Related by context. All words. (Click for frequent words.) 75 microdeletions 75 MLH1 74 missense mutations 74 MSH2 74 PTPN# 72 monogenic 72 mosaicism 72 promoter methylation 71 de novo mutations 71 gene locus 71 orthologs 71 CDKN2A 71 hypermethylated 71 MTHFR 71 gene rearrangements 71 MYH9 gene 70 MGUS 70 allelic variants 70 ABCB1 70 Polymorphisms 70 herpesviruses 70 BRCA1 BRCA2 70 homozygotes 70 TP# mutations 70 heterozygotes 70 microdeletion 70 APOL1 70 IgA deficiency 70 p# mutation 70 C#Y 70 genetic loci 70 haematopoietic 70 chromosomal rearrangement 70 GSTP1 70 KRAS oncogene 69 somatic mutations 69 metaplasia 69 inherited mutations 69 K ras mutations 69 PALB2 69 chromosome #q# [001] 69 rs# [004] 69 CYP#D# gene 69 susceptibility loci 69 spontaneous mutations 69 HLA DRB1 69 TCF#L# gene 69 gene polymorphisms 69 microsatellite instability 68 FGFR2 68 BRAF V#E 68 CDH1 68 hamartomas 68 hepatocellular carcinomas 68 chromosome #p#.# 68 ADPKD 68 susceptibility gene 68 breast cancer genes BRCA1 68 chromosome #q# [002] 68 hypermethylation 68 IKZF1 68 ZNF# 68 ERBB2 68 HLA DQ2 68 spontaneous mutation 68 LPA gene 68 urothelial carcinoma 68 hepatoma 68 COL#A# 68 CCR5 delta# 68 Leydig cells 68 UGT#B# 68 ALK gene 68 activating mutations 68 BRCA1 mutations 68 heterozygous 68 genetic polymorphisms 68 seminomas 68 APOE e4 68 microcephalin 68 susceptibility genes 68 autosomal recessive 68 chromosomal alterations 68 mesotheliomas 68 virulence genes 68 prostate cancer CaP 68 LRAT 68 SLITRK1 68 colorectal carcinoma 68 LRP5 68 Li Fraumeni 68 dinucleotide 68 p# mutations 68 TP# mutation 68 genetic polymorphism 68 PIK3CA 68 Leydig cell 68 CHD7 68 CHEK2 68 #q#.# [001] 68 V#F mutation 68 #p#.# [002] 68 germline mutation 68 #q#.# [002] 67 TET2 67 Clusterin 67 epigenetic alterations 67 Li Fraumeni syndrome 67 Genetic variants 67 polymorphisms 67 etiologic 67 TMEM#B 67 hyperplastic 67 familial pancreatic cancer 67 homozygosity 67 C. trachomatis 67 CagA 67 chromosomal rearrangements 67 sequence homology 67 syngeneic 67 protein tyrosine phosphatase 67 constitutively expressed 67 basal cell nevus syndrome 67 SNP rs# [001] 67 PON1 67 breast carcinomas 67 VNTR 67 HepG2 cells 67 FLT3 67 mutations 67 missense mutation 67 frameshift mutation 67 genes predisposing 67 HbF 67 penetrance 67 null mice 67 FGFs 67 modifier genes 67 karyotypes 67 breast cancer subtypes 67 cytopathic 67 promoter hypermethylation 67 GISTs 67 rs# [002] 67 Immunohistochemical analysis 67 susceptibility locus 67 APOE genotype 67 #q# [001] 67 HLA DRB1 * 67 mutated K ras 67 monozygotic twins 67 Cathepsin B 67 familial clustering 67 JAK2 enzyme 67 functional polymorphism 67 chromosomal translocations 67 DSBs 66 ALK mutations 66 nonhereditary 66 neuroligins 66 epigenetic modification 66 HLA B# 66 JAK2 gene 66 leiomyomas 66 paternally inherited 66 COX2 66 variant alleles 66 nucleotide substitutions 66 heterozygote 66 mRNA expression 66 lymphangiogenesis 66 BARD1 66 myeloproliferative neoplasms 66 maternally inherited 66 TP# gene 66 seropositivity 66 K ras gene 66 lymphocytic 66 somatic mutation 66 mtDNA mutations 66 IPAH 66 myeloproliferative 66 tumorigenicity 66 lysine residues 66 MLL gene 66 chromosomal aberrations 66 sporadic ALS 66 histological subtype 66 epigenetic changes 66 IL#R 66 #p#.# [001] 66 beta amyloid peptides 66 PARP inhibition 66 rs# [001] 66 epistasis 66 VIPR2 66 GBA mutations 66 splice variants 66 phenotypic variation 66 chlamydial 66 aneuploidies 66 transgenic mice expressing 66 HNPCC 66 myopathies 66 chromosomal anomalies 66 mutant alleles 66 #p# [003] 66 serine protease 66 MTHFR gene 66 autosomal recessive disease 66 airway hyperresponsiveness 66 hereditary hemochromatosis 66 ABCB1 gene 66 DRB1 * 66 gastric carcinoma 66 p# activation 66 miRNA expression 66 PTEN mutations 66 Genotypes 66 dopamine transporter gene 66 Genetic variation 66 Trichophyton rubrum 66 Activating mutations 66 MECP2 gene 66 generalized vitiligo 66 #q# [002] 66 renal cell carcinomas 66 PCa 66 β1 66 evolutionarily conserved 66 GIST tumors 66 normal karyotype 66 potent inducer 66 inverse agonist 66 Single Nucleotide Polymorphisms SNPs 66 CD#c 66 metalloprotease 66 methylation patterns 66 IL#B 66 MLL2 66 BMPR2 66 motor neuron degeneration 66 cisplatin resistant 66 gene polymorphism 66 activating mutation 66 LIS1 66 Histone 66 autosomal 66 neoplastic 66 capsular polysaccharide 66 TMPRSS2 ERG fusion 65 Estrogen Receptor 65 lymphoid cells 65 mitochondrial mutations 65 myeloproliferative diseases 65 SNP rs# [002] 65 CpG island 65 genetic variants associated 65 androgen receptor AR 65 HLA genes 65 chemokine receptor 65 KCNH2 65 TGFBR1 * 6A 65 FGFR3 65 constitutively active 65 JAK2 mutation 65 Chlamydia pneumoniae 65 IDH1 mutation 65 X inactivation 65 proto oncogene 65 substrate specificity 65 neoplasias 65 fig. S4 65 SMAD4 65 LRRK2 gene 65 oncogenic mutations 65 HER2 expression 65 lysophosphatidic acid 65 C. pneumoniae 65 NOTCH1 65 Alu elements 65 alleles 65 KLF4 65 D#N 65 transgenic mouse models 65 G6PD deficiency 65 epithelial tumors 65 Fas ligand 65 glomerular 65 M. pneumoniae 65 allele frequency 65 sCJD 65 GPx 65 melanocytic nevi 65 GSTT1 65 genomic alterations 65 mutation 65 causal variants 65 progranulin gene 65 MAPK pathway 65 familial ALS 65 bronchial epithelial cells 65 breast carcinoma 65 TEL AML1 65 differentially expressed genes 65 DNA methylation patterns 65 enolase 65 allele frequencies 65 androgen receptor gene 65 prostate carcinoma 65 pathogenic mutations 65 immunoreactive 65 apolipoprotein E gene 65 osteosarcomas 65 testicular germ cell 65 haplotypes 65 thrombophilia 65 transgene expression 65 amino acid substitutions 65 asymptomatic carriers 65 HGPS 65 antiphospholipid antibodies 65 HLA DR 65 TNFalpha 65 SCN5A 65 mutant allele 65 CAG repeats 65 R#W [002] 65 gene amplification 65 adenocarcinomas 65 #q# deletion 65 isotypes 65 synthases 65 lymphoproliferative disorders 65 ERK signaling 65 malignant phenotype 65 p#INK#a 65 metastatic neuroendocrine tumors 65 dominantly inherited 65 intronic 65 chromosome #p# [001] 65 RASSF1A 65 protein isoforms 65 thyroid carcinoma 65 metabolomic profiles 65 paralogs 65 GSTM1 65 Leukemias 65 deleterious mutation 65 ADAM# 65 VKORC1 65 PTEN gene 65 SPINK1 65 clefting 65 JAK mutations 65 BRAF gene 65 polycystin 65 NKX#.# 65 phosphatases 65 histocompatibility 65 atypical hyperplasia 65 MeCP2 gene 65 replicon 65 chromosome #q#.# [001] 65 amyloid deposition 65 extramedullary 65 SHANK3 64 virulence determinants 64 perilipin 64 microglial 64 erythrocytes 64 STAT4 64 gene APOE 64 KIF6 gene 64 pulmonary metastases 64 plasma kallikrein 64 K#R [002] 64 clade B 64 MnSOD 64 immunoreactivity 64 #S rRNA 64 gastric adenocarcinoma 64 ERalpha 64 pheochromocytoma 64 epigenetically 64 TOP2A 64 MC1R 64 prothrombotic 64 K#N 64 toxoplasma 64 p# MAPK 64 chromosomal regions 64 replicase 64 autosomal dominant disorder 64 WNK1 64 gene MECP2 64 TTR gene 64 CYP#B# 64 mesenchymal cell 64 kDa protein 64 tyrosine phosphorylation 64 BCL#A 64 Fibroblast 64 noncoding RNAs 64 CC genotype 64 apolipoprotein E4 64 SSc 64 NR#A# 64 mucinous 64 Genetic variations 64 malignant transformation 64 MYCN amplification 64 Inactivation 64 BRAF V#E mutation 64 genes encoding 64 phenotype 64 mitochondrial DNA mtDNA 64 alveolar epithelial cells 64 C1q 64 glycosylated 64 transgenic mouse model 64 HGPIN 64 LVNC 64 chromosome #q 64 invasive carcinoma 64 intestinal polyps 64 HER2 positivity 64 micrometastases 64 proband 64 T. vaginalis 64 MMP# 64 neuroblastomas 64 precursor lesions 64 Macrophage 64 IL 1ß 64 immunohistochemical 64 herpes viruses 64 variant allele 64 ADAMTS# 64 APOC3 64 HHV 6 64 NNRTI resistance 64 TNF α 64 S. maltophilia 64 haplogroups 64 Smad3 64 ribosomal protein 64 Trichomonas vaginalis 64 lymphoid tissue 64 von Hippel Lindau 64 chromosomal deletions 64 pDCs 64 alternatively spliced 64 Mycoplasma pneumoniae 64 nodal metastasis 64 FSHR 64 chromosome #p# [002] 64 pRb 64 subclinical 64 mitochondrial metabolism 64 IRAK1 64 causative genes 64 FGF2 64 beta1 integrin 64 ORMDL3 64 differential gene expression 64 adenomatous polyps 64 mammary stem cells 64 PPARγ 64 OGG1 64 genotypic 64 autoinflammatory diseases 64 histologic subtype 64 clinicopathologic 64 GPC5 64 apoE 64 posttranslational modifications 64 nucleoli 64 TT genotype 64 NF1 64 astrocytomas 64 N Myc 64 transmembrane receptor 64 cell adhesion molecule 64 Src kinase 64 hypothalamic pituitary 64 G6PD 64 G allele 64 pathophysiological 64 methyltransferase 64 eotaxin 64 GNAQ 64 squamous cell carcinoma SCC 64 TACI mutations 64 Epstein Barr Virus EBV 64 SLC#A# [001] 64 neuropathologic 64 airway remodeling 64 splice junctions 64 KRAS mutations 64 #p# [001] 64 inactive X chromosome 64 Heterozygous 64 Cytogenetic 64 TCF#L# 64 nonmelanoma skin cancers 64 bexarotene 64 chromosome #q#.# [002] 64 superinfection 64 genomic deletions 64 transgenic rats 64 HER2 overexpression 64 DNA rearrangements 64 caveolin 64 cyclin dependent kinase inhibitor 64 IL #R 64 inducible nitric oxide synthase 64 VHL gene 64 heterozygosity 64 coding genes 64 breast cancer metastasis 64 cervical lymph nodes 64 interferon IFN 64 unmutated 64 CYP#C# [002] 64 causative mutations 64 IDH1 gene 64 etiologic agent 64 premutation 64 FMR1 gene 64 histone acetylation 64 HIV HCV coinfected 64 homozygote 64 Fragile X gene 64 mTOR inhibitors 64 clinicopathological 64 hereditary predisposition 64 inhibin B 64 TIMP 64 Nedd4 64 immunohistochemical analysis 64 prognostic marker 64 histone modifications 64 deacetylation 64 CGG repeats 63 sarcomatoid 63 allelic 63 LPS induced 63 enteroviral 63 mRNA transcripts 63 airway responsiveness 63 endogenous retroviruses 63 pyrimidine 63 prostate cancer PCa 63 Treg cell 63 Aß 63 beta subunit 63 synaptogenesis 63 Sjögren syndrome 63 Papillary 63 GPR# [002] 63 immunocompetent 63 BMP2 63 RRM1 63 DNA methyltransferase 63 APOE ε4 63 epithelia 63 granulosa cell 63 PDGFR 63 PNET 63 SRY gene 63 BRCA2 carriers 63 atopic 63 Dysregulation 63 mitogen activated protein kinases 63 miRNAs miR 63 neurite outgrowth 63 familial aggregation 63 homodimer 63 pathogenic mechanisms 63 E#F# 63 chorioamnionitis 63 C. neoformans 63 telomere dysfunction 63 serine threonine 63 tumor subtypes 63 rs# [003] 63 CEACAM1 63 N. gonorrhoeae 63 micronuclei 63 autosomal dominant 63 microRNA expression 63 Oncogenic 63 CpG islands 63 NPM1 gene 63 amino terminal 63 causative mutation 63 bile acid metabolism 63 subcellular compartments 63 vimentin 63 Aneuploidy 63 H pylori 63 Immunohistochemical staining 63 MYBPC3 63 ADRB2 63 polyglutamine 63 hypogonadotropic hypogonadism 63 linkage disequilibrium 63 CSF biomarkers 63 monoclonal gammopathy 63 HER2 receptor 63 TRAIL induced apoptosis 63 papillary renal cell carcinoma 63 KRAS mutation 63 autoreactive 63 steroidogenic 63 pDC 63 alpha1 63 dermatophytes 63 Upregulation 63 mammary gland tumors 63 S aureus 63 indels 63 heritable variation 63 DLC1 63 CYP#A# gene 63 HSV1 63 EBV infection 63 ESR1 63 oesophageal adenocarcinoma 63 enterococcal 63 proteolytic cleavage 63 Epidermal Growth Factor Receptor 63 Aspergillus species 63 synuclein 63 thiopurine 63 congenital anomalies 63 survivin expression 63 isoenzyme 63 interferon γ 63 c KIT 63 Epstein Barr virus EBV 63 distinct subtypes 63 androgen deficiency 63 malignant neoplasm 63 TSC1 63 peptide antigens 63 Raf MEK ERK 63 malignant prostate 63 indel 63 Amino acid 63 haplotype 63 CALHM1 63 carcinoids 63 HBx 63 PrPSc 63 KIT mutations 63 monocytic 63 folate metabolism 63 H#Y 63 MAPT 63 inbred strains 63 gastrointestinal stromal tumors GISTs 63 hamartoma 63 varicella infection 63 narcolepsy cataplexy 63 ß1 63 gonococcal 63 N acetyltransferase 63 forkhead 63 receptor inhibitor 63 S. enterica 63 microfilariae 63 liver metastasis 63 adipogenic 63 HLA alleles 63 HFE gene 63 FGFR2 gene 63 transthyretin 63 costimulatory 63 genital tract infections 63 germline 63 tumor suppressor protein 63 CFTR gene 63 IgG4 63 Hashimoto thyroiditis 63 paramyxoviruses 63 TOP2A gene 63 ependymomas 63 Autoantibodies 63 genomewide 63 homodimers 63 MC4R gene 63 Cytotoxic T 63 CNTNAP2 63 tryptase 63 TIMP 1 63 thrombospondin 63 medulloblastomas 63 trophoblast cells 63 proline rich 63 lung adenocarcinomas 63 T1D 63 genes differentially expressed 63 micro RNAs 63 dysglycemia 63 coagulase negative staphylococci 63 methylenetetrahydrofolate reductase 63 murine models 63 cyclin E 63 transcriptional regulation 63 INF2 63 pertussis toxin 63 tumoral 63 thrombin receptor 63 chromosomal instability 63 5 HT1A 63 ovarian carcinoma 63 aberrant methylation 63 chromosomal mutations 63 MYH9 63 monozygotic 63 IDH1 63 lung carcinomas 63 NKG2D 63 serous ovarian cancer 63 TNF blocker therapy 63 apolipoprotein E 63 suppressor gene 63 Notch receptor 63 immunoregulatory 63 coinfection 63 Chlamydia trachomatis 63 lipoxygenase 63 retinoic acid receptor 63 Kupffer cells 63 Cryptococcus neoformans 63 cytokeratin 63 melanocyte 63 Peutz Jeghers syndrome 63 CYP #D# 63 morphogen 63 Six3 63 endogenous ligands 63 BALB c mice 63 SOD2 63 leiomyoma 63 melatonin receptor 63 SLC#A# [002] 63 Prox1 63 SCN1A 63 vivax 63 renal fibrosis 63 gastric carcinogenesis 63 Lp PLA 2 63 prognostic indicator 63 IgG1 63 PDGF receptor 63 huntingtin gene 63 cis regulatory 63 HNSCC 63 alpha2 63 genomic imprinting 63 monozygotic twin 63 ABL1 62 dysbindin 62 HER2 amplification 62 inactivating mutations 62 molecular abnormalities 62 Plasmodium vivax 62 4E BP1 62 metachronous 62 apo E 62 piRNAs 62 epigenetic silencing 62 ncRNA 62 proapoptotic 62 multidrug resistance 62 colonic mucosa 62 lymph node metastasis 62 CYP#C# * 62 outer membrane proteins 62 Ehrlichia 62 NPC1 62 CDK4 62 MDR1 62 major histocompatibility complex 62 F#del 62 colorectal adenoma 62 Lymphocytic 62 metazoan 62 Asymptomatic 62 glioblastoma tumors 62 mutant huntingtin protein 62 leucocytes 62 autosomal dominant inheritance 62 #S rRNA gene 62 DNA adducts 62 Germline 62 IgA antibodies 62 MEF2A 62 perivascular 62 polymorphism 62 NR#A# gene 62 QTLs 62 chemokine receptors 62 phenotypic expression 62 CYP#D# 62 differentially regulated 62 coexpression 62 epithelial tissues 62 homolog 62 mesangial 62 FMR1 62 APOA5 62 rotaviruses 62 adenoviral 62 serpin 62 neoplastic cells 62 predisposing factor 62 estrogen receptor beta 62 aminopeptidase 62 muscarinic 62 phospholipase 62 VEGFR1 62 T#I [002] 62 CREBBP 62 dizygotic twins 62 neoplasms 62 CD# expression [001] 62 CpG DNA 62 oncogenic transformation 62 3'UTR 62 brain lesions 62 CNVs 62 colorectal adenocarcinoma 62 childhood leukemias 62 neuronal dysfunction 62 endophenotypes 62 pancreatic prostate 62 prognostic significance 62 UGT#A# * 62 immunofluorescence staining 62 hydrolase 62 Protein Kinase C 62 ductal lobular 62 Streptococcus agalactiae 62 lymphomas leukemias 62 intergenic 62 pancreatic endocrine 62 Homozygous 62 transmembrane protein 62 KIAA# 62 cytokine receptors 62 lysosomal storage diseases 62 uPAR 62 IDH mutations 62 papillomas 62 Mutational 62 paragangliomas 62 multigenic 62 N myc 62 Gorlin syndrome 62 FasL 62 homologs 62 RUNX3 62 cytochrome b 62 genes BRCA1 62 aneuploid 62 Overexpression 62 neuroblastoma tumors 62 Candida species 62 Y chromosomal 62 developmental abnormalities 62 embryonal 62 HBsAg 62 presymptomatic 62 E. faecalis 62 WT1 62 Chronic pancreatitis 62 histone modification 62 pleiotropic effects 62 NKT cells 62 previously undescribed 62 mutant p# 62 thyrotropin 62 NAT2 62 homologues 62 genomic rearrangements 62 NFkB 62 immunodominant 62 proximal colon 62 mGluR 62 gastric carcinomas 62 polyadenylation 62 hyperactivation 62 neuritic 62 choroidal neovascularization 62 OCA2 62 nitrotyrosine 62 genetic determinants 62 gene mutations 62 BRCA2 gene mutation 62 endostatin 62 fetal malformations 62 granzyme B 62 fluoroquinolone resistance 62 PDGFRA 62 vacuolar 62 effector function 62 SMN1 62 human leukocyte antigen 62 endocannabinoid signaling 62 infantile hemangioma 62 ectoderm 62 miR #a [001] 62 cytokine receptor 62 APOE4 62 receptor tyrosine kinase 62 microglial activation 62 ASCUS 62 cytogenetic abnormalities 62 EGFR mutations 62 catechol O methyltransferase COMT 62 Polymorphism 62 radiosensitivity 62 Janus kinase 62 diagnostic biomarker 62 TGF β 62 LRRK2 mutations 62 peptide receptor 62 Adenomas 62 esophageal squamous cell carcinoma 62 mitochondrial gene 62 Apolipoprotein E 62 ortholog 62 respiratory viral infections 62 plasma lipid 62 ccRCC 62 iNOS 62 metalloproteinases 62 orthologous genes 62 myeloproliferative disorders 62 epigenetic modifications 62 BRAC2 62 JAK STAT 62 histone deacetylases 62 CD8 + 62 untreated celiac disease 62 Thyroid nodules 62 colorectal cancer CRC 62 underlying pathophysiology 62 hepato 62 AMACR 62 oligodendrogliomas 62 mediated inhibition 62 methylated DNA 62 polycythemia vera PV 62 melanocortin receptor 62 thymidine kinase 62 isoenzymes 62 clonal expansion 62 selective modulator 62 genes CYP#C# 62 Phosphorylation 62 Proteobacteria 62 neurofibromatosis type 62 orthologous 62 activin 62 paraneoplastic 62 ENaC 62 GSK3B 62 nephrogenic 62 receptor gene 62 MAPKs 62 ploidy 62 downregulation 62 metastatic lesions 62 prion infection 62 transcriptional repressor 62 62 CIN2 + 62 RNA sequences 62 miRNA genes 62 recessive mutations 62 polyomavirus 62 neural progenitor 62 TRAF1 C5 62 CCR2 62 micrometastasis 62 nicotine receptor 62 carotid plaques 62 Chlamydia psittaci 62 kinase inhibition 62 DNA methyltransferases 62 dopamine D4 receptor 62 somatostatin 62 DLX5 62 chromosome aberrations