Related by context. All words. (Click for frequent words.) 72 KCNQ1 71 hypermethylated 71 microcephalin 70 LRAT 70 missense mutations 70 KRAS oncogene 70 MSH2 69 inherited mutations 69 MLL2 69 MECP2 gene 69 GSTP1 69 PTPN# 69 cell adhesion molecule 68 BRCA1 BRCA2 68 Kir#.# 68 JAK2 enzyme 68 TP# gene 68 SCN1A 68 mRNA encoding 68 LMNA 68 chromosome #q#.# [001] 68 SHANK3 68 Cathepsin B 67 LRP5 67 motor neuron degeneration 67 Dystrophin 67 gene MECP2 67 PDGFR 67 transcriptional repressor 67 chromosome #q# [002] 67 regulator CFTR gene 67 BRAF gene 67 cystic fibrosis transmembrane conductance 67 constitutively expressed 67 CDH1 67 BRAF protein 67 KCNH2 67 Kv#.# 67 sortilin 67 APOL1 67 GSTT1 67 GNAQ 67 epigenetically 67 MLH1 67 serine threonine kinase 67 KCNE2 67 K ras mutations 66 TCF#L# gene 66 PDE#A 66 CCR5 delta# 66 frameshift mutation 66 gene locus 66 NR#A# 66 TMEM#B 66 FGFR3 66 CpG island 66 NR#A# gene 66 proto oncogene 66 ADAMTS# 66 LPA gene 66 MYBPC3 66 Clusterin 66 MC4R gene 66 HFE gene 66 upregulating 66 methyltransferase 66 Cyclin D1 66 ALK gene 66 succinate dehydrogenase 66 IgA deficiency 66 serine protease 66 allelic variants 66 CYP#D# gene 66 germline mutation 66 Brugada syndrome 66 ADPKD 66 MTHFR 66 heterozygotes 66 promoter methylation 65 transmembrane receptor 65 apolipoprotein E4 65 SCD1 65 Dysregulation 65 CFTR gene 65 CNTNAP2 65 KLF4 65 BMAL1 65 de novo mutations 65 ENPP1 65 somatic mutations 65 H#K#me# 65 CFTR cystic fibrosis transmembrane 65 non coding RNA 65 TACI 65 IRS1 65 TEL AML1 65 chromosomal rearrangement 65 BMPR2 65 HER2 neu 65 CDKN2A 65 microRNA molecules 65 beta globin 65 MYH9 gene 65 Polymorphisms 65 IDH1 mutation 65 LKB1 65 androgen receptor gene 65 ABCB1 65 lymphangiogenesis 65 germline mutations 65 intracellular signal transduction 65 isoenzyme 65 chemokine receptor 65 neuroligins 65 ZNF# 65 hypothalamic pituitary 65 MEF2A 65 ERBB2 65 micro RNAs 65 PTEN gene 65 NKX#.# 65 eotaxin 65 ectopic expression 65 Epstein Barr Virus EBV 65 gene rearrangements 65 genetic loci 65 cyclic AMP cAMP 65 torsade de pointes 65 ERK signaling 65 circadian clock genes 65 TIMP 1 65 Apolipoprotein E 65 FGFR1 65 methylenetetrahydrofolate reductase 64 mtDNA mutations 64 HLA DRB1 64 metabolizing enzymes 64 Upregulation 64 Six3 64 deacetylation 64 autosomal dominant disorder 64 EGFR protein 64 Hypoxia Inducible Factor 64 STAT4 64 pDC 64 C1q 64 conductance regulator 64 NOTCH1 64 proapoptotic 64 pancreatic endocrine 64 progressive neurodegenerative disorder 64 astrocytic 64 CHD7 64 receptor tyrosine kinase 64 androgen receptor AR 64 NF kB pathway 64 UGT#B# 64 CREBBP 64 monogenic 64 CPVT 64 tryptophan hydroxylase 64 NOD2 64 Inherited mutations 64 chromosomal aberrations 64 microdeletion 64 IL#R 64 tyrosine phosphorylation 64 oncogenic transformation 64 ERK1 2 64 BMP signaling 64 huntingtin gene 64 metaplasia 64 leukocyte adhesion 64 Wwox 64 GATA4 64 VIPR2 64 sinus node 64 autophagic 64 kidney urologic 64 SLITRK1 64 kinase gene 64 Prox1 64 electrical conduction 64 E#F# 64 subventricular zone 64 TRPV4 64 Fibroblasts 64 vanA gene 64 BRAF V#E 64 Dpp 64 ERK pathway 64 Peutz Jeghers syndrome 64 MAP kinases 64 microdeletions 64 MIF protein 64 GPC5 64 apoE 64 RRM1 64 JAK STAT 64 repolarization 64 granule cells 64 sporadic ALS 64 SMAD4 64 mammary duct 64 PALB2 64 ankyrin B 64 Neuregulin 1 64 TOP2A gene 64 aneuploidies 64 p# activation 64 CDK4 64 acyl CoA 64 PIK3CA 64 abnormal methylation 64 myelofibrosis polycythemia vera 64 chromosome #p#.# 63 connexin 63 haematopoietic 63 mosaicism 63 anterior pituitary 63 IRAK1 63 CEACAM1 63 FGFs 63 ErbB4 63 SLC#A# [002] 63 gene polymorphism 63 polymorphic ventricular tachycardia 63 Protein Kinase C 63 p# tumor suppressor 63 GBA mutations 63 NFKBIA 63 IFNg 63 Leydig cells 63 PI3K AKT 63 apoptotic pathway 63 familial pancreatic cancer 63 fatty acid binding 63 renal cysts 63 Immunohistochemical analysis 63 siRNA knockdown 63 constitutive activation 63 parkin gene 63 NF1 gene 63 encodes protein 63 glucokinase 63 downregulated 63 histone methylation 63 muscarinic receptors 63 klotho 63 ryanodine receptor 63 LRRK2 gene 63 N myc 63 peroxisomal 63 ORMDL3 63 HLA DQ2 63 Cytotoxic T 63 KIAA# 63 EAAT2 63 AMPA receptor 63 ERalpha 63 Angiotensin converting enzyme 63 RUNX3 63 p# mitogen activated 63 5 lipoxygenase 63 antiapoptotic 63 familial ALS 63 WDR# 63 mutated K ras 63 autosomal dominant inheritance 63 apoE4 63 rs# [004] 63 upregulates 63 FLT3 63 synaptogenesis 63 hypoperfusion 63 epigenetic modification 63 MAP kinase pathway 63 MMP2 63 podocytes 63 potent inducer 63 tryptase 63 cystic fibrosis transmembrane 63 polyamine 63 ataxias 63 CHEK2 63 C#Y 63 adipogenic 63 HLA DR4 immune 63 Amino acid 63 podocyte 63 CYP#A# [002] 63 constitutively active 63 Janus kinase 63 hypothalamic pituitary adrenal axis 63 circadian genes 63 pituitary hormone 63 promoter hypermethylation 63 urothelial 63 IL6 63 V#F mutation 63 c Myb 63 gene polymorphisms 63 acetylcholine receptor 63 Purkinje cell 63 secretory pathway 63 coding exons 63 lipoxygenase 63 desmin 63 FGFR2 63 pRb 63 gastrointestinal stromal tumors GISTs 63 cypin 63 cagA 63 HbF 63 CYP#A# gene 63 #beta HSD1 63 Secretase 63 hypermethylation 63 Sonic Hedgehog 63 CYP#C# [002] 63 VKORC1 63 protein tyrosine phosphatase 63 R#W [002] 63 protein tyrosine phosphatase 1B 63 HIF 1α 63 nitric oxide synthase 63 TCF#L# 63 JAK2 gene 63 CDH# 63 Purkinje cells 63 neurite outgrowth 63 TXNIP 63 nAChR 63 #q#.# [001] 63 intergenic regions 63 Gata4 63 CaM kinase II 63 Wnt1 63 ErbB1 63 morphogen 63 G6PD 63 #S rRNA 63 costimulatory 63 transthyretin 63 4E BP1 63 BDNF gene 63 progranulin gene 63 genes encoding 63 UGT#A# * 63 narcolepsy cataplexy 63 Genetic variants 63 ENaC 63 lymphatic vasculature 63 #q#.# [002] 63 PAR1 62 5 hydroxytryptamine 62 tumor suppressor protein 62 Rb#/p# 62 microsatellite instability 62 cell adhesion molecules 62 adenylate cyclase 62 hepatoma 62 beta adrenergic receptors 62 hepatic lipase 62 hamartomas 62 synapse formation 62 sinoatrial node 62 Cystic Fibrosis Transmembrane conductance 62 Epstein Barr virus EBV 62 mRNA transcripts 62 CagA 62 chromosome #q# [001] 62 COL#A# 62 atrioventricular 62 electrophysiologic 62 spontaneous mutation 62 OGG1 62 inactivating mutations 62 Notch1 62 dominantly inherited 62 hyperactivation 62 survival motor neuron 62 chromosome #q 62 neuroligin 62 SMN protein 62 beta1 integrin 62 constitutively activated 62 multiprotein complex 62 IKK beta 62 #p#.# [001] 62 phosphorylates 62 CAG repeats 62 chromatin modification 62 LRP6 62 lysyl oxidase 62 cytokine receptor 62 MMP9 62 N. gonorrhoeae 62 kinase domain 62 myeloid 62 GRK5 62 Fibroblast Growth Factor Receptor 62 severe congenital neutropenia 62 caveolin 62 genetic polymorphism 62 TSC1 62 mice lacking 62 GSTM1 62 doublecortin 62 FGF2 62 Thyroid hormone 62 DNA methylation patterns 62 SNP rs# [001] 62 RNA polymerases 62 adenomatous polyposis coli 62 histone modifications 62 PAK1 62 previously uncharacterized 62 molecular abnormalities 62 susceptibility loci 62 chronic eosinophilic leukemia 62 epigenetic alterations 62 MECP2 62 laforin 62 X inactivation 62 LDLR 62 retinoid X 62 leptin deficiency 62 activating mutation 62 HMGA1 62 ankyrin repeat 62 monocytes macrophages 62 methylation patterns 62 potent inhibition 62 PDGF receptor 62 M1 muscarinic 62 overactivation 62 somatostatin 62 Aortic stenosis 62 MLL gene 62 cholesterol homeostasis 62 unstable detrusor muscle 62 Leukemias 62 H#K# methylation 62 PARP1 62 colonic mucosa 62 tumorigenicity 62 DNA methyltransferases 62 TPMT 62 miRNA genes 62 Igf2 62 coexpression 62 AT1R 62 phosphoinositide 62 Rap1 62 histone modification 62 TTR gene 62 vWD 62 CALHM1 62 apolipoprotein E APOE 62 causative mutations 62 cisplatin resistant 62 Lymphocytic 62 PKC beta 62 glutamate receptor 62 Fas ligand 62 TORC2 62 receptor gamma 62 polycystin 62 γ secretase 62 thyrotropin 62 HER2 overexpression 62 Wnt signaling pathway 62 Huntingtin 62 neuronal nitric oxide synthase 62 LIS1 62 CXCR2 62 motoneurons 62 granzyme B 62 virulence determinants 62 basal forebrain 62 5 HT2A serotonin 62 mitogen activated protein kinases 62 IDH1 gene 62 Transcription factors 62 orthologs 62 rs# [002] 62 cyclic nucleotide 62 ADAM# 62 TGF ß 62 catalytic subunit 62 CXCL# 62 protein encoded 62 HOTAIR 62 downregulation 62 histocompatibility 62 Mutational 62 beta globin gene 62 mRNA expression 62 nonsense mutation 62 ApoE gene 62 TrkB 62 MAP#K# 62 endothelial nitric oxide synthase 62 FMR1 gene 62 5 HT1A 62 telomerase reverse transcriptase 62 myopathies 62 chromatin structure 62 Chronic pancreatitis 62 neuronal dysfunction 62 protein tyrosine kinase 62 amyloid deposition 62 S#A# [002] 62 leptin receptor 62 MAPK pathway 62 LDL receptor 62 ribosomal DNA 62 autocrine 62 vacuolar 62 extramedullary 62 DQB1 * 62 gastric carcinogenesis 62 potent inhibitors 62 differential gene expression 62 leukemias lymphomas 62 NF kB signaling 62 lung epithelium 62 carcinoids 62 BMP4 62 hematological relapse 62 ribonucleic acids 62 MMP# 62 vitamin D receptors 62 serine proteases 62 #q# [001] 62 Dopaminergic 62 K#N 62 HepG2 cells 62 SMN1 62 cause cardiac channelopathies 62 autosomal recessive 61 interferon pathway 61 cardiac arrhythmia abnormal 61 pre mRNA splicing 61 fronto temporal dementia 61 peroxisome 61 primary cilia 61 anaplastic lymphoma kinase 61 #ß 61 virulence genes 61 SIRT1 gene 61 proximal tubule 61 gamma globin gene 61 LQTS 61 mGluR5 antagonist 61 IRF6 61 calcium calmodulin dependent 61 p# mutation 61 trophoblast cells 61 TGF beta pathway 61 Alu elements 61 von Hippel Lindau 61 glutamatergic neurons 61 abnormal angiogenesis 61 orthologous genes 61 chitinase 61 susceptibility gene 61 kDa protein 61 Trypanosoma brucei 61 Tasigna prolongs 61 Yamanaka recipe 61 ubiquitinated 61 GPR# [002] 61 regulates gene expression 61 RNase L 61 myo inositol 61 WNK1 61 Overexpression 61 catenin 61 intronic 61 cAMP signaling 61 coiled coil domain 61 Autoantibodies 61 cardiac fibroblasts 61 messenger ribonucleic acid 61 cellular prion protein 61 BCL#A 61 airway hyperresponsiveness 61 MeCP2 gene 61 proline rich 61 GLUT4 61 vWF 61 SMN2 61 lymphocyte activation 61 hydroxylase 61 serine threonine 61 MYH9 61 cyclin dependent kinase inhibitor 61 unmethylated 61 lysophosphatidic acid 61 HepG2 61 adrenal cortex 61 Hh 61 VEGFR1 61 PHLPP 61 hepatocellular carcinomas 61 CYT# potent vascular disrupting 61 PTHrP 61 STK# gene 61 Sjögren syndrome 61 Bardet Biedl syndrome 61 cardiac dysfunction 61 transgenic mouse model 61 coding genes 61 alpha synuclein gene 61 IGFBP2 61 transgenic mouse models 61 CaM 61 homodimer 61 ribosomal protein 61 hyperplastic 61 essential thrombocythemia 61 Angiotensin II 61 Prolactin 61 MAP kinase 61 neuromuscular junction 61 RAS RAF MEK 61 Treg cell 61 microtubule dynamics 61 STAT1 61 colorectal carcinoma 61 systemic amyloidosis 61 AV node 61 fibrin deposition 61 hypoxia inducible factor 61 squamous cell lung cancer 61 XBP1 61 trophoblasts 61 C. pneumoniae 61 atherosclerotic lesions 61 bone marrow lymph nodes 61 Microarray analysis 61 isotypes 61 evolutionarily conserved 61 dysgenesis 61 Immunohistochemical staining 61 mitochondrial metabolism 61 selectively inhibited 61 transient receptor 61 Streptococcus agalactiae 61 glomerular 61 metabolizing enzyme 61 Single Nucleotide Polymorphisms SNPs 61 hypocretin neurons 61 ETV1 61 Phosphorylation 61 E selectin 61 COX2 61 intercellular communication 61 VHL gene 61 folate metabolism 61 Oncogenic 61 colorectal adenoma 61 NAT2 61 telomeric 61 c myc 61 Runx1 61 Cx# [001] 61 mutant worms 61 KLF# 61 hypometabolism 61 renal fibrosis 61 ESR1 61 seminomas 61 paraganglioma 61 downregulates 61 IL 1β 61 posttranslational modifications 61 E3 ligase 61 cyclooxygenase COX 61 dystrophin gene 61 dehydrogenase 61 IDH mutations 61 IFN γ 61 Ribavirin causes 61 ribonucleic acid RNA 61 Drosha 61 HER2 positivity 61 mTOR signaling 61 Activating mutations 61 pDCs 61 NSCLC tumors 61 PER2 61 gene amplification 61 ERBB4 61 FSHR 61 methicillin susceptible Staphylococcus aureus 61 KRAS BRAF 61 dentate gyrus 61 Pten 61 Arrhythmogenic Right Ventricular Cardiomyopathy 61 inhibitory neurotransmitters 61 Notch receptor 61 histone acetylation 61 thyroglobulin 61 chromosome condensation 61 SOCS3 61 EGFR receptor 61 PDGFRA 61 interstitial fibrosis 61 metalloprotease 61 isoenzymes 61 Raf MEK ERK 61 GRNOPC1 contains 61 dopamine transporter 61 polyadenylation 61 palladin 61 Topoisomerase II 61 HBeAg negative 61 clade B 61 transgenic mice expressing 61 adenocarcinomas 61 melanocyte 61 pathophysiological effects 61 Peripheral nerves 61 hypothalamus pituitary 61 β1 61 MGUS 61 tau gene 61 cathepsins 61 HER2 expression 61 microRNA expression 61 autoregulation 61 P2X 61 intracellular signaling 61 spontaneous mutations 61 transcriptional regulators 61 pyruvate kinase 61 isoprenoid 61 PIP2 61 caspase activation 61 autoreactive B 61 alternatively spliced 61 SSc 61 IRE1 61 p# MAPK 61 PHD2 61 thyroid hormone receptor 61 thrombocytopenic 61 pathogenic mutations 61 mitogen activated protein kinase 61 activin 61 NF1 61 ovarian carcinomas 61 Wnt beta catenin 61 impaired glucose metabolism 61 glutamic acid decarboxylase 61 clefting 61 rRNA 61 sequence homology 61 radiosensitivity 61 PON1 61 intracortical 61 adhesion molecule 61 TACI mutations 61 MTHFR gene 61 p# mutations 61 DNA methyltransferase 61 diabetes mellitus DM 61 acyltransferase 61 mediated inhibition 61 X Chromosome 61 fibulin 61 Jhdm2a 61 activated microglia 61 TNFR 61 fibrillin 1 61 autosomal dominant 61 miRNA expression 61 ChR2 61 epigenetic silencing 61 glucocorticoid receptors 61 fascin 61 cultured neurons 61 node metastases 61 decarboxylase 61 ERK2 61 mutant genes 61 transcriptional activation 61 MiRNAs 60 DSBs 60 prolonged QT interval 60 TRAF1 C5 60 C5aR 60 RASSF1A 60 transcriptional silencing 60 nephronophthisis 60 TTR amyloidosis 60 nonischemic 60 erythropoiesis 60 causative genes 60 IKZF1 60 uPAR 60 breast carcinomas 60 susceptibility locus 60 interleukins 60 nephrogenic 60 DGAT1 60 Ventricular fibrillation 60 c MYC 60 Heterozygous 60 myeloproliferative diseases 60 enkephalin 60 TAp# 60 MYCN 60 protein phosphorylation 60 Fragile X gene 60 radial glia 60 NKX2 60 PLX STROKE targeting 60 #S ribosomal RNA 60 VEGF receptor 60 neutrophil recruitment 60 coreceptor 60 NFkB 60 neurofibrillary 60 pituitary adenomas 60 Brugada Syndrome 60 adenylyl cyclase 60 CD#b 60 striated muscle 60 TERT 60 HDAC enzymes 60 paralogs 60 inducible nitric oxide synthase 60 HER2 HER2 60 cholecystokinin CCK 60 Factor Receptor 60 humanin 60 intercellular signaling 60 c KIT 60 Inactivation 60 maternally inherited 60 dysbindin 60 CFTR gene mutations 60 noncoding 60 nucleolar 60 NRTI resistance 60 K#R [002] 60 electrophysiological recordings 60 differentially regulated 60 chromosome rearrangements 60 HLA genes 60 epigenetic changes 60 CYP #D# 60 mGluRs 60 small molecule activators 60 KIF6 gene 60 Epidermal Growth Factor Receptor 60 recessive inheritance 60 proNGF 60 renal cell carcinomas 60 T#M 60 hypomethylation 60 neuroepithelial cells 60 exocrine glands 60 neuronal synapses 60 MTHFD1L gene 60 transcriptional regulation 60 ABCB1 gene 60 breast cancer genes BRCA1 60 copper zinc superoxide 60 normal karyotype 60 prostate carcinoma 60 PKD1 60 DRB1 * 60 aldehyde dehydrogenase 60 histone H3 60 papillary renal cell carcinoma 60 protein tyrosine phosphatases 60 APOE e4 60 ß amyloid 60 SNCA 60 proteolytic cleavage 60 plasmacytoid 60 indels 60 SGPT 60 systolic dysfunction 60 intracellular signaling pathways 60 HMGA2 60 proteins encoded 60 transmembrane protein 60 ALK mutations 60 intraventricular 60 glycogen metabolism 60 cytokine signaling 60 glutamate signaling 60 homeobox gene 60 RCAN1 60 molecular signaling pathway 60 axon guidance 60 immunoglobulin genes 60 RAF kinase VEGFR 60 CYP#D# 60 receptor molecule 60 HLA DRB1 * 60 IgG1 60 G6PD deficiency 60 alpha2 60 DNA rearrangements 60 progranulin 60 SNP rs# [002] 60 TNF α 60 Sonic hedgehog 60 transcriptional activity 60 BRAF V#E mutation 60 lymphatic vessel 60 hypogonadotropic hypogonadism 60 SGLT2 60 heterologous expression 60 Fragile X mental retardation 60 CYP#A# CYP#D# 60 viral nucleic acids 60 Skeletal muscle 60 DISC1 gene 60 Epithelial 60 vimentin 60 HMG CoA reductase 60 colorectal carcinomas 60 endogenous retroviruses 60 ABL1 60 receptor kinase 60 MEK1 60 surgically resected 60 Interferon gamma 60 MDR1 60 Glial 60 SOD1 gene 60 PI3K Akt 60 bronchoalveolar lavage fluid 60 CHFR 60 DLC1 60 MTDH 60 Becker muscular dystrophy 60 beta amyloid peptide 60 NKG2D 60 autosomal 60 gene deletions 60 IDH1 60 colocalization 60 Aâ 60 dopamine D4 receptor 60 euthymic patients 60 ACC2 60 neoplastic transformation 60 C#T [002] 60 kinase pathway 60 untranslated regions 60 tRNA synthetase 60 mRNA molecules 60 Macrophage 60 missense mutation 60 Protein Kinase 60 underlying vasculopathy 60 TCF4 60 TNFalpha 60 FOXO 60 gene encodes protein 60 antibody mediated 60 MT1 MMP 60 splice variants 60 DEAR1 60 hypereosinophilic syndrome 60 PPARg 60 Meckel Gruber 60 IL 1ß 60 tumor suppressor gene 60 HERV 60 microglial 60 CD#c 60 HCV replication 60 TET2 60 mucinous 60 dorsal root ganglion 60 sGC 60 malignant prostate 60 MyD# 60 CHD5 60 micronuclei 60 BRIP1 60 mouse neural stem 60 metastatic neuroendocrine tumors 60 nasal epithelium 60 EBNA1 60 hereditary predisposition 60 intracellular pH 60 ciliated 60 filaggrin