Related by context. All words. (Click for frequent words.) 67 chromosomal translocations 64 translocation 64 chromosomal rearrangements 62 mutations 62 gene rearrangements 62 genetic recombination 62 germline mutations 61 epigenetic modification 61 chromosomal rearrangement 61 hypermethylation 61 malignant transformation 61 orthologs 61 chromosomal deletions 61 DNA rearrangements 60 gene duplications 60 chromosome rearrangements 60 epigenetic alterations 60 genomic instability 60 X inactivation 59 SRY gene 59 mitochondrial gene 59 morphologically 59 segmental duplications 59 somatic mutations 59 missense mutations 59 microdeletions 59 DSBs 59 V#F mutation 59 indels 59 microdeletion 59 de novo mutations 59 telomeric 59 #q#.# [002] 59 LIS1 58 primate genomes 58 Dpp 58 spontaneous mutation 58 homozygosity 58 mRNAs 58 polyploidy 58 Alu elements 58 mitochondrial genomes 58 activating mutations 58 paralogs 58 coevolution 58 cytochrome b 58 introgression 58 polyploids 58 metazoan 58 DNA demethylation 58 cytokinesis 58 MLL gene 58 genomic rearrangements 58 phenotypic variation 58 alleles 57 ncRNAs 57 karyotypes 57 splice variants 57 epigenetic silencing 57 codons 57 genetic alterations 57 mutation 57 prion infection 57 ncRNA 57 chromosome translocations 57 structural rearrangements 57 virulence genes 57 neural crest cells 57 coding genes 57 proto oncogene 57 chromosomal 57 mutational 57 HAR1 57 mRNA expression 57 meiotic 57 mosaicism 57 mutant alleles 57 CHD7 57 mtDNA mutations 57 indel 57 MLL2 56 germline mutation 56 homozygotes 56 piRNAs 56 deacetylation 56 methyltransferases 56 JAK2 gene 56 spontaneous mutations 56 granule cells 56 eusociality 56 chromosomal aberrations 56 heterozygotes 56 radial glia 56 meiotic recombination 56 noncoding 56 polymerases 56 genetic rearrangements 56 nucleotide substitutions 56 MAPK pathway 56 MLH1 56 eukaryote 56 NR#A# gene 56 p# activation 56 hypermethylated 56 epigenetic mechanisms 56 micro RNAs 56 tyrosine phosphorylation 56 germline cells 56 transgene expression 56 CHEK2 56 polyploid 56 genomic alterations 56 MSH2 56 miRNA expression 56 speciation 56 DLC1 56 histone modifications 56 protein phosphorylation 56 genomic imprinting 55 inherited mutations 55 PTPN# 55 genotoxic stress 55 APOL1 55 chromosomal instability 55 Hsp# [001] 55 hyperactivation 55 PDGFR 55 mammary cells 55 HLA alleles 55 insulin signaling pathway 55 X chromosome inactivation 55 homologous recombination 55 proteolytic cleavage 55 proteolysis 55 intron 55 PGCs 55 epigenetic changes 55 phenotypically 55 heterozygous 55 isoforms 55 noncoding RNAs 55 previously undescribed 55 intergenic 55 mitochondrial DNA mtDNA 55 ectopic expression 55 RNA viruses 55 maternally inherited 55 sequence homology 55 seminomas 55 meiosis 55 sexual dimorphism 55 ribosomal proteins 55 primordial germ cells 55 TP# gene 55 missense mutation 55 phenotype 55 Kabuki syndrome 55 non coding RNA 55 phylogenetic analyzes 55 VNTR 55 constitutively expressed 55 germline 55 orthologous genes 55 transposable elements 55 GISTs 55 evolutionarily conserved 55 FGFR2 55 HLA genes 55 metazoans 55 Xenopus 55 Genetic mutations 55 gene mutations 55 distantly related species 55 microcephalin 55 heterozygosity 55 transcriptional regulation 55 amino acid substitutions 54 recombination 54 trypanosome 54 phylogenetically 54 inbreeding depression 54 phthalate syndrome 54 phylogeny 54 motor neuron degeneration 54 STAT4 54 allele frequencies 54 MC4R gene 54 neural crest 54 coding exons 54 intronic 54 centromeres 54 CGG repeats 54 VHL gene 54 untranslated regions 54 downregulation 54 3'UTR 54 aneuploidy 54 genetic loci 54 evolvability 54 evolutionary divergence 54 parthenogenetic 54 TP# mutations 54 nucleotide substitution 54 trophoblast cells 54 morphological 54 caveolae 54 X. laevis 54 monophyletic 54 SOD1 protein 54 Supplementary Fig 54 epistasis 54 heterochromatic 54 upregulation 54 heterochromatin 54 Notch1 54 KIT mutations 54 imprinted genes 54 transcriptomes 54 genetic aberrations 54 PTEN gene 54 Chromosomal 54 telomere shortening 54 RUNX3 54 mRNA transcripts 54 #q#.# [001] 54 synuclein 54 Plasmodium 54 Cyclin D1 54 FLT3 54 conformational changes 54 methyltransferase 54 ChR2 54 unmethylated 54 p# MAPK 54 missense 54 p# mutation 54 LRRK2 gene 54 homologs 54 splice junctions 54 phylogenies 54 PAX5 54 Translocation 54 hair follicle stem cells 54 epigenetic regulation 54 #p#.# [002] 54 H#K#me# 54 chromatin remodeling 54 BARD1 54 subfamilies 54 Hh pathway 54 fungal genomes 54 sexually dimorphic 54 ERK1 2 54 microRNAs miRNAs 54 exomes 54 haplotypes 54 mammalian genomes 54 brood parasitism 54 mouse embryonic fibroblasts 54 gastrulation 54 phenotypic differences 54 genomic deletions 54 nucleotide sequence 54 cytosolic 54 promoter methylation 54 synaptic proteins 54 rDNA 54 neoplastic 54 MECP2 gene 54 outcrossing 54 phenotypic traits 54 introns 53 chromosome #q# [001] 53 catenin 53 phosphatases 53 SCN5A 53 RNA polymerases 53 CYP#B# 53 exons 53 menin 53 Hox gene 53 histone modification 53 ribonucleic acids 53 quasispecies 53 prion gene 53 mutant proteins 53 orthologous 53 aneuploid 53 E#F# 53 dimorphic 53 transcriptional activation 53 chromatin structure 53 mammary stem cells 53 recombinations 53 IKZF1 53 Dysregulation 53 synaptogenesis 53 gambiae 53 globin genes 53 BMP4 53 haplotype 53 chromosomal regions 53 demethylation 53 ALK gene 53 sexually reproducing 53 microarray experiments 53 cellular prion protein 53 ribosomal DNA 53 immunofluorescence microscopy 53 embryoid bodies 53 A. thaliana 53 beta1 integrin 53 epigenetic modifications 53 Chk1 53 somatic mutation 53 prion strains 53 UTRs 53 MAPKs 53 Pten 53 cofactors 53 orangutan genome 53 histone H4 53 Leydig cells 53 monogenic 53 leukaemic stem cells 53 miRNA genes 53 TCF#L# gene 53 Genetic variation 53 chordates 53 hypomethylation 53 taxa 53 miR #a [001] 53 clefting 53 microRNA expression 53 RNA transcripts 53 phenotypes 53 socially monogamous 53 N myc 53 haematopoietic 53 cDNAs 53 Trypanosoma brucei 53 dedifferentiation 53 chimerism 53 tumorigenesis 53 bilaterians 53 PIK3CA 53 retinal neurons 53 deuterostomes 53 downregulated 53 pseudogenes 53 lincRNA 53 Smad3 53 β1 53 Drosophila genome 53 epigenetic inheritance 53 viral genome 53 clonal 53 ontogeny 53 haplogroups 53 genetic polymorphism 53 interconversion 53 acinar 53 Foxp3 53 transactivation 53 astrocytic 53 FGF signaling 53 Ehrlichia 52 mtDNA 52 neuroligins 52 herpesviruses 52 phenotypic 52 CPEB 52 chromosomal DNA 52 FUS1 52 #q# [001] 52 SVZ 52 developmental abnormalities 52 linkage disequilibrium 52 transgenic mouse model 52 acetylation 52 #S rRNA 52 mitochondrial mutations 52 p# mutations 52 #S rDNA 52 hematopoietic cells 52 BRCA1 BRCA2 52 endogenous retroviruses 52 segmental duplication 52 constitutively active 52 SMAD4 52 GSTP1 52 dephosphorylation 52 Phylogenetic analyzes 52 chromosome aberrations 52 insertions deletions 52 cyclins 52 ABCB1 52 chromosome #q#.# [002] 52 BMP signaling 52 epigenetically 52 Jhdm2a 52 CpG islands 52 genes encoding 52 MAP kinase pathway 52 #S rRNA gene 52 recessive mutation 52 reproductively isolated 52 lymphoid cells 52 Wnt signaling 52 MAP kinases 52 mammary tumors 52 heritable traits 52 ERK2 52 oncogenic transformation 52 retrotransposon 52 LRP5 52 exocytosis 52 transcriptional repressor 52 morphogen 52 COL#A# 52 ALK mutations 52 chromosomal translocation 52 KLF4 52 chromosomal anomalies 52 Wnts 52 prokaryote 52 retrotransposons 52 gene fusions 52 nucleolar 52 breast cancer genes BRCA1 52 IgA deficiency 52 testis 52 LKB1 52 peroxisome 52 CpG island 52 operons 52 transmembrane domains 52 coexpression 52 organismal 52 multiprotein complex 52 somites 52 pseudogene 52 histone 52 BRAF gene 52 metaplasia 52 primary cilium 52 genetic mutations 52 gastric carcinogenesis 52 ortholog 52 DNA replication 52 allelic 52 cysteine residues 52 bacterial genomes 52 anaphase 52 reproduce asexually 52 homologous genes 52 methylation 52 HOX genes 52 genetic manipulations 52 CTVT 52 fatty acid synthesis 52 MC1R gene 52 RNA sequences 52 #p# [003] 52 homologous chromosomes 52 polyglutamine 52 PON1 52 microglial 52 functional polymorphism 52 cysteines 52 stathmin 52 mutated protein 52 NR#A# 52 substrate specificity 52 caveolin 52 organogenesis 52 translocated 52 Sonic Hedgehog 52 terrestrial vertebrates 52 polymorphisms 52 ABCB1 gene 52 homodimers 52 MeCP2 gene 52 Sp1 52 Dictyostelium 52 tumor suppressor genes 52 mammary cancers 52 mice lacking 52 guanine G 52 gene inactivation 52 trinucleotide 52 ant genomes 52 gene locus 52 ZEBOV 52 genotypic 52 microRNA molecules 52 Prox1 52 polynucleotides 52 sporadic ALS 52 blastomeres 52 rearrangements 52 TERT 52 transduced 52 Rickettsia 52 homolog 52 motoneurons 52 overactivation 52 mutated genes 52 colocalization 52 c myc 52 tumor suppressor gene 52 6S RNA 51 neoplastic transformation 51 apoptosis pathway 51 allelic variation 51 Phylogenetic analysis 51 melanistic 51 nucleotide sequences 51 KRAS oncogene 51 CDK4 51 genetic abnormalities 51 Hox genes 51 mitochondrial genome 51 eukaryotic organisms 51 cell adhesion molecules 51 endogenous retrovirus 51 neuroblastomas 51 eusocial 51 H#K# methylation 51 hematopoietic progenitors 51 SLC#A# gene [002] 51 karyotype 51 FMR1 51 commensal bacteria 51 immunological responses 51 cyclin E 51 metaphase 51 differentially expressed genes 51 perilipin 51 lineages 51 pRb 51 overexpression 51 HGPS 51 simian immunodeficiency virus 51 #BP# 51 DNA methylation 51 homologues 51 focal adhesions 51 primate evolution 51 endosymbiosis 51 cAMP signaling 51 polyadenylation 51 chromosome condensation 51 mesoderm 51 CDH1 51 Heterodontosaurus 51 overexpressing 51 misfolding 51 microsatellite markers 51 HbF 51 transcriptome 51 antisense oligonucleotides 51 alternatively spliced 51 eukaryotic genomes 51 coding sequences 51 thymocytes 51 PALB2 51 aneuploid cells 51 NKT cells 51 Aspergillus species 51 INF2 51 hammerhead ribozyme 51 recessive trait 51 adult neurogenesis 51 neuronal dysfunction 51 transgenes 51 vertebrate embryos 51 cybrid 51 interneurons 51 PrPSc 51 transfected cells 51 budding yeast 51 ontogenetic 51 transcriptionally 51 JAK2 enzyme 51 pathogenic mutations 51 CRISPR 51 deleterious mutations 51 N Myc 51 microglial cells 51 EBV infection 51 ubiquitination 51 malignant phenotype 51 Cre recombinase 51 ionic currents 51 genetic locus 51 A. gambiae 51 SLITRK1 51 TSC1 51 transmembrane 51 IL 1ß 51 Neandertal DNA 51 activating mutation 51 Htt 51 aneuploidies 51 phylogenetic relationships 51 hybridisation 51 senescent cells 51 etiologic 51 IL 1β 51 glycosylation 51 M. genitalium 51 short hairpin RNAs 51 potent inhibitors 51 CTCF 51 phylogenetic analysis 51 germinal center 51 chromosomal abnormalities 51 Phylogenetic 51 subfamily 51 DNA methylation patterns 51 IDH1 51 Overexpression 51 trematodes 51 BMAL1 51 morphogenesis 51 cellular pathways 51 CEACAM1 51 molecular scissors 51 endocytic 51 microglial activation 51 vasopressin receptor 51 messenger RNAs mRNAs 51 bacterial symbiont 51 Arabidopsis genome 51 mutagenesis 51 Borrelia 51 sister chromatid 51 aberrant methylation 51 signaling cascade 51 ecotypes 51 Kufs disease 51 chimeric mice 51 TMEM#B 51 proteins encoded 51 γδ T cells 51 Xenopus laevis 51 intergenic regions 51 sensu lato 51 transthyretin 51 syngeneic 51 conserved sequences 51 tau gene 51 QTLs 51 leucocytes 51 transgene 51 Immunohistochemical analysis 51 cytosine 51 beta catenin protein 51 cohesin 51 Mcl 1 51 proapoptotic 51 evolutionary lineages 51 protein isoforms 51 primordial follicles 51 tetramers 51 COX2 51 protein tyrosine phosphatase 51 CYP# [002] 51 hamartomas 51 uPAR 51 HLA molecules 51 Mesenchymal 51 heterozygote 51 IGF1 51 beta globin 51 autoinflammatory diseases 51 hermaphroditism 51 PKD1 51 PER2 51 ependymomas 51 genetic alteration 51 viral genomes 51 multi celled organisms 51 SCN1A 51 DNA methyltransferase 51 Fragile X gene 51 amino acid substitution 51 palmitoylation 51 shortened telomeres 51 amyloid fibrils 51 GenBank accession 51 membrane fusion 51 hantaviruses 51 succinate dehydrogenase 51 lysine residues 51 proteomes 51 autosomes 51 CD#c 51 CYP#C# [002] 51 gene deletions 51 mutant protein 51 signaling cascades 51 autophagic 51 sympatric speciation 51 oncogenes 51 hippocampal neurons 51 receptor tyrosine kinase 51 adipogenic 51 lincRNAs 51 At#g# 51 archaeal 51 overexpress 50 hematopoetic stem cells 50 ashy storm petrels 50 GIST tumors 50 haploid 50 C#Y 50 gene expression patterns 50 TTR gene 50 selfing 50 ERK signaling 50 proteins misfold 50 susceptibility genes 50 Akt1 50 nonsense mutation 50 herpes viruses 50 RNA splicing 50 FMR1 gene 50 alanine 50 fig. S1 50 ploidy 50 SERT gene 50 antigenic shift 50 caveolin 1 50 enzymatic activity 50 microsporidia 50 placental mammals 50 GPR# [002] 50 autosomal recessive 50 immunohistochemical analysis 50 BRAF V#E 50 inbred strains 50 EGFR gene 50 mutant p# 50 cis regulatory 50 LRP6 50 susceptibility loci 50 C. neoformans 50 Nf1 50 antigenic variation 50 centrosome 50 K ras 50 ribosomal protein 50 ribozyme 50 dimerization 50 synthases 50 pea aphid 50 neural precursor 50 noncoding RNA 50 Alleles 50 mycoplasmas 50 SMN1 50 mitochondrial proteins 50 KCNH2 50 unicellular organisms 50 genome rearrangements 50 RNAs 50 osteosarcomas 50 gene amplification 50 genetic defects 50 FANCD2 50 dinucleotide 50 embryogenesis 50 Mutations 50 commensal 50 morphogens 50 pre malignant lesions 50 centrioles 50 eukaryotic cells 50 amyloid deposition 50 K ras gene 50 morphologically distinct 50 mangabeys 50 convergent evolution 50 Acanthostega 50 HBx 50 clades 50 opsins 50 Golgi apparatus 50 neurite outgrowth 50 nucleolus 50 da mage 50 allele frequency 50 NFkB 50 MYH9 gene 50 PIP2 50 germ cells 50 unmutated 50 SIV infection 50 paternally inherited 50 transgenic rats 50 allelic variants 50 cisplatin resistant 50 organism genome 50 myofibroblasts 50 KCNE2 50 penetrance 50 thioredoxin 50 outbred 50 melanogaster 50 clonally 50 frameshift mutation 50 methylation patterns 50 olfactory receptor 50 proinflammatory mediators 50 gliosis 50 DEAR1 50 constitutively 50 homologous 50 mediated inhibition 50 gut microbiota 50 mutant SOD1 50 BMP2 50 HOTAIR 50 Fig. 1b 50 nucleotide 50 ZNF# 50 OGG1 50 mitochondrial genome sequence 50 hyperplastic 50 cathepsins 50 MDSCs 50 lung adenocarcinoma 50 striated muscle 50 transgenic mice expressing 50 ribosomal RNA 50 neural cells 50 endostatin 50 receptor gene 50 GAPDH 50 genomic variants 50 NFKBIA 50 tumor suppressor protein 50 plasma kallikrein 50 rRNA 50 faunas 50 podocytes 50 basal cell nevus syndrome 50 parkin gene 50 telomere dysfunction 50 monozygotic twins 50 phylogenetic trees 50 translocates 50 KCNQ1 50 oncogenic 50 dizygotic 50 DNMT1 50 Ets2 50 genetic relatedness 50 EZH2 50 medulloblastomas 50 molecular abnormalities 50 artiodactyls 50 phagocytic cells 50 chromosome #q# [002] 50 kinase domain 50 Chromosomes 50 germline stem cells 50 BDNF gene 50 BRAF protein 50 mRNA molecules 50 antigenic epitopes 50 mutated gene 50 CD1d 50 HERV 50 cDNA libraries 50 Notch signaling pathway 50 MEFs 50 L. pneumophila 50 HSCs 50 Plasmodium parasites 50 TGF beta signaling 50 JAK2 50 morphologic 50 somatic cells 50 cardiac progenitor cells 50 metabolic enzymes 50 endonuclease 50 subcellular compartments 50 FXTAS 50 TRIM5 50 S. enterica 50 Rad# 50 placental mammal 50 eotaxin 50 NKG2D 50 morphological traits 50 dimers 50 micronuclei 50 Cathepsin B 50 copper zinc superoxide 50 normal karyotype 50 Amino acid 50 amplicons 50 effector molecules 50 glutamate receptor 50 ERBB2 50 neuroepithelial cells 50 multipotent 50 Activating mutations 50 ciliated 50 LRAT 50 nonhereditary 50 causal variants 50 isotypes 50 DNA polymerases 50 allele 50 differential gene expression 50 cnidarians 50 Single Nucleotide Polymorphisms SNPs 50 mesenchymal cells 50 transposons 50 progerin 50 leiomyoma 50 chromosome #p#.# 50 superfamily 50 ribonucleic acid RNA 50 tau aggregates 50 T. gondii 50 antigenic 50 MyoD 50 α synuclein 50 NETs 50 transgenic mouse models 50 β catenin 50 SIRT3 50 alternative splicing 50 gene mutation 50 multicellular organisms 50 PTEN protein 50 FasL 50 Entamoeba 50 protein misfolding 50 symbioses 50 #p#.# [001] 50 S. pombe 50 helicases 50 lacZ 50 transcriptional machinery 50 apoE4 50 LPA gene 50 alpha synuclein gene 50 K ras mutations 50 genetic variation 50 AhR 50 Or#b 50 C1q 50 microbiome 50 receptor mediated endocytosis 50 colugos 49 mutant gene 49 lymphatic tissues 49 Skp2 49 receptor kinase 49 miR# 49 HepG2 cells 49 flatfishes 49 recombination hotspots 49 SHANK3 49 LRRK2 mutation 49 Rap1 49 chaperone proteins 49 poly dA 49 EBNA1 49 superior colliculus 49 NF2 49 bdelloids 49 glycoproteins 49 D. melanogaster 49 sRNA 49 TMPRSS2 ERG fusion 49 honeybee genome 49 vesicle fusion 49 leukemic cell 49 histone H3 49 ligand receptor 49 RAR beta 49 Caenorhabditis 49 synapse formation 49 E cadherin 49 cytochrome c oxidase 49 clade C 49 parasitoid 49 R#W [002] 49 ApoE4 49 TP# mutation 49 mesenchymal cell 49 KRAS gene