Related by context. All words. (Click for frequent words.) 70 BRCA2 gene 66 breast cancer genes BRCA1 66 CDKN2A 65 hypermethylated 65 BRCA1 BRCA2 64 MLL2 63 BRCA1 gene 63 mutated BRCA1 63 gene BRCA2 63 BRCA2 gene mutations 63 MSH2 62 BRCA2 62 MLH1 62 BRCA1 mutation 62 microdeletions 62 PALB2 62 germline mutations 62 mutated BRCA 62 CDH1 61 Li Fraumeni 61 genes BRCA1 61 BRCA2 gene mutation 61 BRCA genes 61 LRRK2 gene 61 TRAF1 C5 61 Yamanaka recipe 61 KRAS oncogene 61 non mutated KRAS 61 BRCA gene mutation 61 BRCA2 mutation 60 TCF#L# gene 60 somatic mutations 60 genes BRCA 60 BRCA2 mutations 60 BRIP1 60 BRCA1 mutations 60 TGFBR1 * 6A 60 ERBB2 60 K#N 59 CCR5 delta# 59 maternally inherited 59 missense mutations 59 CYP#D# gene 59 anaplastic lymphoma kinase ALK 59 LRAT 59 promoter methylation 59 KRAS mutations 59 apolipoprotein E4 59 CREBBP 59 atypical hyperplasia 59 F#del 59 BRAF gene 59 BRCA mutation 59 vanA gene 59 androgen receptor gene 58 inherited mutations 58 CETP VV 58 microcephalin 58 gene MECP2 58 TP# gene 58 BRCA mutations 58 Fragile X gene 58 ZNF# 58 JAK2 gene 58 K ras mutations 58 TACI mutations 58 IDH1 gene 58 CDK4 58 MAGE A3 protein 58 breast cancer gene mutation 58 ABCB1 58 BARD1 57 SHANK3 57 BRCA gene 57 SCN5A 57 breast carcinomas 57 FGFR2 gene 57 PTEN gene 57 GNAQ 57 K#R [002] 57 TCF#L# 57 Epstein Barr virus EBV 57 BRAF mutation 57 L. pneumophila 57 familial pancreatic cancer 57 LPA gene 57 GPC5 57 HG PIN 57 spontaneous mutations 57 TP# mutations 57 ALK gene 57 herpesviruses 57 TP# mutation 57 SOD1 gene 57 BRAF V#E 57 promoter hypermethylation 57 M. pneumoniae 57 C#Y 57 HLA DQ2 57 hemagglutinin H 57 mutated K ras 57 heterozygous 57 MYH9 gene 57 NR#A# gene 56 PTPN# 56 p# mutation 56 APOE e4 56 #q# deletion 56 APOE4 56 SLITRK1 56 MTHFR 56 GSTP1 56 medulloblastoma tumors 56 M. genitalium 56 FLT3 56 CFTR cystic fibrosis transmembrane 56 neuroblastoma tumors 56 renal cell carcinomas 56 IgA deficiency 56 ENPP1 56 Fetal heartbeats 56 UGT#A# * 56 familial ALS 56 ApoE4 gene 56 SMAD4 56 chromosomal disorders 56 FMR1 gene 56 R#W [002] 56 breast cancer susceptibility genes 56 c KIT 56 paternally inherited 56 #q#.# [001] 56 CCL#L# 56 CFTR gene mutations 56 APOE ε4 56 subtyped 56 BRCA1 56 sCJD 56 apolipoprotein E gene 56 HFE gene 56 hepatocellular carcinomas 56 T#I [002] 55 GSTT1 55 CFTR gene 55 retinoic acid receptor 55 cisplatin resistant 55 UGT#B# 55 aneuploid 55 FLT3 mutations 55 p# mutations 55 Immunohistochemical staining 55 K ras gene 55 APOL1 55 pilocytic astrocytomas 55 invasive lobular 55 antinuclear antibodies 55 mammary duct 55 reverse transcriptase inhibitors 55 MSH6 55 previously uncharacterized 55 JAK2 mutation 55 splice junctions 55 NNRTI resistance 55 untreated metastatic melanoma 55 MECP2 gene 55 IDH1 55 MEF2A 55 aneuploidies 55 microdeletion 55 mosaicism 55 IDH1 mutation 55 de novo mutations 55 HER2 receptor 55 MLL gene 55 WDR# 55 GBA mutations 55 mesotheliomas 55 LungAlert TM 55 M#V 55 HER2 neu 55 NF1 gene 55 BRCA 55 vesicular stomatitis virus 55 HLA DRB1 55 HNPCC 55 HBsAg 55 CHEK2 55 chromosome #q# [001] 55 glutamic acid decarboxylase 55 Li Fraumeni syndrome 55 spontaneous mutation 55 mitochondrial DNA mtDNA 54 nonsense mutations 54 methylation markers 54 microsatellite instability 54 Immunohistochemical analysis 54 proband 54 lung adenocarcinomas 54 coding exons 54 frameshift mutation 54 progranulin gene 54 mRNA transcripts 54 gene predisposing 54 oligodendrogliomas 54 fruitfly Drosophila 54 malignant polyps 54 #S rRNA 54 KCNQ1 54 allelic variants 54 EGFR mutations 54 NPC1 54 Single Nucleotide Polymorphisms SNPs 54 TET2 54 MCAD deficiency 54 pool dies unwept 54 chromosomal abnormalities 54 parkin gene 54 genetic variants associated 54 MC4R gene 54 mouse mammary tumor 54 KIF6 gene 54 Leydig cells 54 EGFR gene 54 RUNX3 54 PALB2 gene 54 causal variants 54 HER2 overexpression 54 abnormal methylation 54 Kufs disease 54 obstructive coronary artery 54 Cytogenetic 54 precancers 54 severe congenital neutropenia 54 G#S mutation 54 gene rearrangements 54 lung adenocarcinoma 54 chromosomal aberration 54 TMEM#B 54 indels 54 MAP#K# 54 SCN1A 54 colorectal carcinomas 54 urine cytology 54 NKX#.# 54 enteroviral 54 bloodborne 54 genetic abnormalities 54 LRP5 54 chromosomal aberrations 54 ABCB1 gene 54 FXTAS 54 NPM1 gene 54 CALHM1 54 Alzheimer's linked 53 intergenic regions 53 gene amplification 53 MC1R gene 53 APOE epsilon 4 53 chromosomal defect 53 nonmelanoma skin cancers 53 #S ribosomal RNA 53 WT1 53 testicular germ cell 53 lymph node biopsies 53 gene APOE4 53 Squamous 53 ApoE4 53 SPINK1 53 HER2 gene 53 CYT# potent vascular disrupting 53 causative mutations 53 GBM tumors 53 deleterious mutation 53 EGFR protein 53 chromosomal anomalies 53 British dadA 53 sentinel nodes 53 susceptibility loci 53 ORMDL3 53 IKZF1 53 Epidermal Growth Factor Receptor 53 Meckel Gruber 53 S. aureus isolates 53 virulence genes 53 basal cell nevus syndrome 53 TTR gene 53 BRAF protein 53 mutated genes 53 succinate dehydrogenase 53 HPV vaccine protects 53 NOTCH1 53 gene APOE 53 susceptibility gene 53 ETV1 53 p# deficient 53 chromosomal deletions 53 asymptomatic carriers 53 regulator CFTR gene 53 Bordetella pertussis 53 KCNE2 53 chromosomal rearrangement 53 T. vaginalis 53 mutant allele 53 tumors GIST 53 receptor CCR5 53 endostatin 53 ductal lobular 53 endometrial cancers 53 recessive mutations 53 TMPRSS2 ERG fusion 53 sporadic ALS 53 transthyretin TTR 53 childhood leukemias 53 chromosome #q# [002] 53 MGUS 53 Gorlin syndrome 53 causative gene 53 papillary renal cell carcinoma 53 KIAA# 53 rifamycins 53 nonmelanoma 53 IDH2 53 genotypic resistance 53 pigtail macaques 53 autosomal 53 Rh factor 53 murine leukemia virus 53 JAK mutations 53 vimentin 53 holoprosencephaly 53 Her2/neu 53 SMN1 gene 53 benign polyps 53 ankyrin B 53 alpha folate receptor 53 HUMIRA resembles 53 MYBPC3 53 modifier genes 53 bacterium Mycobacterium tuberculosis 53 nasopharyngeal swabs 53 Clusterin 53 chromosomal alterations 53 VHL gene 53 immunochemical 53 noncancerous prostate 53 humanised antibody 53 abnormal chromosomes 53 Endometrial 53 hypereosinophilic syndrome 53 ARID1A 53 HPV genotypes 53 CISH 53 Serologic 53 Acute myeloid leukemia 53 precancerous polyp 53 dopamine D4 receptor 53 cardiac channelopathies 52 transiently transfected 52 curable cancers 52 Cathepsin B 52 heterozygotes 52 splice variants 52 fetal chromosomal 52 mutant worms 52 PB2 gene 52 doublecortin 52 LMNA 52 mutated gene 52 #p#.# [001] 52 genetic loci 52 sporadic Creutzfeldt Jakob 52 Amniocentesis 52 CNTNAP2 52 immunoblotting 52 PNET 52 Colon polyps 52 #q# [001] 52 #.#ng/ml 52 NFKBIA 52 histocompatibility 52 Plasmodium ovale 52 pathogenic mutations 52 causative genes 52 squamous intraepithelial lesions 52 genus Plasmodium 52 Dpp 52 colonoscopy flexible sigmoidoscopy 52 nucleotide substitutions 52 GATA4 52 fronto temporal dementia 52 nephronophthisis 52 RNA ribonucleic acid 52 HPV# 52 virulence determinants 52 paramyxoviruses 52 klotho 52 advanced adenoma 52 myelofibrosis polycythemia vera 52 conductance regulator 52 bronchial lavage 52 Septin9 52 mda 7 52 human leukocyte antigens 52 CHD7 52 FDG PET scans 52 Microarray analysis 52 FGFR2 52 COL#A# 52 TSC1 52 NR#A# 52 commonly mutated genes 52 gene locus 52 activating mutations 52 toxoplasma 52 apolipoprotein E APOE 52 BCG vaccinated 52 VIPR2 52 epigenetic modifications 52 chromosomal mutations 52 Mycobacterium tuberculosis MTB 52 BMPR2 52 chromosome #p# [001] 52 USA# strain 52 Ultrasensitive 52 variant alleles 52 mutations 52 gene mutations 52 germline mutation 52 GBMs 52 rs# [004] 52 immunized mice 52 PTEN mutations 52 lung cancer NSCLC 52 collagen VII 52 PENNVAX ™ B 52 genomic alterations 52 Hutchinson Gilford progeria 52 asymptomatically 52 gastric carcinoma 52 APOE gene 52 Trichophyton rubrum 52 ELISPOT assay 52 genomic deletions 52 genes predisposing 52 PICALM 52 Folfox 52 neuroligins 52 MiRNAs 52 C1q 52 receptor tyrosine kinase inhibitor 52 APOE e4 gene 52 Brugada syndrome 52 Multidrug resistant 52 Rb gene 52 homologous genes 52 NRTI resistance 52 hMPV 52 muscular dystrophy cystic fibrosis 52 DICER1 gene 52 mutation 52 cTnT 52 micrometastasis 52 TOMM# 52 epigenetic silencing 52 glutamic acid decarboxylase GAD 52 epigenetic modification 52 densest breasts 52 intronic 52 chromosome abnormality 52 HLA loci 52 coding genes 52 ASCUS 52 FASPS 52 endometrial ovarian 52 human metapneumovirus 52 Roche AmpliChip 52 heterozygote 52 Mutation Detection 52 seronegative 52 serologically 51 sentinel lymph nodes 51 CYP#C# [002] 51 penetrance 51 MC1R 51 viral nucleic acids 51 tuberculin skin testing 51 detecting precancerous 51 retinoblastoma Rb 51 bladder cancers 51 genetic polymorphisms 51 syngeneic 51 genes CYP#C# 51 exomes 51 M. capricolum 51 LQTS 51 Apolipoprotein E 51 APOC3 51 molecular abnormalities 51 HHV 6 51 Oncotype DX colon cancer 51 STK# gene 51 APOA5 51 radiation chemoradiation 51 genetic rearrangements 51 underarm lymph nodes 51 methicillin sensitive 51 heterosexually acquired 51 genetic abnormality 51 melanoma basal cell 51 abnormal cytology 51 precancerous cervical 51 Liver biopsies 51 chromosome abnormalities 51 Situ Hybridization 51 ELISpot 51 PARP inhibition 51 DEAR1 51 chromosome #q#.# [001] 51 p# tumor suppressor 51 F#del mutation 51 APTIMA HPV 51 narcolepsy cataplexy 51 chromosomal regions 51 sickle cell cystic fibrosis 51 revealed multivessel coronary 51 miRNAs miR 51 Basal cell 51 monogenic 51 Peutz Jeghers syndrome 51 PIK3CA 51 SOD2 gene 51 Goltz syndrome 51 APOE allele 51 mutant genes 51 causative mutation 51 chromosomal defects 51 Smallpox vaccines 51 IL#R 51 mtDNA mutations 51 SMN1 51 Vesivirus 51 lymphogranuloma venereum 51 CYP#A# gene 51 latent tuberculosis TB 51 cytokeratin 51 BRCA gene mutations 51 CMV antibodies 51 Epstein Barr Virus EBV 51 Chlamydia trachomatis 51 autosomal dominant disorder 51 positional cloning 51 chromosomal anomaly 51 HLA B# 51 HPVs 51 underwent surgical resection 51 conserved sequences 51 APOE4 gene 51 epigenetic changes 51 vancomycin resistant enterococcus 51 cynomolgus macaques 51 malignant prostate 51 phylogenetic analyzes 51 chromosome translocations 51 polyadenylation 51 non coding RNA 51 Ribavirin causes 51 homozygote 51 Trypanosoma 51 HLA genes 51 cyclin dependent kinase inhibitor 51 miRview ™ squamous 51 downregulated 51 nucleoside analogues 51 anti PlGF 51 Leukemias 51 Human papillomaviruses 51 cysteines 51 constitutively expressed 51 Vidaza ® 51 specific CD8 + 51 genetic alterations 51 cells overexpressing 51 KIBRA 51 rs# [002] 51 spontaneously aborted 51 protein encoded 51 Entamoeba histolytica 51 colorectal carcinoma 51 E7 proteins 51 tryptophan hydroxylase 51 induced tumor regression 51 autosomes 51 apoE 51 vaginal lesions 51 hemagglutinin gene 51 neisseria 51 autopsied brains 51 mutant alleles 51 microalbumin test 51 HIV reverse transcriptase 51 granulosa cell 51 Hepatitis C Viral 51 spinal muscle atrophy 51 metastatic lymph nodes 51 Genotypes 51 TNF blocker therapy 51 dual tropic 51 Wnt signaling pathway 51 diagnose coronary artery 51 hepatoma 51 deafness neurological 51 miRNA expression 51 ALK mutations 51 virus XMRV 51 potent inducer 51 linkage disequilibrium 51 GRNOPC1 contains 51 RASSF1A 51 Human papillomavirus 51 Circulating tumor cells 51 Cervista HPV HR 51 methylenetetrahydrofolate reductase 51 attach auristatin 51 noninvasive prenatal genetic 51 alternatively spliced 51 HBeAg negative 51 Neisseria 50 anionic backbone 50 HER2/neu 50 Plasmodium vivax 50 Tanespimycin KOS 50 siRNA knockdown 50 gondii 50 abnormal prions 50 faulty BRCA1 gene 50 rs# rs# 50 precancerous tumors 50 CpG island 50 antisense therapies 50 Wwox 50 HBV genotype 50 pneumococci 50 genes encoding 50 STK# [002] 50 interferon pathway 50 epithelial tumors 50 immunohistochemical analysis 50 sequence homology 50 chronic myeloid 50 OGG1 50 dyskeratosis congenita 50 MTHFR gene 50 serratia 50 connexin 50 Tay Sachs thalassemia 50 proto oncogene 50 genetic mutations 50 CIN3 50 medulloblastomas 50 colorectal polyp 50 hypermethylation 50 DNA rearrangements 50 MeCP2 gene 50 micro RNAs 50 Genital HPV 50 monocytic 50 pRb 50 autism susceptibility genes 50 PFOS PFOA 50 Moraxella catarrhalis 50 bacteria Escherichia coli 50 OCT4 50 Chlamydia psittaci 50 cytopathic 50 #p#.# [002] 50 DNA methylation patterns 50 latently infected 50 H. pylori infections 50 transgenic rats 50 RT PCR assay 50 histopathologic examination 50 premutation 50 SETDB1 50 quantitative reverse transcriptase 50 NF1 50 Hormone receptor 50 XLHED 50 MIF protein 50 Or#b 50 ncRNA 50 Plasmodium falciparum parasite 50 faecal occult blood 50 vacuolar 50 malignant nodules 50 relapsed MM 50 recessive genetic 50 leukaemias 50 intestinal polyps 50 RNA viruses 50 preferentially bind 50 CYP#A# [002] 50 S. pyogenes 50 neuroblastomas 50 ApoE gene 50 Infectivity 50 short hairpin RNAs 50 JAK2 enzyme 50 autosomal recessive 50 anterior pituitary 50 Janus kinase 50 inactive X chromosome 50 thyroglobulin 50 test FOBT 50 hyperplastic 50 Kabuki syndrome 50 SE alleles 50 protein tyrosine phosphatase 1B 50 urine dipstick 50 suppressor gene 50 UCRs 50 adeno associated viruses 50 Immunohistochemistry IHC 50 TMPRSS2 ERG 50 androgen receptor AR 50 Cryptococcus neoformans 50 monozygotic twins 50 MYCN amplification 50 precancerous stem cells 50 anti JCV antibodies 50 systemic ALCL 50 chromosome #p#.# 50 CYT# vascular disrupting 50 cell nuclei 50 ovarian carcinomas 50 mycobacterium tuberculosis 50 karyotype 50 apoE4 50 gene fusions 50 #p# [001] 50 neuraminidases 50 Tissue Factor 50 forkhead 50 Arabidopsis genome 50 reverse transcriptase 50 haematopoietic 50 unmutated 50 pulmonary metastases 50 invasive carcinomas 50 RhuDex R 50 CGG repeats 50 adenocarcinomas 50 Trichomonas vaginalis 50 abnormal pap 50 dizygotic twins 50 A/Brisbane/#/# H#N# 50 Viral RNA 50 lincRNAs 50 HER1 50 HOX genes 50 sputum specimens 50 vancomycin resistant 50 histone deacetylases 50 Genetic variants 50 RNA polymerases 50 primary cilia 50 Thorough cooking kills 50 clinically detectable 50 genetic syndromes 50 hereditary breast cancer 50 Chromosomal 50 Y STR 50 abnormal pap smear 50 #S rRNA gene 50 sarcosine 50 Varicella zoster virus 50 campylobacter jejuni 50 p# antigen 50 SIVcpz 50 epithelial tissues 50 carboxyl terminal 50 biopsied tissue 50 DLC1 50 Trypanosoma brucei 50 autosomal recessive disorder 50 CYP#A# CYP#D# 50 ano genital warts 50 #q# [002] 50 TSC2 50 familial adenomatous polyposis 50 Biopsies 50 Enterobacter cloacae 50 hematopoietic cancers 49 INF2 49 FUS1 49 lavage fluid 49 HAAH 49 Nosema apis 49 Ehrlichia 49 Six3 49 index assay IVDMIA 49 BDNF gene 49 eotaxin 49 allele frequencies 49 brivanib 49 Lafora disease 49 HIV coinfected 49 xenotropic murine leukemia 49 Hepatitis B Virus 49 kinase gene 49 NMP# 49 Shp2 49 bacterium Neisseria meningitidis 49 D#N 49 human leukocyte antigen 49 P. reichenowi 49 Drosophila genome 49 anti HBs 49 gene mutation 49 Mycoplasma pneumoniae 49 vancomycin resistant Staphylococcus aureus 49 prevalent sexually transmitted 49 chromosome aberrations 49 Leydig cell 49 methicillin resistant staph 49 assay detects 49 Prostate specific antigen 49 bronchial epithelial cells 49 genomewide 49 subclinical hyperthyroidism 49 E#F# 49 FMR1 49 coagulase negative staphylococci 49 infects pigs 49 mRNA molecules 49 chlamydial 49 Brugada Syndrome 49 MAGE A3 ASCI 49 Protein Kinase C 49 #q#.# [002] 49 ADH1B * 49 major histocompatibility complex 49 Escherichia coli Klebsiella pneumoniae 49 Entamoeba 49 methylation patterns 49 germline 49 IRF6 gene 49 estrogen receptor 49 proximal colon 49 microRNA expression 49 differentially regulated 49 GSTM1 gene 49 CCR5 receptors 49 HMGA2 49 achromatopsia 49 recurrent metastatic 49 HLA alleles 49 mammographically 49 mutations conferring 49 HDACs 49 GSTM1 49 Lassa virus 49 Vaxfectin formulated 49 SLC#A# [001] 49 P. knowlesi 49 Prox1 49 Zolinza 49 Drosha 49 CAG repeats 49 recurrent NSCLC 49 pneumocystis 49 5q chromosome 49 HepG2 cells 49 P. ovale 49 Small RNAs 49 engineered bladders 49 lymphocytic 49 dioxin Zimpfer 49 adipogenic 49 epistasis 49 tumor suppressor genes 49 KIT mutations 49 Panton Valentine Leukocidin PVL 49 S aureus 49 lamivudine resistant 49 methylated 49 #p# [003] 49 non coding RNAs 49 cystic fibrosis transmembrane conductance 49 germline cells 49 ribosomal RNA 49 glioblastoma tumors 49 miRNA genes 49 Transcription factors 49 pelvic ultrasound 49 congenital disorders 49 prostate carcinomas 49 MDR1 49 imprinted genes 49 Chlamydia pneumoniae 49 flavopiridol 49 ERK signaling 49 dengue serotype 49 ADAMTS# 49 missense mutation 49 BEXXAR Therapeutic Regimen 49 vivax 49 VNTR 49 DNA adducts 49 HSV1 49 Histopathologic examination 49 Bcl2 49 CyPath ® assay 49 parainfluenza viruses 49 STAT4 49 staphylococci 49 Hair follicle 49 DNA methyltransferase 49 LKB1 49 tumor xenograft models 49 serine threonine kinases 49 rRNA 49 palladin 49 M. leprae 49 karyotypes 49 nephropathy kidney 49 Genetic variations 49 endogenous ligands 49 protozoan parasite 49 Pelvic inflammatory 49 cyclin E 49 viral nucleic acid 49 Fecal occult blood 49 M#V mutation 49 nestin 49 NS5b 49 missense 49 Estrogen receptor positive 49 cervical vaginal 49 FUS TLS 49 epigenetic alterations 49 aneuploidy 49 HAR1 49 Amyloid beta protein 49 HGPS 49 orally administered inhibitor 49 Upregulation 49 spontaneous miscarriages 49 genetic aberrations 49 IRF6 49 telomerase reverse transcriptase 49 mitochondrial DNA mutations 49 cervicovaginal 49 hereditary hemochromatosis 49 tumor suppressor protein 49 histone demethylase 49 PARP inhibitor 49 Oncotype 49 abnormal proteins 49 TRAIL induced apoptosis 49 nonidentical 49 Micromonas 49 CSF Tf 49 V#F mutation 49 primate genomes 49 somatic mutation 49 Telik logo TELINTRA 49 DISC1 gene 49 NMIBC 49 beta lactams 49 smallest extrasolar planet 49 beta1 integrin 49 mitochondrial genomes 49 chromosomal rearrangements 49 targeting moieties 49 parainfluenza virus 49 KCNH2 49 clade B 49 mammary cells 49 gene variants 48 centromeric 48 Crizotinib 48 Paraffin Embedded FFPE 48 noncoding RNAs 48 thyroid peroxidase 48 progestagen 48 paralogs 48 orthologous genes 48 ankyrin repeat 48 FGFR3 48 TAp# 48 Gleevec resistant 48 tyrosine kinases 48 recurrent miscarriages 48 DU# [002] 48 Xelox 48 FLT3 kinase 48 Alfacell proprietary ribonuclease 48 Sanger sequencing 48 tissue biopsies