Neurodegenerative DiseasesDisease SusceptibilityGenetic Predisposition to DiseaseLungNerve DegenerationPolymorphism, Single NucleotideGenotypeAlzheimer DiseaseBrainAllelesAmyotrophic Lateral SclerosisNeuronsHaplotypestau ProteinsHuntington DiseaseParkinson DiseasePolymorphism, Geneticalpha-SynucleinDisease Models, AnimalMutationLung DiseasesGenome-Wide Association StudyGene FrequencyCase-Control StudiesNerve Tissue ProteinsPrionsLung NeoplasmsTauopathiesNeuroprotective AgentsPhenotypeMice, Inbred C57BLPrion DiseasesMice, TransgenicGenetic VariationLinkage DisequilibriumInclusion BodiesHeredodegenerative Disorders, Nervous SystemProteostasis DeficienciesGenetic LinkageChromosome MappingMicrogliaMolecular Sequence DataMicrobial Sensitivity TestsGenetic MarkersOxidative StressCells, CulturedSynucleinsCell DeathAmyloid beta-PeptidesLung InjurySpinocerebellar AtaxiasGenome, HumanFrontotemporal Lobar DegenerationGene Expression RegulationAgingSignal TransductionMitochondriaTrinucleotide Repeat ExpansionCarcinoma, Non-Small-Cell LungImmunity, InnateModels, BiologicalMice, KnockoutFrontotemporal DementiaFriedreich AtaxiaHLA-DQ AntigensModels, GeneticGenetic Association StudiesAmino Acid SequenceLung TransplantationNod2 Signaling Adaptor ProteinAutophagyEpistasis, GeneticCrohn DiseaseHLA-DRB1 ChainsGuamHLA-DR3 AntigenAmyloidHLA-DQ beta-ChainsNeuronal Ceroid-LipofuscinosesComplement C4aPlant DiseasesHLA-DR AntigensCell LineAnti-Bacterial AgentsPeptidesGenetic LociSuperoxide DismutaseProtein FoldingPedigreeApoptosisBase SequenceDementiaNeurofibrillary TanglesGenetic Diseases, InbornAge of OnsetAstrocytesNeurotoxinsLewy Body DiseaseRNA, MessengerGene Expression Profiling