Related by context. All words. (Click for frequent words.) 73 VHL gene 72 DICER1 gene 72 SHANK3 72 HFE gene 70 histocompatibility 70 MECP2 gene 70 ZNF# 70 CHD7 69 LIS1 69 Cathepsin B 69 Ets2 69 prion gene 69 mRNA transcripts 69 TP# gene 68 CDH1 68 gene MECP2 68 GPC5 68 HLA DRB1 68 transmembrane receptor 68 KIAA# 68 LMNA 68 de novo mutations 68 HMGCR 68 missense mutation 68 DEAR1 68 LRAT 68 C#Y 67 SLITRK1 67 MLL2 67 SMN2 gene 67 MC4R gene 67 TCF#L# gene 67 NF1 gene 67 maternally inherited 67 neural progenitor 67 BARD1 67 Genetic variation 67 JAK2 enzyme 67 Prox1 67 alternatively spliced 67 promoter hypermethylation 67 hypermethylated 67 mutated K ras 67 Cyclin D1 67 somatic mutation 67 NKX#.# 67 prodynorphin 67 CCL#L# 67 Single Nucleotide Polymorphisms SNPs 67 parkin gene 66 LKB1 66 IL#R 66 von Hippel Lindau 66 gastrointestinal stromal tumors GISTs 66 apoE 66 CCR5 delta# 66 gene rearrangements 66 severe congenital neutropenia 66 genetic polymorphism 66 histone modification 66 ALK gene 66 CFTR gene 66 microcephalin 66 mutant allele 65 causative mutations 65 constitutively expressed 65 C EBP alpha 65 BRCA1 BRCA2 65 splice variant 65 PTPN# 65 mutated p# 65 BRAF V#E 65 COL#A# 65 recessive mutation 65 glutamic acid decarboxylase 65 mosaicism 65 LRP5 65 tumorigenicity 65 KRAS oncogene 65 alpha synuclein gene 65 MEF2A 65 SOD1 gene 65 pathogenic mutations 65 LRRK2 gene 65 orthologs 65 germline mutations 65 R#W [002] 65 PTEN gene 65 E#F# 65 Upregulation 65 abnormal hemoglobin 65 BRIP1 65 UGT#B# 65 Shp2 65 SHANK3 gene 65 peroxisome 65 spontaneous mutation 65 CDKN2A 65 Clusterin 65 familial ALS 65 monogenic 65 Kufs disease 65 hemagglutinin H 65 HER2 neu 65 virulence genes 65 endogenous ligands 65 chromosomal translocations 65 sequence homology 65 murine leukemia virus 65 transgenic mouse models 65 breast cancer genes BRCA1 65 CFTR cystic fibrosis transmembrane 65 WAGR syndrome 65 chromosome rearrangements 65 DLX5 65 neurite outgrowth 65 FUS1 65 melanocyte 64 fronto temporal dementia 64 MLH1 64 Epstein Barr Virus EBV 64 Htt 64 Genetic mutation 64 HLA DQ2 64 MC1R gene 64 Wwox 64 recessive trait 64 NFKBIA 64 DGAT1 64 genus Plasmodium 64 neuroD2 64 pancreatic endocrine 64 MYH9 gene 64 paternally inherited 64 outer membrane proteins 64 MSH2 64 oncogenic transformation 64 vesicular stomatitis virus 64 replicon 64 Six3 64 SMN1 gene 64 epigenetic modifications 64 Trypanosoma brucei 64 FGFs 64 virulence determinants 64 GSTM1 gene 64 androgen receptor AR 64 retinoblastoma Rb 64 #p#.# [001] 64 abnormal proteins 64 mouse neural stem 64 medulloblastoma tumors 64 chromosomal aberrations 64 STAT4 64 uPAR 64 NR#A# gene 64 VIPR2 64 EGFR gene 64 colorectal adenocarcinoma 64 olfactory receptor 64 BRAF gene 64 BRAF protein 64 Cyclin E 64 autoreactive 64 GNAQ 64 CD#c 64 somatic mutations 64 neurofibrillary 64 TTR gene 64 FGFR2 64 Aromatase 64 mitogen activated protein kinases 64 missense mutations 64 inherited mutations 63 PDGFRA 63 epigenetic regulation 63 PALB2 63 chromosome #q# [002] 63 multiply uncontrollably 63 deacetylation 63 neuroligins 63 Entamoeba 63 number variations CNVs 63 gamma globin gene 63 recombinantly 63 MeCP2 gene 63 transcriptional repressor 63 number variation CNV 63 transiently transfected 63 epigenetic silencing 63 Thorough cooking kills 63 trypanosome 63 aneuploidies 63 Nf1 63 KCNQ1 63 beta globin 63 PKD1 63 ribosomal protein 63 RPE# gene 63 RCAN1 63 pRb 63 Epstein Barr virus EBV 63 F#del 63 ortholog 63 RRM1 63 splice variants 63 connexin 63 Apc 63 Arabidopsis genome 63 PGC 1α 63 Hutchinson Gilford progeria 63 potent inducer 63 Cryptococcus neoformans 63 metalloprotease 63 IRAK1 63 TRAIL induced apoptosis 63 ectopic expression 63 TMPRSS2 ERG fusion 63 alpha synuclein protein 63 MAPK pathway 63 Irs2 63 miRNA genes 63 c KIT 63 mutation 63 ribosomal RNA rRNA 63 chromosomal instability 63 serine threonine kinase 63 SMAD4 63 sphingolipid 63 NPM1 gene 63 C. neoformans 63 At#g# 63 Inactivation 63 regulates gene expression 63 BCL#A 63 MC1R 63 Cytotoxic T 63 dyskeratosis congenita 63 beta globin gene 63 apoE4 63 RNA polymerases 63 Wnt signaling pathway 63 Glut1 63 Polymorphisms 63 Foxp2 63 microdeletions 63 intronic 63 exocrine glands 63 RKIP 63 fruitfly Drosophila 63 hepatoma 63 NPHP 63 telomere DNA 63 chronic granulomatous disease 63 SCN5A 63 lymphangiogenesis 63 alpha syn 63 PrPC 63 Ras oncogene 63 DNMT1 62 cytopathic 62 spontaneous mutations 62 genetic rearrangements 62 Genetic mutations 62 p# deficient 62 androgen receptor gene 62 hyperactivated 62 WDR# 62 K ras mutations 62 CDK4 62 ChR2 62 RUNX3 62 Jhdm2a 62 constitutively 62 GRNOPC1 contains 62 polyploid 62 tumor suppressor protein 62 K ras gene 62 palladin 62 hemagglutinin gene 62 endogenous retroviruses 62 apolipoprotein E gene 62 Karayiorgou 62 bacterium Mycobacterium tuberculosis 62 genetic loci 62 DNA methylation patterns 62 intergenic regions 62 primordial germ cells 62 segmental duplications 62 HLA DQ 62 siRNA knockdown 62 FLT3 62 sickle cell hemoglobin 62 mRNA decay 62 Polycomb proteins 62 Genetic variants 62 PCA3 gene 62 IDH1 gene 62 constitutively active 62 CYP #D# 62 ABCB1 62 PrPSc 62 glucocerebrosidase 62 SMN1 62 M. pneumoniae 62 CD# expression [001] 62 piRNAs 62 trophoblast 62 5 HT2A serotonin 62 rDNA 62 Sox9 62 Heterozygous 62 transcriptional silencing 62 annexin 62 germline mutation 62 transgenic rats 62 thymidine kinase 62 unmutated 62 Sonic Hedgehog 62 aldehyde dehydrogenase 62 MAPK signaling pathway 62 Histopathologic examination 62 genotoxic stress 62 Microarray analysis 62 Homozygous 62 lymphomas leukemias 62 H#Y 62 transgenic mouse model 62 ductal adenocarcinoma 62 suppressor gene 62 TLE3 62 misregulation 62 epigenetic markers 62 carboxy terminal 62 epigenetic modification 62 Rb gene 62 clonally 62 survival motor neuron 62 variant allele 62 HLA B# 62 Fas ligand 62 cyclin dependent kinase inhibitor 62 mitochondrial gene 62 mtDNA mutations 62 Alu elements 62 transcriptional repression 62 4E BP1 62 HepG2 cells 62 Foxp3 62 aneuploid 62 protein encoded 62 autoinflammatory 62 GSTT1 62 sortilin 62 syngeneic 62 anterior pituitary 62 Leukemias 62 obligate intracellular 62 ERK2 62 TET2 62 RNA ribonucleic acid 62 chromosomal regions 62 dopamine D4 receptor 62 T#I [002] 62 tryptase 62 FGFR3 62 Leydig cells 62 Fibroblast 62 HLA DR4 immune 62 GFP gene 62 protein tyrosine phosphatase 1B 62 TAp# 62 epigenetic changes 62 copper zinc superoxide 62 Moraxella bovis 62 autosomal dominant disorder 62 postnatal foreskin fibroblasts 62 malignant prostate 62 CpG island 62 Inappropriate activation 62 chromatin structure 62 Induced pluripotent stem cells 62 TRIM5 62 Ehrlichia 62 forkhead 62 HCMV 62 thymidylate synthase TS 62 IDH2 62 CpG DNA 62 epigenetically 62 Li Fraumeni syndrome 62 LPA gene 62 Lyn kinase 62 Adenoviral 62 BCL2 62 OCT4 62 transthyretin 62 histone demethylase 62 coding exons 62 A. fumigatus 62 MECP2 62 Phylogenetic analysis 62 microdeletion 62 protein phosphorylation 61 autosomal recessive disease 61 SMN2 61 synovial cells 61 paralogs 61 IRS1 61 laforin 61 transgenic mice expressing 61 mammaglobin 61 dependent RNA polymerase 61 observable traits 61 naturally occurring neuroprotective 61 enolase 61 tumor specific antigen 61 ADAMTS# 61 retinoic acid receptor 61 gene locus 61 Oncogenic 61 ß amyloid 61 activin 61 frataxin gene 61 SCN1A 61 anaplastic lymphoma kinase ALK 61 collagen VI 61 clade B 61 γ secretase 61 TMPRSS2 ERG 61 non coding RNA 61 adenomatous polyposis coli 61 ABCB1 gene 61 filaggrin 61 WNK1 61 Pten 61 epithelial cells lining 61 lacZ 61 APOE e4 61 upregulates 61 FOXP2 gene 61 abnormal methylation 61 germline cells 61 phosphorylates 61 MDR1 61 PKM2 61 #S ribosomal RNA 61 melanocyte stimulating hormone 61 Treg cell 61 genomic variants 61 BCR ABL protein 61 gene p# 61 Pier Paolo Pandolfi 61 PARP inhibition 61 MLL gene 61 APOE4 61 chloroplast genome 61 PB1 F2 61 CagA 61 phenotypic expression 61 histone acetylation 61 Apobec3 61 cisplatin resistant 61 dominantly inherited 61 hnRNP 61 TMPRSS6 61 mutant SOD1 61 mutated protein 61 Confocal microscopy 61 microRNA expression 61 Rh factor 61 #q#.# [001] 61 NPC1 61 DNA methyltransferase 61 furin 61 recessive mutations 61 CALHM1 61 lymphoblastoid cell lines 61 Chlamydia pneumoniae 61 spore formation 61 KIF6 gene 61 melanin pigments 61 DUX4 61 vacuolar 61 IgA deficiency 61 MIF protein 61 IFNg 61 IKK beta 61 gene amplification 61 IRF6 61 S. sanguinis 61 HIV reverse transcriptase 61 transmembrane protein 61 neuregulin 1 61 vitamin D receptor 61 UGT#A# * 61 Variant Creutzfeldt Jakob Disease 61 Mycoplasma pneumoniae 61 herpesviruses 61 Streptococcus agalactiae 61 number variants CNVs 61 uniparental 61 glutamic acid decarboxylase GAD 61 remains mystery Yairi 61 ubiquitylation 61 SOD2 gene 61 Rap1 61 Pten gene 61 miRNA expression profiles 61 superoxide dismutase 61 potently inhibit 61 Coxiella burnetii 61 mda 7 61 genetic alteration 61 A. thaliana 61 causal variants 61 C1q 61 bone marrow mesenchymal stem 61 iPSC lines 61 cause cardiac channelopathies 61 M. capricolum 61 intracellular bacteria 61 globin 61 methylation patterns 61 granulosa cell 61 autosomal recessive 61 CYP#D# gene 61 metalloproteinase 61 DQB1 * 61 sCD# 61 mice lacking 61 Dystrophin 61 subcellular localization 61 CYP#B# 61 chromosome aberrations 61 #S rRNA 61 kappa B 61 E. faecalis 61 hepatic lipase 61 lincRNA 61 LPA receptors 61 pleiotropic effects 61 sporadic ALS 61 neoplastic cells 61 beta actin 61 E1A 61 Nkx#.# 61 GAB2 61 ankyrin B 61 nonsense mutations 61 vimentin 61 rRNA 61 allelic variants 61 polyomavirus 61 dihydrofolate reductase 61 tRNA synthetase 61 tumor suppressor PTEN 61 nephronophthisis 61 cell adhesion molecule 61 colorectal tumor 61 epigenetic alterations 61 STK# [002] 61 luciferase gene 61 clefting 61 venom peptides 61 C. pneumoniae 61 embryonal 61 lysyl oxidase 61 protein p# 61 TMEM#B 61 mediated inhibition 61 trimeric 61 Wnt#b 61 IGFBP2 61 phenotypic variation 61 Propionibacterium acnes 61 Meckel Gruber 61 p# mutations 61 Nf1 gene 61 replicase 61 mutant alleles 61 Myb 61 GPI anchored 61 Creutzfeld Jakob disease 61 HOTAIR 61 osteoprotegerin 61 human leukocyte antigen HLA 61 caveolin 61 huntingtin gene 61 cryopyrin 61 differential gene expression 61 MMP# 61 SCD1 61 chromosomal rearrangement 61 Nedd4 61 telomere dysfunction 61 GATA4 61 CDK8 61 MALAT1 61 molecular determinants 61 mutant gene 61 LMNA gene 61 chromosome #q 61 mammary cells 61 insertions deletions 61 mutant proteins 61 mesenchymal cell 61 SGK1 61 Dr. Karsenty 61 cells overexpressing 60 pluripotent embryonic 60 susceptibility gene 60 III EGFRvIII 60 telomerase reverse transcriptase 60 Smad3 60 klotho 60 ERBB4 60 p# MAPK 60 infective agent 60 paramyxoviruses 60 Genetic variations 60 metabolomic profiles 60 HLA molecules 60 DNA hypermethylation 60 #beta HSD1 60 Dendritic cell 60 Staphylococcus epidermidis 60 inherited maternally 60 lymphocytic choriomeningitis virus LCMV 60 RNA binding 60 MMP9 60 #q# deletion 60 ApoE gene 60 Lrp5 60 estrogen receptor alpha 60 prion protein PrP 60 Helicobacter 60 p# mutation 60 Entamoeba histolytica 60 nonhereditary 60 TSC1 60 Immunohistochemical analysis 60 noncoding RNA 60 S. pombe 60 CREBBP 60 Leptospira 60 rifamycins 60 GSTP1 60 p# activation 60 focal adhesion kinase 60 PON1 gene 60 Janus kinase 60 transcriptional regulation 60 regulator CFTR gene 60 mutant huntingtin protein 60 histone deacetylase HDAC 60 Monoclonal 60 molecular abnormalities 60 #p# [003] 60 huntingtin protein 60 Coronaviruses 60 Fibroblasts 60 ribonucleic acids 60 telomerase gene 60 retrovirus XMRV 60 mitochondrial DNA mtDNA 60 myopathies 60 inactivating mutations 60 NEIL1 60 cellular prion protein 60 E3 ligase 60 p#/CBP 60 synaptogenesis 60 underlying pathophysiology 60 multiprotein complex 60 TACI mutations 60 posttranslational modifications 60 inactive X chromosome 60 transcriptional regulators 60 cybrid 60 recessive genetic 60 evolutionarily conserved 60 genomic rearrangement 60 Pax3 60 DNA rearrangements 60 neuroblastoma tumors 60 chromosomal anomalies 60 COX2 60 Mycobacterium paratuberculosis 60 defensins 60 fibrous tangles 60 overactivation 60 HMGA2 60 Trypanosoma cruzi 60 GATA3 60 amyloid cascade 60 cypin 60 survivin expression 60 GRP# 60 homeobox gene 60 antisense inhibition 60 adipogenic 60 enteroviral 60 prostate epithelial cells 60 ADPKD 60 eotaxin 60 kidney urologic 60 endogenous retrovirus 60 alpha MSH 60 familial pancreatic cancer 60 proteinase 60 mitochondrial disorders 60 biologic pathway 60 autistic enterocolitis 60 G#S [002] 60 genomic alterations 60 CNTNAP2 gene 60 transthyretin TTR 60 oncogenesis 60 HSF1 60 #q#.# [002] 60 Huntingtin 60 ADAM# 60 amyloid peptide 60 immunopathology 60 sporadic Creutzfeldt Jakob 60 P. reichenowi 60 Prion proteins 60 tumor suppressor p# 60 embryonal carcinoma 60 receptor ligand 60 misfolded protein 60 Sporadic CJD 60 amyloid plaque formation 60 chromosome #q#.# [002] 60 fatty acid binding 60 apolipoprotein E4 60 JAK2 gene 60 Eukaryotic 60 metabolome 60 Nod1 60 fungal genomes 60 indels 60 chimeric mice 60 mutated gene 60 histone methylation 60 antisense therapies 60 JAK mutations 60 autophagic 60 HGPS 60 genomic deletions 60 CETP VV 60 protein fragment 60 CEACAM1 60 HLA DRB1 * 60 ABL1 60 miRNA expression 60 nonvascular 60 neural progenitor cells 60 quantitative trait loci 60 pDC 60 genomic imprinting 60 upregulating 60 ErbB4 60 chitinase 60 FMR1 gene 60 segmental duplication 60 herpes viruses 60 microchimerism 60 KCNH2 60 Streptococcus pneumonia 60 leptin deficiency 60 FOXP3 gene 60 neuritic 60 pleiotropic 60 proteosome 60 p# tumor suppressor 60 immunotoxin 60 C. burnetii 60 CXCL5 60 Mycobacterium bovis 60 RNA splicing 60 SIRT1 gene 60 K#R [002] 60 operons 60 short hairpin RNA 60 Histone deacetylase 60 specific CD8 + 60 Plasmodium parasite 60 SLC#A# [001] 60 genetic recombination 60 malignant transformation 60 PARP1 60 multigenic 60 COMT gene 60 insulin secreting beta 60 medulloblastomas 60 progressive neurodegenerative disorders 60 leptin receptors 60 DAT1 60 conductance regulator 60 Hashimoto thyroiditis 60 BALB c 60 neuronal dysfunction 60 calcium calmodulin dependent 60 gene encodes 60 Single Nucleotide Polymorphisms 60 chromosomal rearrangements 60 chimeric 60 ABCA1 gene 60 steroidogenic 60 BRCA2 gene 60 PLA2 60 FGFR4 60 c Myb 60 pylori 60 Trichophyton rubrum 60 tyrosine phosphorylation 60 leukaemias 60 abnormal p# 60 NOD2 60 Cry1Ab 60 Notch1 60 DEC2 60 variant rs# 60 X inactivation 60 KATP channel 60 gastric carcinomas 60 ankyrin repeat 60 DUX4 gene 60 thyrotropin 60 hydrolase 60 CDK5 60 phagocytic cells 60 Spinal muscular atrophy 60 deaminase 60 mycobacterium tuberculosis 60 pancreatic islet 60 multigene 60 Polymerase 60 non mutated KRAS 60 lymphoid organs 60 squamous cell lung cancer 60 MTHFR 60 cathepsins 60 anti microbial peptides 60 ribonucleic acid RNA 60 Germline 60 PIK3CA 60 proliferative disorders 60 SLC#A# gene [001] 60 3'UTR 60 PDE#A 60 BubR1 60 downregulation 60 #S rDNA 59 pathological hallmarks 59 phylogenetic analyzes 59 #beta HSD 1 59 Dpp 59 ncRNAs 59 GPR# [002] 59 Rickettsia 59 genetically mapped 59 Her2 gene 59 Simian Immunodeficiency Virus 59 dedifferentiation 59 frameshift mutation 59 serovar 59 CYP#E# gene 59 S#A# [002] 59 IL #R 59 Arf gene 59 haematopoietic 59 Neisseria 59 metalloproteinases 59 NOTCH1 59 subcellular compartments 59 experimentally validated 59 #S rRNA gene 59 beta1 integrin 59 SNP rs# [001] 59 bacterial pathogen 59 C. trachomatis 59 Pdx1 59 PTP1B 59 bronchial epithelial cells 59 ARF1 59 RefSeq 59 activating mutations 59 Sandhoff disease 59 STK# gene 59 CHRNA5 59 Candida species 59 Panton Valentine leukocidin 59 granzyme 59 KRAS BRAF 59 lung epithelium 59 amino acid sequences 59 methylation markers 59 pseudogene 59 oncoprotein 59 wasting Creutzfeldt Jakob 59 Nup# 59 HuCNS SC ® 59 Vaxfectin formulated 59 osteopontin OPN 59 gliosis 59 granzyme B 59 heterozygosity 59 KIBRA 59 nucleus Chinnery 59 G#S mutation 59 homocystinuria 59 S. enterica 59 defective mitochondria 59 miR #a [002] 59 nucleotide sequence 59 hypereosinophilic syndrome 59 Monoamine oxidase 59 glutathione S transferase 59 doublecortin 59 gp# protein [002] 59 CCR1 59 podocytes 59 crystallin 59 #p#.# [002] 59 presenilin 59 c myb 59 simian virus 59 histone code 59 SRY gene 59 INF2 59 redox active 59 splice junctions 59 Id1 59 malayi 59 hematopoietic progenitor cells 59 Li Fraumeni 59 normal prion protein 59 X4 viruses 59 intracellular signal transduction 59 protein synthesis machinery 59 exocrine 59 gamma glutamyl 59 APOBEC3G 59 OGG1 59 small RNAs encoded 59 mutations 59 tubercle bacillus 59 resistin 59 tau gene 59 FKBP# 59 monocytes macrophages 59 budding yeast Saccharomyces 59 T#M 59 nasal epithelium 59 CNTNAP2 59 STAT3 signaling 59 HIF 1α 59 Amyloid plaques 59 N Myc 59 bacterium Listeria 59 NR#A# 59 epigenetic mechanisms 59 Protein Kinase C 59 EF Tu 59 potent inhibition 59 Epigenetics refers 59 CIB1 59 Fanconi anemia FA 59 spongiform encephalopathies 59 Beta thalassemia 59 mutant genes 59 transcriptional machinery 59 TIR1 59 cyclophilin D 59 distinct subtypes 59 Topoisomerase II 59 LRP6 59 autosomal 59 BRAF V#E mutation 59 cystic fibrosis transmembrane 59 cynomolgus macaques 59 bacterium Neisseria meningitidis 59 hypomethylation 59 glucocerebroside primarily 59 DNA demethylation 59 PI3K signaling 59 secreted proteins 59 Plasmodium parasites 59 Transcriptome 59 proapoptotic 59 aT cell 59 TEL AML1 59 mitochondrial proteins 59 heterochromatic 59 Corynebacterium 59 cholesteryl ester transfer