Related by context. All words. (Click for frequent words.) 70 TCF#L# gene 69 TCF#L# 69 LRP5 69 FGFs 67 retinoid X 67 Clusterin 67 KIAA# 67 Cathepsin B 67 KRAS oncogene 67 genetic loci 67 STAT4 67 familial pancreatic cancer 66 airway hyperresponsiveness 66 CYP#A# gene 66 chromosome #q# [002] 66 JAK2 enzyme 66 neuroligins 66 apoE4 66 GPC5 66 thyrotropin 66 TMEM#B 66 histone deacetylases 66 ENPP1 66 missense mutations 66 ZNF# 66 FGFR2 66 HLA DRB1 65 PTPN# 65 susceptibility loci 65 BMPR2 65 K ras mutations 65 oxysterols 65 NR#A# 65 STK# gene 65 MC1R 65 epigenetic modification 65 Genetic predisposition 65 chromosome #q# [001] 65 familial clustering 65 PI3K AKT 65 non coding RNA 65 ABCB1 gene 65 fatty acid synthase 65 FGF2 65 ADAM# 65 IKK2 65 monogenic 65 gene polymorphisms 65 MYH9 gene 65 CYP#D# gene 65 cyclic AMP cAMP 65 LRRK2 gene 65 Genetic variants 65 IL#R 64 NF kB signaling 64 APOL1 64 epigenetic markers 64 clefting 64 VIPR2 64 DNA methylation patterns 64 p#/CBP 64 myo inositol 64 amyloid deposition 64 #q#.# [001] 64 hypermethylated 64 MAPK pathway 64 PIK3CA 64 CDH1 64 gastrointestinal stromal tumors GISTs 64 thymidylate synthase 64 Genetic variations 64 genetic variants associated 64 Darapladib 64 SORL1 64 kidney urologic 64 GSTP1 64 #p# [001] 64 BRAF V#E 64 abnormal glucose metabolism 64 germline mutations 64 MYH9 64 breast cancer subtypes 64 SMAD4 64 CNTNAP2 64 apoE 64 tryptase 64 micro RNAs 64 dehydrogenases 64 ERK signaling 64 androgen receptor gene 64 OGG1 64 protein tyrosine kinase 64 ABCB1 64 C#Y 64 inherited mutations 64 Fas ligand 64 HLA DQ2 64 γ secretase 64 COX enzymes 64 metabolomic profiles 64 ankyrin B 64 COX2 63 Kufs disease 63 microdeletions 63 narcolepsy cataplexy 63 MC4R gene 63 BARD1 63 gastric carcinoma 63 SNP rs# [002] 63 apolipoprotein E4 63 motor neuron degeneration 63 CB2 receptor 63 ERBB2 63 underlying pathophysiology 63 SCD1 63 SCN5A 63 CALHM1 63 microcephalin 63 SNP rs# [001] 63 thyrotropin levels 63 LPA gene 63 sFlt 1 63 Mitochondrial dysfunction 63 sphingolipid 63 WDR# 63 APOE4 63 HER2 overexpression 63 lipoprotein metabolism 63 PPARγ 63 PPARg 63 trans palmitoleate 63 TSP1 63 rs# [002] 63 MEF2A 63 Angiotensin receptor blockers 63 cAMP signaling 63 protein kinase C 63 xenobiotic 63 HMGCR 63 Topoisomerase II 63 autism susceptibility genes 63 etiologic 63 chromosome #p#.# 63 IgA deficiency 63 ALDH2 63 biologic pathways 63 INF2 63 elevated CRP 63 FKBP# 63 amyloid cascade 63 Alpha synuclein 63 CHRNA5 63 apolipoprotein E gene 63 Peptide YY 63 nonhereditary 63 clusterin 63 Mycoplasma pneumoniae 63 serous ovarian cancer 63 paraoxonase 63 epigenetic changes 63 lymphomas leukemias 63 HIF 1α 63 obesity insulin resistance 63 copper zinc superoxide 63 bronchial hyperresponsiveness 63 KIF6 gene 63 CHD7 63 mitogen activated protein kinases 63 B7 H3 63 CDK4 63 CCR5 delta# 63 posttranslational modifications 63 chitinase 63 IGFBP2 63 basal cell nevus syndrome 63 pathogenic mutations 63 vitamin D receptors 63 TTR gene 63 sarcosine 62 S#A# [002] 62 BCL#A 62 WNK1 62 #q# deletion 62 intracellular signal transduction 62 ALK gene 62 osteopontin 62 sortilin 62 eotaxin 62 SIRT1 gene 62 protein tyrosine phosphatase 1B 62 Src kinase 62 MTHFR 62 KLF4 62 #q# [001] 62 type2 diabetes 62 Epstein Barr Virus EBV 62 MSH2 62 BRAF gene 62 multi factorial disease 62 airway remodeling 62 myelofibrosis polycythemia vera 62 GSTT1 62 pre mRNA splicing 62 CYP #A# 62 histone methylation 62 pathogenic mechanisms 62 eosinophil count 62 amyloid protein plaques 62 CYP#A# [002] 62 EphA2 62 GNAQ 62 alpha synuclein protein 62 beta carotene supplementation 62 breast carcinogenesis 62 hematopoietic cancers 62 MLL2 62 Amino acid 62 PHD2 62 gastric carcinogenesis 62 inhibitory neurotransmitters 62 GSTM1 62 dysbindin 62 Shortened telomeres 62 colorectal carcinogenesis 62 BRCA1 BRCA2 62 KCNH2 62 trans palmitoleic acid 62 adipokines 62 spermidine 62 Elevated CRP 62 C1q 62 isotypes 62 Amyloid plaques 62 prodynorphin 62 fat hormone leptin 62 microRNA molecules 62 adipogenic 62 LDL receptor 62 sterol regulatory 62 IGFBP 3 62 myopathies 62 MAP kinase 62 causative mutations 62 subclinical hyperthyroidism 62 somatic mutations 62 XMRV infection 62 cathepsins 62 PDE7B 62 hypovitaminosis D 62 ADPKD 62 klotho 62 amyloid beta plaques 62 filaggrin 62 impaired glucose metabolism 62 MECP2 gene 62 evolutionary conserved 62 neurite outgrowth 62 predisposing factor 62 intercellular signaling 62 FUS1 62 chromosomal rearrangement 62 Preimplantation Factor 62 PKM2 62 amyloid ß 62 DNA methyltransferases 62 Six3 62 HLA DR4 immune 62 MAP kinases 62 demethylase 62 Hashimoto thyroiditis 62 Wnt signaling pathway 62 synovial cells 62 susceptibility gene 62 PDGFR 62 palladin 62 VKORC1 62 inverse agonist 62 histone deacetylase inhibitors 62 serine proteases 62 nondemented 62 serum BDNF 62 IgE antibody 62 remains mystery Yairi 62 potent inducer 62 circulating endothelial cells 62 CYP#A# CYP#D# 62 anterior pituitary 62 tryptophan hydroxylase 62 Cyclin E 62 nicotinic receptor 62 microRNA expression 62 endoplasmic reticulum stress 62 MIF protein 62 Aromatase 62 glycolipids 62 virulence genes 61 cell adhesion molecules 61 AMACR 61 histone demethylase 61 SIRT3 61 TGF beta pathway 61 EoE 61 Helicobacter pylori infection 61 SOD1 gene 61 elevated homocysteine 61 Chlamydia pneumoniae 61 Upregulation 61 peroxisomal 61 squamous cell lung cancer 61 NFkappaB 61 primary biliary cirrhosis 61 GRK5 61 Yamanaka recipe 61 mutated K ras 61 papillary renal cell carcinoma 61 GRNOPC1 contains 61 Brd4 61 fibrillin 1 61 Treg cell 61 TRAF1 C5 61 IKZF1 61 neuropathologic 61 arterial inflammation 61 Eosinophils 61 proto oncogene 61 SCN9A 61 CagA 61 5 HT1A receptor 61 Celiac sprue 61 unstable detrusor muscle 61 genomic alterations 61 CDK5 61 hypertensive rats 61 HCV replication 61 GSTM1 gene 61 glucocorticoid receptors 61 epigenetic regulation 61 Ets2 61 Homocysteine 61 mitogen activated protein kinase 61 NKX#.# 61 promoter methylation 61 redox active 61 cholesterol biosynthesis 61 ependymomas 61 UCP1 61 serine protease 61 #q#.# [002] 61 c KIT 61 cyclin E 61 TGFBR1 * 6A 61 4E BP1 61 sphingolipids 61 soluble CD# ligand 61 tNOX 61 SLC#A# [001] 61 Teriflunomide 61 familial ALS 61 plasma lipid 61 dysglycemia 61 dopamine D4 receptor 61 elevated triglyceride levels 61 histone acetylation 61 sickle cell hemoglobin 61 IL #R 61 CYP#C# [002] 61 mGluR5 antagonist 61 SSc 61 LKB1 61 pathophysiological effects 61 C5aR 61 chronic myeloid 61 hyperinsulinism 61 monoamines 61 GRP# 61 carotid plaque 61 immunoregulatory 61 CRTC3 61 Vidaza ® 61 Protein Kinase C 61 MECP2 61 Cryptococcus neoformans 61 resistin 61 melanocortin receptor 61 Lyn kinase 61 TP# gene 61 interleukins 61 Helicobacter 61 heparanase 61 tumor suppressor protein 61 Smad3 61 diagnostic biomarker 61 hereditary predisposition 61 epigenetically 61 Oxidative damage 61 PEDF 61 hamartomas 61 Hutchinson Gilford progeria 61 FGFR1 61 overt hypothyroidism 61 prostate carcinogenesis 61 serine threonine kinase 61 nucleus Chinnery 61 hypereosinophilic syndrome 61 cypin 61 Ki# 61 5 HT2A serotonin 61 folate metabolism 61 aP2 61 VLDL cholesterol 61 telomere dysfunction 61 CYP#C# gene 61 NR#A# gene 61 Undesirable alterations 61 G6PD 61 NS4B 61 gene loci 61 idiopathic myelofibrosis 61 #p#.# [001] 61 Karayiorgou 61 CYP#D# 61 leukemias lymphomas 61 activated microglia 61 androgen receptor AR 61 Thyroid hormone 61 COL#A# 61 alpha synuclein gene 61 H#K#me# 61 mitochondrial proteins 61 Elevated serum 61 AGTR1 61 endogenous ligands 61 microRNAs miRNAs 61 LSD1 61 CFTR cystic fibrosis transmembrane 61 basophils 61 p#INK#a 61 histone H4 61 de novo mutations 61 HLA genes 61 KRAS variant 61 Jhdm2a 61 p# mutations 61 histone modifications 61 antiphospholipid syndrome 61 HDAC2 61 C. pneumoniae 61 SORL1 gene 61 KATP channel 61 sporadic ALS 61 PON1 61 LRRK2 mutation 61 CYP#B# 61 Nampt 61 oxidized phospholipids 61 subclinical atherosclerosis 61 hormone angiotensin II 61 sCJD 61 interleukin 1beta 61 Li Fraumeni 61 phospholipase A2 61 inducible nitric oxide synthase 61 neurexins 61 chromosomal aberrations 61 ATG#L# 61 chromosome #p# [002] 60 SERCA2a 60 autonomic dysfunction 60 macrophage migration inhibitory 60 ALK mutations 60 CYP#E# gene 60 PGC 1α 60 colorectal carcinoma 60 periodontal infections 60 nonnucleoside reverse transcriptase inhibitors 60 hypermethylation 60 mitochondrial disorders 60 leukaemias 60 pancreatic prostate 60 APOE gene 60 glutamic acid decarboxylase 60 testicular germ cell 60 NO synthase 60 HMG CoA reductase 60 AT1R 60 HMGA1 60 thrombophilia 60 apolipoprotein E 60 TEL AML1 60 GATA4 60 hay fever allergic rhinitis 60 aminotransferase 60 rs# [003] 60 cell adhesion molecule 60 IGF IR 60 genes encode proteins 60 ataxias 60 #ß HSD1 60 neuroinflammation 60 APOE e4 60 SHANK3 60 BMP2 60 polyamines 60 PALB2 60 tRNA synthetase 60 maternally inherited 60 APOE genotype 60 TMPRSS2 ERG fusion 60 Glucocorticoids 60 STIM1 60 beta1 integrin 60 Aß 60 cTnT 60 clinicopathological 60 PTHrP 60 Oxidative stress 60 apoptotic pathway 60 histone deacetylation 60 HbF 60 MYBPC3 60 susceptibility locus 60 nanobacteria 60 receptor tyrosine kinase 60 nicotine receptor 60 protein kinases 60 IRS1 60 peroxisome 60 inherited predisposition 60 ERK1 2 60 hormonal abnormalities 60 circadian clock genes 60 macrophage migration 60 oncogenic transformation 60 p# MAPK 60 Amyloid beta protein 60 FBPase 60 alpha defensins 60 Raf MEK ERK 60 Aâ 60 Alu elements 60 methylenetetrahydrofolate reductase 60 granulosa cell 60 mitochondrial DNA mtDNA 60 excitatory neurotransmitter glutamate 60 hypothalamic pituitary adrenal axis 60 inborn errors 60 extramedullary 60 genetic polymorphism 60 metalloprotease 60 SOD2 gene 60 CYP#E# 60 DLC1 60 genotoxic stress 60 PI3K Akt 60 adrenal hormone 60 PTEN mutations 60 intronic 60 WT1 60 dimeric 60 microdeletion 60 RUNX3 60 chemokine receptor 60 Dr. Bezprozvanny 60 epigenetic alterations 60 histocompatibility 60 enzymatic pathways 60 germline mutation 60 HER2 expression 60 apo E 60 SLC#A# [002] 60 PON1 gene 60 neurosensory 60 HOX genes 60 cystatin C 60 5 lipoxygenase 60 gene APOE4 60 c MET 60 LPA1 60 neuritic 60 G6PD deficiency 60 protein tyrosine phosphatase 60 Chronic pancreatitis 60 p# alpha [002] 60 Hypercholesterolemia 60 prostate cancer CaP 60 Adiponectin 60 cholesterol homeostasis 60 Apolipoprotein E 60 ovarian pancreatic 60 neuroinflammatory 60 CaM kinase II 60 gene locus 60 SE alleles 60 cryptogenic 60 immune modulating 60 polyamine 60 congenital toxoplasmosis 60 CETP VV 60 E#F# 60 H#K# [001] 60 MiRNAs 60 Tasigna prolongs 60 Brain derived neurotrophic 60 methylation patterns 60 TERT 60 Oncogenic 60 transcriptional activation 60 glycolipid 60 DICER1 gene 60 nonfasting triglycerides 60 #p#.# [002] 60 progranulin 60 Uncontrolled hypertension 60 PKD1 60 NR2B subunit 60 B7 H4 60 #beta HSD 1 60 myeloproliferative diseases 60 DQB1 * 60 obstructive coronary 60 multiprotein complex 60 HAAH 60 5 HTTLPR 60 allelic variants 60 albumin excretion 60 fatty acid oxidation 60 Leukemias 60 TGF ß 60 NAT2 60 homodimers 60 deacetylase 60 miRNA genes 60 T#I [002] 60 neuropeptide Y NPY 60 NKG2D 60 Dysregulation 60 chromosomal instability 60 monocyte chemoattractant protein 60 Sjögren syndrome 60 CD#c 60 COMT gene 60 toxic amyloid beta 60 acetylcholine receptor 60 IMiDs ® 60 vWF 60 KCNQ1 60 etiologic factors 60 allergic inflammation 60 ApoE gene 60 anaplastic lymphoma kinase ALK 60 antiproliferative effects 60 Polymorphisms 60 NF kB pathway 60 deacetylation 60 cholesteryl ester transfer 60 hepatic lipase 60 cytokines chemokines 60 mechanotransduction 60 NRG1 60 gene rearrangements 60 idiopathic pulmonary 60 gene APOE 60 GPIHBP1 60 von Willebrand factor 60 selective modulator 60 astrocytomas 60 oxidases 60 virulence determinants 60 HOTAIR 60 serum IGF 60 stress cardiomyopathy 60 androgenic hormones 60 Nonalcoholic fatty liver 60 HSF1 60 Systemic lupus erythematosus 60 MEK ERK 60 mitochondrial mutations 60 CREB protein 60 genetic determinants 60 steroidogenic 60 dopamine D2 60 PDE#A 60 ADAMTS# 60 atherothrombosis 60 BRAF protein 60 PKC beta 60 somatic mutation 60 uPAR 60 childhood leukemias 60 SLITRK1 60 TNFalpha 60 PI 3K 60 EBV infection 60 APOE ε4 60 calcium calmodulin dependent 60 Klotho gene 60 renal fibrosis 60 renal cell carcinomas 60 amyloid plaque formation 60 protein alpha synuclein 60 genetic polymorphisms 60 microvascular disease 60 CEACAM1 60 VCAM 1 60 MMP# 60 PDGF alpha receptor 60 MLH1 60 FGFR3 60 hormone aldosterone 59 ribosomal RNA rRNA 59 transcriptional silencing 59 A3 adenosine receptor 59 HLA B# 59 c Myb 59 phosphoinositide 59 NOTCH1 59 florbetaben 59 constitutively expressed 59 #S rRNA 59 fetuin 59 serine threonine 59 mediated inhibition 59 thromboxane A2 59 PICALM 59 catechol O methyltransferase 59 epigenetic inheritance 59 Froguel 59 MDM2 59 IL6 59 CYP#A# substrate 59 HMGA2 59 IRF6 59 modifier genes 59 cardiolipin 59 mda 7 59 epilepsies 59 serum PTH 59 phosphorylated tau 59 beta amyloid peptides 59 receptor tyrosine kinase inhibitor 59 angiotensin receptor blockers ARBs 59 prostate carcinoma 59 prostanoid 59 Brodmann Area 59 differential gene expression 59 MGUS 59 VEGF receptor 59 EGFR protein 59 CXCR2 59 AML MDS 59 costimulation 59 nitric oxide synthase 59 DRD2 gene 59 impaired endothelial 59 UGT#A# * 59 promoter hypermethylation 59 Short telomeres 59 FOXO3a 59 ACh 59 granzyme B 59 Brugada syndrome 59 ovarian endometrial 59 hypothalamic pituitary 59 GST pi 59 KLF# 59 ApoE4 gene 59 Fibroblast 59 p# activation 59 hyperphenylalaninemia HPA due 59 TRAIL induced apoptosis 59 NOD2 59 impaired insulin secretion 59 INTERHEART study 59 upregulates 59 Leydig cells 59 furin 59 protein tyrosine phosphatases 59 lipid concentrations 59 peptidic 59 autistic regression 59 potent inhibitors 59 HG PIN 59 neurofibrillary tangles 59 progressive neurodegenerative disorder 59 cytokine receptor 59 Pseudomonas aeruginosa infections 59 CDKN2A 59 IDH1 mutation 59 mtDNA mutations 59 TET2 59 JAK mutations 59 folate folic acid 59 RAS RAF MEK 59 MetAP2 59 epithelial tumors 59 Rb gene 59 E3 ubiquitin ligase 59 TP# mutation 59 bone marrow mesenchymal stem 59 Haptoglobin 59 corticotrophin releasing hormone 59 DLX5 59 troponin T 59 lipid elevations 59 pyrimidines 59 genetic locus 59 cdk5 59 miR #b [001] 59 ARID1A 59 serotonin receptor 59 coronary microvascular 59 CARDIA study 59 angiotensin converting enzyme 59 genes predisposing 59 antiphospholipid antibodies 59 epigenetic silencing 59 Lipoprotein 59 colorectal adenoma 59 NMDA receptor 59 JAK STAT 59 LRAT 59 causal variants 59 estrogen metabolism 59 autoantigens 59 bile acid metabolism 59 Lp PLA 2 59 Angiotensin II 59 observable traits 59 Dr. Loeken 59 MAPKs 59 chromosome #p# [001] 59 catechol O methyltransferase COMT 59 RIP1 59 CHD5 59 5 HT6 receptor 59 major histocompatibility complex 59 humanised antibody 59 CYP#C# [001] 59 Serum calcium 59 pathological hallmark 59 transgenic mouse models 59 pleiotropic effects 59 assay detects 59 GLI1 59 pathogenetic 59 coagulation cascade 59 glycosylated 59 transmembrane receptor 59 oxidized cysteine 59 affective psychoses 59 adrenocortical cancer 59 LMNA 59 micro RNA 59 polyadenylation 59 HIF 1a 59 periodontal pathogens 59 cyclooxygenase 2 59 mGluR2 NAM 59 TIMP 1 59 Genetic variation 59 PLX STROKE targeting 59 sirtuin activators 59 inhibin B 59 calcineurin 59 miRNA expression 59 BEXXAR Therapeutic Regimen 59 phenotypic expression 59 mitochondrial metabolism 59 cortisol concentrations 59 gene BRCA2 59 Abeta# 59 EGFR pathway 59 DNA demethylation 59 interferon pathway 59 GATA3 59 PrPSc 59 familial hypercholesterolemia 59 NFkB 59 Akt1 59 brain derived neurotrophic 59 Tumor Necrosis Factor 59 SGK1 59 familial predisposition 59 Janus kinase 59 non cirrhotic portal 59 rs# [001] 59 metabolizing enzymes 59 neuroblastomas 59 BRIP1 59 SHANK3 gene 59 apoC III 59 somatostatin 59 inactive X chromosome 59 Foxp3 59 demyelinating disease 59 penetrance 59 endoglin 59 Fragile X gene 59 Lrp5 59 morphogen 59 diabetic kidney 59 prostaglandin synthesis 59 chromosomal anomalies 59 EEG abnormalities 59 lactate dehydrogenase LDH 59 T1DM 59 berberine 59 NKT cells 59 primary hyperparathyroidism 59 synapse formation 59 CYT# potent vascular disrupting 59 circadian genes 59 GPI anchored 59 hepatic steatosis 59 ovarian hormones 59 CNTNAP2 gene 59 FUS protein 59 WAGR syndrome 59 neuropsychiatric disorder 59 CHEK2 59 pretreatment serum 59 FOXM1 59 microscopic colitis 59 von Willebrand 59 apolipoprotein B 59 modifiable lifestyle 59 MTDH 59 PPAR gamma 59 klotho gene 59 synaptogenesis 59 primary cilia 59 Transcription factors 59 humanin 59 anticholinergic effects 59 functional polymorphism 59 ANCA associated 59 urocortin 59 activate SIRT1 59 SETDB1 59 teratogens 59 molecular biomarkers 59 chromatin structure 59 euthymic patients 59 TGF b 59 BDNF gene 59 insulin signaling pathway 59 clusterin protein 59 NQO1 59 neuropeptide Y 59 Shp2 59 aldose reductase 59 breast endometrial 59 cystic fibrosis transmembrane conductance 59 enkephalin 59 rs# [004] 59 metabolite concentrations 59 intact parathyroid hormone 59 glial tumors 59 PCNSL 59 activin 59 beta globin gene 59 Cotinine 59 oncogenesis 59 eicosanoid 59 mTOR mammalian target 59 HLA molecules 59 plasma selenium 59 downregulated 59 serum leptin 59 EphB2 59 miR# 59 alpha glucans 59 fatty acid binding 59 FLT3 59 genomic imprinting 59 myocardial ischaemia 59 uric acid levels 59 CXCL# 59 microchimerism 59 myeloproliferative disorders 59 MSMB 59 PARP inhibition 59 underlying molecular mechanisms 59 HER signaling pathway 59 transgenic rats 59 cisplatin resistant 59 XBP1 59 pulmonary hypertension PH 59 bought Glaxo Serevent 59 alpha7 NNR 59 chromosome #q#.# [001] 59 microscopic lesions 59 proapoptotic 59 Autoantibodies 59 non fasting triglycerides 59 stratifying patients 59 nephronophthisis 59 tyrosine phosphorylation 59 mitochondrial dysfunction