Related by context. All words. (Click for frequent words.) 70 LIS1 70 gene rearrangements 70 chromosomal rearrangements 69 VHL gene 69 mitochondrial dysfunction 68 chromosomal rearrangement 68 genomic instability 68 virulence genes 68 Alu elements 68 missense mutations 67 chromosomal aberrations 67 mosaicism 67 microdeletion 67 epigenetic regulation 67 spontaneous mutations 67 translocations 67 de novo mutations 67 MECP2 gene 67 mutations 67 neural crest 67 germline mutations 66 mtDNA mutations 66 splice variants 66 epigenetic silencing 66 epigenetic alterations 66 somatic mutations 66 genomic alterations 66 V#F mutation 66 DNA demethylation 66 malignant transformation 66 PTPN# 66 sporadic ALS 66 chromatin structure 66 chromosome translocations 66 somatic mutation 66 splice junctions 65 molecular abnormalities 65 #q#.# [002] 65 synaptogenesis 65 transcriptional regulation 65 histone modifications 65 neuroligins 65 evolutionarily conserved 65 non coding RNA 65 cellular pathways 65 serine protease 65 progranulin gene 65 metabolic enzymes 65 protein misfolding 65 epigenetic mechanisms 64 CHD7 64 genomic imprinting 64 noncoding RNAs 64 gene duplications 64 Fas ligand 64 chromosomal regions 64 epigenetic modification 64 genetic loci 64 STAT4 64 genomic deletions 64 MSH2 64 genotoxic stress 64 proto oncogene 64 apoptotic pathway 64 APOL1 64 BARD1 64 Genetic variation 64 genetic polymorphism 64 mitochondrial gene 64 genomic rearrangements 64 missense mutation 64 Smad3 64 clefting 64 segmental duplications 64 DNA rearrangements 64 chromosomal instability 64 LRP5 63 BRAF gene 63 TCF#L# gene 63 microdeletions 63 neuronal dysfunction 63 nucleotide sequence 63 primate genomes 63 alpha synuclein gene 63 posttranslational modifications 63 DNA methylation patterns 63 polyploidy 63 3'UTR 63 gene locus 63 miRNA genes 63 Wnt signaling pathway 63 RNA sequences 63 MC4R gene 63 motor neuron degeneration 63 mutant alleles 63 meiotic recombination 63 chromosomal deletions 63 tyrosine phosphorylation 63 epigenetic changes 63 Cathepsin B 63 p# activation 63 p# mutations 63 MLL gene 63 airway remodeling 63 genetic mutations 63 PTEN gene 63 hypermethylation 63 RUNX3 63 acetylation 63 activating mutations 63 Prox1 63 signaling cascades 63 tumor suppressor protein 63 LRRK2 gene 63 phenotypic variation 63 substrate specificity 63 phenotypic expression 63 Htt 63 HGPS 63 metazoan 63 MDR1 63 MLH1 63 neurite outgrowth 62 paralogs 62 p# MAPK 62 micro RNAs 62 susceptibility genes 62 mitochondrial mutations 62 medulloblastomas 62 orthologs 62 LRRK2 62 KLF4 62 methyltransferases 62 amino acid substitutions 62 apoE 62 CNTNAP2 62 pRb 62 #q#.# [001] 62 rDNA 62 H#Y 62 tumorigenicity 62 phenotypic differences 62 chromosome aberrations 62 Genetic mutations 62 microRNAs miRNAs 62 airway hyperresponsiveness 62 MAPK pathway 62 mesenchymal cell 62 radial glia 62 epigenetic inheritance 62 alternatively spliced 62 genetic recombination 62 herpesviruses 62 cell signaling pathways 62 Kufs disease 62 hypermethylated 62 miRNA expression 62 Activating mutations 62 mRNA transcripts 62 FGFR2 62 autoinflammatory diseases 62 mitochondrial disorders 62 genetic alterations 62 transmembrane receptor 62 mutant proteins 62 HSF1 62 Genetic variants 62 renal fibrosis 62 PON1 61 histone acetylation 61 CYP#D# gene 61 neuropilin 61 NF kB pathway 61 protein phosphorylation 61 Notch pathway 61 FGFs 61 aneuploidies 61 Ets2 61 mutated protein 61 podocytes 61 etiologic 61 proteolysis 61 autism susceptibility genes 61 histocompatibility 61 oncogenic transformation 61 TMEM#B 61 EBV infection 61 epigenetic modifications 61 PIK3CA 61 causative genes 61 nucleolar 61 LKB1 61 piRNAs 61 Cyclin D1 61 AhR 61 M. pneumoniae 61 monogenic 61 ALK gene 61 membrane fusion 61 causal variants 61 glycolipids 61 germline mutation 61 Skp2 61 NF1 gene 61 epithelial tissues 61 HCV replication 61 Kv#.# 61 E#F# 61 deacetylation 61 ABCB1 61 FLT3 61 phosphatases 61 pathogenic mechanisms 61 X inactivation 61 homozygosity 61 JAK2 gene 61 viral genomes 61 mutation 61 VIPR2 61 catenin 61 c KIT 61 #p#.# [002] 61 microcephalin 61 NEIL1 61 synuclein 61 FUS1 61 inherited mutations 61 SMAD4 61 sphingolipid 61 GRP# 61 Hsp# [001] 61 alternative splicing 61 JAK mutations 61 ribonucleic acids 61 lysosomal storage diseases 61 HAR1 61 downregulation 61 outer membrane proteins 61 CDH1 61 ERK signaling 61 Clusterin 61 adipogenic 61 pharmacodynamic biomarkers 61 FTLD 61 maternally inherited 61 PARP inhibition 61 microRNA molecules 61 genomic rearrangement 61 tumor suppressor gene 61 modifier genes 61 cell adhesion molecules 61 APOE e4 61 protein coding RNAs 61 chromosome #q 61 MAP kinases 61 Foxp2 61 ARID1A 61 protein isoforms 61 genetic rearrangements 61 biogenesis 61 metazoans 61 proapoptotic 61 messenger RNAs mRNAs 61 DICER1 61 transactivation 61 DNA methyltransferase 61 LMNA 60 potent inhibitors 60 epigenetic markers 60 tRNA synthetases 60 sequence homology 60 granule cells 60 telomere dysfunction 60 hammerhead ribozyme 60 insertions deletions 60 tumorigenesis 60 oncogenesis 60 histone modification 60 haematopoietic 60 ubiquitylation 60 #BP# 60 RNA viruses 60 vimentin 60 HLA B# 60 neuroendocrine cells 60 methylation patterns 60 gene fusions 60 hypomethylation 60 primary cilia 60 parkin gene 60 prion infection 60 underlying molecular mechanisms 60 CFTR gene 60 nongenetic 60 epistasis 60 JAK2 enzyme 60 intracellular bacteria 60 previously undescribed 60 CNVs 60 DSBs 60 GPR# [002] 60 receptor gamma 60 spontaneous mutation 60 telomeric 60 Notch1 60 ABCA1 60 EGFR gene 60 NF κB 60 HLA alleles 60 myopathies 60 MMP# 60 insulin signaling pathway 60 untranslated regions 60 fatty acid synthase 60 ADAM# 60 transcriptional machinery 60 IRAK1 60 TCF4 60 apoE4 60 genetic determinants 60 ERK2 60 autosomal recessive 60 Hashimoto thyroiditis 60 NFkB 60 ribosomal protein 60 HLA DRB1 60 ubiquitination 60 PDGFR 60 myeloproliferative diseases 60 MAP kinase pathway 60 PB1 F2 60 transcriptional repressor 60 Notch signaling 60 protein tyrosine phosphatases 60 metalloprotease 60 serine threonine kinase 60 USP# 60 synapse formation 60 pDCs 60 beta amyloid peptides 60 tyrosine kinases 60 mammalian genomes 60 gene inactivation 60 enolase 60 neoplastic 60 proteolytic cleavage 60 TMPRSS2 ERG fusion 60 genetic polymorphisms 60 mammary stem cells 60 cathepsins 60 DLX5 60 COX enzymes 60 herpes viruses 60 RNA splicing 60 phenotypes 60 lymphoid cells 60 glycosylated 60 IgA deficiency 60 Kabuki syndrome 60 MLL2 60 CHEK2 60 ribosomal RNA 60 genes encode proteins 60 c myc 60 peroxisome 60 constitutively expressed 60 proliferative disorders 60 prion gene 60 SRY gene 60 pleiotropic 60 neuroinflammation 60 aneuploidy 60 tRNA synthetase 60 Wwox 60 NKX#.# 60 immunoregulatory 60 neuropsychiatric disorders 60 intracellular signal transduction 60 Hedgehog signaling 60 mitochondrial respiration 60 histone deacetylases 60 γ secretase 60 ribosomal proteins 60 pathophysiologic 60 microglial activation 60 pathogenic mutations 60 SERT gene 60 uncharacterized 60 glycosylation 60 K ras mutations 60 chromatin remodeling 60 nucleosome positioning 60 KRAS oncogene 60 plasma kallikrein 60 molecular biomarkers 60 mitochondrial proteins 60 SLC#A# [002] 60 OGG1 60 lymphoid 60 cis regulatory 60 pathophysiological 60 myeloid 60 HOTAIR 59 microsatellite instability 59 transgene expression 59 ribonucleic acid RNA 59 γδ T cells 59 mRNA decay 59 gliosis 59 endogenous retroviruses 59 ubiquitin ligases 59 ependymomas 59 DLC1 59 CDK4 59 familial ALS 59 SGK1 59 CHD5 59 IL#R 59 coding RNA 59 C1q 59 globin genes 59 homologous recombination 59 Sonic Hedgehog 59 receptor molecule 59 riboswitches 59 beta globin gene 59 mammary cells 59 ADAMTS# 59 TP# gene 59 pseudogene 59 genes encoding 59 neuropsychiatric diseases 59 β1 59 demethylation 59 previously uncharacterized 59 E3 ubiquitin ligase 59 Gorlin syndrome 59 childhood leukemias 59 histone code 59 TGF β 59 molecular mechanisms underlying 59 phenotype 59 genetic aberrations 59 chromosomal DNA 59 coding genes 59 ALK mutations 59 autophagic 59 PINK1 59 MAPCs 59 amyloid formation 59 susceptibility gene 59 MYH9 gene 59 epigenetically 59 E3 ligase 59 gastric carcinogenesis 59 epithelial mesenchymal transition 59 beta1 integrin 59 lysosomal storage disease 59 mutated genes 59 mitogen activated protein kinases 59 Nedd4 59 estrogen receptor alpha 59 Inappropriate activation 59 mucins 59 ncRNAs 59 neuronal plasticity 59 cohesin 59 heterozygosity 59 drug metabolizing enzymes 59 cardiac hypertrophy 59 TLR9 agonists 59 genetic abnormalities 59 dermatophytes 59 indels 59 gene amplification 59 myotonic dystrophy 59 Ehrlichia 59 PI3K pathway 59 IKZF1 59 oncogenic 59 COL#A# 59 Mdm2 59 gene mutations 59 histone H4 59 NF2 59 muscular dystrophies 59 SMN2 gene 59 neuronal degeneration 59 mTOR inhibitors 59 HipA 59 SHANK3 59 metalloproteinases 59 granzyme B 59 constitutively active 59 eotaxin 59 molecular determinants 59 sRNA 59 Wnt signaling 59 abnormal proteins 59 fibrocytes 59 mitochondrial DNA mtDNA 59 Wnt pathway 59 pathogenetic 59 HbF 59 gamma H2AX 59 WAGR syndrome 59 molecular pathways 59 Cyclin E 59 rifamycins 59 chromosome #p#.# 59 MALAT1 59 Dysregulation 59 gene polymorphisms 59 etiological 59 overactivation 59 Dpp 59 hematopoetic stem cells 59 6S RNA 59 crystallin 59 T#M 59 innate immune responses 59 caveolin 59 mutational status 59 amino acid sequence 59 activin 59 E1A 59 kinase domain 59 CYP#C# [002] 59 costimulatory 59 TRP channels 59 oncogenes 59 Rap1 59 familial pancreatic cancer 59 Helicobacter 59 biochemical pathways 59 LPA gene 59 nicotinic receptor 59 receptor tyrosine kinase 59 JAK STAT pathway 59 microglial 59 synthases 59 Apc 59 G#S mutation 59 S. sanguinis 59 Pten 59 neurodegeneration 59 amyloid cascade 59 RNA polymerases 59 dedifferentiation 59 functional polymorphism 59 mutant protein 59 PrP 59 micro RNA 59 protein tyrosine phosphatase 59 ZNF# 59 Oxidative stress 59 NKT cells 59 synaptic transmission 59 polycystin 59 nucleotide sequences 59 polyglutamine 59 alpha synuclein protein 59 isoforms 59 Mitochondrial 59 mitogen activated protein kinase 59 noncoding 59 neurexins 59 underlying pathophysiology 59 protein tau 59 BCL6 gene 59 RNA silencing 59 protein encoded 59 X chromosome inactivation 59 autosomal 59 tumor suppressors 59 DISC1 59 genetic alteration 59 melanocyte 59 lincRNAs 59 RNA transcripts 59 fronto temporal dementia 59 generalized vitiligo 59 Foxp3 59 microRNA expression 59 HLA genes 58 TXNIP 58 cAMP signaling 58 BMP signaling 58 transcriptional repression 58 gene mutation 58 genomic variation 58 Vpu 58 commensal bacteria 58 NFκB 58 leukemic stem cells 58 IDH1 58 oligomerization 58 apoptosis pathway 58 TLR8 58 chromosome rearrangements 58 fungal genomes 58 tumor suppressor genes 58 mitochondrial metabolism 58 inactivating mutations 58 Apobec3 58 glycolipid 58 prostaglandin synthesis 58 MC1R 58 CagA 58 PALB2 58 enzymatic activity 58 TAp# 58 amyloid deposits 58 KLF# 58 Upregulation 58 HMGCR 58 Chlamydia pneumoniae 58 gene expression patterns 58 Mycoplasma pneumoniae 58 Li Fraumeni syndrome 58 Genetic variations 58 S. pombe 58 neuropathologic 58 cyclin E 58 lung epithelial cells 58 genome rearrangements 58 LRAT 58 MAPKs 58 IKKa 58 metabolizing enzymes 58 tau aggregates 58 breast cancer metastasis 58 DEAR1 58 IGF1 58 Jhdm2a 58 Hh pathway 58 oncoprotein 58 immunopathology 58 Borrelia 58 isoenzymes 58 MT1 MMP 58 ABCB1 gene 58 eukaryotic cells 58 MEF2A 58 topoisomerases 58 axonal degeneration 58 endosymbiosis 58 mutational analysis 58 focal adhesions 58 JAK2 58 chromosome condensation 58 chromosome #q# [001] 58 precancerous stem cells 58 signaling molecule 58 neural cells 58 myelination 58 APOE4 58 ribosomal DNA 58 protein kinases 58 methylated DNA 58 myeloproliferative disorders 58 biochemical abnormalities 58 MDSCs 58 cellular prion protein 58 CALHM1 58 polypeptides 58 endogenous retrovirus 58 mammary cancers 58 lymphangiogenesis 58 Arp2 3 58 nucleotide substitutions 58 intestinal epithelium 58 neuroblastomas 58 receptor gene 58 endogenous ligands 58 phylogenetic analyzes 58 structural rearrangements 58 HFE gene 58 GPC5 58 Treg cell 58 aetiological 58 allelic variation 58 adult neurogenesis 58 thymosin 58 BRAF V#E 58 mesenchymal transition 58 paraganglioma 58 intron 58 leukaemias 58 DNA polymerases 58 C. neoformans 58 cyclins 58 genetic variation 58 systemic inflammation 58 morphological traits 58 Francisella 58 short hairpin RNAs 58 dyskeratosis congenita 58 Prion diseases 58 polycystin 1 58 Chk1 58 NF1 58 C. pneumoniae 58 telomere maintenance 58 pre malignant lesions 58 chromosomal translocation 58 Wnt proteins 58 chromosome #q# [002] 58 amino acid substitution 58 GSK 3ß 58 hyperactivation 58 breast cancer subtypes 58 #S rRNA gene 58 PTEN mutations 58 subcellular compartments 58 SOD1 gene 58 MGUS 58 PrPSc 58 osteogenic differentiation 58 EGFR pathway 58 Six3 58 NR#A# 58 ligases 58 XBP1 58 FOXP2 gene 58 Entamoeba 58 fatty acid biosynthesis 58 WNK1 58 cytolytic 58 constitutively activated 58 nonvascular 58 COX2 58 Cockayne syndrome 58 kinase pathway 58 phosphorylates 58 RNA polymerase II 58 Sonic hedgehog 58 beta lactamases 58 prognostic marker 58 chromosomal 58 LRRK2 mutation 58 FGFR3 58 gamma globin gene 58 p#/CBP 58 genetic heterogeneity 58 replicon 58 KCNH2 58 vacuolar 58 coding sequences 58 huntingtin 58 number variations CNVs 58 forkhead 58 nucleases 58 cypin 58 hyperactivated 58 susceptibility loci 58 transgenic mouse models 58 congenital disorders 58 miR #a [002] 58 centromeres 58 thyroid hormone receptor 58 osteopontin 58 BMP2 58 TRAIL induced apoptosis 58 osteoclast 58 FGFR1 58 gene loci 58 viral genome 58 pre mRNA splicing 58 NOTCH1 58 aminoacyl tRNA synthetases 58 NFKBIA 58 opportunistic pathogens 58 biochemical mechanisms 58 astrocytic 58 Sjögren syndrome 58 intergenic 58 mRNA sequences 58 lysine residues 58 SLITRK1 58 clonal expansion 58 tropomyosin 58 PAK1 58 #q# [001] 58 uPAR 58 viral proteins 58 proliferative diseases 58 GIST tumors 58 androgen receptor gene 58 evolvability 58 CCL#L# 58 susceptibility locus 58 BDNF gene 58 downstream effectors 58 neural progenitor 58 nerve degeneration 58 H#K# methylation 58 HLA molecules 58 epigenetic 58 receptor signaling 58 condensin 58 DUX4 58 FOXP3 58 SCN5A 58 GATA4 58 BCL#A 58 overactivated 58 ApoE gene 58 TSLP 58 telomere DNA 58 TGF b 58 synthetic analogues 58 BMAL1 58 copper zinc superoxide 58 KCNQ1 58 DNA methylation 58 developmental abnormalities 58 bilaterians 58 hereditary deafness 58 NPM1 gene 58 Stat3 57 isotypes 57 neuromuscular junction 57 MYH9 57 imprinted genes 57 tetherin 57 antibody mediated 57 carcinogenesis 57 Sox9 57 endocannabinoid signaling 57 synaptic proteins 57 GAPDH 57 unmutated 57 NF kB signaling 57 molecular pathway 57 transmembrane protein 57 EBNA1 57 KIAA# 57 superoxide dismutase 57 ERK1 2 57 virulence factors 57 pancreatic endocrine 57 antigenic epitopes 57 monozygotic twins 57 morphogens 57 transdifferentiation 57 ALDH2 57 FGF signaling 57 SIRT2 57 kinase gene 57 lysosomal 57 SMN2 57 anterior pituitary 57 clonally 57 Epstein Barr Virus EBV 57 PGC 1α 57 mutant huntingtin protein 57 sortilin 57 metabolic abnormalities 57 glycosyltransferase 57 ependymal cells 57 acinar 57 IGFBP2 57 SOD1 57 homologs 57 oncoproteins 57 DNMT1 57 T#I [002] 57 phylogenetically 57 N myc 57 palladin 57 protein conformation 57 lymphocytic 57 HBx 57 genetic variants associated 57 chromosomal anomalies 57 promoter methylation 57 JAK STAT 57 eukaryote 57 PI3K AKT 57 molecular underpinnings 57 GSTP1 57 FMRP protein 57 polyglutamine diseases 57 regulates gene expression 57 aT cell 57 ectopic expression 57 genomic variants 57 Neuregulin 1 57 RNA ribonucleic acid 57 HLA DQ2 57 transcriptional activation 57 Nod1 57 TET2 57 BRCA1 BRCA2 57 NQO1 57 germline cells 57 BRAF protein 57 TLR antagonists 57 cell adhesion molecule 57 kinase enzymes 57 primary cilium 57 GSTT1 57 antigenic 57 PPAR γ 57 subcellular localization 57 EGF receptor 57 genes CYP#C# 57 ncRNA 57 beta globin 57 MC1R gene 57 multidrug resistance 57 OPHN1 57 hyperinsulinemia 57 remyelination 57 LDL receptor 57 cellular senescence 57 penetrance 57 Phosphorylation 57 NFTs 57 demethylase 57 TGF ß 57 Oncogenic 57 vascular endothelial cells 57 Trichophyton rubrum 57 NPY gene 57 heterologous expression 57 Hh 57 genetic modifiers 57 number variation CNV 57 mitotic catastrophe 57 ankyrin B 57 APOE genotype 57 neural crest stem cells 57 TRPV3 57 drugable 57 mitochondrial enzyme 57 intronic 57 cytochrome P#s 57 noncoding RNA 57 myeloma cells 57 polyploid 57 synovial cells 57 CD# expression [001] 57 GISTs 57 bacterial toxins 57 conformational changes 57 atherogenesis 57 plasminogen 57 centrosome 57 bone marrow mesenchymal stem 57 miR #a [001] 57 transcriptomes 57 prothrombotic 57 medulloblastoma 57 chromosomal abnormalities 57 murine leukemia virus 57 neuronal differentiation 57 transgenic mouse model 57 guanine G 57 adhesion proteins 57 yeast prions 57 autocrine 57 N Myc 57 genital tract infections 57 peroxisomes 57 enzymatic pathways 57 osteoblastic 57 Akt1 57 melanocortin receptors 57 subventricular zone 57 SIRT3 57 lipid metabolism 57 matrix metalloproteinases MMPs 57 aneuploid cells 57 APOBEC3G 57 osteosarcomas 57 monogenic disorders 57 karyotypes 57 WDR# 57 lysosomal diseases 57 malignant phenotype 57 beta amyloid peptide 57 introns 57 nNOS 57 klotho 57 quantitative trait loci 57 prostate carcinogenesis 57 LRP6 57 kallikrein 57 Pseudomonas aeruginosa infections 57 androgen receptor AR 57 C EBP alpha 57 lymphoproliferative disorders 57 clusterin 57 tumor suppressive 57 antisense oligonucleotides 57 vertebrate embryos 57 SOD1 protein