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(Click for frequent words.) 85 mutation 82 genetic mutations 79 gene mutations 76 genes 75 alleles 74 mutated genes 73 genetic mutation 72 gene 72 gene mutation 72 genetic alterations 71 mutated gene 71 genetic variants 70 spontaneous mutations 70 polymorphisms 69 gene variants 69 genetic variations 69 genetic abnormalities 68 mtDNA mutations 67 susceptibility genes 67 mutant gene 67 germline mutations 67 methylation 67 missense mutations 67 chromosomal translocations 67 genetic variation 67 miRNAs 66 tumor suppressor genes 66 somatic mutations 66 LRRK2 gene 66 phenotype 66 genotypes 66 genetic variant 66 proteins 66 BRAF gene 66 genomes 66 CNVs 65 SNPs 65 mutational 65 genes encoding 65 mitochondrial mutations 65 chromosomal 65 loci 65 genetic defects 65 BRCA1 gene 65 VHL gene 65 tumor suppressor gene 65 spontaneous mutation 65 mRNAs 65 virulence genes 65 inherited mutations 65 phenotypes 65 BRCA2 gene 65 genomic rearrangements 64 mutant alleles 64 noncoding RNAs 64 FMR1 gene 64 hypermethylation 64 TP# mutation 64 genetic alteration 64 genomic instability 64 mutant genes 64 Alu elements 64 MLH1 64 breast cancer genes BRCA1 64 MSH2 64 heterozygous 64 C#Y 64 chromosomal abnormalities 64 chromosomal rearrangements 64 PTPN# 64 microcephalin 64 RNAs 64 epigenetic changes 64 gene variant 64 polymorphism 64 microdeletions 63 miRNA genes 63 HLA genes 63 epigenetic alterations 63 p# mutations 63 chromosomal aberrations 63 MTHFR 63 mitochondrial dysfunction 63 haplotype 63 micro RNAs 63 FGFR2 63 de novo mutations 63 X chromosome 63 medulloblastomas 63 mutant protein 63 germline mutation 63 NF1 gene 63 imprinted genes 63 susceptibility gene 63 LRRK2 63 G#S mutation 63 PTEN gene 62 translocations 62 epigenetic silencing 62 genomic alterations 62 mosaicism 62 gene rearrangements 62 familial ALS 62 microRNA molecules 62 LIS1 62 genetic defect 62 PALB2 62 epigenetic mechanisms 62 EGFR gene 62 chromosomal rearrangement 62 microRNAs 62 chromosomal instability 62 chromosomes 62 CDH1 62 MECP2 gene 62 defective gene 62 deleterious mutations 62 pathogenic mutations 62 aneuploidy 62 TACI mutations 62 kinases 62 herpesviruses 62 nonsense mutations 62 mRNA molecules 62 genetic abnormality 62 parkin gene 62 causal variants 62 mammary cells 62 coding sequences 62 ncRNAs 62 genes BRCA1 61 CHD7 61 Mutations 61 endogenous retroviruses 61 DNA methylation 61 proto oncogene 61 genetic 61 epigenetically 61 H#Y 61 overexpression 61 TP# gene 61 gene expression patterns 61 gene expression 61 heterozygotes 61 RNA viruses 61 enzymatic activity 61 mutated protein 61 APOE4 61 BRCA1 61 TMEM#B 61 PTEN mutations 61 chromosome 61 RUNX3 61 CFTR gene 61 chromosomal regions 61 MeCP2 gene 61 genome 61 heterozygote 61 EGFR mutations 61 acetylation 61 mutant proteins 61 malignant transformation 61 epigenetic 61 DSBs 61 allele 61 mtDNA 60 oncogenes 60 BRCA1 mutations 60 BRCA2 60 homozygosity 60 missense mutation 60 transgene 60 haplotypes 60 HGPS 60 RNA molecules 60 WT1 60 LRAT 60 ApoE4 gene 60 paralogs 60 familial pancreatic cancer 60 ALK gene 60 genetic markers 60 MC1R gene 60 suppressor gene 60 Foxp3 60 methylation patterns 60 Skp2 60 mutated 60 #q#.# [001] 60 metabolic enzymes 60 causative genes 60 #q# [001] 60 introns 60 IKZF1 60 homologs 60 KRAS oncogene 60 homozygous 60 histone modifications 60 oncogenic 60 bacterial genomes 60 beta1 integrin 60 protein kinases 60 Mycobacterium tuberculosis 60 yeast genome 60 tyrosine phosphorylation 60 IDH2 60 MTHFR gene 60 molecular abnormalities 60 MLL gene 60 monogenic 60 maternally inherited 60 autoantibodies 60 genetic aberrations 60 chromosome rearrangements 60 huntingtin gene 60 Notch1 60 protein encoded 60 HbF 60 cystic fibrosis transmembrane conductance 60 DNA sequences 60 nucleotide sequence 60 GBM tumors 60 NF1 60 multidrug resistance 60 MLL2 60 huntingtin protein 60 PIK3CA 60 uPAR 60 ZNF# 60 subtypes 60 basal cell nevus syndrome 60 germline 59 Akt1 59 SOD1 gene 59 genomic deletions 59 genotype 59 APOL1 59 Jhdm2a 59 MYH9 gene 59 sporadic ALS 59 transcription factors 59 IDH1 59 ubiquitination 59 nucleotide substitutions 59 miRNA expression 59 pseudogenes 59 tumor suppressor protein 59 K#R [002] 59 endostatin 59 chromosomal alterations 59 alpha synuclein gene 59 DLX5 59 globin genes 59 histone modification 59 CGG repeats 59 Prox1 59 TCF#L# gene 59 progranulin gene 59 viral genomes 59 heterochromatin 59 herpes viruses 59 germ cells 59 aneuploidies 59 MAPK pathway 59 molecular pathways 59 splice junctions 59 EBNA1 59 exons 59 activating mutations 59 mitochondrial 59 mice lacking 59 hypermethylated 59 Genetic mutations 59 genetic makeup 59 somatic mutation 59 genetic polymorphisms 59 autosomal recessive 59 progranulin 59 SORL1 59 segmental duplications 59 mRNA transcripts 59 GSTP1 59 FTLD 59 Htt 59 LQTS 59 SCN5A 59 IgA deficiency 59 CYP#D# gene 59 microdeletion 59 chromosome #q# [001] 59 promoter methylation 59 phenotypic variation 59 miRNA 59 CDKN2A 59 telomere shortening 59 RNA sequences 59 Fragile X gene 59 Plasmodium 59 cyclin D1 59 homozygotes 59 nonsense mutation 59 ALK mutations 59 primary cilia 59 isoforms 59 nucleotide 58 chromatin structure 58 H#K# methylation 58 Methylation 58 DNA rearrangements 58 neuroblastomas 58 deacetylation 58 Wwox 58 pRb 58 mammalian cells 58 pneumococci 58 beta catenin 58 HNPCC 58 mitochondrial gene 58 outer membrane proteins 58 p# [001] 58 FLT3 58 commensal bacteria 58 #q#.# [002] 58 genetic rearrangements 58 autism susceptibility genes 58 E#F# 58 chromosomal deletions 58 autosomal 58 SOD1 protein 58 gene amplification 58 genetically 58 small RNAs 58 cellular pathways 58 chromosome abnormalities 58 viral genome 58 EZH2 58 MDM2 58 glycoproteins 58 BRAF V#E 58 LKB1 58 BRAF protein 58 chromosome aberrations 58 T. gondii 58 SRY gene 58 IDH1 mutation 58 centromeres 58 mutated BRCA1 58 alternatively spliced 58 EBV infection 58 non coding RNA 58 epigenetic modifications 58 STK# [002] 58 single nucleotide polymorphism 58 HLA alleles 58 BRAF mutation 58 BRIP1 58 HLA B# 58 LMNA 58 codons 58 CHEK2 58 oncoproteins 58 amino acid substitutions 58 PON1 58 linkage disequilibrium 58 non coding RNAs 58 viral proteins 58 Cyclin D1 58 karyotypes 58 Six3 58 polymerases 58 GSTM1 58 eukaryotic cells 58 CCR5 delta# 58 Mutation 58 C. neoformans 58 exomes 58 PKM2 58 orthologs 58 alpha synuclein 58 Plasmodium parasites 58 transgenes 58 gene sequences 58 signaling pathway 58 tumors 58 piRNAs 58 Pten 58 Pin1 58 microRNAs miRNAs 58 splice variants 58 K ras gene 58 BRCA1 BRCA2 58 recombination 58 Rad# 58 breast cancer metastasis 58 kinase gene 58 methyltransferases 58 KRAS gene 58 retrovirus 58 GNAQ 58 shRNAs 58 transgene expression 58 K ras mutations 58 oncogene 58 mutant worms 58 transcriptional repressor 58 HMGA2 58 BRCA mutations 58 tumorigenesis 58 RASSF1A 58 p# gene 58 Wnt signaling 58 genetic recombination 58 BRCA genes 58 germline cells 58 lincRNAs 58 V#F mutation 58 protein isoforms 58 ovarian tumors 58 unmethylated 58 epithelial tissues 58 gene locus 58 mitochondrial proteins 58 NFKBIA 58 ERK2 58 conserved sequences 58 bacterial strains 57 mesotheliomas 57 SGK1 57 Epstein Barr virus EBV 57 medulloblastoma 57 MGUS 57 transposable elements 57 recessive mutations 57 activating mutation 57 estrogen receptor 57 N. gonorrhoeae 57 SMN1 57 micro RNA 57 KIT mutations 57 IGF2 57 sRNA 57 NKT cells 57 misfolding 57 amino acid sequence 57 E cadherin 57 Clusterin 57 evolutionarily conserved 57 APOE e4 57 mitochondrial genes 57 X inactivation 57 primate genomes 57 indels 57 N Myc 57 CYP#E# gene 57 signaling pathways 57 neuroligins 57 JAK mutations 57 FMR1 57 CDK4 57 chromatin proteins 57 heritable 57 epigenetic modification 57 BRCA mutation 57 epigenetic regulation 57 myostatin gene 57 cDNAs 57 amino acid sequences 57 mycobacterium 57 CAG repeats 57 gene duplications 57 SMN1 gene 57 genes predisposing 57 molecular pathway 57 intron 57 Smad3 57 ADPKD 57 promoter hypermethylation 57 tyrosine kinases 57 transcription factor 57 TAp# 57 genetic polymorphism 57 lung adenocarcinoma 57 Plasmodium falciparum 57 glycosylation 57 miR #b [001] 57 chromosome #q#.# [001] 57 M. pneumoniae 57 synapse formation 57 trypanosomes 57 CRISPR Cas 57 coding genes 57 frameshift mutation 57 mammary cancers 57 microglial cells 57 tumor suppressors 57 senescent cells 57 lymphomas 57 IDH1 gene 57 HOTAIR 57 gut microbes 57 #q# [002] 57 untranslated regions 57 short hairpin RNAs 57 SMN2 gene 57 HPV# 57 ERBB2 57 BARD1 57 Activating mutations 57 CCL#L# 57 amyloid deposits 57 proteases 57 synaptogenesis 57 MSH6 57 Apobec3 57 beta globin gene 57 SMN2 57 coding exons 57 chromosome abnormality 57 chromosome translocations 57 X chromosomes 57 KRAS mutations 57 genes CYP#C# 57 Wolbachia 57 FANCD2 57 oncoprotein 57 Tregs 57 PAX5 57 recessive trait 57 alternative splicing 57 melanocyte 57 p# protein 57 GFP gene 57 subtype 57 overexpress 57 ectopic expression 57 chitinase 57 familial adenomatous polyposis 57 clusterin 57 recessive mutation 57 VIPR2 57 amino acid substitution 57 antibodies 57 mammalian genomes 57 genomic 57 proteolysis 57 androgen receptor 57 ubiquitylation 57 JAK2 mutation 57 NR#A# gene 57 tumor suppressor 57 palladin 57 autosomal dominant 57 unmutated 57 A. thaliana 57 noncoding 57 DLC1 57 NKX#.# 57 antisense RNA 57 TSC1 57 amino acid residues 57 vimentin 57 TRIM5 57 breast carcinomas 57 epigenetic marks 57 Hsp# [001] 57 genotoxic stress 57 neuroinflammation 57 protein p# 57 neuroblastoma tumors 57 microRNA expression 57 nestin 57 recessive genes 57 SLITRK1 57 genetic determinants 57 beta thalassemia 56 cyclin E 56 homologous recombination 56 menin 56 TET2 56 variants 56 APOE 56 epigenetic markers 56 STAT3 56 genetic loci 56 HDACs 56 Drosophila genome 56 Dpp 56 intergenic 56 NFkB 56 OGG1 56 sequence homology 56 Wnts 56 receptor protein 56 RNA transcripts 56 HLA molecules 56 globin 56 TGFBR1 * 6A 56 synuclein 56 H#K# [001] 56 suppressor genes 56 gene fusions 56 caveolin 56 trypanosome 56 upregulation 56 transgenic rats 56 allelic variants 56 Velculescu 56 ependymomas 56 genetic susceptibility 56 virulence factors 56 #p#.# [002] 56 Candida species 56 transcriptional repression 56 genetic traits 56 abnormalities 56 genetic manipulations 56 mitochondrial genome 56 causative gene 56 gene variation 56 primordial germ cells 56 Cx# [001] 56 QTLs 56 APOC3 56 TFIIH 56 presenilin 56 BCL#A 56 PAK1 56 rs# [003] 56 mutant allele 56 constitutively 56 gene loci 56 leukemic cells 56 neural crest 56 antigenic 56 Vpu 56 homodimers 56 M. genitalium 56 motor neuron degeneration 56 5 hydroxymethylcytosine 56 genetic variants associated 56 phenotypic 56 transthyretin 56 prion strains 56 neoplastic 56 granule cells 56 Rap1 56 Helicobacter 56 mitochondria 56 MYCN amplification 56 penetrance 56 SMAD4 56 mRNA 56 CagA 56 allele frequencies 56 HLA DQ2 56 PrPSc 56 SATB1 56 BMPR2 56 TTR gene 56 transactivation 56 TP# mutations 56 mutagenesis 56 JAK2 gene 56 progerin 56 defensin 56 DNA methylation patterns 56 modifier genes 56 mitochondrial genomes 56 sortilin 56 enteroviruses 56 apoE4 56 Kufs disease 56 Peutz Jeghers syndrome 56 p# activation 56 DNMT1 56 epigenomes 56 hematopoetic stem cells 56 Aβ 56 SIRT3 56 MC1R 56 Mitochondrial 56 tau mutation 56 chromosome #q# [002] 56 yeast cells 56 K#N 56 epitopes 56 apolipoprotein E gene 56 ultraconserved elements 56 immunoglobulin genes 56 HCMV 56 substrate specificity 56 lung tumors 56 MC4R gene 56 neural cells 56 aneuploid cells 56 B lymphocytes 56 RNA splicing 56 phosphatases 56 fungal genomes 56 FOXP2 gene 56 EGFR mutation 56 eukaryote 56 overexpressing 56 gene APOE4 56 DNA replication 56 shortened telomeres 56 retroviruses 56 parainfluenza virus 56 metastasis 56 GPx 56 transcriptional regulation 56 EGFRvIII 56 phosphorylation 56 miR 56 metalloprotease 56 connexin 56 regulator CFTR gene 56 progenitor cells 56 colorectal tumors 56 HSCs 56 HFE gene 56 mutant huntingtin protein 56 proteins encoded 56 basal cells 56 SLC#A# [002] 56 prion protein gene 56 CFTR 56 CHD5 56 P. falciparum 56 Bcl2 56 Li Fraumeni syndrome 56 resistant isolates 56 ARID1A 56 Tumours 56 Hox gene 56 tau protein 56 brain lesions 56 #S rRNA 56 cyclins 56 tau gene 56 ABCA1 56 PTEN mutation 56 biochemical pathways 56 genomic variants 56 phenotypically 56 ApoE4 56 HLA DRB1 55 gamma globin gene 55 ApoE 55 Genetic variation 55 tumor cells 55 abnormal proteins 55 nicotinamide 55 PKD1 55 PTEN protein 55 LRP5 55 aneuploid 55 E1A 55 cancers 55 C1q 55 prion proteins 55 IL#R 55 FGFR3 55 androgen receptor gene 55 catenin 55 KCNQ1 55 amyloid deposition 55 PTP1B 55 mitochondrial DNA mtDNA 55 Akt 55 APOE ε4 55 Leydig cells 55 tRNAs 55 narcolepsy cataplexy 55 SORL1 gene 55 IFN gamma 55 neuraminidases 55 Arabidopsis 55 chloroplasts 55 BRCA2 mutation 55 KCNE2 55 GSTT1 55 telomere length 55 OCT4 55 #S rRNA gene 55 Hox genes 55 intronic 55 telomere dysfunction 55 premalignant 55 transcriptome 55 hypomethylation 55 BRCA1 mutation 55 APOE gene 55 isotypes 55 RNA molecule 55 Wnt pathway 55 virulence determinants 55 HOX genes 55 mutant strains 55 constitutively expressed 55 iNOS 55 PHLPP 55 miR #a [001] 55 CYP#C# [002] 55 invadopodia 55 Epstein Barr virus 55 MAPCs 55 JAK2 enzyme 55 CYP#B# 55 recombinants 55 phosphorylate 55 ERCC1 55 DHFR 55 variant alleles 55 histone deacetylases 55 downregulated 55 KLF4 55 MIF protein 55 pDCs 55 GISTs 55 microRNA 55 genetic variability 55 AAV2 55 ubiquitinated 55 tRNA synthetase 55 transfected cells 55 STAT4 55 epistasis 55 miR# 55 GAPDH 55 FMRP protein 55 sCJD 55 PALB2 gene 55 mesenchymal cells 55 abnormal chromosome 55 gene encoding 55 organism genome 55 clonally 55 metabolic abnormalities 55 HTLV 55 intracellular bacteria 55 palmitoylation 55 leukaemias 55 RPE# 55 SPINK1 55 aberrant methylation 55 leukemic stem cells 55 RNA polymerase II 55 operons 55 GIST tumors 55 genomic imprinting 55 ABCB1 55 neurones 55 precursor lesions 55 staphylococci 55 HSF1 55 PP2A 55 protein fragment 55 carcinogenesis 55 Polymorphisms 55 kinase 55 myelination 55 BDNF gene 55 molecular mechanism 55 enterotypes 55 osteopontin 55 signaling molecule 55 abnormal prions 55 membrane fusion 55 Genetic variants 55 prion gene 55 activin 55 FGFR1 55 p# mutation 55 laforin 55 clades 55 PrP 55 Hh 55 IGFBP2 55 HepG2 cells 55 prion protein 55 c Myc 55 mRNA expression 55 INF2 55 Th# cells 55 FXTAS 55 isoform 55 homozygote 55 KLF# 55 mutant strain 55 KIF6 gene 55 Stat5 55 diploid cells 55 L. pneumophila 55 prion infection 55 SLC#A# [001] 55 endometrial cancers 55 homologues 55 rifamycins 55 methylenetetrahydrofolate reductase 55 apoE 55 polymerase 55 synthases 55 Src 55 BRCA2 gene mutations 55 fusion protein 55 APOE4 gene 55 pilocytic astrocytomas 55 meiotic recombination 55 microsatellite instability 55 genetic modifiers 55 microglial 55 lymphoid 55 lysosomal 55 c Myb 55 LRRK2 mutation 55 gene expression profiles 55 protein 55 MEF2D 55 colon tumors 55 CD8 + 55 PDGFR 55 allelic variation 55 Ets2 55 replicative 55 malaria parasite 55 CD8 cells 55 GPC5 55 transmembrane protein 55 immune responses 55 innate immune responses 55 hyperactivation 55 PML RARA 55 methylated 55 genetic sequences 55 mitochondrial disorders 55 CEACAM1 55 epigenome 55 peroxisome 55 ubiquitin ligases 55 colocalization 55 anaplastic lymphoma kinase 55 lineages 55 short hairpin RNA 55 ADAM# 55 MIF gene 55 globin gene 55 #p#.# [001] 55 metazoan 55 transgenic mice 55 IGF 1R 55 EphB4 55 thioredoxin 55 ribosomal protein 55 CREBBP 55 chromosomal anomalies 55 XBP1 55 HDAC inhibitors 55 FOXP3 55 NEDD9 55 osteosarcomas 55 GPR# [002] 55 nucleoli 55 transgenic mouse model 55 monozygotic twins 55 PARP inhibition 55 Myc 55 GBA mutations 54 TGF β 54 HPVs 54 JAK STAT 54 metastases 54 SOD1 54 Chromosomes 54 p# MAPK 54 receptor gene 54 crystallin 54 mutant mice 54 NF2 54 MYH9 54 lymphocytes 54 CCR5 gene 54 PDGFRA 54 transcriptional 54 BCR ABL 54 riboswitches 54 ribosomal proteins 54 Y chromosome 54 RAR beta 54 EGF receptors 54 receptor molecule 54 clefting 54 c myc 54 VKORC1 54 PB1 F2 54 secretory pathway 54 succinate dehydrogenase 54 T lymphocytes 54 Inactivation