Related by context. All words. (Click for frequent words.) 73 SORL1 gene 69 TCF#L# gene 68 progranulin 68 apoE4 68 BARD1 68 CNTNAP2 67 TCF#L# 67 APOE4 66 TMEM#B 66 CALHM1 65 MTHFR 65 dopamine D4 receptor 65 SH#B# 65 KIAA# 65 neuroglobin 65 alpha synuclein gene 65 amyloid beta peptides 65 LRP5 65 MC1R 65 LKB1 64 kalirin 64 APOE gene 64 MAOA gene 64 susceptibility gene 64 synuclein 64 MYH9 gene 64 ApoE4 gene 64 BCL#A 64 ORMDL3 64 MLL2 64 sporadic ALS 64 tumor suppressor protein 64 gene variants 64 PTPN# 64 ApoE4 64 SLC#A# [002] 64 micro RNAs 63 TGFBR1 * 6A 63 CYP#A# gene 63 apoE 63 microcephalin 63 clusterin 63 CNTNAP2 gene 63 Pin1 63 estrogen metabolism 63 chromosomal rearrangement 63 epigenetic modification 63 genes CYP#C# 63 hypermethylation 63 Klotho gene 63 DISC1 63 miRNA genes 63 Genetic variants 63 protein tau 63 MIF protein 63 KRAS oncogene 63 lipin 63 FGFR2 63 ZNF# 63 hypocretin 62 fetal hemoglobin 62 inherited mutations 62 SGK1 62 ABCB1 62 MDM2 62 BRAF gene 62 FTLD 62 factor BDNF 62 dysbindin 62 presenilin 62 TSP1 62 NPY gene 62 protein alpha synuclein 62 CYP#D# gene 62 UCP2 62 IRF5 62 mitochondrial function 62 APOE4 gene 62 mitochondrial dysfunction 62 FMR1 gene 62 LRRK2 gene 62 gene variant 62 p# protein 62 Alzheimer pathology 62 IL#R 62 protein encoded 62 narcolepsy cataplexy 62 mutated genes 62 regulates gene expression 62 APOE e4 62 protein kinase C 62 KLF# 62 missense mutations 62 CCR5 delta# 62 methylation patterns 62 Amyloid plaques 62 CYP#C# gene 62 brain derived neurotrophic 62 BDNF gene 62 DQB1 * 62 CHD7 62 Abeta# 62 PDE#A 62 Amyloid Precursor Protein 62 IDH1 62 KIBRA 62 PTEN mutations 61 ApoE gene 61 LIS1 61 MSH2 61 RBP4 61 K ras mutations 61 Prox1 61 CatB 61 PTEN gene 61 GSTP1 61 EZH2 61 familial ALS 61 neuroligins 61 Neuregulin 1 61 NKX2 61 apolipoprotein E gene 61 polyamines 61 Aβ 61 histone modifications 61 SHANK3 61 genetic variant 61 rs# [002] 61 gene APOE4 61 klotho 61 tau proteins 61 FGFR1 61 apolipoprotein E APOE 61 amyloid peptide 61 calcium homeostasis 61 FGF2 61 MTHFR gene 61 prodynorphin 61 SIRT1 61 tumor suppressor gene 61 hypermethylated 61 HLA genes 61 JAK2 enzyme 61 ALDH2 61 genetic variants 61 amyloid beta plaque 61 CETP gene 61 GSTM1 61 thyrotropin 61 DRD2 gene 61 RUNX3 61 microRNA molecules 61 tau protein 61 MECP2 61 resistin 61 DISC1 gene 61 microscopic lesions 61 GNAQ 61 ovarian hormones 61 LRP6 61 MC4R gene 61 CETP VV 61 genes BRCA1 61 FTO gene 61 ERK2 61 KCNH2 61 sarcosine 61 neurofibrillary tangles 61 MAPK pathway 60 epigenetic changes 60 CFTR gene 60 DNA methylation patterns 60 androgen receptor gene 60 TGF beta pathway 60 KCNQ1 60 ABCA1 60 metabolic abnormalities 60 POMC neurons 60 #q#.# [001] 60 mutant protein 60 vitamin D receptors 60 Srcasm 60 progranulin protein 60 PALB2 60 MC4R 60 osteopontin 60 BDNF protein 60 DICER1 gene 60 fatty acid metabolism 60 ApoE 60 TAp# 60 synapse formation 60 amyloid deposition 60 FOXP3 60 genetic polymorphisms 60 apoC III 60 adiponectin 60 MMP# 60 collagen VI 60 folate deficiency 60 tumor suppressor genes 60 COMT gene 60 MECP2 gene 60 primary cilia 60 gene locus 60 SIRT3 60 MEF2A 60 CagA 60 PICALM 60 Aß 60 STAT4 60 uPAR 60 fetuin 60 DLC1 60 sortilin 60 serotonin transporter gene 60 FMRP protein 60 alpha synuclein protein 60 HGPS 60 missense mutation 60 causal variants 60 MYH9 60 HbF 60 alpha synuclein 60 Sp1 60 non coding RNA 60 Cyclin D1 60 IgA deficiency 60 GSTT1 60 5 HTTLPR 60 KIF6 gene 60 APOE ε4 60 ENPP1 60 glutamate signaling 60 GAB2 60 proto oncogene 60 KLF4 60 tyrosine phosphorylation 60 parkin gene 60 BRCA2 gene 59 SCN5A 59 beta amyloid peptide 59 gene mutation 59 LPA gene 59 SOD1 59 Wnt pathway 59 cyclin E 59 amyloid beta plaques 59 prostate carcinogenesis 59 β amyloid 59 mitochondrial mutations 59 adiponectin levels 59 γ secretase 59 mtDNA mutations 59 Alpha synuclein 59 CYP#E# 59 CNVs 59 synaptic function 59 NF1 gene 59 apolipoprotein E4 59 p# gene 59 causative genes 59 excitatory neurotransmitter glutamate 59 p#INK#a 59 dopamine receptor gene 59 chromosome #q# [002] 59 c Myb 59 inflammatory cytokines 59 HBx 59 PPAR γ 59 motor neuron degeneration 59 mutated gene 59 C1q 59 SLC#A# [001] 59 cardiolipin 59 TXNIP 59 tyrosine kinases 59 BRIP1 59 HOTAIR 59 CYP#C# [001] 59 CYP#D# 59 TOMM# 59 TP# gene 59 GPC5 59 shorter telomeres 59 FANCD2 59 mutations 59 myo inositol 59 transgenic mouse models 59 NADPH oxidase 59 neurotransmitter GABA 59 fatty acid synthase 59 IGF2 59 abnormal proteins 59 CaM kinase II 59 B7 H3 59 Abeta 59 TSC1 59 aromatase 59 BRCA1 gene 59 Clusterin 59 ankyrin B 59 chitinase 59 cystatin C 59 amyloids 59 MSMB 59 LDLs 59 SHANK3 gene 59 CIB1 59 huntingtin 59 WNK1 59 amino acid homocysteine 59 BACE1 59 HLA DRB1 59 activin 59 spermidine 59 dopamine signaling 59 PTP1B 59 endocannabinoids 59 HMGA2 59 COX2 59 APOE 59 amyloid beta proteins 59 Pten 59 ADAM# 58 CYP#A# [002] 58 sCJD 58 Smad3 58 TNFAIP3 58 IGF1 58 nicotinamide 58 genes predisposing 58 PHLPP 58 microglial cells 58 #p# [001] 58 APOC3 58 Alzheimer disease pathology 58 metapneumovirus 58 CCL5 58 telomere lengths 58 SMN2 gene 58 palladin 58 GSTM1 gene 58 NKX#.# 58 oncoprotein 58 epigenetic regulation 58 HMGCR 58 BRCA1 mutations 58 genetic mutation 58 interferon gamma 58 hepatic lipase 58 protein beta amyloid 58 CaMKII 58 endothelial nitric oxide 58 de novo mutations 58 CHD5 58 nestin 58 hyperphosphorylated tau 58 NF kB 58 thyrotropin levels 58 gamma tocopherol 58 histone deacetylases 58 C. pneumoniae 58 amyloid β 58 Lp PLA2 58 MALAT1 58 PTEN protein 58 transthyretin 58 hereditary predisposition 58 LDL receptor 58 S#A# [002] 58 G#S mutation 58 HSF1 58 HFE gene 58 ALK gene 58 telomere length 58 ApoB 58 biochemical pathway 58 Genetic variation 58 lipoprotein metabolism 58 copper zinc superoxide 58 Wnt signaling 58 Alzheimer's linked 58 folate intake 58 Hashimoto thyroiditis 58 dysregulation 58 IKZF1 58 chromosomal instability 58 histone acetylation 58 Wwox 58 SMN2 58 JAK STAT 58 Lrp5 58 IFNg 58 epigenetic silencing 58 FMR1 58 trans palmitoleate 58 BMPR2 58 amyloidogenic 58 osteocalcin 58 insulin receptors 58 penetrance 58 HMG CoA reductase 58 miRNAs 58 FUS protein 58 Wnt#b 58 dentate gyrus 58 COMT 58 NR#A# 58 lipoprotein 58 rs# [001] 58 PARP inhibition 58 gene APOE 58 Runx2 58 aldehyde dehydrogenase 58 MAOA 58 NRG1 58 FOXP2 58 TGF b 58 Notch1 58 receptor protein 58 miRNA expression 58 IRAK1 58 filaggrin 58 mice lacking 58 UGT#A# * 58 prostaglandin E2 58 Sir2 58 MLL gene 58 sFlt1 58 chromatin structure 58 FGF# 58 TSLP 58 CXCL5 58 beta1 integrin 58 endoxifen 58 transcriptional machinery 58 E#F# 58 Cyclin E 58 CAG repeats 58 NAFLD 58 GRK2 58 Smad7 58 C#Y 58 gene rearrangements 58 CCR3 58 PIK3CA 58 G6PD 58 #q# [001] 58 huntingtin protein 58 GBA mutations 58 Notch signaling 58 STAT3 58 S#K# 58 HPA axis 58 GLI1 58 IGFBP 58 GATA4 58 genes encoding 58 aP2 58 dysregulated 57 Lewy bodies 57 ADDLs 57 Alu elements 57 TMPRSS6 57 caveolin 57 mutant mouse 57 gut microbes 57 SOD1 protein 57 evolutionary conserved 57 beta catenin 57 pathogenic mechanisms 57 amyloid cascade 57 microRNA expression 57 underlying pathophysiology 57 VHL gene 57 signaling molecule 57 FGFs 57 eNOS 57 PKM2 57 Sirt1 57 vitamin D receptor 57 ACh 57 uric acid levels 57 amyloid ß 57 GPR# [002] 57 APOE allele 57 epigenetic alterations 57 TGF beta 57 calcineurin 57 hyperinsulinemia 57 leptin receptors 57 beta catenin protein 57 kinase gene 57 mitochondrial metabolism 57 APOL1 57 Ras pathway 57 genetic mutations 57 disulfide bond 57 Akt1 57 homocysteine 57 IDH mutations 57 enterovirus infection 57 MDR1 57 Hedgehog signaling 57 BRAF protein 57 gene 57 MnSOD 57 ERBB2 57 Apobec3 57 p# MAPK 57 cholesterol metabolism 57 breast cancer metastasis 57 SOCS1 57 Six3 57 furin 57 p# mutations 57 neurofibromin 57 DEAR1 57 UGT#B# 57 NFKBIA 57 TGF β 57 vimentin 57 CYP#E# gene 57 normal prion proteins 57 gene p# 57 BMP signaling 57 VKORC1 57 gastric carcinogenesis 57 familial pancreatic cancer 57 SCD1 57 Stat5 57 amyloid proteins 57 neuroligin 57 KCNE2 57 neuronal degeneration 57 MIF gene 57 GABA receptor 57 palmitoylation 57 Brain derived neurotrophic 57 evolutionarily conserved 57 OGG1 57 RIP1 57 ERK signaling 57 mutation 57 Pol IV 57 functional polymorphism 57 MTHFD1L gene 57 TGF ß 57 Prolactin 57 ARF1 57 autoantibody 57 Apolipoprotein E 57 fibrillin 1 57 astrocyte 57 abnormal methylation 57 cyclic AMP cAMP 57 Fas ligand 57 gene mutations 57 RKIP 57 FoxO1 57 neurite outgrowth 57 TLR4 57 mutant proteins 57 TGF beta signaling 57 cardiac fibroblasts 57 phenotypic variability 57 basal cell nevus syndrome 57 WWP2 57 leptin hormone 57 PON1 57 chromosome #q# [001] 57 elevated triglyceride levels 57 DEC2 57 subclinical hyperthyroidism 57 UCP1 57 MC1R gene 57 MAO B 57 PDGFR 57 GRP# 57 beta amyloid plaques 57 IRF6 57 4E BP1 57 metabolizing enzymes 57 pathogenic mutations 57 DGAT1 57 nAChR 57 receptor gene 57 alleles 57 SMN protein 57 nicotinic receptor 57 FGFR2 gene 57 genomic variants 57 molecular pathway 57 folate metabolism 57 p# activation 57 myelination 57 TP# mutation 57 SIRT6 57 neuropeptide Y 57 rs# [003] 57 GRK5 57 mutated protein 57 VLDL cholesterol 57 neuronal stem cells 57 neurotransmitter acetylcholine 57 squamous cell lung cancer 57 PlGF 57 PCSK9 gene 57 susceptibility genes 57 filaggrin gene 57 oxysterols 57 CFH gene 57 axon guidance 57 SOD1 gene 57 gene amplification 57 Genetic mutations 57 progranulin gene 57 chromosomal aberrations 57 nicotinic receptors 57 disease NAFLD 57 stathmin 57 genetic loci 57 FOXP2 gene 57 TET2 57 cholecystokinin CCK 57 promoter methylation 57 Skp2 57 alpha secretase 57 meiotic recombination 57 oxidized LDL 57 CYP#C# [002] 57 progressive neurodegenerative disorder 57 SOD2 gene 57 cryopyrin 57 genotoxic stress 57 NRF2 gene 57 abnormal prions 57 Ets2 57 SH2 B 57 somatic mutations 57 Stat3 57 TCF4 57 dopamine transporter 57 HDAC2 57 #q#.# [002] 57 serotonin receptor 57 EphB2 57 peroxisome proliferator activated 57 ARID1A 57 thioredoxin 57 hormone estrogen 57 TEL AML1 57 transcriptional repressor 57 circadian clock genes 57 NAT2 56 SIR2 56 NF kB signaling 56 antioxidant compounds 56 genetic polymorphism 56 PRDM# 56 Genetic variations 56 FKBP# 56 microdeletions 56 p# mutation 56 mutant alleles 56 catechol O methyltransferase 56 TOP2A 56 C EBP alpha 56 amyloid precursor protein 56 leptin 56 ERK1 56 EBV infection 56 ADPKD 56 PPARg 56 vascular dysfunction 56 ß amyloid 56 DHEAS 56 abnormal tau 56 Foxp3 56 beta globin 56 Oxidative stress 56 tau tangles 56 Aâ 56 BRCA2 mutations 56 PrPSc 56 glycogen metabolism 56 CYP#B# 56 progerin 56 monogenic 56 Cathepsin B 56 endogenous retroviruses 56 amyloid protein 56 monozygotic twins 56 urate 56 genes 56 nitrotyrosine 56 NF κB 56 SNCA 56 lung adenocarcinoma 56 LDLR 56 elevated CRP 56 Nrf2 56 endothelial dysfunction 56 Akt pathway 56 elevated cortisol 56 CXCR2 56 dystrophin gene 56 CCL#L# 56 FCGR3A 56 protein kinases 56 cholinergic tone 56 IRS1 56 PPARγ 56 oncogenic 56 genetic variants associated 56 huntingtin gene 56 leptin receptor 56 neurotransmitter glutamate 56 estrogen receptors 56 gene encodes protein 56 SETDB1 56 caveolin 1 56 G#S [002] 56 IGFBP2 56 miR #b [001] 56 UCRs 56 GPx 56 3'UTR 56 MiRNAs 56 toxic amyloid beta 56 dysbindin gene 56 LMNA 56 alternatively spliced 56 chromosomal rearrangements 56 #beta HSD1 56 morphogen 56 hormone ghrelin 56 COX enzymes 56 plasma lipid 56 enzymatic activity 56 gene DRD4 56 neuroinflammation 56 PKC beta 56 Hsp# [001] 56 androgen receptor AR 56 RNA sequences 56 neuropeptide Y NPY 56 demethylase 56 regulating gene expression 56 pleiotropic 56 SIRT1 gene 56 angiotensinogen 56 spontaneous mutations 56 NR2B 56 frataxin 56 PEDF 56 H#K# [001] 56 alternative splicing 56 anaplastic lymphoma kinase 56 GATA3 56 genetic variations 56 FOXO1 56 NFκB 56 genomic instability 56 Htt 56 arginase 56 Wnt signaling pathway 56 untranslated regions 56 colorectal carcinogenesis 56 breast cancer genes BRCA1 56 MLH1 56 HLA G 56 5 HTT gene 56 CDH1 56 dystrophin 56 beta amyloid 56 NOD2 56 protein p# 56 caspases 56 MMPs 56 LTB4 56 Brd4 56 cell adhesion molecules 56 cyclin D1 56 Lyn kinase 56 microRNAs miRNAs 56 allelic variants 56 FXTAS 56 CHI#L# 56 SNP rs# [001] 56 hormone leptin 56 galanin 56 airway remodeling 56 trans palmitoleic acid 56 lymphocyte activation 56 HDACs 56 ribosomal protein 56 transgene expression 56 Akt 56 polymorphisms 56 noncoding RNA 56 TH# cells 56 activated microglia 56 eosinophil count 56 SR B1 56 mucins 56 neurofibrillary 56 soluble CD# ligand 56 intronic 56 PP2A 56 CDH# 56 Nod1 56 autoantibodies 56 SPINK1 56 molecular pathways 56 nonalcoholic fatty liver 56 hormone adiponectin 56 SCN1A 56 VIPR2 56 CHRNA5 56 EphA2 56 #q# deletion 56 genetic susceptibility 56 SRY gene 56 mutant huntingtin 56 peroxisome 56 MMP2 56 amino acid methionine 56 Nf1 56 Peutz Jeghers syndrome 56 Treg cell 56 ncRNAs 56 costimulatory 56 bcl 2 56 MeCP2 56 Bcl xL 56 inherited predisposition 56 gene variation 56 Hedgehog pathway 56 RANKL 56 estrogen receptor alpha 56 frontotemporal dementia 56 genetic variation 56 neuronal plasticity 56 chromosomal regions 56 beta amyloid peptides 56 ependymomas 56 paralogs 56 defensin 56 receptor gamma 56 connexin 56 ADDL 56 chromosome #p#.# 56 aneuploidy 56 HLA B# 56 mutated BRCA1 56 gluconeogenesis 56 misfolded protein 56 sequence homology 56 serum BDNF 56 PAR1 56 defective gene 56 laforin 56 calmodulin 56 DUX4 56 mitochondrial enzyme 56 kisspeptin 56 amyloid beta protein 56 protein misfolding 56 adult neurogenesis 56 familial hypercholesterolemia 56 epigenetic inheritance 56 MGUS 56 SOX3 gene 56 mitochondrial fusion 56 EAAT2 56 urocortin 56 cypin 56 flavonoids 56 SLITRK1 56 miR# 56 bone resorption 56 exfoliation glaucoma 56 polymorphism 56 fructose intake 56 leptin signaling 56 DLX5 56 antioxidant enzyme 56 nonsense mutations 56 virulence genes 56 adiponectin hormone 56 cardiac hypertrophy 56 LRP1 56 sex hormone estrogen 56 Hypoxia Inducible Factor 56 chemical serotonin 56 eotaxin 56 PrP 56 glucose metabolism 56 ipRGCs 56 monocyte chemoattractant protein 56 familial clustering 55 Jhdm2a 55 vasopressin receptors 55 microdeletion 55 Th1 type 55 Yamanaka recipe 55 APOA5 55 IRF6 gene 55 ADAMTS# 55 adrenal cortex 55 white matter hyperintensities 55 plasminogen 55 PGE2 55 Siglec 8 55 gamma aminobutyric acid 55 LQTS 55 NKT cells 55 albuminuria 55 ACAT2 55 pathological hallmark 55 glycolipids 55 haplotypes 55 interferon pathway 55 elevated homocysteine 55 TRIM5 55 PON1 gene 55 SE alleles 55 micro RNA 55 epigenetic mechanisms 55 genetic abnormality 55 IKK2 55 APOE e4 gene 55 oncogene 55 gamma secretase 55 chromosomal deletions 55 RAR beta 55 oxidized phospholipids 55 Rap1 55 PPAR alpha 55 androgen receptor 55 DNA methylation 55 mutant gene 55 HDL2 55 neuropathologic 55 LXRs 55 beta amyloid proteins 55 DNMT1 55 amyloid deposits 55 utrophin 55 protein fragment 55 MUFAs 55 enterotypes 55 fronto temporal dementia 55 fewer dopamine receptors 55 VLDL 55 p#Kip# 55 neuritic plaques 55 HMMR 55 triptolide 55 encodes protein 55 histone modification 55 Sonic Hedgehog 55 angiotensin converting enzyme 55 iNOS 55 amyloid plaque formation 55 airway hyper responsiveness 55 TGFBR1 55 EphB2 levels 55 GBM tumors 55 adipokines 55 Froguel 55 WDR# 55 CDK8 55 c MYC 55 Karayiorgou 55 hedgehog signaling 55 Mendelian disorders 55 tau protein tangles 55 glutamatergic 55 anandamide 55 Chlamydia pneumoniae 55 chromosomal abnormalities 55 glycogen synthase kinase 55 homodimers 55 Adiponectin 55 benfotiamine 55 c Abl 55 biochemical pathways 55 lamin 55 IL #p# 55 tau mutation 55 GABA receptors 55 DARPP 55 Beta thalassemia 55 nNOS 55 leptin deficient 55 cathelicidin