAmyloid beta-PeptidesMicrobial Sensitivity TestsSynucleinsGenetic MarkersCell DeathCells, CulturedOxidative StressFrontotemporal Lobar DegenerationSpinocerebellar AtaxiasGenome, HumanAgingSignal TransductionGene Expression RegulationMitochondriaTrinucleotide Repeat ExpansionModels, BiologicalFrontotemporal DementiaAutophagyAmino Acid SequenceImmunity, InnateModels, GeneticFriedreich AtaxiaHLA-DQ AntigensMice, KnockoutGenetic Association StudiesNod2 Signaling Adaptor ProteinAmyloidEpistasis, GeneticCrohn DiseaseNeurofibrillary TanglesHLA-DRB1 ChainsPlant DiseasesGuamHLA-DR3 AntigenHLA-DQ beta-ChainsNeuronal Ceroid-LipofuscinosesComplement C4aHLA-DR AntigensCell LinePeptidesGenetic LociProtein FoldingAnti-Bacterial AgentsAstrocytesApoptosisPedigreeDementiaSuperoxide DismutaseLewy Body DiseaseBase SequenceNeurotoxinsGenetic Diseases, InbornAge of OnsetLewy BodiesParkinsonian DisordersBahrainChromosomes, Human, Pair 6DiseaseGene Expression ProfilingSalicylic AcidGenetic Testing