Related by context. All words. (Click for frequent words.) 57 LRAT 56 IDH2 56 homozygotes 56 HFE gene 55 mutated K ras 55 K ras mutations 55 heterozygotes 55 PTPN# 55 leukemic stem cells 54 chromosomal alterations 54 UGT#B# 54 SMAD4 54 CREBBP 54 TP# mutations 54 TOP2A gene 53 normal karyotype 53 CDH1 53 parkin gene 53 Notch1 53 missense mutations 53 ADAM# 53 germline mutations 53 multidrug resistance 53 mutation 53 JAK2 mutation 53 Akt1 53 ERBB2 53 MYCN amplification 53 C1q 53 sporadic ALS 53 missense mutation 53 spontaneous mutation 53 MTHFR 53 apoE 52 PDE#A 52 TACI mutations 52 PTEN gene 52 tumor suppressor protein 52 eotaxin 52 PTP1B 52 histone deacetylases 52 heterozygote 52 MSH2 52 hypermethylated 52 NFkB 52 Bcl2 52 mutated protein 52 APOC3 52 microdeletions 52 unmutated 52 MeCP2 gene 52 APOL1 52 APOE e4 gene 52 IGF1 52 mutant worms 52 LRRK2 gene 52 autosomal dominant disorder 52 K ras gene 52 inherited mutations 52 TP# mutation 52 gene MECP2 52 pathogenic mutations 52 BRCA1 BRCA2 52 p# mutation 52 PON1 52 mitochondrial DNA mutations 52 homozygote 52 CEACAM1 52 receptor blocker 52 mutant huntingtin protein 52 ABCB1 51 immunodeficient 51 ZNF# 51 enzymatic activity 51 CDK4 51 VHL gene 51 TP# gene 51 leukemic cell 51 GSTP1 51 apoE4 51 MEF2A 51 SOD2 gene 51 p# mutations 51 germline mutation 51 receptor gene 51 gene rearrangements 51 alternatively spliced 51 KRAS oncogene 51 FLT3 51 mutations 51 nonischemic 51 ApoE4 gene 51 karyotypes 51 kinase gene 51 JAK2 enzyme 51 CFTR gene 51 granzyme B 51 ApoE gene 51 FGFs 51 5q 51 microsatellite instability 51 cytoplasmic tail 51 epigenetic silencing 51 lymphoid tissues 51 heterozygous 51 DNA methyltransferase 51 ApoE4 51 apolipoprotein E gene 51 atypical hyperplasia 51 tau gene 51 neuroblastoma tumors 51 PDGFR 51 rs# [004] 51 GISTs 51 APOE4 51 transthyretin 51 TET2 51 melanocyte 51 β cells 51 chromosome #q# [002] 51 pancreatic endocrine 51 ADPKD 51 ApoE4 allele 51 neoplastic 51 pRb 51 APOE e4 51 chromosome #q#.# [001] 50 TTR gene 50 NFKBIA 50 monogenic 50 progranulin gene 50 mice lacking 50 FGFR2 50 IL #R 50 downregulated 50 aldehyde dehydrogenase 50 huntingtin gene 50 BRCA2 gene mutation 50 palladin 50 EGFR mutations 50 phenotype 50 downstream effectors 50 amyloid deposits 50 Smad3 50 somatic mutations 50 homozygous 50 CFH gene 50 chitinase 50 caveolin 50 HLA DRB1 * 50 LRP5 50 TT genotype 50 SCN5A 50 RCAN1 50 outer membrane proteins 50 brain lesions 50 Vpu 50 clade B 50 GBM tumors 50 autoreactive 50 variant alleles 50 chromosome #q 50 C#Y 50 FMR1 gene 50 PALB2 gene 50 HLA DQ2 50 herpesviruses 50 CHD7 50 GPC5 50 Dystrophin 50 microcephalin 50 cervical lymph nodes 50 T#I [002] 50 #q#.# [001] 50 MC4R gene 50 SHANK3 49 NR#A# 49 UGT#A# * 49 Helicobacter 49 Prox1 49 iNOS 49 PKD1 49 prion protein gene 49 human leukocyte antigens 49 MIF gene 49 tumor suppressor gene 49 N Myc 49 Ets2 49 virulence genes 49 colorectal carcinoma 49 chromosomal rearrangement 49 c KIT 49 lymphocytic 49 Irs2 49 MnSOD 49 Clusterin 49 herpes viruses 49 WT1 49 globin 49 ataxin 49 SPINK1 49 HMGA2 49 COL#A# 49 NQO1 49 FMR1 49 thioredoxin 49 MLH1 49 gene amplification 49 BRAF gene 49 BDNF gene 49 NF2 49 receptor subunits 49 KLF4 49 CYP#C# * 49 HLA DRB1 49 genes encoding 49 Li Fraumeni syndrome 49 hyperplastic 49 transcriptional repressor 49 IGFBP 49 activin 49 genetic abnormality 49 CD#c 49 HLA DR4 immune 49 CHEK2 49 familial adenomatous polyposis 49 apo E 49 NNRTI resistance 49 VIPR2 49 alleles 49 RKIP 49 beta globin gene 49 FANCD2 49 TGFBR1 * 6A 49 susceptibility genes 49 GSTT1 49 synaptogenesis 49 CDKN2A 49 NF1 gene 49 uPAR 49 familial ALS 49 C EBP alpha 49 NKX#.# 49 Heterozygous 49 LRP6 49 granulocyte 49 peroxisome 49 BRAF V#E 49 chromosomal deletions 49 SOD1 gene 49 DGAT1 49 SMN1 49 klotho 49 LKB1 49 FMRP protein 49 progranulin 49 asymptomatically 49 FHIT 49 elevated triglyceride levels 49 HCV genotype 49 gene 49 polymorphisms 49 G#S [002] 49 thyroid carcinoma 49 C. neoformans 49 caveolin 1 49 tyrosine phosphorylation 49 AAV2 49 PTEN mutations 48 EGFR gene 48 IgA deficiency 48 TMEM#B 48 MYH9 gene 48 JAK mutations 48 epigenetic modifications 48 nonsense mutation 48 MECP2 gene 48 HLA B# 48 FLT3 ITD 48 substrate specificity 48 breast carcinomas 48 ADH1B * 48 allelic variants 48 OCA2 48 aggrecan 48 microdeletion 48 cyclin D1 48 aneuploidies 48 thrombospondin 48 Pten 48 mutant gene 48 de novo mutations 48 neuraminidases 48 NF1 48 KRAS gene 48 nonsense mutations 48 GNAQ 48 Genetic variation 48 CYP#D# gene 48 genes predisposing 48 subtype 48 cystic fibrosis transmembrane conductance 48 clefting 48 genetic alteration 48 transmembrane protein 48 claudin 48 superoxide dismutase 48 chromosome #q#.# [002] 48 G6PD 48 cytogenetic abnormalities 48 TCF4 48 genetic mutation 48 NOTCH1 48 CD8 + 48 TCF#L# 48 MTHFR gene 48 spontaneous mutations 48 sequence homology 48 colorectal tumors 48 mutated gene 48 miRNA expression 48 catenin 48 endostatin 48 Immunohistochemical analysis 48 BRCA1 mutations 48 SLC#A# [002] 48 mtDNA mutations 48 JAK2 gene 48 gene deletions 48 mesotheliomas 48 K ras 48 BRAF protein 48 activating mutations 48 E#F# 48 EGFR mutation 48 EBV infection 48 LIS1 48 Genetic mutations 48 nondemented 48 huntingtin protein 48 GRK5 48 IDH1 48 cyclophilin D 48 recessive mutations 48 #p#.# [001] 48 human leukocyte antigen 48 Estrogen receptor 48 rs# [002] 48 Wwox 48 pneumococci 48 vimentin 48 myostatin gene 48 K#N 48 prion gene 48 transcriptional activation 48 SOCS3 48 SOX3 gene 48 GRP# 48 Bcl 48 abnormal clotting 48 BRCA2 gene 48 chromosomal instability 48 variant allele 48 Pten gene 48 ERK2 48 Cryptococcus neoformans 48 chromosome #q# [001] 48 miR #b [001] 48 periventricular 48 dorsal root ganglia 48 mosaicism 48 polymorphism 48 MAPK pathway 48 untreated celiac disease 48 familial dysautonomia 48 hamartomas 48 adipogenic 47 TOP2A 47 Glioblastoma multiforme GBM 47 PCSK9 gene 47 severe congenital neutropenia 47 HMGCR 47 replicon 47 evolutionarily conserved 47 mutated genes 47 mitochondrial proteins 47 mutant allele 47 RUNX3 47 miRNA genes 47 proto oncogene 47 IGF2 47 replicase 47 HOX genes 47 resistant isolates 47 nestin 47 penetrance 47 mRNA expression 47 #q# [001] 47 functional polymorphism 47 defensin 47 genotypes 47 MIF protein 47 MC1R 47 CCR5 delta# 47 APOE gene 47 resistin 47 Jhdm2a 47 molecular abnormalities 47 bile acid metabolism 47 lung adenocarcinoma 47 polyomavirus 47 glycogen storage 47 Foxp3 47 GPR# [002] 47 ABCA1 gene 47 SOD1 protein 47 CLL cells 47 astrocytomas 47 FUS TLS 47 phenotypic expression 47 mRNA transcripts 47 epigenetic alterations 47 TAp# 47 receptor protein 47 SCN1A 47 transfected cells 47 maternally inherited 47 osteocalcin 47 IgA antibodies 47 IDH mutations 47 autosomal recessive disease 47 OCT4 47 immunoreactivity 47 clusterin 47 microglial 47 transcriptional machinery 47 osteopontin 47 infected macrophages 47 YKL 47 gene mutations 47 familial pancreatic cancer 47 histocompatibility 47 FUS1 47 PARP inhibition 47 genotype 47 constitutively active 47 epigenetic mechanisms 47 HERV K 47 deleterious mutations 47 carotid plaque 47 clade C 47 KCNE2 47 NRTI resistance 47 neuroblastomas 47 COX2 47 alpha synuclein gene 47 HbF 47 NF κB activation 47 recessive trait 47 chromosomal regions 47 gene p# 47 gene mutation 47 genomic alterations 47 Brugada syndrome 47 COMT gene 47 histone demethylase 47 BRCA2 breast cancer 47 NKT cells 47 cofilin 47 cyclin E 47 anaplastic lymphoma kinase 47 metalloprotease 47 DHFR 47 paralogs 47 rs# [003] 47 micro RNAs 47 Epstein Barr virus EBV 47 leptin receptor 47 DLX5 47 hormone receptor negative 47 lymph node involvement 47 Htt 47 malignant transformation 47 viral proteins 47 PTEN mutation 47 cytopathic 47 resistant mutants 47 isotype 47 transcriptional regulation 47 chromosome #p# [001] 47 coding genes 47 EBNA1 47 BRCA mutation 47 mRNA decay 47 mitochondrial mutations 47 chromosome abnormality 47 Dpp 47 phosphatases 47 susceptibility gene 46 chromosome #p#.# 46 gene locus 46 ALDH2 46 DICER1 46 proteolysis 46 fusogen 46 gene expression patterns 46 subclinical 46 pheochromocytoma 46 vesicular stomatitis virus 46 transgene expression 46 ± SEM 46 epigenetic markers 46 APOE ε4 46 beta1 integrin 46 dystrophin gene 46 #q# [002] 46 BRCA1 gene 46 Aß 46 μ opioid receptor 46 ectopic expression 46 androgen receptor gene 46 gene variant 46 dopamine receptor gene 46 leukemic cells 46 LMNA 46 Sp1 46 frameshift mutation 46 luminal 46 CYP# [002] 46 PKM2 46 chromosomal translocations 46 ABCB1 gene 46 homolog 46 R#W [002] 46 lymphoid 46 coinfected 46 isoform 46 autoantibody 46 Fragile X gene 46 NPC1 46 transmembrane receptor 46 inactivating mutations 46 p tau 46 G#S mutation 46 GSTM1 46 HCMV 46 ABCA1 46 HGPS 46 M. pneumoniae 46 TNF blocker therapy 46 overexpress 46 BRIP1 46 MLL2 46 suppressor gene 46 hTERT 46 #q#.# [002] 46 FGFR2 gene 46 gene expression 46 mutant genes 46 connexin 46 intronic 46 DLC1 46 genetic polymorphism 46 mutant protein 46 orthologs 46 virulence determinants 46 miRNAs 46 RASSF1A 46 CXCL# 46 breast cancer metastasis 46 RPE# 46 HMGA2 gene 46 ALK gene 46 Cyclin D1 46 miR 46 PrP 46 Rap1 46 globin genes 46 Bcl xL 46 transactivation 46 monozygotic twins 46 mutant alleles 46 autosomal recessive 46 proband 46 TRIM5 46 pseudogene 46 #p# [001] 46 IKZF1 46 Cockayne syndrome 46 GlcNAc 46 protein p# 46 hepatic enzymes 46 CAG repeats 46 transgenic rats 46 cytoprotective 46 precancerous polyp 46 T1c 46 #p#.# [002] 46 constitutively 46 KRAS wild 46 staphylococci 46 N. gonorrhoeae 46 proteolytic cleavage 46 TCF#L# gene 46 CHD5 46 thrombin receptor 46 major histocompatibility complex 46 methylation patterns 46 tumor suppressor genes 46 downregulation 46 mPGES 1 46 malaria parasite Plasmodium falciparum 45 CagA 45 mutated BRCA1 45 mitochondrial 45 CD4 + cells 45 PDGFRA 45 chromosomal aberrations 45 V#F mutation 45 medulloblastomas 45 tumor suppressor PTEN 45 MSH6 45 succinate dehydrogenase 45 epigenetically 45 medulloblastoma 45 KLF# 45 p# MAPK 45 protein encoded 45 transgenic mouse model 45 hematopoietic cancers 45 dystrophin protein 45 FGFR4 45 phosphorylated 45 oncogenic 45 mutant p# 45 osteosarcomas 45 polyglutamine 45 pDCs 45 IL# [001] 45 gene loci 45 Amino acid 45 poorer prognosis 45 antiphospholipid antibodies 45 beta thalassemia 45 chromosomal defect 45 murine leukemia virus 45 genes 45 BRCA1 mutation 45 serum BDNF 45 Cx# [001] 45 intraoperative complications 45 Rb gene 45 breast cancer genes BRCA1 45 Bcl XL 45 neurodegenerative disorder 45 Candida species 45 micro RNA 45 SMN protein 45 inactive X chromosome 45 neuroD2 45 HER2 gene 45 encodes protein 45 morphologic 45 PrPSc 45 palmitoylation 45 overexpression 45 defective gene 45 TERT 45 K#R [002] 45 HSF1 45 Ph chromosome 45 CFTR protein 45 IL#R 45 beta globin 45 C#Y mutation 45 aneuploid 45 genes BRCA1 45 K ras mutation 45 KSHV 45 telomere shortening 45 DNA methylation patterns 45 collagen VI 45 anterior pituitary 45 eukaryotic cells 45 monocyte chemoattractant protein 45 overactivated 45 lesional 45 splice junctions 45 melanocytic nevi 45 histologic 45 beta catenin 45 hematologic abnormalities 45 genetic alterations 45 ovarian tumors 45 CYP#E# gene 45 SLITRK1 45 mitochondrial gene 45 Toxoplasma 45 histone modifications 45 SMN1 gene 45 EGFR 45 CaM kinase II 45 MECP2 45 causal variants 45 proteins 45 IDH1 gene 45 ALK mutations 45 Wnt signaling 45 curative therapy 45 PBMCs 45 HNPCC 45 FOXP3 45 phosphorylate 45 GSTM1 gene 45 MC1R gene 45 CRTAP 45 congenital deficiency 45 CCR5 mutation 45 transcriptional repression 45 CYP#C# [002] 45 Apobec3 45 genetic variant 45 protein 45 cytosolic 45 APOE4 gene 45 estrogen receptor 45 serine threonine kinase 45 GAB2 45 antisense RNA 45 BMP2 45 autoantibodies 45 glycosylation 45 Trypanosoma brucei 45 neoplastic lesions 45 filaggrin gene 45 mycobacterium 45 tumorigenesis 45 TSC1 45 G allele 45 presenilin 45 lipid rafts 45 hematologic toxicity 45 mutant proteins 45 causative genes 45 factor HGF 45 EGFRvIII 44 narcolepsy cataplexy 44 histone modification 44 lymphocyte subsets 44 perineural invasion 44 myotonic dystrophy 44 intestinal mucosa 44 ncRNAs 44 MDM2 44 MHC molecules 44 H#Y 44 arterial thrombotic 44 ChR2 44 GDNF gene 44 HLA genes 44 acute leukemias 44 apolipoprotein E APOE 44 oncoproteins 44 chromatin remodeling 44 glycogen synthase kinase 44 trypanosome 44 CCL#L# 44 polyadenylation 44 endogenous retroviruses 44 atherothrombosis 44 unknown etiology 44 chromosome translocations 44 Supplementary Table 44 syngeneic 44 Leydig cells 44 At#g# 44 Dicer enzyme 44 CC genotype 44 APOE allele 44 antigenicity 44 p# protein 44 unmethylated 44 allele frequencies 44 ribosomal protein 44 JAK2 44 pro angiogenic 44 unfavorable prognostic 44 tumor suppressor 44 allele frequency 44 dephosphorylation 44 protein kinases 44 DRD2 gene 44 #HC 44 short hairpin RNA 44 genetic variation 44 rifamycins 44 acute GvHD 44 SLC#A# [001] 44 deacetylation 44 mitochondrial dysfunction 44 non coding RNA 44 metastatic bladder 44 IRF6 44 MLL gene 44 acetylation 44 deleterious mutation 44 dyskeratosis congenita 44 HGPIN 44 H#K# methylation 44 POMC neurons 44 genetic polymorphisms 44 myeloid cells 44 allele 44 serum lipid 44 gene encoding 44 microRNA miR 44 paternally inherited 44 advanced neoplasia 44 Fibroblast growth 44 tumor suppressor p# 44 coexpression 44 microRNA molecules 44 ENPP1 44 CALHM1 44 T. gondii 44 RNA splicing 44 mesenchymal cell 44 RNA viruses 44 STAT1 44 genetic loci 44 epigenetic changes 44 trypanosomes 44 Skp2 44 exon 44 p# gene 44 Lkb1 44 MiRNAs 44 TB bacterium 44 CNTNAP2 44 quasispecies 44 cirrhotic 44 leptin receptors 44 radiosensitive 44 lacZ 44 myeloid derived 44 ubiquitination 44 nondiabetic 44 EZH2 44 PALB2 44 STAT4 44 chromosomal abnormality 44 phenotypes 44 homozygosity 44 kinase 44 promoter hypermethylation 44 HLA B 44 chromosomal rearrangements 44 BRCA mutations 44 karyotype 44 recessive mutation 44 sRNA 44 TMPRSS2 ERG 44 MAOA gene 44 allelic 44 cervical carcinoma 44 genetic defect 44 homologues 44 FXTAS 43 HLA identical 43 dopamine D4 receptor 43 regulator CFTR gene 43 PB1 F2 43 ALDH2 enzyme 43 dysbindin 43 CYP #D# 43 SGK1 43 noncoding DNA 43 congenital anomalies 43 genotoxic stress 43 hypomethylation 43 SMN2 43 perioperative complications 43 DNMT1 43 immuno suppressive 43 prion infection 43 number variation CNV 43 segmental duplications 43 proapoptotic 43 homodimers 43 follistatin 43 CGG repeats 43 hyperinsulinemic 43 dystrophin 43 apolipoprotein E 43 holoprosencephaly 43 V Leiden 43 CD# + [001] 43 histologies 43 chromosome #p# [002] 43 protein fragment 43 BCL#A 43 #p# [003] 43 Mitochondrial 43 Postoperative complications 43 neural crest 43 promoter methylation 43 neonatal lupus 43 kinases 43 SMN2 gene 43 abnormal hemoglobin 43 prostate bladder 43 Argonaute 43 adrenocortical carcinoma 43 genomic imprinting 43 outcrossing 43 phenotypic variation 43 short hairpin RNAs 43 clinically insignificant 43 PCSK9 protein 43 immuno suppressed 43 receptors EGFR 43 neuropathological 43 sexually dimorphic 43 H5 viruses 43 mitochondrial genes 43 FASPS 43 prepubertal 43 bone marrow lymph nodes 43 homologs 43 etiologic 43 oncoprotein 43 RhoA 43 methylation 43 ECOG PS 43 metazoan 43 osteoblast 43 IKK beta 43 HTLV 43 HBx 43 adenomatous polyps 43 demethylation 43 MYBPC3 43 noncoding RNAs 43 gene variation 43 NPM1 gene 43 signaling pathway 43 RPE# gene 43 aberrant methylation 43 intergenic regions 43 ras gene 43 GBV C 43 dysplastic 43 E1A 43 sCJD 43 epicardium 43 colorectal polyp 43 abnormal chromosomes 43 Plasmodium falciparum 43 ubiquitylation 43 supratentorial 43 hormone secreting 43 Peutz Jeghers syndrome 43 S. cerevisiae 43 heterozygosity 43 Synovial sarcoma 43 WNK1 43 gene variants 43 ARID1A 43 poxvirus 43 Wnt#b 43 hypermethylation 43 malignant polyps 43 LPA gene 43 progerin 43 HPV# 43 3'UTR 43 Kufs disease 43 X inactivation 43 P. falciparum 43 synuclein 43 nucleotide substitutions 43 HLA alleles 43 gamma globin gene 43 neurodevelopmental outcome 42 BRAF mutation 42 elevated LDL 42 HLA molecules 42 premutation 42 M. leprae 42 KIF6 gene 42 SNPs pronounced snips 42 chromatin structure 42 receptor molecule 42 activating mutation 42 regulates gene expression 42 HRAS 42 bcl 2 42 mutated 42 circulating endothelial cells