Related by context. All words. (Click for frequent words.) 74 somatic mutations 74 PTPN# 73 mtDNA mutations 73 transgene expression 73 K ras mutations 72 gene rearrangements 72 MAPK pathway 72 chromosomal aberrations 71 microdeletion 71 monogenic 71 KRAS oncogene 70 myeloproliferative diseases 70 BRAF gene 70 hamartomas 70 tyrosine phosphorylation 70 cyclin E 70 missense mutations 70 germline mutations 70 protein tyrosine phosphatase 69 DNA methylation patterns 69 de novo mutations 69 virulence genes 69 penetrance 69 Fas ligand 69 molecular abnormalities 69 inherited mutations 69 chromosomal instability 69 miRNA genes 69 phenotypic variation 69 genomic alterations 69 motor neuron degeneration 69 SMAD4 69 LRP5 69 p# activation 69 primary cilia 69 ERK signaling 69 PHD2 69 p# mutations 69 TCF#L# gene 69 genetic polymorphism 69 Genetic variants 69 plasma kallikrein 68 CYP#D# gene 68 oncogenic transformation 68 PARP inhibition 68 chromosomal translocations 68 TMEM#B 68 neuronal dysfunction 68 beta1 integrin 68 TP# gene 68 beta amyloid peptides 68 osteosarcomas 68 PTEN gene 68 Genetic predisposition 68 carcinoids 68 MGUS 68 potent inhibitors 68 etiologic 68 CYP #A# 68 proto oncogene 68 lymphocytic 68 autophagic 68 STAT4 68 VHL gene 68 KLF4 68 epigenetic silencing 68 missense mutation 68 trophoblast cells 68 CYP #D# 68 PPARg 68 gene amplification 68 posttranslational modifications 68 sequence homology 68 pleiotropic 68 cellular prion protein 68 #q#.# [002] 68 microdeletions 68 epigenetic alterations 68 DSBs 68 DNA demethylation 68 HER2 overexpression 68 gastrointestinal stromal tumors GISTs 68 inactivating mutations 68 gastric carcinoma 67 FUS1 67 mucinous 67 Telomere length 67 ABCB1 67 hypermethylated 67 genetic aberrations 67 eotaxin 67 OGG1 67 Notch1 67 NF kB pathway 67 hematopoietic cancers 67 GISTs 67 hyperplastic 67 Smad3 67 potent inhibition 67 haematopoietic 67 clefting 67 MMP# 67 synaptogenesis 67 nucleoli 67 Clusterin 67 aneuploidies 67 ZNF# 67 hepatic stellate cells 67 sCJD 67 FGFR2 67 isoenzymes 67 pharmacokinetic interactions 67 HbF 67 ALK mutations 67 MSH2 67 chromosomal rearrangements 67 prion infection 67 GPx 67 aneuploid cells 67 arterial calcification 67 Genetic mutations 67 CDK4 67 uPAR 67 IDH mutations 67 microglial activation 67 micro RNAs 67 heterozygotes 67 testicular dysgenesis syndrome 67 underlying pathophysiology 67 extramedullary 67 TGF beta signaling 67 TRPV4 67 gliosis 67 glycolipids 67 JAK2 enzyme 67 TMPRSS2 ERG fusion 67 germline mutation 67 PDGFR 67 previously uncharacterized 67 neuroinflammation 67 transgenic mice expressing 67 coexpression 67 mitochondrial metabolism 67 oncogenic mutations 67 V#F mutation 67 astrocytic 67 epigenetic modification 67 renal fibrosis 67 tumorigenicity 66 Treg cell 66 mRNA transcripts 66 amyloid deposition 66 neuroblastomas 66 MECP2 gene 66 liver metastasis 66 PrPSc 66 Alu elements 66 osteoblastic 66 PON1 66 allelic variants 66 DNMT1 66 Htt 66 histone acetylation 66 Aspergillus species 66 p# mutation 66 neurite outgrowth 66 MTHFR 66 chemosensitivity 66 leiomyomas 66 metaplasia 66 differential gene expression 66 p# MAPK 66 ADAMTS# 66 hypermethylation 66 precursor lesions 66 lymphocyte activation 66 mitochondrial enzyme 66 Cyclin E 66 genetic loci 66 malignant transformation 66 #q# deletion 66 Hashimoto thyroiditis 66 hepatic lipase 66 axonal degeneration 66 NKX#.# 66 STAT3 signaling 66 TPMT 66 caveolin 1 66 B7 H3 66 miRNA expression 66 myopathies 66 DLC1 66 metalloprotease 66 biochemical abnormalities 66 paralogs 66 EBV infection 66 genomic deletions 66 ß amyloid 66 TNF blocker therapy 66 pituitary adenomas 66 untranslated regions 66 susceptibility gene 66 CREBBP 66 hyperinsulinemia 66 LIS1 66 C1q 66 urothelial carcinoma 66 infantile hemangioma 66 airway hyperresponsiveness 66 antiphospholipid syndrome 66 TGF ß 66 PIK3CA 66 CHD7 66 Cathepsin B 66 androgen receptor AR 66 TCF#L# 66 colorectal carcinogenesis 66 microRNA expression 66 causative mutations 66 protein tyrosine phosphatases 66 proline rich 66 H#Y 66 IL 1ß 66 activating mutations 66 cysteines 66 ADPKD 66 transcriptional repressor 66 mutant huntingtin protein 66 Activating mutations 66 #beta HSD1 66 cell adhesion molecules 66 hyperalgesia 66 ERK1 2 66 P cadherin 66 fluoroquinolone resistance 66 HMGA1 66 epithelial tissues 66 intracranial hemorrhage ICH 66 osteogenic differentiation 66 pleiotropic effects 66 Leydig cell 66 structural rearrangements 66 nonsense mutations 66 hepatocellular carcinomas 66 neurofibrillary 66 mosaicism 66 renal cysts 66 seminomas 66 CD# expression [001] 66 thyrotropin 66 genotoxic stress 66 alpha synuclein protein 66 serine protease 66 amyloid peptide 66 Hedgehog signaling 66 atypical hyperplasia 66 prostate carcinogenesis 66 metabolic abnormalities 66 myeloid 65 SHANK3 65 chromosomal anomalies 65 innate immune responses 65 cAMP signaling 65 CALHM1 65 epigenetic changes 65 functional polymorphism 65 genital tract infections 65 prostate cancer CaP 65 FGFs 65 immunoreactivity 65 overactivation 65 MYH9 gene 65 LPA gene 65 somatic mutation 65 T#M 65 mitochondrial mutations 65 underlying molecular mechanisms 65 CYP#C# gene 65 tryptase 65 hydrops 65 genetic polymorphisms 65 secretory pathway 65 CNTNAP2 65 CHD5 65 Genetic variation 65 CD#c 65 ERBB2 65 β catenin 65 ABCA1 65 sarcosine 65 intracellular signal transduction 65 histone deacetylases 65 small molecule activators 65 NADPH oxidase 65 epithelial tumors 65 Prion diseases 65 β amyloid 65 clonal expansion 65 splice variants 65 Trichophyton rubrum 65 protein alpha synuclein 65 proteoglycan 65 microglial 65 proteolytic cleavage 65 Cyclin D1 65 basal cell nevus syndrome 65 IgA deficiency 65 SCN5A 65 abnormal proteins 65 FMRP protein 65 hypoperfusion 65 Raf MEK ERK 65 TSLP 65 TGF ß1 65 CPEB 65 predisposing factor 65 vimentin 65 Leydig cells 65 chromosomal deletions 65 MLL gene 65 subclinical 65 amyloid deposits 65 thiopurine 65 M. pneumoniae 65 secretase 65 serine threonine kinase 65 myelofibrosis polycythemia vera 65 Sjögren syndrome 65 mTOR inhibitors 65 homozygosity 65 RUNX3 65 brain lesions 65 Notch signaling 65 insulin signaling pathway 65 HER2 expression 65 stratifying patients 65 chromosome aberrations 65 MLH1 65 E#F# 65 diagnostic biomarker 65 pathogenic mutations 65 gene polymorphisms 65 NFκB 65 chronicity 65 cisplatin resistant 65 Gorlin syndrome 65 chromosome #p#.# 65 hypomethylation 65 hyperactivation 65 #q#.# [001] 65 glycosylated 65 neurofibromas 65 mitochondrial toxicity 65 pancreatic endocrine 65 drug metabolizing enzymes 65 shortened telomeres 65 TOP2A gene 65 Foxp3 65 synovial cells 65 Chronic pancreatitis 65 tumor suppressor protein 65 γ secretase 65 CFTR gene 65 tumoral 65 ligand receptor 65 nephrogenic 65 BCL#A 65 3'UTR 65 familial pancreatic cancer 65 p# alpha [002] 65 ncRNA 65 H#K#me# 65 HOTAIR 65 herpesviruses 65 MIF protein 65 lactate dehydrogenase LDH 65 BARD1 65 pathogenetic 65 incidentalomas 65 chromatin structure 65 conserved sequences 65 teratogens 65 epithelial barrier 65 Jhdm2a 65 methylation patterns 65 Oncogenic 65 ALK gene 65 gene deletions 65 CEACAM1 65 BRCA1 BRCA2 65 atherosclerotic lesions 65 caveolin 65 mutant alleles 65 metastatic neuroendocrine tumors 65 nAChR 65 lung epithelium 65 childhood leukemias 65 chromosomal mutations 65 demyelinating 65 c myc 65 prognostic markers 65 receptor kinase 65 LRRK2 gene 65 beta subunit 65 oxidized phospholipids 64 deacetylation 64 granulosa cell 64 WT1 64 pre malignant lesions 64 ADAM# 64 MC4R gene 64 neoplastic transformation 64 endocannabinoid signaling 64 substrate specificity 64 neoplastic 64 calculi 64 MTHFR gene 64 PHLPP 64 non coding RNA 64 promoter hypermethylation 64 histone methylation 64 causal variants 64 genetic determinants 64 adrenocortical cancer 64 COX2 64 karyotypes 64 CHEK2 64 Hurthle cell 64 activating mutation 64 AMACR 64 oncoproteins 64 constitutively expressed 64 glomerulonephritis 64 TNF α 64 spontaneous mutations 64 HER2 neu 64 Telomere shortening 64 atherosclerotic lesion 64 genomic instability 64 IFN γ 64 protein tau 64 FGF2 64 NEIL1 64 granzyme B 64 apoE4 64 benign neoplasms 64 Pten 64 RAS RAF MEK 64 oncogene addiction 64 segmental duplications 64 pulmonary metastases 64 receptor tyrosine kinase 64 modifier genes 64 atherogenesis 64 FGFR2 gene 64 huntingtin gene 64 matrix metalloproteinases 64 epistasis 64 normal karyotype 64 sarcomatoid 64 anemias 64 hypometabolism 64 HCV replication 64 osteolytic 64 JAK STAT signaling 64 FLT3 64 TSC1 64 Prox1 64 mesenchymal cell 64 neurocognitive impairment 64 mutant proteins 64 BMP signaling 64 lysosomal enzyme 64 choroidal neovascularization CNV 64 cis regulatory 64 MT1 MMP 64 epigenetic mechanisms 64 PI3K pathway 64 squamous cell lung cancer 64 effector function 64 immunofluorescence staining 64 Upregulation 64 morphogen 64 beta globin gene 64 NKG2D 64 Flt3 64 immunological responses 64 mRNA expression 64 Lyn kinase 64 TAp# 64 BRAF V#E 64 malignant phenotype 64 tumor necrosis 64 Estrogen Receptor 64 CDH1 64 neuroligins 64 pressure natriuresis 64 plasminogen 64 immunomodulation 64 epigenetic modifications 64 Akt activation 64 metabolic disturbances 64 lymphomas leukemias 64 L. pneumophila 64 pituitary hormone 64 gene APOE 64 PTEN mutations 64 Epstein Barr Virus EBV 64 renal cell carcinomas 64 4E BP1 64 node metastases 64 thyroid carcinoma 64 ataxias 64 desmosomes 64 TEL AML1 64 papillomas 64 TNFa 64 NFKBIA 64 COL#A# 64 somatostatin 64 virulence determinants 64 CpG island 64 leiomyoma 64 haematologic 64 TCF4 64 metabolizing enzymes 64 interferon IFN 64 hereditary predisposition 64 lichen planus 64 C. pneumoniae 64 hypothalamic pituitary 64 progranulin 64 Fibroblast 64 Skeletal muscle 64 malignant lesions 64 nucleotide substitutions 64 airway remodeling 64 microsatellite instability 64 Smac mimetic 64 proapoptotic 64 xenobiotic 64 proteolysis 64 mitochondrial dysfunction 64 oncogenesis 64 Chlamydia pneumoniae 64 etiologic factors 64 glial tumors 64 p tau 64 IL 1β 64 selective antagonists 64 amyloid β 64 oligomerization 64 neurofibroma 64 familial clustering 64 Cdc7 64 multidrug resistance 64 KCNH2 64 phenotypic variability 64 C#Y 64 TNFalpha 64 multigenic 64 indel 64 nitrotyrosine 64 apoE 64 colorectal adenoma 64 filaggrin 64 KIT mutations 64 promoter methylation 64 CagA 64 aneuploidy 64 LRAT 64 methicillin susceptible Staphylococcus aureus 64 p# Shc 64 Dysregulation 64 methylenetetrahydrofolate reductase 64 endocrine tumors 64 BMP2 64 osteopontin 64 humoral immunity 64 pRb 64 downregulation 64 amyloid beta plaques 64 rs# [004] 64 caspase activation 64 Papillary 64 Wnt signaling pathway 64 osteoid 64 immunohistochemical analysis 64 chlamydial 64 histone modifications 64 TGFBR1 * 6A 64 ABL1 64 GBA mutations 64 N Myc 64 adipogenic 64 infectious prion proteins 64 nonhereditary 64 Vangl2 64 ultrastructural 64 cardiac troponin 64 autoinflammatory diseases 64 nodal metastasis 64 CCR3 64 #BP# 64 protein misfolding 64 GPIHBP1 64 p#INK#a 64 candida infections 64 occludin 64 Hh pathway 64 skeletal metastases 64 gene locus 64 HER2 positive cancers 64 cytolytic 64 CYP#E# 64 miRs 64 E. faecalis 64 aberrant activation 64 telomere dysfunction 64 meiotic recombination 64 intracellular bacteria 64 GRP# 64 intestinal epithelium 64 cathepsin K 64 arrhythmogenic 64 molecular biomarkers 64 Abeta# 64 PCNSL 64 isotypes 64 isoenzyme 64 Immunohistochemical staining 64 MAPKs 64 LKB1 64 radiographic findings 64 lymphoid cells 64 amyloidogenic 64 pheochromocytoma 64 neurological abnormalities 63 deleterious mutations 63 transcriptional regulation 63 Abeta protein 63 ABCB1 gene 63 prostate carcinoma 63 hypogonadotropic hypogonadism 63 MMP9 63 pathophysiologic 63 quasispecies 63 gastric adenocarcinoma 63 ACh 63 prothrombotic 63 chromosome #q# [002] 63 NFAT 63 LRP6 63 ectopic expression 63 selective inhibition 63 serum antibodies 63 GABAB receptors 63 bone morphogenetic proteins 63 APOL1 63 CD1d 63 NPM1 mutation 63 NNRTI resistance 63 orthologous genes 63 choroidal neovascularization 63 endogenous ligands 63 metastatic lesions 63 antibody mediated 63 tRNA synthetases 63 activin 63 hepatic enzymes 63 chromosome translocations 63 MTHFD1L gene 63 collagen degradation 63 HFE gene 63 Pseudomonas aeruginosa infections 63 osteoclast activity 63 CYT# potent vascular disrupting 63 neural crest 63 N. gonorrhoeae 63 PTEN protein 63 MYCN amplification 63 EGFR pathway 63 FGFR3 63 hypothalamic pituitary adrenal axis 63 colocalization 63 ribosomal DNA 63 Kufs disease 63 USP# 63 cardiac fibrosis 63 osteogenic 63 nonvascular 63 PALB2 63 Brugada syndrome 63 polyploidy 63 myeloperoxidase 63 IRAK1 63 kidney urologic 63 Vitamin B# deficiency 63 G6PD deficiency 63 putative biomarkers 63 amine oxidase 63 GIST tumors 63 adrenocortical 63 NF kB signaling 63 Peutz Jeghers syndrome 63 PEDF 63 cardiac troponin T 63 receptor molecule 63 tau protein tangles 63 intercellular signaling 63 mutated protein 63 biologic pathway 63 malignant lymphomas 63 Imprinted genes 63 PI3K AKT 63 TGF β 63 sphingolipid 63 microcephalin 63 hypercalcemia 63 neoplastic diseases 63 microRNA molecules 63 peroxisomal 63 rs# [002] 63 synuclein 63 phenotypic expression 63 malignant prostate 63 indels 63 cholinergic tone 63 genes differentially expressed 63 WNK1 63 morphologic 63 aggrecan 63 Cryptococcus neoformans 63 hepatocellular 63 splice junctions 63 SGK1 63 leukaemic stem cells 63 myofibroblasts 63 CYP#B# 63 CCR1 63 alveolar epithelial cells 63 gastric cardia 63 overactivated 63 polyploid 63 IDH1 mutation 63 amino acid substitutions 63 podocyte 63 airway hyper responsiveness 63 c KIT 63 adenocarcinomas 63 gene APOE4 63 histopathological 63 TTR gene 63 plastid 63 anti angiogenic drugs 63 molecular determinants 63 ouabain 63 immunocompetent 63 tunica vaginalis 63 BRAF mutations 63 ependymomas 63 hepatoma 63 genomic rearrangements 63 fibrotic disease 63 mediated inhibition 63 SORL1 63 mutant allele 63 Aß 63 upregulating 63 cTnT 63 prognostic marker 63 IgG4 63 CYP#C# [002] 63 gene fusions 63 COX enzymes 63 von Willebrand 63 XMRV infection 63 penile fibrosis 63 kinase gene 63 immune dysregulation 63 nucleases 63 pDCs 63 lethal arrhythmias 63 Fragile X gene 63 MC1R 63 Sp1 63 glomerular 63 immunotoxicity 63 LDL receptor 63 Fc receptor 63 glycolytic pathway 63 constitutively active 63 superinfection 63 EGFR tyrosine kinase inhibitors 63 γδ T cells 63 neuropsychological impairments 63 tumor subtypes 63 presymptomatic 63 fatty acid synthase 63 sporadic ALS 63 bronchial epithelial cells 63 quantitative trait loci 63 aetiological 63 hyperprolactinemia 63 colorectal carcinoma 63 prolonged QT interval 63 C. albicans 63 epigenetic markers 63 epigenetic inheritance 63 mammary stem cells 63 Immunohistochemical analysis 63 MC1R gene 63 neurosensory 63 gastric carcinomas 63 autoregulation 63 Metastases 63 RIP1 63 developmental abnormalities 63 EGFR protein 63 sporadic Creutzfeldt Jakob 63 ionic currents 63 PARP1 63 p#Kip# 63 radiosensitivity 63 transgenic mouse model 63 immunopathology 63 TGF b 63 FGF signaling 63 APOE4 63 pertussis toxin 63 chitinase 63 steroidogenic 63 lysosomal storage diseases 63 podocytes 63 subclinical disease 63 phosphatases 63 serous ovarian cancer 63 biomarker identification 63 microglial cells 63 carotid plaques 63 adrenal hormone 63 hypercoagulable 63 pyrimidines 63 prostanoid 63 Gleevec resistant 63 allelic variation 63 fungal genomes 63 melanocyte 63 basal cell carcinoma BCC 63 myeloproliferative 63 CFTR protein 63 ventricular myocardium 63 dimeric 63 paragangliomas 63 breast carcinoma 63 bacterial virulence 63 fig. S4 63 developmental neurotoxicity 63 myo inositol 63 tissue fibrosis 63 fetal malformations 63 Shp2 63 CXCL5 63 repolarization 63 heterologous expression 63 miR #b [002] 63 GSTP1 63 oligomeric 63 NOD2 63 SLC#A# [002] 63 fibrin deposition 63 unmeasured confounders 63 VEGF receptor 63 disulfide bond 63 MDR1 63 methylated DNA 63 Polymorphisms 63 Protein Kinase C 63 spermidine 63 T2DM 63 mTOR inhibition 63 Sezary syndrome 63 histologic subtype 63 hereditary hemochromatosis 63 FXTAS 63 tau protein 63 cytokine signaling 63 prostaglandin synthesis 63 miR #a [002] 63 impair fertility 63 vacuolar 63 Systemic lupus erythematosus 63 malignant nodules 63 protein kinase C 63 druggable targets 63 post translational modifications 63 dopaminergic cells 63 ribonucleic acids 63 Aβ 63 lactate dehydrogenase 63 chromosome condensation 63 NR#A# 63 NR2B subunit 63 mitogen activated protein kinase 63 apoptotic pathway 63 NF KB 63 AhR 63 epithelia 63 polyglutamine 63 homozygotes 63 acinar 63 BCR ABL mutations 63 invasive carcinoma 63 NF kappaB activation 63 GABAA receptors 63 FTLD 63 SOCS3 63 necrotic core 63 mutated EGFR 63 vasogenic edema 63 lymphangiogenesis 63 maternally inherited 63 APOE e4 63 susceptibility loci 63 HSF1 63 cerebral ischemia 63 JAK mutations 63 Aâ 63 NKT cells 63 lung adenocarcinoma 63 HBx 63 systemic toxicity 63 neurologic complications 63 cyclophilin D 63 tau aggregates 63 costimulatory 63 misregulation 63 neuropathologic 63 neuritic 63 cDNAs 62 EGFR mutations 62 Amino acid 62 TRPV3 62 GSTT1 62 IKK2 62 nonmelanoma skin cancers 62 methyltransferase 62 perivascular 62 GPC5 62 vascular dysfunction 62 lymphoid 62 cyclic AMP cAMP 62 β1 62 aminopeptidase 62 agonist antagonist 62 Genetic mutation 62 miR #a [001] 62 PlGF 62 PCA3 gene 62 recessive trait 62 autosomal dominant disorder 62 Hutchinson Gilford progeria 62 Wnts 62 rRNA 62 adult neurogenesis 62 ascertainment bias 62 leukocyte adhesion 62 autoantibodies 62 SNP rs# [002] 62 hermaphroditism 62 BMPR2 62 gastric carcinogenesis 62 Neurodegenerative diseases 62 lymphatic vasculature 62 testicular tumors 62 breast cancer subtypes 62 WDR# 62 homodimers 62 mGluR 62 nodulation 62 Zollinger Ellison Syndrome 62 NP CRNs 62 GPI anchored 62 Eg5 62 inactive X chromosome 62 c MET 62 perfusion abnormalities 62 ß1 62 VEGFR1 62 inhibitory receptor 62 demethylase 62 abnormal prion protein 62 neuroblastoma tumors 62 VIPR2 62 SSc 62 endonuclease 62 receptor mediated endocytosis 62 MLL2 62 EoE