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(Click for frequent words.) 68 microdeletions 68 virulence genes 67 somatic mutations 67 microdeletion 67 splice junctions 67 chromosome #q#.# [001] 67 pathogenic mutations 67 #q#.# [002] 67 #p#.# [001] 66 #p#.# [002] 66 chromosomal aberrations 66 KCNH2 66 K ras mutations 66 chromosomal rearrangement 66 chromosomal deletions 66 missense mutations 65 de novo mutations 65 #q#.# [001] 64 SHANK3 64 Alu elements 64 chromosomal translocations 64 spontaneous mutations 64 genomic rearrangements 64 monogenic 64 germline mutations 64 IgA deficiency 63 PTPN# 63 miRNA genes 63 MLH1 63 causative mutations 63 FUS1 63 M. pneumoniae 63 genetic polymorphism 63 KRAS oncogene 63 chromosome translocations 63 herpesviruses 63 somatic mutation 63 hypermethylated 63 splice variants 62 gene rearrangements 62 NFKBIA 62 molecular abnormalities 62 chromosome #q# [001] 62 orthologs 62 causal variants 62 Trichophyton rubrum 62 chromosome rearrangements 62 #q# [001] 62 mtDNA mutations 62 LIS1 62 mRNA transcripts 62 mosaicism 62 ABCB1 62 #q# deletion 62 MECP2 gene 62 paralogs 62 #q# [002] 62 segmental duplications 61 GBA mutations 61 hamartomas 61 BRCA1 BRCA2 61 epithelial tumors 61 chromosome #q 61 V#F mutation 61 MSH2 61 MLL2 61 CDH1 61 Entamoeba histolytica 61 mutated K ras 61 D#N 61 CYP#D# gene 61 genetic loci 61 SLITRK1 61 susceptibility gene 61 LRRK2 gene 61 sCJD 61 #p# [003] 61 MLL gene 61 inherited mutations 61 eosinophilia 61 VHL gene 61 oxysterols 61 Sjögren syndrome 61 OGG1 61 microsatellite instability 61 chromosomal regions 61 3'UTR 61 SHANK3 gene 61 nucleotide substitutions 61 coding exons 60 ABCB1 gene 60 neuronal dysfunction 60 Activating mutations 60 DQB1 * 60 G#S mutation 60 JAK mutations 60 gene deletions 60 biochemical abnormalities 60 FGFR2 60 rs# [004] 60 SOD1 gene 60 FLT3 60 chromosomal rearrangements 60 chromosome #q# [002] 60 dominantly inherited 60 mutant alleles 60 chromosome abnormalities 60 NRTI resistance 60 MYCN amplification 60 susceptibility genes 60 PTEN gene 60 non coding RNA 60 missense mutation 60 gene duplications 60 nucleotide sequence 60 DNMT1 60 ADAMTS# 60 GBM tumors 60 sporadic ALS 60 metalloprotease 60 progranulin gene 60 APOE e4 60 chromosomal anomaly 60 phylogenetic analyzes 60 LRAT 60 KRAS mutations 60 ALK mutations 60 promoter hypermethylation 60 cytochrome b 60 chromosome aberrations 60 TTR gene 60 splice variant 60 chromosomal alterations 60 cDNAs 60 heterozygosity 60 neuroblastoma tumors 60 TCF#L# gene 60 #S rRNA gene 60 selective antagonists 60 A3 adenosine receptor 60 NF1 gene 60 hepatocellular carcinomas 59 renal cell carcinomas 59 Clusterin 59 FMR1 59 mutations 59 EGFR mutant 59 chromosome #q#.# [002] 59 globin genes 59 diagnostic biomarker 59 epigenetic markers 59 TMPRSS2 ERG fusion 59 adenoviral 59 mRNA molecules 59 CHD7 59 indels 59 karyotype 59 polyglutamine 59 huntingtin gene 59 RNA sequences 59 NKX#.# 59 MAPK pathway 59 germline mutation 59 susceptibility loci 59 synuclein 59 aneuploidies 59 chromosomal anomalies 59 VNTR 59 ataxias 59 Corynebacterium 59 nucleotide sequences 59 tryptase 59 genes differentially expressed 59 generalized vitiligo 59 clade B 59 gene MECP2 59 ALK gene 59 CALHM1 59 quasispecies 59 neuropsychiatric diseases 59 noncoding 59 #S rRNA 59 inactivating mutations 59 protein encoded 59 HLA B# 59 gene amplification 59 Microarray analysis 59 pRb 59 osteosarcomas 59 MTHFR 59 immunodeficiencies 59 CagA 59 proto oncogene 59 conserved sequences 59 mitochondrial toxicity 59 biologic pathway 59 XL# inhibits 59 heterozygotes 59 DEAR1 59 viral proteins 59 neuro developmental disorders 59 immunohistochemical staining 59 varicella infection 59 potent inhibition 59 BRAF V#E mutation 59 EGF receptors 59 HER2 expression 59 Plasmodium vivax 59 indel 59 genomic alterations 59 p# mutations 59 familial ALS 59 constitutively expressed 59 T#I [002] 59 K ras gene 59 penetrance 59 predisposing factor 59 K#N 58 BRAF V#E 58 myelofibrosis polycythemia vera 58 noncoding RNAs 58 sporadic Creutzfeldt Jakob 58 maternally inherited 58 p# activation 58 susceptibility locus 58 myeloproliferative 58 genetic polymorphisms 58 Leukemias 58 hemagglutinin gene 58 posttranslational modifications 58 bronchial epithelial cells 58 EBV infection 58 PALB2 58 CD# expression [001] 58 BRAF mutation 58 cytogenetic abnormalities 58 hypoperfusion 58 Arabidopsis genome 58 NSCLC tumors 58 apoE4 58 hyperplastic 58 SCN5A 58 Wwox 58 circadian genes 58 PDGFR alpha 58 distinct subtypes 58 PON1 58 C. neoformans 58 Upregulation 58 dopamine D4 receptor 58 substrate specificity 58 alternatively spliced 58 allelic variants 58 beta1 integrin 58 extramedullary 58 Escherichia coli Klebsiella pneumoniae 58 breast carcinomas 58 ABL1 58 GPC5 58 bacterium Neisseria meningitidis 58 B7 H3 58 CDKN2A 58 HLA DRB1 58 IgG antibody 58 kinase gene 58 E. faecalis 58 BMPR2 58 Candida species 58 CDK4 58 familial aggregation 58 differentially expressed genes 58 PCA3 gene 58 karyotypes 58 intergenic 58 fetal chromosomal 58 activating mutations 58 coding sequences 58 medulloblastomas 58 mGluR5 antagonist 58 MTHFR gene 58 amino acid substitution 58 polyploid 58 potent inhibitors 58 EGFR gene 58 myeloproliferative diseases 58 MDR1 58 5q 58 WDR# 58 ncRNAs 58 ribosomal RNA rRNA 58 genetic locus 58 CRISPR Cas 58 endogenous ligands 58 nonsense mutations 58 CFTR gene 58 E#F# 58 Cytogenetic 58 chromosome #p#.# 58 Mycoplasma pneumoniae 58 epigenetic alterations 58 glutamic acid decarboxylase 58 dysbindin 58 genetic variants associated 58 asymptomatic carriers 58 replicon 58 intergenic regions 58 etiologic 58 cellular prion protein 58 outer membrane proteins 58 intronic 58 apolipoprotein E gene 58 XMRV infection 58 functional polymorphism 58 apoptotic pathway 58 NF kB pathway 58 meningiomas 58 p# biomarker 58 Cryptococcus neoformans 58 UGT#A# * 58 H#Y 58 normal karyotype 58 hepatoma 58 catechol O methyltransferase 58 transgenic mouse models 58 murine models 58 demyelinating 58 Entamoeba 58 molecular determinants 58 pathogenetic mechanisms 58 c KIT 58 MeCP2 gene 58 immunological responses 58 gp# protein [002] 58 G6PD deficiency 58 microRNA expression 58 mitochondrial gene 58 overactivation 58 L. pneumophila 57 Hashimoto thyroiditis 57 hepatic enzyme 57 LRP5 57 MYH9 gene 57 HbF 57 myeloproliferative neoplasms 57 uPAR 57 choroid 57 gene APOE4 57 mucinous 57 cisplatin resistant 57 Genetic predisposition 57 receptor ligand 57 carcinoids 57 ribosomal DNA 57 sequence homology 57 APOA5 57 picornavirus 57 NPY gene 57 mammalian genomes 57 colorectal carcinoma 57 neurodevelopmental disorders 57 genes BRCA1 57 gene loci 57 androgen receptor gene 57 deacetylation 57 vimentin 57 KLF4 57 Immunohistochemical analysis 57 Cathepsin B 57 C#Y 57 gastric carcinoma 57 ERBB2 57 dinucleotide 57 BRAF protein 57 Apc 57 Genetic mutations 57 polyploidy 57 hypomethylation 57 BRAF gene 57 rRNA 57 chromosomal mutations 57 gliosis 57 CYP #D# 57 paragangliomas 57 arterial calcification 57 sphingolipid 57 mitochondrial disorders 57 epigenetic modification 57 previously uncharacterized 57 NNRTI resistance 57 gastrointestinal stromal tumors GISTs 57 transmembrane receptor 57 Li Fraumeni syndrome 57 mitochondrial proteins 57 H#K#me# 57 Vesivirus 57 N. gonorrhoeae 57 fluconazole resistant 57 JAK2 enzyme 57 replicase 57 alleles 57 Epstein Barr virus EBV 57 cyclin E 57 monocytogenes 57 TOP2A 57 DNA methylation patterns 57 neoplastic 57 thymidine kinase 57 seminomas 57 gastrointestinal dysfunction 57 GLUT1 57 tumorigenicity 57 antiphospholipid antibodies 57 PIK3CA 57 immunohistochemical analysis 57 von Hippel Lindau 57 CD#c 57 #S rDNA 57 MGUS 57 prion infection 57 Chlamydia trachomatis infection 57 BDNF gene 57 IDH1 57 microcephalin 57 Li Fraumeni 57 immunoreactive 57 GSTT1 57 genomic variants 57 neurological abnormalities 57 globin 57 immunoreactivity 57 pancreatic endocrine 57 thyroid carcinoma 57 filaggrin 57 epigenetic silencing 57 methylation markers 57 QT interval prolongation 57 fluoroquinolone resistance 57 echogenic foci 57 bacterial genomes 57 K#R [002] 57 allelic 57 lymphocytic 57 spontaneous mutation 57 unknown etiology 57 SNP rs# [001] 57 Squamous 57 CYP#C# [002] 57 tumor specific antigen 57 genetic syndromes 57 homozygosity 57 assay detects 57 Immunohistochemical staining 57 FSHR 57 homologies 57 allele frequencies 57 neuroimaging studies 57 Anaplasma 57 untranslated regions 57 plasma kallikrein 57 histone acetylation 57 proteolytic cleavage 57 CNTNAP2 57 IL#B 57 CHEK2 57 differential gene expression 57 autosomal dominant inheritance 57 PBMCs 57 monoclonal gammopathy 57 familial pancreatic cancer 57 colorectal neoplasms 57 IDH mutations 57 GISTs 57 protein p# 57 modifier genes 57 lymphoid cells 57 mesotheliomas 57 SMAD4 57 NP CRNs 57 nucleoli 57 PTEN protein 57 protein tyrosine phosphatase 57 aneuploid cells 57 phosphoprotein 57 Htt 57 TP# mutations 57 genomic rearrangement 57 quantitative trait loci 57 G#S [002] 57 nucleotide variations 57 eotaxin 57 anterior pituitary 56 NR#A# 56 malignant transformation 56 gene polymorphisms 56 mitochondrial DNA mtDNA 56 A. thaliana 56 C#T [002] 56 isotype 56 selective agonists 56 urolithiasis 56 Prox1 56 intracellular bacteria 56 holoprosencephaly 56 autism susceptibility genes 56 vacuolar 56 CNVs 56 demethylase 56 SLC#A# [002] 56 somatostatin 56 multiprotein complex 56 Ribavirin causes 56 thyrotropin levels 56 ascertainment bias 56 DSBs 56 hepatic enzymes 56 mutant allele 56 viral genomes 56 GFP gene 56 cAMP signaling 56 SOCS3 56 synovial tissue 56 T#M 56 papillomas 56 HER2 gene 56 Alleles 56 ERK2 56 mediated inhibition 56 herpes viruses 56 motor neuron degeneration 56 gene APOE 56 microarray experiments 56 Janus kinase 56 histologic examination 56 microglial activation 56 molecular biomarkers 56 antinuclear antibodies 56 TPMT 56 myeloproliferative disorders 56 UCRs 56 phenotypic variation 56 β1 56 precursor lesions 56 mutated p# 56 anatomical abnormalities 56 γ secretase 56 nongenetic 56 Treg cell 56 retrovirus XMRV 56 JAK2 mutation 56 unmutated 56 mTOR inhibitors 56 linkage disequilibrium 56 rheumatoid arthritis lupus 56 autosomal dominant disorder 56 immunocompetent 56 viral isolates 56 #p# [001] 56 transthyretin amyloidosis 56 PDGFRA 56 orthologous genes 56 xenograft tumors 56 MTHFD1L gene 56 HIV HCV coinfected 56 methylenetetrahydrofolate reductase 56 ribosomal protein 56 pathological hallmark 56 monozygotic twin 56 apoE 56 CCL#L# 56 PTEN mutations 56 Transcriptome 56 TGFBR1 * 6A 56 GSTM1 56 PDE#A 56 primary cilia 56 kilobases 56 coagulopathy 56 aneuploid 56 serous ovarian cancer 56 airway hyperresponsiveness 56 nanomolar 56 polyglutamine diseases 56 genes encoding 56 causative gene 56 HER2 neu 56 MYBPC3 56 APOL1 56 histocompatibility 56 dissociative disorders 56 5 HTTLPR 56 deleterious mutations 56 mice lacking 56 renal cysts 56 ductal adenocarcinoma 56 tissue biopsies 56 syngeneic 56 autoinflammatory diseases 56 HER2 receptor 56 effector molecules 56 chromosome #p# [002] 56 rifamycins 56 globin gene 56 neurosteroid 56 homozygotes 56 breast cancer subtypes 56 Gleevec resistant 56 astrocytic 56 hypermethylation 56 drug metabolizing enzymes 56 glycosylated 56 genetic aberrations 56 brain lesions 56 Kabuki syndrome 56 number variations CNVs 56 leiomyomas 56 histologic subtypes 56 thyrotropin 56 lymphoid tumors 56 FXTAS 56 serum biomarkers 56 histone modification 56 mutated genes 56 CEACAM1 56 pentamidine 56 chromosomal instability 56 striatal neurons 56 Mechanistic studies 56 HMGCR 56 immunopathology 56 genomic loci 56 Genetic variation 56 tRNA synthetases 56 4E BP1 56 ERK signaling 56 serum antibodies 56 Multidrug resistant 56 toxoplasma 56 clefting 56 DLC1 56 NPM1 gene 56 circulating endothelial cells 56 lung carcinomas 56 coding genes 56 Enterobacter cloacae 56 euthymic patients 56 micro RNAs 56 methylated DNA 56 CYP#B# 56 BRCA1 mutation carriers 56 downstream effectors 56 neurodevelopmental disorder 56 microsatellite loci 56 intercellular signaling 56 KIAA# 56 PARP inhibition 56 phenotypic expression 56 melatonin receptor 56 hyperalgesia 56 genotypic 56 EBNA1 56 antisense RNA 56 p# Shc 56 cytopathic 56 Enterobacteriaceae 56 ataxin 56 LRRK2 mutations 56 PDGFR 56 C. trachomatis 56 familial adenomatous polyposis 56 Salmonella enterica 56 SNCA 56 TRIM5 56 HepG2 cells 56 familial clustering 56 etiologic agent 56 MMP# 56 lung epithelium 56 miR #a [002] 56 autosomal 56 M. genitalium 56 TTR amyloidosis 56 oligonucleotide probes 56 transgenic rats 56 HLA DQ2 56 Phenotypic 56 TRAIL induced apoptosis 56 HLA DQ 56 histone modifications 56 perilipin 56 receptor subtypes 56 pyogenes 56 metaplasia 56 insertions deletions 56 colocalization 56 RRM1 56 hypothalamic pituitary 56 affective psychosis 56 CYP#D# 56 KIF6 gene 56 HER2 overexpression 56 Aβ peptides 56 tau aggregates 56 Pten 56 COL#A# 56 mouse xenograft models 56 murine leukemia virus 56 unmethylated DNA 56 BRAF mutations 56 oncogenic HPV types 56 signaling cascades 56 granzyme B 56 LPA gene 56 chlamydial infection 56 phosphorylated tau 56 ZNF# 56 Supplementary Table 56 cutaneous lesions 56 carcinoid tumors 56 Chlamydia trachomatis 56 fronto temporal dementia 56 exons 56 monozygotic twins 56 5q chromosome 56 methylation patterns 56 FGFs 56 ADPKD 56 BCL#A 56 VIPR2 56 mitochondrial dysfunction 56 monocytic 56 cagA 56 promoter methylation 56 C1q 56 SCN1A 56 androgen receptor AR 56 ERalpha 56 IRAK1 56 leukaemias 56 adenylate cyclase 56 ANCA associated 56 adrenal cortex 56 TNF α 55 anti androgens 55 neuropsychiatric disorder 55 gene locus 55 Epstein Barr Virus EBV 55 protein misfolding diseases 55 CHD5 55 S/GSK# 55 dyskeratosis congenita 55 fungal genomes 55 RUNX3 55 proteomic analysis 55 Genetic variants 55 miRNA expression 55 cardioembolic stroke 55 TP# gene 55 D#G 55 neurite outgrowth 55 DISC1 gene 55 vanA gene 55 primate genomes 55 tumor regressions 55 PI3K Akt 55 microglial 55 abnormal proteins 55 pseudogene 55 genomewide 55 amino acid substitutions 55 immunostaining 55 mitogen activated protein kinase 55 homodimer 55 GSTP1 55 proapoptotic 55 melanocytic nevi 55 mammary stem cells 55 neuroligins 55 piRNAs 55 uniparental 55 mammographically 55 periodontal pathogens 55 glial tumors 55 UGT#B# 55 immunoblotting 55 C. pneumoniae 55 subcellular compartments 55 pyrimidine 55 alpha synuclein gene 55 conductance regulator 55 coexpression 55 chromatin structure 55 Gorlin syndrome 55 glycolipid 55 sequenced genomes 55 nonmelanoma skin cancers 55 GPx 55 lung adenocarcinomas 55 Cyclin E 55 FGFR2 gene 55 ß amyloid 55 IDH2 55 TMPRSS2 ERG 55 Chlamydia pneumoniae 55 dermatophytes 55 QTLs 55 nucleases 55 microvessels 55 siRNA knockdown 55 mutational analysis 55 osteochondromas 55 HGPS 55 rotaviruses 55 histologic subtype 55 polynucleotides 55 EAAT2 55 GNAQ 55 vivax 55 neurologic symptoms 55 colonic mucosa 55 nephronophthisis 55 Tay Sachs thalassemia 55 CYP#C# * 55 transgenic mouse model 55 P. ovale 55 genes CYP#C# 55 Francisella 55 malignant lesions 55 methyltransferase 55 microRNA miR 55 genetic alterations 55 ependymomas 55 nAChR 55 Brugada syndrome 55 tau protein tangles 55 SMN2 gene 55 mitochondrial mutations 55 mycobacterium tuberculosis 55 antidepressants SSRIs 55 lysine residues 55 innate immune responses 55 BARD1 55 gonococcal 55 Oncogenic 55 Ehrlichia 55 short hairpin RNAs 55 chromatogram 55 Trichomonas vaginalis 55 chromosome abnormality 55 Heritability 55 perivascular 55 polymorphisms 55 apolipoprotein E4 55 Foxp3 55 NF1 55 tumor biopsies 55 Raman spectra 55 Cre recombinase 55 epistasis 55 Chlamydophila pneumoniae 55 thioredoxin 55 DNA methyltransferase 55 EGFR protein 55 SMN1 gene 55 KCNQ1 55 commensal bacteria 55 HFE gene 55 cDNA sequences 55 pre malignant lesions 55 eosinophilic 55 AMACR 55 SLC#A# [001] 55 Genetic mutation 55 basal cell nevus syndrome 55 RAF kinase VEGFR 55 mda 7 55 antisense inhibition 55 miRs 55 immunohistochemical 55 heritable variation 55 leptin deficiency 55 epigenetic modifications 55 proviral DNA 55 lysosomal storage diseases 55 Phylogenetic analysis 55 mutation 55 extracolonic 55 RNA viruses 55 ORFs 55 protein tyrosine phosphatases 55 previously undescribed 55 BCR ABL1 55 genomewide association studies 55 Glucocorticoids 55 malaria parasite genome 55 pituitary adenomas 55 Leptospira 55 breast cancer genes BRCA1 55 homocystinuria 55 segmental duplication 55 ciliopathies 55 recombinants 55 histopathologic diagnosis 55 neurosensory 55 #HT#A 55 serine protease 55 MMP9 55 caveolin 55 invasive lobular 55 centromeric 55 variant alleles 55 post transplant lymphoproliferative 55 congenital anomalies 55 SNP rs# [002] 55 chromosome #p# [001] 55 mesothelin 55 metabolomic profiles 55 serine threonine kinase 55 ultrastructural 55 Apolipoprotein E 55 mutant huntingtin protein 55 causative mutation 55 FMR1 gene 55 tumor antigen 55 NS4A 55 underlying molecular mechanisms 55 neuritic 55 kilobase 55 genetic rearrangements 55 SNPs pronounced snips 55 morphological abnormalities 55 gastric carcinomas 55 commonly mutated genes 55 coinfections 55 NFTs 55 connective tissue diseases 55 JAK2 gene 55 LRRK2 mutation 55 ribonucleic acids 55 Jhdm2a 55 hypereosinophilic syndrome 55 histone methylation 55 S. enterica 55 NS5B 55 potent inducer 55 inactive X chromosome 55 virulence determinants 55 gastric adenocarcinoma 55 Enterobacter 55 myopathies 55 papillary renal cell carcinoma 55 luciferase gene 55 Epidermal Growth Factor Receptor 55 hereditary predisposition 55 isogenic 55 amyloid cascade 55 RNA ribonucleic acid 55 MECP2 55 lesional 55 IgG4 55 humoral immune response 55 glioblastoma tumors 55 gene fusions 55 nucleolar 55 hepatic lipase 55 microRNA molecules 55 S. maltophilia 55 secretory pathway 55 pleiotropic effects 55 phylogenetic analysis 55 filoviruses 55 Cyclin D1 55 Protein Kinase C 55 NPM1 mutations 55 protein isoforms 55 polynucleotide 55 p#/CBP 55 At#g# 55 Colon polyps 55 cyclophilin D 55 monogenic disorders 55 T. vaginalis 55 Fas ligand 55 antigenic epitopes 55 intracellular protein 55 HMPV 55 Rap1 55 genetic recombination 55 IGF1 55 beta globin gene 55 genetic abnormalities 55 clonally 55 TFIIH 55 Babesia 55 polyomavirus 55 H#N# isolates 55 P. gingivalis 55 polymorphonuclear leukocytes 55 isotypes 55 catenin