Related by context. All words. (Click for frequent words.) 82 APOE4 74 ApoE4 gene 74 APOE e4 72 ApoE4 allele 71 APOE gene 71 APOE4 gene 71 APOE 71 APOE allele 71 APOE e4 gene 70 apoE4 69 CYP#C# * 68 APOE ε4 67 apolipoprotein E 67 CYP#C# [001] 67 BRCA1 mutations 67 variant alleles 66 apolipoprotein E4 66 ApoE gene 66 TCF#L# gene 66 ε4 66 Fragile X gene 66 BRCA mutation 66 ABCB1 66 gene variant 66 genetic variant 65 MSH2 65 sporadic ALS 65 APOC3 65 HLA B# 65 IGF2 65 apolipoprotein E gene 64 KIF6 gene 64 klotho 64 ApoE 64 TGFBR1 * 6A 64 MYH9 gene 64 TCF#L# 64 STAT4 64 elevated triglyceride levels 64 mutated gene 64 noncarriers 64 tau protein 64 SORL1 64 narcolepsy cataplexy 64 PTPN# 63 FTO gene 63 MTHFR 63 BRCA2 gene 63 G allele 63 apoC III 63 genes predisposing 63 BARD1 63 C#Y 63 GSTM1 63 LRP5 63 MnSOD 63 heterozygous 63 DRD2 63 mutated BRCA1 63 G#S mutation 63 BRCA1 mutation 63 Wwox 63 mtDNA mutations 62 BRAF gene 62 leptin receptor 62 homozygotes 62 BMPR2 62 MLH1 62 CNTNAP2 62 RBP4 62 SHANK3 62 BRCA2 mutation 62 BRCA1 gene 62 UGT#A# * 62 apoE 62 GSTM1 gene 62 BRAF mutation 62 KRAS mutations 62 familial ALS 62 HNPCC 62 TP# mutation 62 PTEN gene 62 basal cell nevus syndrome 62 familial pancreatic cancer 62 CDKN2A 62 CFTR gene 62 LRAT 62 APOE genotype 62 BRCA gene mutation 62 genetic polymorphism 62 tarenflurbil 62 EGFR mutation 62 susceptibility gene 62 missense mutations 62 MIF gene 62 DQB1 * 62 SLC#A# [002] 61 germline mutations 61 COMT gene 61 e4 allele 61 Foxp3 61 FGFR2 61 IGF1 61 subclinical hyperthyroidism 61 GPR# [002] 61 CALHM1 61 BRCA2 gene mutation 61 chromosomal rearrangement 61 Aβ 61 SLC#A# [001] 61 APOL1 61 BRCA mutations 61 KIBRA 61 mutated K ras 61 lung adenocarcinoma 61 GBM tumors 61 rs# [002] 61 β amyloid 61 amyloid ß 61 MC4R gene 61 ADH1B * 61 MIF protein 61 GSTT1 61 LDL receptor 61 allele 61 adenoma 61 Genetic variants 61 amnestic mild cognitive impairment 61 #q# deletion 61 familial hypercholesterolemia 61 LRP6 61 CAG repeats 61 neurofibrillary tangles 61 anaplastic lymphoma kinase 60 NR#A# 60 heterozygotes 60 GSTP1 60 OPRM1 gene 60 TMEM#B 60 Aß 60 Aß# 60 HER2 overexpression 60 vasogenic edema 60 gene APOE4 60 BRCA1 60 homozygous 60 microcephalin 60 BRAF mutations 60 #p# [001] 60 DRD4 60 deleterious mutation 60 mutant protein 60 BRCA2 mutations 60 amyloid protein 60 variant allele 60 mutant allele 60 SOD2 gene 60 androgen receptor gene 60 FGF2 60 WNK1 60 fibrous tangles 60 gene APOE 60 HMGA2 60 NNRTI resistance 60 p# mutations 60 cAMP signaling 60 genomic imprinting 60 resistin 60 gene mutation 60 transthyretin 60 FXTAS 60 T#I [002] 60 autoantibody 60 lipin 60 p#INK#a 60 mutation 60 familial adenomatous polyposis 60 Akt1 60 progranulin 60 CETP gene 60 V Leiden 60 SNP rs# [002] 60 ALDH2 60 EGFR mutations 60 breast cancer gene mutation 60 p# mutation 60 K ras mutations 60 amyloid peptide 60 autoantibodies 60 alpha synuclein 60 DFMO 60 FMR1 gene 60 ATG#L# 60 progerin 60 Li Fraumeni 59 CDH1 59 TP# mutations 59 breast cancer genes BRCA1 59 eotaxin 59 amyloid deposits 59 clusterin 59 pDCs 59 fetuin 59 poorer prognosis 59 melatonin receptor 59 rs# [004] 59 prostate cancer CaP 59 PTHrP 59 HBsAg 59 GPC5 59 MC1R 59 HFE gene 59 elevated CRP 59 shorter telomeres 59 rs# [003] 59 TT genotype 59 OGG1 59 Leydig cells 59 NFkB 59 COX2 59 HDL2 59 LKB1 59 missense mutation 59 malignant transformation 59 osteocalcin 59 KLF# 59 clinically detectable 59 Abeta 59 LPA gene 59 LRRK2 gene 59 SORL1 gene 59 activin 59 selenium supplementation 59 mutant gene 59 nondemented 59 IFN beta 59 elevated triglycerides 59 subclinical 59 cystatin C 59 TLR3 59 LQTS 59 chromosomal aberrations 59 HbF 59 ADAM# 59 progranulin protein 59 synuclein 59 TGF β 59 phosphorylated tau 59 apolipoprotein B 59 fluvastatin 59 lipoprotein cholesterol 59 PALB2 59 CaM kinase II 59 angiotensin converting enzyme 59 osteopontin 59 5 HTTLPR 59 K ras mutation 59 tumor suppressor protein 59 EBV infection 59 MetS 59 BRCA2 mutation carriers 59 haptoglobin 59 dopamine receptor gene 59 oxysterols 59 TSP1 59 BRCA2 carriers 59 SGK1 59 ß amyloid 59 premutation 59 gallstone disease 59 postmenopausal breast cancer 59 CXCL5 59 paricalcitol 59 SIRT6 59 chromosomal instability 59 microalbuminuria 59 CC genotype 59 germline mutation 59 thyrotropin 59 glucose metabolism 59 Aβ# 59 GBV C 59 subclinical hypothyroidism 59 rs# [001] 59 PCa 59 proband 59 BRAF V#E 59 CXCL# 59 homozygote 59 genetic variants associated 58 T2DM 58 receptor gene 58 DRB1 * 58 MGUS 58 ovarian hormones 58 GBA mutations 58 homozygosity 58 elevated homocysteine 58 hyperinsulinemia 58 SNP rs# [001] 58 Notch signaling 58 poor metabolizers 58 BDNF protein 58 MC1R gene 58 dysbindin 58 alleles 58 KRAS gene 58 Hashimoto thyroiditis 58 vimentin 58 activating mutations 58 K ras gene 58 KLF4 58 GNAQ 58 neuroblastoma tumors 58 ABCA1 58 EphA2 58 amyloid beta plaques 58 FMR1 58 caveolin 1 58 mutant alleles 58 HIV HCV coinfected 58 Bcr Abl 58 RANKL 58 T1DM 58 mice lacking 58 Prox1 58 ZNF# 58 alpha synuclein gene 58 uPA 58 defective gene 58 intravenous bisphosphonates 58 penetrance 58 SH#B# 58 IGFBP 3 58 SE alleles 58 A1 allele 58 beta amyloid plaques 58 Stat5 58 TACI mutations 58 LIS1 58 serum BDNF 58 Apolipoprotein E 58 leukaemias 58 BDNF gene 58 apolipoprotein E APOE 58 pCR 58 Fas ligand 58 IDH1 58 MUC1 * 58 CDK4 58 PKCi 58 TNFα 58 estrogen receptor alpha 58 Genetic variation 58 fasting glucose levels 58 endoxifen 58 motor neuron degeneration 58 CETP VV 58 ORMDL3 58 gene variation 58 E4 variant 58 nonalcoholic steatohepatitis NASH 58 TEL AML1 58 adiponectin 58 IL# [001] 58 HOTAIR 58 mammary tumors 58 brain derived neurotrophic 58 osteoblast 58 advanced adenomas 58 sCJD 58 HGPIN 58 gene locus 58 FGF# 58 gene variants 58 HLA DRB1 * 58 microglial 58 CYP#D# gene 58 SIDS infants 58 primary cilia 58 thyrotropin levels 58 AGTR1 58 de novo mutations 58 CHEK2 58 atherosclerotic lesions 58 CYP#A# [002] 58 serotonin receptor 58 TOMM# 58 acute myelogenous leukemia AML 58 abnormal proteins 58 FLT3 58 Abeta# 58 CCR5 delta# 58 TAp# 58 huntingtin protein 58 dopamine D4 receptor 58 glycated hemoglobin levels 58 cognitively normal 58 huntingtin gene 58 adiponectin levels 58 NKT cells 58 somatic mutations 58 humanin 58 hypermethylated 58 APOE e4 allele 58 glucocorticoids 58 NR2B 58 Notch1 58 chromosome #p# [001] 58 protein tau 58 BRCA2 58 serum calcium 58 neutrophil counts 58 mitochondrial dysfunction 58 MAOA 58 mutant huntingtin 58 ERBB2 58 VKORC1 58 K#N 58 IGFBP 58 G6PD 58 HER2/neu 58 telomere lengths 58 5 HTT gene 58 albumin excretion 58 cardiolipin 58 FTO variant 58 dopamine transporter 58 PPARγ 58 amyloid plaque 58 PDGFR 58 beta catenin protein 58 TGF ß 58 late onset hypogonadism 58 serotonin transporter gene 58 CYP#C# gene 58 type2 diabetes 58 CYP#D# 58 mutated protein 58 troponin T 58 MTHFR gene 58 ENaC 58 pancreatic adenocarcinoma 58 repeat allele 58 CLA supplementation 58 granzyme B 57 hypermethylation 57 cyclin E 57 mitochondrial mutations 57 atypical hyperplasia 57 glycosylated 57 microglial activation 57 enzymatic activity 57 E selectin 57 Bcl xL 57 ERK signaling 57 latent TB infection 57 DEC2 57 beta amyloid 57 protein kinase C 57 IgA deficiency 57 G#S [002] 57 PKC beta 57 morphogen 57 HER2 expression 57 Ras pathway 57 prothrombotic 57 HDL particles 57 nestin 57 progressive neurodegenerative disorder 57 dentate gyrus 57 EAAT2 57 NPC1 57 BMP2 57 genes BRCA1 57 BRCA1 BRCA2 57 Treg cell 57 ADAMTS# 57 nelfinavir 57 ENPP1 57 micrometastases 57 PROSTVAC VF 57 APOE epsilon 4 57 EGFR gene 57 tau tangles 57 advanced adenoma 57 KCNE2 57 chemokine receptor 57 #q#.# [001] 57 Neuregulin 1 57 HLA B 57 FGFR1 57 dysglycemia 57 colorectal tumor 57 macroalbuminuria 57 ataxin 57 FGFR2 gene 57 DAT1 57 ApoE4 carriers 57 atherosclerotic lesion 57 gastric carcinogenesis 57 amyloid 57 Clusterin 57 caveolin 57 MAOA gene 57 CYP#C# [002] 57 folate deficiency 57 CagA 57 estrogen receptor negative 57 HMGCR 57 heterozygosity 57 KIAA# 57 Akt 57 p# activation 57 PARP inhibition 57 colorectal adenomas 57 DNMT1 57 MDM2 57 serum creatinine levels 57 impaired fasting glucose 57 epigenetic modification 57 Heterozygous 57 Smad7 57 aldehyde dehydrogenase 57 PlGF 57 VLDL cholesterol 57 ERCC1 57 inherited mutations 57 isoform 57 plasma lipid 57 MLL2 57 prion infection 57 eosinophil count 57 antioxidant supplementation 57 gastrointestinal stromal tumors GISTs 57 KRAS mutation 57 dyskeratosis congenita 57 antibody titer 57 E cadherin 57 TNF α 57 MYH9 57 atherogenic dyslipidemia 57 folate intake 57 CYP#A# gene 57 uveal melanoma 57 heritable genetic 57 S#A# [002] 57 systemic lupus erythematosus SLE 57 HBeAg 57 phenotype 57 estrogen receptor ER 57 CIB1 57 testosterone supplementation 57 MEF2A 57 Hsp# [001] 57 receptor inhibitor 57 urate 57 HER2 neu 57 colorectal adenoma 57 HER2 receptor 57 renal fibrosis 57 leukemic cell 57 erythrocytes 57 colorectal neoplasia 57 NFKBIA 57 adipogenic 57 cholesteryl ester transfer 57 gene polymorphism 57 fatty acid synthase 57 DRD2 gene 57 SIRT1 gene 57 hedgehog signaling 57 vWF 57 C. pneumoniae 57 ERK1 2 57 parkinsonism 57 insulin secreting cells 57 GABRA2 57 mutated KRAS 57 IL#B 57 ApoB 57 T2D 57 HDAC6 57 Prehypertension 57 astrocyte 57 SCD1 57 serous ovarian cancer 57 MAPK pathway 57 EGFR protein 57 microdeletion 57 Alzheimer pathology 57 palladin 57 TRAF1 C5 57 BRAF V#E mutation 57 p# MAPK 57 serum IGF 57 nonischemic 57 SMAD4 57 remyelination 57 microsatellite instability 57 mosaicism 57 CHD7 57 squamous cell lung cancer 57 diabetic kidney 57 KRAS oncogene 57 CNTNAP2 gene 57 genetic loci 57 retinol binding protein 57 riociguat 57 plasma folate 57 glucocorticoid 57 osteoclast 57 elevated LDL cholesterol 57 NF1 57 PON1 57 placental function 57 NRG1 57 cardioembolic stroke 57 aldosterone 57 WT1 56 MYCN amplification 56 hTERT 56 ADPKD 56 amyloid deposition 56 MAO B 56 protein alpha synuclein 56 VHL gene 56 estrogen receptor 56 untreated celiac disease 56 HLA molecules 56 insulin resistance syndrome 56 NPY expression 56 FMRP protein 56 bowel polyps 56 GATA4 56 Dpp 56 hormone receptor negative 56 mGluR 56 prostate carcinogenesis 56 IKZF1 56 hepatoma 56 Alu elements 56 c Myb 56 thyroxine 56 chromosome #q# [002] 56 LRRK2 mutation 56 p# protein 56 BRCA mutation carriers 56 nonalcoholic fatty liver 56 reticulocytes 56 PTEN mutations 56 mild cognitive impairment 56 DISC1 gene 56 fetal hemoglobin 56 TH# cells 56 tyrosine phosphorylation 56 IFNg 56 TrkB 56 colorectal carcinoma 56 TNFa 56 HLA DQ2 56 airway remodeling 56 CYP #D# 56 insulin sensitizers 56 HGPS 56 IL#R 56 SOD1 gene 56 carotid plaque 56 leptin 56 cyclooxygenase 56 monocyte 56 MHC molecules 56 clinically insignificant 56 estrogen metabolism 56 cyclin D1 56 brain lesions 56 glucose intolerance 56 VEGF receptor 56 liver metastasis 56 olmesartan 56 apelin 56 ACh 56 soluble CD# ligand 56 Her2/neu 56 immunized mice 56 EGFRvIII 56 familial clustering 56 synaptic function 56 microbleeds 56 PrP 56 TP# gene 56 PPAR gamma 56 FANCD2 56 nonsense mutations 56 genetic polymorphisms 56 PTEN protein 56 HbF levels 56 TERT 56 BRAF protein 56 BACE1 56 hypocretin 56 xenograft tumors 56 T1D 56 BRIP1 56 herpesviruses 56 transgenic mouse model 56 epigenetic changes 56 NRTI resistance 56 haemochromatosis 56 bone resorption 56 NKX#.# 56 sarcosine 56 presymptomatic 56 valine 56 hippocampal volume 56 chromosomal translocations 56 APOE4 variant 56 iNOS 56 allostatic load 56 insulin resistance 56 p#Kip# 56 palmitoleate 56 serum leptin 56 serum selenium 56 glioblastoma tumors 56 inducible nitric oxide synthase 56 DISC1 56 Haptoglobin 56 N Myc 56 EZH2 56 microdeletions 56 mesotheliomas 56 BCL#A 56 clade B 56 allele frequencies 56 airway responsiveness 56 K#R [002] 56 t# c# CLA 56 APOA5 56 Klotho gene 56 androgen deficiency 56 telomerase activation 56 EoE 56 pancreatic islet 56 EGFr 56 KRAS wild 56 POMC neurons 56 KRAS status 56 cysteines 56 aneuploidy 56 proteinuria 56 SOX3 gene 56 #beta HSD1 56 PI3K pathway 56 haplotype 56 UGT#A# 56 frataxin 56 HPV# 56 histological subtype 56 metabolic syndrome MetS 56 MECP2 gene 56 dystrophin 56 haematopoietic 56 UCP2 56 leptin hormone 56 TGF beta 56 LPA1 56 Asymptomatic 56 sFlt1 56 CHRNA5 gene 56 intestinal polyps 56 clioquinol 56 Cyclin D1 56 SIRT3 56 #ß 56 NKX2 56 null mice 56 nNOS 56 Avandia Actos 56 HER2 gene 56 CYP# [002] 56 thyroglobulin 56 interferon gamma 56 JAK2 enzyme 56 ß1 56 polymorphism 56 DLX5 56 PHD2 56 parkin gene 56 UGT#B# 56 ALK gene 56 plasminogen 56 KIF6 56 AAT deficiency 56 beta carotene supplementation 56 type 1diabetes 56 monoclonal gammopathy 56 Sir2 56 autocrine 56 lactate dehydrogenase LDH 56 #q# [002] 56 monocyte chemoattractant protein 56 disease NAFLD 56 Kufs disease 56 MMSE scores 56 ceruloplasmin 56 CYP #A# 56 impaired glucose tolerance 56 transgenic rats 56 plasma kallikrein 56 homozygous familial hypercholesterolemia 56 PTP1B 56 factor BDNF 56 genes CYP#C# 56 beta amyloid peptides 56 JAK2 mutation 56 Irs2 56 HER2 positive cancers 56 baseline HbA1c 56 recessive mutations 56 beta1 integrin 56 adenocarcinomas 56 telomere shortening 56 HER2 positivity 56 apolipoproteins 56 IRF5 56 amnestic MCI 56 lymphocytosis 56 hereditary hemochromatosis 56 hepatitis B infection 56 HLA DRB1 56 CYP#E# gene 56 nondiabetic 56 p#NTR 56 hippocampal neurons 56 T. vaginalis 56 neuronal plasticity 56 Lafora disease 56 pathological hallmark 56 dexrazoxane 56 airway hyperresponsiveness 56 MMP# 56 NOD mice 56 beta globin 56 inherited predisposition 56 5 HT1A 56 serum urate levels 56 DLC1 56 synovial cells 56 Raf MEK ERK 56 cardioprotective effects 56 GRP# 56 hypercoagulable 56 IL6 56 genetic mutation 56 fasting triglyceride levels 56 SGS# 56 FTO allele 56 FUS1 56 infarcts 56 metabolically healthy 56 NF1 gene 56 KIF6 gene variant 56 phthalate syndrome 56 granulocytes 56 linoleic acids 56 mitochondrial proteins 56 hydroxyvitamin D levels 56 c myc 56 C EBP alpha 56 HNSCC 56 advanced neoplasia 56 FTLD 56 chromosomal alterations 56 grade cervical intraepithelial 56 periodontal infection 56 Smad3 56 Subgroup analysis 56 LDLR 56 Lyn kinase 56 chlamydial infection 56 Telomere length 56 K ras 56 GABA receptor 56 medullary thyroid cancer 56 neuronal dysfunction 56 mutations 56 IRAK1 56 neovascular 55 alpha synuclein protein 55 urate levels 55 esophageal squamous cell carcinoma 55 SHBG 55 diabetes mellitus T2DM 55 monogenic 55 glucocorticoid receptors 55 PGE2 55 gene p# 55 VMAT2 55 renal cell carcinomas 55 enterolactone 55 pharmacokinetic interactions 55 transmembrane receptor 55 cell adhesion molecule 55 NP CRNs 55 Pin1 55 SATB1 55 flavopiridol 55 heterozygous FH 55 adrenal cortex 55 ARF1 55 trophoblast cells 55 LRRK2 55 GISTs 55 ER alpha 55 rheumatoid factor 55 mammary cells 55 chromosome #q# [001] 55 TRAIL induced apoptosis 55 COX enzymes 55 Aldosterone 55 nonmelanoma skin cancers 55 hippocampal atrophy 55 genetic variation 55 dopamine transporter gene 55 amyloid beta protein 55 Lewy bodies 55 airway hyper responsiveness 55 COL#A# 55 CLL cells 55 hormone therapy estrogen 55 colon tumors 55 neuritic 55 primary aldosteronism 55 TNFalpha 55 breast epithelial cells 55 miR #a [002] 55 Chlamydia pneumoniae 55 hormone adiponectin 55 dopamine D2 receptors 55 Leydig cell 55 STAT3 55 PITX2 55 CD#c 55 topoisomerase 55 retinoic acid 55 eNOS 55 systemic inflammation 55 HeFH 55 glitazones 55 IGFBP2 55 hematopoietic cells 55 calcium homeostasis 55 sCD# 55 DNA methylation patterns 55 genotype 55 white matter hyperintensities 55 genetic alteration 55 mutated genes 55 genetic mutations 55 insulin receptors 55 salpingo oophorectomy 55 lipoatrophy 55 gastric adenocarcinoma 55 thymosin 55 RUNX3 55 chemoresistant 55 DGAT1 55 PECAM 1 55 transgene expression 55 interleukin IL -# 55 myo inositol 55 amyloid cascade 55 oesophageal adenocarcinoma 55 PKM2 55 tryptase 55 DRD4 gene 55 FOXP3 55 NPY gene 55 folate metabolism 55 amyloid plaque formation 55 epigenetic silencing 55 thyroid hormone levels 55 IDH1 mutation 55 adrenal function 55 MCF7 cells 55 elevated serum creatinine 55 pituitary hormone 55 Hurthle cell 55 R#W [002] 55 immunodeficient 55 micronuclei 55 hyperoxia 55 postmenopausal estrogen 55 hepatic steatosis 55 endoplasmic reticulum stress 55 C1q 55 RKIP 55 monozygotic twin