Related by context. All words. (Click for frequent words.) 64 K ras mutations 61 chromosomal translocation 61 gene rearrangements 61 MSH2 60 microdeletion 60 constitutively active 60 mutated K ras 60 MLH1 59 missense mutation 59 NPM1 mutations 59 PTPN# 59 CREBBP 59 JAK mutations 59 IgA deficiency 58 bcl 2 58 monogenic 58 anterior pituitary 58 Clusterin 58 TP# gene 57 hypermethylated 57 FUS1 57 activating mutations 57 C1q 57 Heterozygous 57 normal karyotype 57 isotype 57 BCR ABL 57 missense mutations 57 chromosome #q#.# [001] 57 K#N 57 TOP2A gene 57 Cytogenetic 57 alternatively spliced 57 GSTP1 57 hamartomas 57 SOD1 gene 56 hTERT 56 breast carcinomas 56 DNMT1 56 karyotypes 56 p# mutation 56 hypermethylation 56 filaggrin 56 amino acid substitution 56 IRAK1 56 germline mutations 56 H#K#me# 56 frataxin gene 56 TMPRSS2 ERG 56 NFKBIA 56 Wnt signaling pathway 56 proto oncogene 56 GNAQ 56 MECP2 gene 56 unmethylated 56 epigenetic modification 56 JAK2 enzyme 56 promoter methylation 56 pRb 55 sporadic ALS 55 CHD7 55 TOP2A 55 somatic mutation 55 mRNA transcripts 55 CDK4 55 deacetylation 55 dyskeratosis congenita 55 chromosomal abnormality 55 replicon 55 vimentin 55 cytokeratin 55 Amino acid 55 ZNF# 55 somatic mutations 55 TP# mutations 55 cyclin E 55 quasispecies 55 HLA DRB1 * 55 MDM2 55 huntingtin gene 55 spontaneous mutations 55 maternally inherited 55 PTEN gene 55 IKZF1 55 NPM1 gene 55 VHL gene 55 eotaxin 55 IDH1 55 LRAT 54 protein encoded 54 gene amplification 54 Htt 54 SMN protein 54 thyroid carcinoma 54 ribosomal proteins 54 missense 54 DLX5 54 lymphoid tissue 54 FMR1 54 ABCB1 54 ALK gene 54 E#F# 54 PARP inhibition 54 β amyloid 54 #p#.# [002] 54 MLL2 54 EZH2 54 catenin 54 rs# [004] 54 microdeletions 54 granule cells 54 mutated protein 54 K ras gene 54 HER2 neu 54 proteoglycan 54 microglial 54 beta globin gene 54 inactivating mutations 54 functional polymorphism 54 ERBB2 54 WNK1 54 chromosomal aberrations 54 FLT3 ITD 54 TMPRSS2 ERG fusion 54 autosomal dominant 54 mutant alleles 54 rRNA 54 phosphatases 54 epigenetic alterations 53 SNP rs# [001] 53 WT1 53 iNOS 53 polyglutamine 53 TGF ß 53 cytogenetic abnormalities 53 blastomeres 53 HMGA2 53 autosomal 53 MIF protein 53 colocalization 53 #q#.# [001] 53 variant allele 53 histopathological 53 DEAR1 53 MLL gene 53 MeCP2 gene 53 chromosome #q 53 Li Fraumeni syndrome 53 brain lesions 53 uPAR 53 Dpp 53 HLA DR4 immune 53 MYCN 53 BRCA1 BRCA2 53 endostatin 53 nucleotide substitutions 53 HER2 receptor 53 DNA rearrangements 53 p# MAPK 53 lysine residues 53 progranulin gene 53 PBMCs 53 tRNA synthetase 53 splice junctions 53 FGFR1 53 collagen VII 53 immunoreactivity 53 genotoxic stress 53 intestinal mucosa 53 micrometastasis 53 downstream effectors 53 HER2 gene 53 KLF4 53 transcriptional repressor 53 coding exons 53 CDH1 53 chromosome aberrations 53 LRP5 53 activin 53 CYP #D# 53 gene locus 53 chromosome abnormality 53 nonsense mutations 53 KRAS oncogene 53 nucleoli 53 SMN1 53 thrombospondin 53 splice variants 53 epigenetic markers 53 coding genes 53 microRNA expression 53 chemokine receptor 53 CagA 52 pathogenic mutations 52 mRNA expression 52 NQO1 52 COL#A# 52 Histologic 52 Chromosomal 52 apoE4 52 factor HGF 52 receptor gene 52 SMAD4 52 transcriptional activation 52 phosphorylates 52 MTHFR 52 adipogenic 52 medulloblastomas 52 globin 52 calcineurin 52 autosomal dominant disorder 52 MAPK pathway 52 lymphoid 52 GSTT1 52 cell adhesion molecule 52 frameshift mutation 52 transcriptionally active 52 PKD1 52 MYH9 gene 52 astrocytic 52 untranslated regions 52 cysteines 52 antiphospholipid antibodies 52 PON1 52 Cyclin D1 52 methyltransferase 52 DNA methylation patterns 52 polyadenylation 52 genomic deletions 52 aldehyde dehydrogenase 52 mutant protein 52 inherited mutations 52 OGG1 52 c KIT 52 PIK3CA 52 SCN5A 52 IL #p# 52 huntingtin 52 TERT 52 myotonic dystrophy 52 FOXP3 52 UGT#B# 52 p# mutations 52 heterozygous 52 CYP#C# [002] 52 transcriptional repression 52 Jhdm2a 52 synuclein 52 DNA methyltransferase 52 heterozygotes 52 ectopic expression 52 CAG repeats 52 SPINK1 52 extracellular matrix protein 52 Irs2 52 glycogen synthase kinase 52 HLA B# 52 HMGCR 52 miRNA expression 52 chromosomal alterations 51 TSC1 51 short hairpin RNAs 51 M. genitalium 51 EGFR gene 51 #q#.# [002] 51 homodimer 51 Aß 51 melanocyte 51 de novo mutations 51 Akt1 51 segmental duplications 51 alpha synuclein gene 51 TAp# 51 Prox1 51 Aβ 51 CFTR gene 51 β cells 51 UGT#A# * 51 mitochondrial dysfunction 51 GAPDH 51 CHD5 51 noncoding 51 tyrosine kinase 51 mitochondrial DNA mtDNA 51 gene deletions 51 #p#.# [001] 51 ERK2 51 chromosomal DNA 51 germline mutation 51 genetic loci 51 transcriptional machinery 51 TACI 51 amyloid deposits 51 RNA splicing 51 clinicopathologic 51 VEGF receptor 51 mtDNA mutations 51 intronic 51 aneuploidies 51 uracil 51 microRNA molecules 51 thioredoxin 51 aneuploidy 51 FGFR2 51 non coding RNA 51 chromosomal rearrangement 51 ataxin 51 miRNA genes 51 beta globin 51 HLA DRB1 51 mosaicism 51 histologic examination 51 virulence genes 51 Corynebacterium 51 DLC1 51 APOL1 51 ERK1 51 #q deletion 51 #q# deletion 51 p tau 51 microRNA miR 51 LDL receptor 51 F#del mutation 51 5 hmC 51 perineural invasion 51 DSBs 51 transiently transfected 51 Estrogen receptor 51 immunodominant 51 cyclophilin D 51 SHANK3 51 chromosome deletion 51 E3 ubiquitin ligase 51 hyperactivation 50 etiologic 50 FGFs 50 chromosomal instability 50 TYMS 50 ERCC1 50 TP# mutation 50 haplotypes 50 Single Nucleotide Polymorphisms SNPs 50 DICER1 gene 50 CYP#D# gene 50 LIS1 50 SLITRK1 50 RPE# gene 50 subcellular localization 50 MMP9 50 GPC5 50 histologic 50 substrate specificity 50 aberrant methylation 50 prion gene 50 Foxp3 50 caveolin 50 Aß peptide 50 neoplastic 50 causal variants 50 dysbindin 50 c myc 50 dystrophin gene 50 CDKN2A 50 mutant allele 50 SOCS3 50 cyclin dependent kinase 50 breast epithelial cells 50 VNTR 50 #p# [003] 50 abnormal prion protein 50 NR#A# gene 50 Fragile X mental retardation 50 monocyte 50 intestinal biopsy 50 Skp2 50 nucleotide sequence 50 subtype 50 FMR1 gene 50 #S rRNA gene 50 allelic variants 50 estrogen receptor alpha 50 Nup# 50 valine 50 Pten 50 LMNA 50 K ras 50 LKB1 50 orthologs 50 chromosomal deletions 50 supratentorial 50 autoantibodies 50 SMN2 gene 50 HGPS 50 radiographic findings 50 TMEM#B 50 ADAM# 50 CpG 50 neuroligins 50 extracellular domain 50 c Myb 50 Chromosome 50 chromosomal anomaly 50 CD8 ^ sup 50 myeloid cells 50 circulating endothelial cells 50 coagulation parameters 50 ALDH2 50 chromosome #q#.# [002] 50 C#Y 50 KRAS gene 50 trypanosome 50 tumor suppressor protein 50 Rap1 50 micro RNAs 50 SOD1 protein 50 epigenetic silencing 50 globin genes 50 cystic fibrosis transmembrane conductance 50 PDE#A 50 histopathologic 50 pancreatic endocrine 50 NR#A# 50 biochemical pathway 49 RhoA 49 genetic abnormality 49 RCAN1 49 clusterin 49 GenBank accession 49 IDH1 gene 49 mammary cells 49 serotonin receptor 49 progranulin 49 inactive X chromosome 49 transgenic mice expressing 49 chromosome #q# [002] 49 epigenetically 49 prion proteins 49 spontaneous mutation 49 sequence homology 49 DLTs 49 IL #R 49 stem progenitor cells 49 3'UTR 49 mice lacking 49 endogenous retroviruses 49 MEF2A 49 BDNF gene 49 ribosomal DNA 49 neuroblastoma cells 49 myocyte 49 selective agonists 49 MECP2 49 pharmacodynamic biomarkers 49 HFE gene 49 tumor suppressor gene 49 aneuploid 49 regulates gene expression 49 Wwox 49 paternally inherited 49 chromosome rearrangements 49 protein kinases 49 PAK1 49 primordial germ cells 49 #S rRNA 49 proapoptotic 49 suppressor gene 49 LRRK2 gene 49 Postoperative complications 49 mitochondrial proteins 49 Mitochondrial 49 histone H3 49 DISC1 49 beta subunit 49 5q chromosome 49 miR #a [002] 49 lesional 49 Bcl XL 49 At#g# 49 casein kinase 49 protein p# 49 CCL#L# 49 MSH6 49 neuropathological 49 enzymatic activity 49 radial glia 49 fusion protein 49 amino acid substitutions 49 TACI mutations 49 polyposis 49 CYP#B# 49 GLI1 49 C EBP alpha 49 SATB1 49 chromosome #p# [002] 49 Neuregulin 1 49 ± SEM 49 mitochondrial genes 49 amino acid sequence 49 monozygotic twins 49 metabolic enzymes 49 carboxy terminal 49 mitochondrial mutations 49 methylation patterns 49 micro RNA 49 dinucleotide 49 apoptosis pathway 49 INF2 49 NF1 49 PALB2 49 paralogs 49 leptin receptor 49 ectopic 49 Rab# 49 NFkB 49 Smad3 49 lung cancer NSCLC 49 apolipoprotein E APOE 49 chromosomal regions 49 NF1 gene 49 mutant proteins 49 pseudogenes 49 phosphorylate 49 SOD1 49 indels 49 cytopathic 49 malignant polyps 49 cytosine 49 morphologic 49 lacZ 49 cytochrome c oxidase 48 IKK beta 48 HSF1 48 SLC#A# [002] 48 holoprosencephaly 48 3' UTR 48 ubiquitylation 48 DGAT1 48 dystrophin protein 48 tumor suppressor p# 48 JAK STAT 48 exons 48 Bcl 48 #BP# 48 c myb 48 APOE e4 48 MC4R gene 48 RNA sequences 48 clinically insignificant 48 extracellular domains 48 B7 H1 48 neuregulin 48 LMNA gene 48 HERV K 48 Rb gene 48 HRAS 48 chromosomal translocations 48 endonuclease 48 atherosclerotic lesions 48 dystrophin 48 heterochromatin 48 tyrosine kinases 48 Sp1 48 RUNX3 48 maturational 48 karyotype 48 cytochrome b 48 tetramer 48 histone modifications 48 proband 48 cytosolic 48 PrP 48 SMN2 48 chromosome 48 GSTM1 48 genes encoding 48 μ opioid receptor 48 palladin 48 VIPR2 48 p# protein 48 MYBPC3 48 XBP1 48 quantitative trait loci 48 X inactivation 48 transcriptional regulation 48 Arabidopsis genome 48 heterozygosity 48 ribosomal protein 48 genetic variants associated 48 tau protein 48 chaperone proteins 48 mitochondrial gene 48 microcephalin 48 Wnt#b 48 glycosylation 48 transactivation 48 familial aggregation 48 NKX2 48 genomic variants 48 interferon pathway 48 PTP1B 48 tubule 48 MDMX 48 #p# [001] 48 chromosome translocation 48 androgen receptor gene 48 protein fragment 48 ciliated 48 apolipoprotein E gene 48 allele frequency 48 heterochromatic 48 IRS1 48 FANCD2 48 D#N 48 KIAA# 48 polynucleotide 48 protein isoforms 48 neuronal cell 48 oncogenic 48 encodes protein 48 connexin 48 Bifidobacterium infantis # 48 homozygosity 48 intergenic regions 48 matrix metalloproteinase 48 allelic 47 5 hydroxymethylcytosine 47 deleterious mutations 47 ubiquitin ligase 47 mutated genes 47 Notch signaling 47 fibrillin 1 47 microRNAs miRNAs 47 phosphorylated 47 histone demethylase 47 gag pol 47 periventricular 47 germline 47 STAT4 47 chromosome #p#.# 47 clade C 47 nicotinic receptor 47 adenoma 47 intergenic 47 adhesion molecule 47 BARD1 47 mutated gene 47 receptor tyrosine kinase 47 subventricular zone 47 histone H4 47 amino acid residues 47 cytogenetic 47 uncoupling protein 47 #q# [001] 47 gene loci 47 antisense RNA 47 OCT4 47 superoxide dismutase 47 nuclease 47 telomere DNA 47 serum lipid 47 tumor suppressor PTEN 47 kinase domain 47 V3 loop 47 GSK 3ß 47 SGK1 47 amplicons 47 RNA binding 47 5 methylcytosine 47 chromosome abnormalities 47 cohesin 47 genetic rearrangements 47 multiprotein complex 47 isoform 47 disulfide bond 47 Pax6 47 gp# [002] 47 p# gene 47 phylogenetic analyzes 47 homozygous 47 viral genomes 47 EBNA1 47 gene encodes protein 47 interfering RNA 47 histone modification 47 telomeric 47 5q 47 clefting 47 fascin 47 nucleotide sequences 47 ependymomas 47 segmental duplication 47 epigenetic modifications 47 SMN1 gene 47 Cx# [001] 47 exonuclease 47 genetic alteration 47 mRNA molecules 47 neurodevelopmental outcome 47 rs# [003] 47 hypomethylation 47 CDH# 47 transmembrane 47 cDNAs 47 presynaptic 47 penetrance 47 DNA glycosylase 47 homozygote 47 mutant gene 47 oxidative lesions 47 cytochrome 47 tumor suppressor genes 47 neuroligin 47 metalloproteases 47 PALB2 gene 47 transmembrane receptor 47 CYP#C# * 46 Klotho gene 46 viral proteins 46 polypeptide 46 DUX4 gene 46 POMC neurons 46 PTEN phosphatase 46 pseudogene 46 genomic loci 46 mutant genes 46 mRNA sequences 46 MTHFR gene 46 receptor protein 46 provirus 46 chromosome translocations 46 neurofibromatosis type 46 imprinted genes 46 genomic imprinting 46 progerin 46 bacterial genomes 46 gene encoding 46 overexpression 46 CNVs 46 prion protein 46 MC1R 46 claudin 46 SHANK3 gene 46 HBx 46 intron 46 unknown etiology 46 cyclins 46 Exclusion criteria 46 gene duplications 46 HAR1 46 filaggrin gene 46 #q# [002] 46 chromosomal rearrangements 46 thymine 46 demethylase 46 podocytes 46 guanine 46 Lewy bodies 46 catalytic subunit 46 calpain 46 amino terminal 46 GlcNAc 46 biogenesis 46 antigenic 46 variola 46 gene expression patterns 46 H#K# [002] 46 receptor subunits 46 alpha synuclein 46 dopamine transporter gene 46 CTL epitopes 46 phenotype 46 microRNA molecule 46 Single Nucleotide Polymorphism 46 serum BDNF 46 intraoperative complications 46 mPGES 1 46 ABCB1 gene 46 Sox9 46 mitochondrial genomes 46 chromatin structure 46 SLC#A# [001] 46 methylated 46 C. neoformans 46 Caspase 46 breast cancer genes BRCA1 46 autosomes 46 Alleles 46 hepatic enzymes 46 genomic rearrangements 46 subtyped 46 SWI SNF 46 MYH# 46 dynamin 46 SLC#A# gene [001] 46 neuroD2 46 XMRV infection 46 Pten gene 45 actin binding 45 epigenetic changes 45 cyclin D1 45 Math1 45 SIRT6 45 CNTNAP2 gene 45 mutations 45 susceptibility gene 45 nestin 45 genomic instability 45 ribosomal RNA 45 Wnt pathway 45 CRTAP 45 MIF gene 45 syncope fainting 45 #q 45 cDNA 45 receptor molecule 45 APOE4 45 fig. S1 45 miR #b [001] 45 hexamer 45 ZFN TM 45 Alu elements 45 RNA polymerases 45 haplotype 45 aggrecan 45 2' O methyl 45 EGFR 45 Supplementary Fig 45 CRISPR 45 eukaryotic cells 45 homologous recombination 45 CFH gene 45 phylogenetically 45 E cadherin 45 noncoding RNAs 45 overexpressed 45 Dicer enzyme 45 acetyl groups 45 isoforms 45 glycoproteins 45 major histocompatibility complex 45 cis regulatory 45 DNMT3A 45 Fragile X gene 45 rDNA 45 STAT3 45 mutation 45 viral genome 45 constitutively 45 Bonferroni correction 45 budding yeast 45 alternative splicing 45 gastric antrum 45 Karayiorgou 45 myelination 45 mesoderm 45 cytoplasmic tail 45 Gag protein 45 chromatid 45 linkage disequilibrium 45 F#del 45 bile acid metabolism 45 rs# [002] 45 chromosome #p# [001] 45 Golgi apparatus 45 epigenetic regulation 45 glial cell 45 sister chromatid 45 dorsal root ganglia 45 human leukocyte antigen 45 congenital anomalies 45 centromeric 45 ultraconserved elements 45 T1 weighted images 45 A. thaliana 45 serine 45 gene mutations 45 beta catenin 45 Wnt signaling 45 NF2 45 HOTAIR 45 retrotransposon 45 Akt 45 PGRN 45 APOC3 45 fibroblast cells 45 Hox gene 45 single nucleotide polymorphism 45 forkhead 45 PTEN protein 45 PIP3 45 BRCA2 gene 45 dopamine D4 receptor 45 HLA molecules 45 interfering RNAs siRNAs 45 IKKa 44 trisomy 44 abnormal hemoglobin 44 proline rich 44 kilobase 44 antigenicity 44 genetic abnormalities 44 presenilin 44 membrane proximal 44 recombination hotspots 44 RASSF1A 44 H#Y 44 gene p# 44 FXTAS 44 lincRNA 44 ascertainment bias 44 non coding RNAs 44 aromatase 44 transmembrane domain 44 mutational 44 ApoE gene 44 CHEK2 44 SRY gene 44 knockout mice 44 messenger RNA mRNA 44 neuroblasts 44 glycan 44 telomerase RNA 44 Src 44 lymphocyte subsets 44 causative genes 44 caveolae 44 WAGR syndrome 44 histone 44 piRNAs 44 Her2 gene 44 de novo lipogenesis 44 C#BL/#J 44 dentate gyrus 44 meiotic recombination 44 cytoplasmic 44 CCR5 gene 44 FGFR2 gene 44 haploid 44 polymorphisms 44 KLF# 44 type II pneumocytes 44 ultraconserved 44 myostatin gene 44 insertions deletions 44 genetic mutations 44 serotonin transporter 44 mRNAs 44 sRNA 44 Nat Biotechnol 44 laminin 44 CpG islands 44 NHEJ 44 centrosome 44 neural crest 44 allele frequencies 44 luminal 44 RAD# [001] 44 Hh 44 menadione 44 FHIT 44 cAMP 44 CYP#E# gene 44 APOE gene 44 chromosome segregation 44 TGF beta 44 Argonaute 44 ncRNAs 44 acetylation 44 signaling molecule 44 ADH1B * 44 plasma lipoprotein 44 lamin 44 BMP signaling 44 diploid 44 histone protein 44 spontaneous miscarriages 44 RNA strand 44 codons 44 ectoderm 44 amino acid glutamine 43 GTPase 43 heterodimer 43 SEQ ID 43 5 HTTLPR 43 Smad 43 dysmorphic features 43 chromosome #q# [001] 43 epithelial markers 43 subconjunctival hemorrhage 43 chromosomal abnormalities 43 coding sequences 43 ribonucleic acid RNA 43 IGF2 43 cyclin 43 uniparental 43 ORFs 43 translocations 43 SORL1 43 klotho