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(Click for frequent words.) 55 MLH1 54 SLITRK1 54 Overexpression 54 IL#B gene 53 5q 52 enteroviral 52 Upregulation 51 rs# [004] 51 PTPN# 51 Supplementary Table 51 #p#.# [002] 50 gag pol 50 mutated K ras 50 Supplemental Figure 50 echocardiographic parameters 49 nitrotyrosine 49 Subtype 49 IL#B 49 phosphorylase 49 constitutively expressed 49 #q# [002] 49 #p# [003] 49 CD# CD# 49 progranulin gene 49 heterozygotes 49 amino acid residue 49 SMN1 49 rs# [002] 48 Estrogen receptor 48 LPS induced 48 GTP binding 48 FSHR 48 C#Y 48 BRAF V#E 48 Interferon gamma 48 NS5B 48 hepatocellular carcinomas 48 Akt signaling 48 SSc 48 MSH2 48 Meckel Gruber syndrome 48 sequence homology 48 VEGFR1 48 isoenzyme 48 CagA 48 TYMS 48 allele frequency 48 hepatic lipase 48 phosphorylated tau 48 protein tyrosine phosphatase 1B 48 missense mutations 48 XLHED 48 methyltransferase 48 Activating mutations 48 DQB1 * 48 immunoreactivity 48 Apc 48 #q#.# [001] 47 missense mutation 47 FGFR3 47 tyrosine residues 47 polycystin 47 mosaicism 47 CCR5 delta# 47 chromosome #q# [002] 47 Genetic variation 47 CYP#C# * 47 cell adhesion molecule 47 dysbindin 47 At#g# 47 germline mutations 47 indels 47 dependent protein kinase 47 rs# rs# 47 GSTP1 47 heterozygote 47 KIF6 gene 47 autosomal recessive disease 47 microdeletions 47 null mice 47 homozygotes 47 humoral responses 47 inherited maternally 47 mediated inhibition 47 variant allele 47 Dysregulation 47 Replikin Count 47 methylenetetrahydrofolate reductase 47 FLT3 47 rs# [001] 47 JAK2 V#F 47 CD4 + CD8 + 46 Spinal muscular atrophy 46 cagA 46 tryptase 46 allelic variants 46 thyroid carcinoma 46 allele frequencies 46 hydroxylase 46 glutamyl 46 MTHFR 46 orthologous 46 ABL1 46 N acetyltransferase 46 glycogen synthase 46 Caveolin 1 46 melatonin receptor 46 RRM1 46 ERBB2 46 gene polymorphism 46 Polymorphisms 46 interleukin IL 46 del 5q 46 ß1 46 glucocorticoid induced 46 Angiotensin converting enzyme 46 adiponectin concentrations 46 cytokines chemokines 46 hydrolase 46 SMAD4 46 plasminogen activator inhibitor 46 ABCB1 46 cytidine 46 osteoprotegerin 46 Hcrt 46 gastric carcinogenesis 46 #OHD 46 PGC 1b 46 glutathione S transferase 46 TSH receptor 46 transiently transfected 46 chromosome #p# [001] 46 immunostaining 46 Heterozygous 46 glyceraldehyde 3 46 Leydig cell 46 promoter polymorphism 46 villous atrophy 46 functional polymorphism 46 interferon γ 46 GenBank accession 46 constitutively active 46 guanosine 46 CYP# [002] 46 Amino acid 46 Clusterin 46 affective psychosis 46 ubiquitinated 46 p# MAPK 46 CDKN2A 46 colorectal carcinoma 45 microdeletion 45 APOA5 45 retinol binding protein 45 CD# expression [001] 45 BCL2 45 chromosomal aberrations 45 DRB1 * 45 mitotic progression 45 Monocyte 45 BRCA1 BRCA2 45 MLL2 45 linkage disequilibrium 45 transgenic mice expressing 45 catechol O methyltransferase 45 MLL gene 45 PLA2 45 ERK1 2 45 NFkB 45 BMPR2 45 CD8 + 45 Fig. 3b 45 receptor alpha 45 HLA DRB1 * 45 autosomal dominant disorder 45 genetic polymorphism 45 CYP #D# 45 upregulates 45 PDGFR alpha 45 extracellular domain 45 fig. S2 45 myeloid lineage 45 mRNA expression 45 autosomal dominant 45 myopathies 45 ankyrin repeat 45 #bps qoq [001] 45 PON1 gene 45 collagenous colitis 45 transcriptional activity 45 chromosome #q#.# [002] 45 transferase 45 mineralocorticoid receptor 45 chromosome #q# [001] 45 pancreatic endocrine 45 p# activation 45 COL#A# 45 syngeneic 45 striatal 45 spontaneous mutation 45 genomic deletions 45 coding genes 45 thrombospondin 45 CYP#C# [002] 45 cysteines 45 myocardial fibrosis 45 mutant BRAF 45 homolog 45 chromosome #q#.# [001] 45 periventricular 45 induced platelet aggregation 45 FGFR4 45 HLA DR4 45 IL 1ß 45 IgG antibody 44 Platelet counts 44 steroidogenic 44 pN 44 apolipoprotein E gene 44 cyclin dependent kinase 44 Flt3 44 ERalpha 44 CEACAM1 44 colony stimulating factor 44 C#BL/#J 44 Immunohistochemical staining 44 dominantly inherited 44 LV dysfunction 44 maternally transmitted 44 Serum concentrations 44 potently inhibits 44 metalloproteinase 44 actinin 44 Haplotype 44 endothelial activation 44 renal fibrosis 44 ORFs 44 PDGFR 44 downregulation 44 independent prognostic marker 44 Congenital Muscular Dystrophy 44 PARP1 44 paraoxonase 44 Cyclin D1 44 CC genotype 44 HER2 expression 44 mitogen activated protein 44 glutamic acid decarboxylase 44 homozygote 44 de novo mutations 44 Chromosomal 44 apolipoprotein E4 44 HLA DRB1 44 #q# [001] 44 hemagglutinin H 44 microsatellite instability 44 striatal dopamine 44 CFTR cystic fibrosis transmembrane 44 gene MECP2 44 serogroup 44 p# mutation 44 inactivating mutations 44 hypermethylated 44 leucocytes 44 overactivation 44 IgG4 44 autosomes 44 mRNA encoding 44 ADPKD 44 #.# +#.# +#.# [006] 44 poly ADP ribose polymerase 44 granulocyte 44 neuronal dysfunction 44 Apolipoprotein 44 Fig. 4a 44 susceptibility locus 44 visceral adiposity 44 monogenic 44 Mice deficient 44 mitochondrial gene 44 gastric carcinoma 44 phospholipase A2 44 GPI anchored 44 plasminogen activator 44 unmethylated DNA 44 APOE e4 44 DNA methyltransferase 44 clade B 44 #S rRNA gene 44 SNP rs# [001] 44 TIMP 44 AMACR 44 VEGF receptor 44 myeloproliferative 44 substrate specificity 43 succinate dehydrogenase 43 p tau 43 Dehydrogenase 43 immunodeficiencies 43 extracapsular extension 43 Supplementary Fig 43 ductal adenocarcinoma 43 circadian genes 43 hypothalamic pituitary 43 polyomavirus 43 monocyte 43 PTHrP 43 cytochrome b 43 phospholipase 43 CYP#D# genotype 43 pancreatic islet 43 Treg cell 43 Gln 43 forkhead 43 trinucleotide 43 protein tyrosine phosphatase 43 splenocytes 43 coinfection 43 glycosyltransferase 43 antitrypsin 43 multivariable adjusted 43 caveolin 43 leptin receptor 43 acetylcholine receptor 43 gene APOE 43 rs# [003] 43 Jhdm2a 43 pneumoniae 43 Phylogenetic analysis 43 membrane proximal 43 Î ² 43 alanine aminotransferase 43 autosomal recessive genetic 43 aneuploid 43 germline mutation 43 HbF 43 inducible nitric oxide synthase 43 #ß 43 mice lacking 43 PCA3 gene 43 apolipoprotein B 43 heterozygosity 43 autosomal dominant inheritance 43 paternally inherited 43 43 plasma lipids 43 gastric adenocarcinoma 43 conductance regulator 43 overexpressing 43 PDGF B 43 SNP rs# [002] 43 MYH9 gene 43 Genotypic 43 transmembrane receptor 43 histologic subtype 43 junctional 43 maternal serum 43 TMEM#B 43 Single nucleotide polymorphisms 43 homozygosity 43 mRNA transcripts 43 Lipodystrophy 43 muscarinic receptor 43 eotaxin 43 PON1 43 metabolizing enzyme 43 PGC 1α 43 MIF gene 43 ligand induced 43 tumor infiltrating lymphocytes 43 HLA DQ2 43 fig. S1 43 dinucleotide 43 cells transfected 43 MYBPC3 43 chemokine receptor 43 subcellular compartments 43 MMP# 43 leukocyte counts 43 vesicular stomatitis virus 43 Human Leukocyte Antigen 43 pathophysiological effects 43 GSTT1 43 triiodothyronine 43 hepatoma 43 amino acid substitutions 43 immunoreactive 43 MECP2 gene 43 normal karyotype 43 Western blotting 43 epithelial tumors 42 TT genotype 42 autoantibody levels 42 proto oncogene 42 haematopoietic 42 chromosomal deletions 42 cytogenetic abnormalities 42 kDa protein 42 autoregulation 42 inhibin 42 NS3 42 HOXB# 42 HepG2 cells 42 COX2 42 immunotoxin 42 somatic mutations 42 TOP2A gene 42 D2 dopamine receptor 42 globin genes 42 coexpression 42 ADAMTS# 42 IFN γ 42 myeloproliferative neoplasms 42 ;) CO 42 deacetylation 42 ADH1B * 42 rapamycin kinase 42 coagulopathy 42 GLUT1 42 Rho kinase 42 carboxy terminal 42 lipoxygenase 42 lactate dehydrogenase 42 VKORC1 42 APOC3 42 SOCS3 42 indel 42 Fig. 1E 42 genes predisposing 42 ß = 42 post transplant lymphoproliferative 42 SOD2 gene 42 hyper IgE syndrome 42 hypoperfusion 42 Entered Ichimoku Cloud 42 catalytic subunit 42 apolipoprotein E 42 karyotypes 42 thyrotropin 42 virulence genes 42 metaplasia 42 capillary endothelial cells 42 CAG repeats 42 intergenic 42 E selectin 42 IgG1 42 lysine residues 42 cytomegalovirus infection 42 catenin 42 sporadic ALS 42 Single Nucleotide Polymorphisms 42 ß amyloid 42 CHD7 42 β = 42 chromosome #p# [002] 42 MMP2 42 PUFA intake 42 epistasis 42 HFE gene 42 N. gonorrhoeae 42 monozygotic twins 42 isotypes 42 BMAL1 42 claudin 42 hypometabolism 42 FasL 42 histone modification 42 chromosome #q 42 multivariable analysis 42 c fos 42 SOD2 42 ptau 42 CYP#D# gene 42 Protein Kinase C 42 hypothalamus pituitary 42 euthymic patients 42 beta globin 42 oligodendrogliomas 42 inherited mutations 42 phosphatase 42 quantitative trait loci 42 #p# [001] 42 gene polymorphisms 42 HIV reverse transcriptase 42 FDG uptake 42 autosomal recessive 42 arachidonic acid AA 42 IgA deficiency 42 cyclin E 42 VLDL cholesterol 42 ERK signaling 42 ploidy 42 myeloperoxidase 42 β1 41 BARD1 41 monozygotic twin 41 apo AI 41 apolipoprotein E APOE 41 5 HTTLPR 41 replicase 41 #q#.# [002] 41 Microarray analysis 41 transgene expression 41 UPSIDE MOVERS + 41 Cadherin 41 parasitaemia 41 Fig. 1D 41 Dopaminergic 41 intraepithelial neoplasia 41 MECP2 41 variant rs# 41 demyelinating 41 resistin 41 IFN gamma 41 umbilical artery 41 pulmonary vascular 41 lupus anticoagulant 41 renal tubular 41 preeclamptic 41 H#K#me# 41 ribosomal protein 41 subcellular localization 41 multivariate Cox 41 NMDAR 41 childhood acute lymphoblastic 41 HLA B# 41 isomerase 41 cytochrome c oxidase 41 cytomegalovirus CMV 41 Htt 41 lung epithelial cells 41 Oncogenic 41 hnRNP 41 MnSOD 41 multifactorial disease 41 IPAH 41 hemagglutinin gene 41 polygenic 41 Rap1 41 alanine aminotransferase ALT 41 isoprostane 41 statistically significant predictor 41 microglial 41 ectopic expression 41 receptor gene 41 hyperresponsiveness 41 virus HBV 41 CNTNAP2 gene 41 intraventricular hemorrhage 41 neurofibrillary 41 liver histology 41 pyridoxal 5' phosphate 41 kidney allograft 41 karyotype 41 CYP#A# [002] 41 glomerular 41 TNFalpha 41 Tumor shrinkage 41 causative mutations 41 γ secretase 41 matrix metalloproteinase 41 HMGCR 41 neuroligins 41 guanine nucleotide exchange 41 CDH1 41 metabolic abnormality 41 Selected constructors 41 anterior temporal 41 neuro developmental disorders 41 Notch receptor 41 heterodimer 41 bronchial epithelial cells 41 heparanase 41 tw telecom NASDAQ TWTC 41 phenotype 41 hyperplastic 41 antibody mediated 41 thymic 41 NKT cell 41 Fig. 3a 41 nAChR 41 downregulates 41 pRb 41 neuro endocrine 41 Williams Beuren syndrome 41 leukemic cell 41 hyperparathyroidism 41 penetrance 41 PRNP 41 HbF levels 41 proband 41 dorsal root ganglia 41 uPAR 41 transcriptional repressor 41 IRF6 41 transmembrane protein 41 haplotype 41 CHEK2 41 urothelial carcinoma 41 adenylate cyclase 41 Estimates Boosted 41 annexin 41 gastric cardia 41 airway hyperresponsiveness 40 alveolar epithelial cells 40 G6PD deficiency 40 #p#.# [001] 40 p# Shc 40 esophageal carcinoma 40 alpha4 40 dephosphorylation 40 KRAS oncogene 40 O methyltransferase 40 4E BP1 40 serovar 40 amino terminal 40 #β estradiol 40 apo B 40 rRNA 40 ESR1 40 VNTR 40 platelet receptor 40 STAT4 40 nicotinic receptor 40 Neurofibromatosis type 40 CYP#B# 40 hematological relapse 40 Fig. 1B 40 ornithine decarboxylase 40 SLC#A# [001] 40 Analysts Upgrades Downgrades 40 colocalization 40 antibody titer 40 neuropsychiatric diseases 40 neuritic 40 Neisseria gonorrhoeae 40 N Myc 40 immunopathology 40 GABRA2 40 MTHFD1L gene 40 regression coefficient 40 LIS1 40 PCR amplified 40 inverse agonist 40 cruzi 40 eIF4E 40 ventilation perfusion 40 striated muscle 40 peroxisomal 40 pg ml 40 bronchopulmonary dysplasia 40 beta globin gene 40 immunoblotting 40 Placental 40 fasting plasma 40 arterial calcification 40 alpha defensin 40 hamartoma 40 homeobox gene 40 HCMV 40 tumor suppressor PTEN 40 serum cortisol 40 folate concentrations 40 intronic 40 ANGPTL4 40 proteolytic cleavage 40 clonal expansion 40 c Fos 40 antiphospholipid antibodies 40 differentially regulated 40 Cognitive dysfunction 40 SCN1A 40 prefrontal cortical 40 multivariable Cox 40 HLA B 40 proximal tubule 40 dsDNA 40 demethylation 40 LRP5 40 noradrenergic 40 miRNA expression 40 hippocampal atrophy 40 cystatin 40 SPINK1 40 enkephalin 40 cerevisiae 40 MTHFR gene 40 DAT1 40 alleles 40 chromosomal anomalies 40 EF Tu 40 potent inducer 40 lymphocytic 40 PEDF 40 protein phosphatase 40 serpin 40 serum homocysteine 40 lactis 40 AT1R 40 Hp2 2 40 genes differentially expressed 39 tertile 39 antinuclear antibodies 39 SMase 39 attain statistical significance 39 obstructive coronary artery 39 chromosomal regions 39 kinase domain 39 Histologic 39 orthologs 39 trisomic 39 fourteenth consecutive 39 metabolomic profiles 39 Fig. 1C 39 MAPK pathway 39 ADRB2 39 superantigens 39 FGFs 39 allergic eczema 39 IKZF1 39 protein glycosylation 39 monocyte chemoattractant protein 39 artery stenosis 39 Cre recombinase 39 RASSF1A 39 cardiac myocytes 39 JNK1 39 DRD2 39 NPC1 39 histological subtype 39 chromosomal anomaly 39 allelic 39 FMR1 gene 39 differential gene expression 39 androgen receptor AR 39 C. trachomatis 39 mineralocorticoid 39 secretase 39 prothrombotic 39 S. cerevisiae 39 glycated 39 paxillin 39 diabetes mellitus DM 39 Hippocampal 39 aberrantly activated 39 protein kinase C 39 susceptibility gene 39 predisposing factor 39 oncogenesis 39 PI3K signaling 39 PCR RFLP 39 chromosomal alterations 39 immunodominant 39 acyl CoA 39 hyperactivation 39 SLC#A# gene [002] 39 G allele 39 paraneoplastic 39 neonatal lupus 39 intestinal microflora 39 #q#.# deletion syndrome 39 IGF1 39 endophenotypes 39 dopamine receptor gene 39 ligand receptor 39 ADAM# 39 APOE genotype 39 chromosomal rearrangement 39 apo E 39 fig. S8 39 prostatic acid phosphatase 39 aneuploidy 39 capsular polysaccharide 39 transcriptional silencing 39 lymphatic vessel 38 neuroinflammation 38 nephron 38 PALB2 38 cadherin 38 Wiskott Aldrich syndrome 38 gene locus 38 periventricular leukomalacia 38 surfactant protein 38 TNF α 38 pre eclamptic 38 multisystemic 38 DHFR 38 p# p# 38 thyroid peroxidase 38 Phenotypic 38 erythrocytes 38 phenotypes 38 mCRPC 38 gene DRD4 38 -#.# -#.# % [003] 38 qRT PCR 38 total thyroidectomy 38 Elevated serum 38 hyperinsulinism 38 ANCOVA 38 apoE 38 R#W [002] 38 Sequentially 38 centromeric 38 STAT3 activation 38 hemoglobin molecule 38 multigenic 38 heterozygous 38 receptor signaling 38 synaptogenesis 38 atypical hyperplasia 38 -#.# mm Hg 38 fig. S# 38 G6PD 38 FEV ^ sub 38 proviral 38 polyglutamine 38 overt hypothyroidism 38 serotonin uptake 38 Inc NASDAQ NFLX 38 chorionic villi 38 STAT1 38 pulmonary hypoplasia 38 Compellent Technologies NYSE 38 tumorigenicity 38 familial aggregation 38 protonated 38 lymph node metastasis 38 isoenzymes 38 Genetic variants 38 GABAergic interneurons 38 postoperative delirium 38 tumor suppressor protein 38 C. neoformans 38 beta1 integrin 38 kinase gene 38 #.# +#.# +#.# [001] 38 WNK1 38 pyogenes 38 haemolytic 38 ciliary 38 α 38 mGluR 38 adenosine deaminase 38 recessive mutations 38 cells multiply uncontrollably 38 selective estrogen receptor modulator 38 ectodomain 38 P Midcap 38 gonadotrophin releasing hormone 38 multivariate analyzes 38 P cadherin 38 genetic loci 38 transthyretin 38 IgA antibodies 38 HERV 38 stratifying patients 38 DNA methylation patterns 38 NPY gene 38 dehydrogenase deficiency 38 mutant huntingtin protein 38 cystic kidney 38 quasispecies 38 nonhereditary 38 RothmanResearch.com Stock Review 38 premutation 37 paratuberculosis 37 plasma kallikrein 37 IL 1β 37 Vic Wisemann report 37 neurodevelopmental disorder 37 type natriuretic peptide 37 TrkB 37 muscarinic receptors 37 lymphocyte activation 37 alkaline phosphatase 37 Hypothalamic 37 human leukocyte antigen HLA 37 fig. S4 37 synovial cells 37 receptor ligand 37 endocannabinoid signaling 37 Prefrontal 37 SLC#A# [002] 37 histocompatibility 37 NR#A# 37 β thalassemia 37 MEF2A 37 hypothalamic pituitary adrenal axis 37 genotypic 37 phenotypic expression 37 urinary excretion 37 transgenic mouse models 37 polymorphism 37 D. melanogaster 37 medium chain acyl 37 FOXO3a 37 neuroendocrine 37 #Q# [003] 37 HHV 6 37 globin 37 arcuate nucleus 37 heritable 37 anti cyclic citrullinated 37 tubule 37 anogenital 37 CALHM1 37 Thyroid hormone 37 left ventricular diastolic 37 urethritis 37 genes CYP#C# 37 autoantigen 37 chlamydial 37 antiphospholipid syndrome 37 causative genes 37 Fig. 1A 37 DLX5 37 PTEN gene 37 MYCN amplification 37 autonomic dysfunction 37 receptor CD# 37 gastric carcinomas 37 transcriptional activation 37 EBNA1 37 fibrillin 1 37 HLA gene 37 myocyte 36 psychosocial functioning 36 Inc TICKER 36 apoE4 36 chromosome #p#.# 36 genomewide 36 PB1 F2 36 endogenous opioid 36 hereditary hemochromatosis 36 β actin 36 clusterin 36 ABCB1 gene 36 PIGF 36 chromosome condensation 36 Apolipoprotein E 36 DRD4 36 intron 36 allele 36 histone methylation 36 interindividual differences 36 regulates gene expression 36 Hh 36 HBV genotypes 36 = -#.# 36 BullMarket.com Previews Earnings 36 plexiform 36 multi factorial disease 36 PCa 36 serotonin transporter 36 KLF4 36 etiologic 36 SCD1 36 CFVR 36 Troj Dloadr 36 Asterisks indicate 36 Cognitive impairment 36 autoantibody 36 prostate cancer CaP 36 T. vaginalis 36 causative mutation 36 major histocompatibility complex 36 APOE4 36 statistically indistinguishable 36 ofloxacin 36 Fragile X gene 36 susceptibility loci 36 aggrecan 36 Univariate analysis 36 Sclerosing 36 #S rDNA 36 APOE gene 36 nonalcoholic steatohepatitis NASH 36 Vps# 36 receptor mediated endocytosis 36 dopamine transporter gene 36 double digit growths 36 Genetic susceptibility 36 genomic imprinting 36 bupropion HCl 36 endonuclease 35 3'UTR 35 etiologic agent 35 susceptibility genes 35 cerebellar vermis 35 FGFR2 gene 35 amino acid residues 35 baroreceptor reflex 35 plasmids encoding 35 CGG repeats 35 Excluding 35 Habitual snoring 35 NSYE 35 ProShares NYSEArca