Related by context. All words. (Click for frequent words.) 67 BRIP1 65 BRCA1 BRCA2 64 breast cancer genes BRCA1 63 CDK4 63 MSH2 62 mutated BRCA1 62 KRAS oncogene 62 gene BRCA2 62 PALB2 62 HER2 neu 61 mutated BRCA 61 deCODE ProstateCancer TM 61 CDH1 61 mutated K ras 61 TP# gene 61 susceptibility gene 61 BRAF gene 61 MTHFR 61 MLH1 60 BRCA2 carriers 60 Yamanaka recipe 60 MLL2 60 LRAT 60 BRAC2 60 BARD1 60 BRAF V#E 60 cisplatin resistant 60 CDKN2A 59 CCR5 delta# 59 BRCA1 gene 59 BRCA2 gene 59 AGTR1 59 cells overexpressing 59 pancreatic lung 59 mammary duct 59 C#Y 59 PTPN# 59 TP# mutation 59 antisense therapies 59 GAB2 58 Li Fraumeni 58 NFKB 58 deCODE AF TM 58 CFTR gene 58 BRCA genes 58 CHEK2 58 causative genes 58 Gene Mutations 58 ApoE 58 promoter hypermethylation 58 interferon pathway 58 PTEN gene 57 FGFR1 57 genes BRCA1 57 HER2 receptor 57 GSTP1 57 Janus kinase 57 Oncogenes 57 p# deficient 57 inherited mutations 57 KIF6 gene 57 MECP2 gene 57 LRRK2 gene 57 Single Nucleotide Polymorphisms SNPs 57 Genes Identified 57 endostatin 57 Sox9 57 gamma globin gene 57 MYH9 gene 57 gene amplification 57 III EGFRvIII 57 mRNA transcripts 57 genes predisposing 57 aneuploidy 57 HFE gene 57 gene predisposing 57 apolipoprotein E4 57 testicular germ cell 57 BRCA2 gene mutations 57 gag pol 56 mammary cells 56 NFkB 56 collagen VII 56 Estrogen Receptor 56 MEF2A 56 ALK gene 56 SOD1 gene 56 hypermethylated 56 ERBB2 56 MTHFR gene 56 Cystic fibrosis CF 56 p# mutation 56 K ras mutations 56 Human Leukocyte Antigen 56 TEL AML1 56 ANGPTL4 56 Gene Mutation 56 APOL1 56 mosaicism 56 muscular dystrophy cystic fibrosis 56 HLA DQ2 56 IDH2 56 Wwox 56 methylation markers 56 Signaling Pathway 56 Chromosome 56 CALHM1 56 CYP#D# gene 56 glycogen synthase kinase 56 SHANK3 56 FGFR2 gene 56 radiolabeled antibodies 56 OCT4 56 granulosa cell 56 comparative genomic hybridization CGH 56 apolipoprotein E gene 56 Tumor Suppressor 56 MECP2 56 ZNF# 56 tumor suppressor gene 56 Leukemias 56 Roche AmpliChip 56 Genetic mutation 56 PIK3CA 56 modifier genes 56 TET2 56 IRS1 56 SPINK1 56 NF1 gene 56 breast cancer metastasis 56 #q#.# [001] 56 SOD2 gene 55 microdeletion 55 LRP5 55 BRAF protein 55 connexin 55 ENPP1 55 Cyclin D1 55 progranulin gene 55 mutant genes 55 DU# [002] 55 deCODE BreastCancer TM 55 Genetic mutations 55 DGAT1 55 SMAD4 55 telomere DNA 55 microcephalin 55 HMMR 55 Transcription Factor 55 microsatellite instability 55 SCN5A 55 #S rRNA 55 SMN1 55 methylenetetrahydrofolate reductase 55 Chromosomal 55 tumor suppressors cytokines 55 IRAK1 55 HER2 gene 55 FLT3 55 Metastases 55 PALB2 gene 55 gastrointestinal stromal tumors GISTs 55 missense mutations 55 atypical hyperplasia 55 filaggrin gene 55 LMNA 55 Homozygous 55 somatic mutations 55 chromosome #q# [001] 55 Gene Linked 55 fronto temporal dementia 55 SETDB1 55 cell adhesion molecule 55 methyltransferase 55 CpG island 55 JAK2 enzyme 55 PTP1B 55 germline mutations 55 R#W [002] 55 MLL gene 55 human leukocyte antigen HLA 55 Vaccine Shows Promise 55 neuroblastoma tumors 55 aneuploidies 55 genetic mutations 55 ovarian colon 55 genes CYP#C# 55 VKORC1 55 mutated genes 55 cyclin dependent kinase 55 aneuploid 55 STAT4 55 microdeletions 55 breast carcinomas 55 Colon polyps 54 breast epithelial cells 54 #p# [003] 54 susceptibility loci 54 Notch signaling 54 suppressor gene 54 fruitfly Drosophila 54 FGFR2 54 diagnostic biomarker 54 abnormal methylation 54 Platinum Resistant Ovarian 54 BRCA1 mutations 54 FMR1 gene 54 pyruvate kinase 54 Li Fraumeni syndrome 54 NPC1 54 deCODE T2 TM 54 DHFR 54 monocytic 54 Genes Discovered 54 gene BRCA1 54 Fragile X gene 54 genetic aberrations 54 Scorpion venom 54 Glioblastoma multiforme GBM 54 von Hippel Lindau 54 BRCA2 gene mutation 54 Cell Non Hodgkin 54 KIAA# 54 Susceptibility Gene 54 COX2 54 chromosome #p# [001] 54 V Leiden 54 EGFR protein 54 proto oncogene 54 epigenetic regulation 54 capsular polysaccharide 54 Test Detects 54 MeCP2 gene 54 Caveolin 54 VHL gene 54 MSH6 54 klotho 54 PTEN protein 54 positional cloning 54 chemo resistant 54 transcriptionally active 54 INF2 54 transgenic mouse model 54 micro RNAs 54 commonly mutated genes 54 cardiac channelopathies 54 Naive Patients 54 molecular abnormalities 54 chimeric mice 54 cyclin D1 54 Subtypes 54 HMGCR 54 Squamous Cell 54 Pten 54 C#T [002] 54 Shows Promise Against 54 thrombospondin 54 breast cancer gene mutation 54 UGT#B# 54 coding exons 54 preoperative staging 54 MC1R gene 54 paternally inherited 54 BRCA2 54 Germline 53 plasminogen activator inhibitor 53 genetic alteration 53 NKX2 53 gene rearrangements 53 X Chromosome 53 VIPR2 53 progressive neurodegenerative disorder 53 eotaxin 53 APOE epsilon 4 53 E#F# 53 antisense strand 53 virulence genes 53 Mesenchymal 53 IgA deficiency 53 Genes Linked 53 transgenic rats 53 germline mutation 53 autoinflammatory 53 Aneuploidy 53 vesicular stomatitis virus 53 alpha synuclein toxicity 53 monogenic disorders 53 p# mutations 53 multiply uncontrollably 53 Estrogen receptor 53 suppresses tumor 53 Genetic variants 53 Premature Aging 53 TP# mutations 53 LKB1 53 ImmunoGen TAP technology 53 HG PIN 53 bisulfite sequencing 53 CFTR gene mutations 53 gene locus 53 ferroportin levels 53 CEP# 53 genetic variants associated 53 TCF#L# gene 53 IL#R 53 cause cardiac channelopathies 53 HLA DRB1 53 susceptibility alleles 53 Epidermal Growth Factor 53 MEK1 53 Kufs disease 53 Epidermal Growth Factor Receptor 53 Epithelial 53 microRNA molecules 53 cystic fibrosis transmembrane conductance 53 autosomal recessive disease 53 epigenetic changes 53 Genetic variation 53 MIF protein 53 RAD# [001] 53 Akt1 53 methyl CpG binding 53 SATB1 53 IKZF1 53 kidney urologic 53 IDH1 53 tumor suppressor protein 53 Ets2 53 MYBPC3 53 BRCA gene mutation 53 single nucleotide polymorphism 53 gene fusions 53 Meckel Gruber 53 NR#A# 53 monogenic 53 Interferon gamma 53 TACI mutations 53 BRCA1 53 uterus womb 53 TAp# 53 NSCLC tumors 53 SOD1 protein 53 Mitochondrial 53 MicroRNA 53 Dystrophin 53 PITX2 53 PARP inhibition 53 APOE e4 53 susceptibility locus 53 chromosome #p# [002] 53 HLA loci 53 DLX5 53 TGFBR1 * 6A 53 estrogen receptor alpha 53 TYMS 53 palladin 53 TNFAIP3 53 de novo mutations 53 fatty acid binding 53 TGFBR1 53 MeCP2 protein 53 parkin gene 53 gene polymorphism 53 dopamine receptor gene 53 BRCA 53 melanocyte 53 hereditary breast 53 leukemia lymphomas 53 Spinal muscular atrophy 53 Transcriptome 53 Muscular dystrophies 52 monozygotic twin 52 p# gene 52 Basal Cell 52 GATA3 52 CCL#L# 52 receptor tyrosine kinase 52 Suppl. 52 chromosomal aberrations 52 Helps Diagnose 52 HLA markers 52 NFKBIA 52 regulates gene expression 52 SNP rs# [001] 52 APOC3 52 SMN1 gene 52 colonic mucosa 52 Epstein Barr virus EBV 52 neurofibromatosis type 52 Nedd4 52 cyclin E 52 protein tyrosine phosphatase 52 spontaneous mutations 52 BMPR2 52 PICALM 52 Von Willebrand 52 allelic variants 52 recessive mutations 52 Six3 52 Gnant consults 52 RRM1 52 Neuronal 52 IDH mutations 52 NKX#.# 52 CETP VV 52 Clusterin 52 Breast Cancer Cells 52 breast cancer subtypes 52 Tibolone 52 K ras gene 52 mutant allele 52 mutations 52 Nf1 52 C EBP alpha 52 ductal breast cancer 52 GNAQ 52 Telomere 52 gene APOE 52 primordial germ cells 52 genetic loci 52 CHD7 52 castration resistant 52 progressive retinal degenerative 52 BRCA2 genes 52 SORL1 gene 52 BRCA2 mutation 52 Glioma 52 kinase gene 52 Drug Shows Promise 52 chemokine receptor 52 colorectal carcinomas 52 Hutchinson Gilford progeria 52 endogenous retroviruses 52 channelopathies 52 pDC 52 ApoE gene 52 genetic abnormalities 52 chromosome #q# [002] 52 Screening mammography 52 protein fragment 52 dopamine D4 receptor 52 Slow Progression 52 chromosome #p#.# 52 colorectal tumor 52 nucleus Chinnery 52 LPA gene 52 SPORE grant 52 Chemokine Receptor 52 tests miRview TM 52 IDH1 gene 52 Hypertrophy 52 mitochondrial mutations 52 Medullary thyroid cancer 52 abnormal chromosomes 52 caveolin 52 ADAM# 52 peptide antigens 52 apolipoprotein E 52 Apolipoprotein E 52 ARF1 52 MC4R gene 52 KRAS variant 52 dedifferentiation 52 nonsense mutations 52 nephronophthisis 52 uPAR 52 Researchers Identify 52 Breast Cancer Recurrence 52 KRAS mutations 52 ADPKD 52 genome rearrangements 52 proline rich 52 lung adenocarcinoma 52 KRAS mutation 52 intestinal polyps 52 mitochondrial gene 52 causative gene 52 Wnt signaling pathway 52 Nonalcoholic fatty liver 52 EZH2 52 Tumor Suppressor Gene 52 virulence determinants 52 severe congenital neutropenia 52 ABCB1 52 CIB1 52 Apobec3 52 human leukocyte antigens 52 extracellular domain 52 pancreatic islet 52 TCF4 52 GPC5 52 BRCA1 mutation 52 mutation 52 TRIM5a 52 TOP2A gene 52 NR#A# gene 52 Dr. Victor Velculescu 52 HMGA2 52 Protein Kinase 52 cystic fibrosis sickle cell 52 Klotho gene 52 Biomarker Panel 52 metabolizing enzyme 52 HLA DR4 52 chromosome abnormality 52 mutant gene 52 Scientists Identify 52 transgenic mouse models 52 M. genitalium 52 susceptibility genes 52 human T lymphotropic 52 Epstein Barr Virus 52 mutated gene 52 DNA rearrangements 52 Src 52 frameshift mutation 52 BRCA1 gene mutation 52 haematopoietic 52 Expression Profiling 52 genomewide 52 heterozygotes 52 protein encoded 52 Breast Tumors 52 Chlamydia psittaci 52 Notch1 52 Bone marrow transplantation 51 DNA Methylation 51 Pre implantation genetic 51 vimentin 51 huntingtin gene 51 Histone 51 GSTT1 51 mitochondrial DNA mtDNA 51 SLITRK1 51 genome decoded 51 PD# [005] 51 ErbB4 51 Endothelial Cells 51 Activating mutations 51 immunized mice 51 PON1 51 BRAF mutation 51 HOUSE Remains 51 #q# deletion 51 #p#.# [002] 51 EGFR gene 51 TSC1 51 Fragile X mental retardation 51 Polymorphisms 51 Gene Variants 51 chitinase 51 mineralocorticoid receptor 51 Agilent microarrays 51 nonsmall cell lung cancer 51 Epstein Barr Virus EBV 51 hypermethylation 51 causal variants 51 tumor suppressor genes 51 STK# gene 51 GATA4 51 herpesviruses 51 #/#/# Appendix 3Y Page 51 pulmonary metastases 51 TCF#L# 51 radiosensitivity 51 genetic alterations 51 dysbindin 51 Situ Hybridization 51 Transcription factors 51 V#E 51 papillary RCC 51 multigene 51 Arabidopsis genome 51 NF kappaB 51 p# biomarker 51 Rearrangements 51 GISTs 51 Protein Linked 51 Autoantibodies 51 RASSF1A 51 flavopiridol 51 hereditary breast cancer 51 murine leukemia virus 51 #p# [001] 51 human leukocyte antigen 51 epigenetically 51 underarm lymph nodes 51 LDL receptor 51 inherited maternally 51 micro RNA 51 MAPK pathway 51 neurofibromas 51 catenin 51 Squamous 51 aneuploid cells 51 KIT mutations 51 ovarian cervical 51 Methylation 51 Oncogenic 51 Neural stem cells 51 CYP#C# * 51 MYCN 51 Genetic Variations 51 Id1 51 melanoma basal cell 51 Sanger sequencing 51 GFP gene 51 Brugada Syndrome 51 faulty BRCA1 gene 51 deCODE Glaucoma TM 51 CHD5 51 Mutational 51 genetic rearrangements 51 OGG1 51 Major Histocompatibility Complex 51 MC1R 51 Breast Cancers 51 HNPCC 51 beta globin 51 Systemic lupus erythematosus SLE 51 KLF4 51 HPRT gene 51 chromosomal mutations 51 Mutation Detection 51 Hyperplasia 51 matrix metalloproteinase 51 MDM2 51 DNA methylation patterns 51 chromosome #q 51 Predict Risk 51 Brd4 51 HER2 expression 51 carboxy terminal 51 genes 51 Supplemental Figure 51 pathogenic mutations 51 Prox1 51 GSTM1 51 gene mutations 51 polyunsat 51 sCJD 51 Genetic predisposition 51 Fibroblast 51 chromatin proteins 51 NFAT 51 cytokeratin 51 IGF2 51 p# MAPK 51 Mycoplasma genitalium 51 prognostic markers 51 #p#.# [001] 51 ubiquitylation 51 c KIT 51 cancerous nodules 51 AVEO proprietary 51 transmembrane receptor 51 dbSNP 51 ribosomal protein 51 Genetic variations 51 DNA methylation biomarker 51 NEDD9 51 phosphorylates 51 autosomal 51 autosomal dominant disorder 51 Genetic Predisposition 51 Alleles 51 content VENDOR WHITE PAPER 51 tegafur 51 casein kinase 51 LIS1 51 molecular biomarkers 51 PKM2 51 transactivation 51 BDNF gene 51 pilocytic astrocytoma 51 IDH1 mutation 51 cervical precancers 51 gene polymorphisms 51 Basal cell 51 beta1 integrin 51 FUS protein 51 VNTR 51 Tay Sachs thalassemia 51 CCR3 51 Glial 51 chromosomal rearrangement 51 thymine T 51 dystrophin gene 51 kilobases 51 Mouse Model 51 Benign breast 51 polycystic kidneys 51 TMEM#B 51 genotoxic stress 51 Inactivation 51 CHO K1 51 Systemic Delivery 51 HLA B# 51 DNA methyltransferases 51 Circulating Tumor Cells 50 PKD1 50 Subtype 50 Patrick Swayze Dies 50 Ivanhoe Newswire Patients 50 Bucindolol 50 molecular subtypes 50 neural progenitor cells 50 multiforme 50 autosomal recessive disorder 50 FGFs 50 chromosomal anomalies 50 WT1 50 molecular pathway 50 nonmelanoma 50 oncogenic mutations 50 estrogen receptor 50 GLUT1 50 Velculescu 50 Microtubule 50 epigenetic markers 50 KCNQ1 50 metastatic bladder 50 Aromatase 50 UGT#A# * 50 APOE gene 50 Whole Genome 50 Genetic Variant 50 Neuregulin 1 50 pilocytic astrocytomas 50 receptor protein 50 Apolipoprotein 50 chromosomal abnormalities 50 Transgenic Mice 50 forkhead 50 gene mutation 50 severe NCI Grades 50 pre malignant lesions 50 genomic rearrangements 50 Fibroblasts 50 Inhaling asbestos fibers 50 infects pigs 50 urothelial cells 50 epithelial tissues 50 Cytotoxic T 50 COL#A# 50 nucleic acid sequence 50 fetal aneuploidy 50 Oncotype DX colon cancer 50 K#R [002] 50 armpit lymph nodes 50 Cell Adhesion 50 Breast Cancer Risk 50 MMP# 50 genomic instability 50 receptor molecule 50 K#N 50 medulloblastoma tumors 50 Parathyroid 50 myostatin gene 50 ALK inhibitors 50 HLAs 50 Hp2 2 50 thymine 50 genetic polymorphisms 50 DISC1 gene 50 PCA3 gene 50 leukaemic cells 50 NF KappaB 50 mutant proteins 50 Bleomycin 50 * 1F 50 immunodeficiency disorders 50 Estrogen fuels 50 neuro endocrine 50 short hairpin RNAs 50 tumor suppressors 50 diagnose coronary artery 50 Sonic Hedgehog 50 HDACs 50 familial adenomatous polyposis 50 neuroligins 50 homolog 50 HLA DQ 50 promoter methylation 50 C#T [001] 50 tumor biopsies 50 amyloid protein plaques 50 Healthbeat Report 50 ChR2 50 VEGF receptor 50 DICER1 gene 50 Cancer Cells 50 splice variant 50 FCGR3A 50 gene expression profiles 50 heterozygote 50 CTCF 50 chromosome #q#.# [001] 50 causative mutations 50 Adenoma 50 lymphoid tissue 50 coding genes 50 globin genes 50 Sipuleucel T 50 Multidrug Resistance 50 7F 9V 50 LPS induced 50 hereditary predisposition 50 Single Nucleotide Polymorphism 50 Her2/neu 50 Chronic HCV 50 squamous cell lung cancer 50 comparative genomic hybridization 50 tau gene 50 #S ribosomal RNA 50 malignant astrocytoma 50 benign polyps 50 chromosomal disorders 50 autosomal recessive 50 BRCA mutations 50 T#M 50 C1q 50 cysteines 50 transcriptional repressor 50 PTEN mutations 50 Single Nucleotide Polymorphisms 50 RNA splicing 50 BRCA2 mutations 50 tumor suppressing 50 chromatin immunoprecipitation ChIP 50 Neurofibromatosis type 50 Artificial Pancreas 50 cervical lymph node 50 #q# [001] 50 Glucagon Like Peptide 50 amino acid substitution 50 IRF6 50 Ultrasensitive 50 Myostatin 50 T1D 50 TRAF6 50 tests miRview ™ 50 CAG repeats 50 differentially expressed proteins 50 epigenetic alterations 50 ectopic expression 50 histone deacetylases 50 pancreatic ductal 50 pool dies unwept 50 aromatase 50 chromosome rearrangements 50 Lafora disease 50 human herpesvirus 50 exome sequencing 50 JAK STAT 50 gene 50 prognostic marker 50 DLC1 50 Tumor Growth 50 seminomas 50 leptin receptor 50 IGFBP 50 acute lymphoid leukemia 50 pRb 50 autism susceptibility genes 50 SLC#A# gene [001] 50 leukaemias 50 polyps growths 50 protein p# 50 commercialize deforolimus 50 NPM1 gene 50 Breast Ovarian Cancer 50 CYP#E# gene 50 replicase 50 p#NTR 50 5 hmC 50 Inflammatory Markers 49 genetic biomarkers 49 dyskeratosis congenita 49 IL#B 49 CYP#C# [001] 49 multiplex ligation dependent 49 Cloning embryos 49 BRCA mutation 49 precancers 49 oncogenes 49 Chronic pancreatitis 49 #S rRNA gene 49 H#D 49 mRNA expression 49 MAP#K# 49 Small Intestine 49 squamous miRview TM 49 telomere dysfunction 49 ESR1 49 uracil 49 Myotonic dystrophy 49 homozygosity 49 mRNA molecules 49 exonuclease 49 Epithelial Cell 49 KRAS BRAF 49 neuregulin 1 49 microRNA expression 49 holoprosencephaly 49 Inhibits 49 splice variants 49 quantitative trait loci 49 missense mutation 49 DICER1 49 mouse fibroblasts 49 indels 49 Trichomonas 49 gene deletions 49 Antigens 49 BRCA gene 49 Fanconi anemia FA 49 KRT# 49 Gleevec resistant 49 cynomolgus macaques 49 KIBRA 49 alpha synuclein gene 49 bought Glaxo Serevent 49 F#del 49 hedgehog pathway 49 NNRTI resistant virus 49 Mutation Analysis 49 Wnt#b 49 Resequencing 49 Phosphatase 49 Amniocentesis 49 Deoxyribonucleic acid 49 missense 49 APOE4 49 TOMM# 49 NRG1 49 transcriptional repression 49 amyloid plaque formation 49 circadian genes 49 spinal muscular atrophy SMA 49 transfusion syndrome 49 microRNAs miRNAs 49 demethylase 49 Peripheral Blood 49 ApoE4 gene 49 methylation profiling 49 receptor ligand 49 lupus anticoagulant 49 rs# [001] 49 estrogen receptor ER 49 tau protein tangles 49 Predict Prostate Cancer 49 chromosomal aberration 49 genetic markers 49 GLI1 49 alternatively spliced 49 enteroviral 49 nucleotide substitutions 49 SIRT1 gene 49 phenotypic expression 49 Obesity Linked 49 claudin 49 chromosomal anomaly 49 HBV HCV 49 invadopodia 49 Glucocorticoid 49 costimulatory 49 #q#.# [002] 49 SCN1A 49 Von Willebrand disease 49 deacetylation 49 Help Predict 49 neoplastic cells 49 CGG repeats 49 karyotype 49 miRNAs miR 49 sortilin 49 Prenatal Diagnosis 49 CNTNAP2 gene 49 Squamous cell 49 Synthase 49 progestagen 49 fatal neuromuscular disorder 49 shortened telomeres 49 Protease 49 Genetic Mutation 49 Tr DNA 49 P2X 49 gastrin analogue TT 49 abnormal proteins 49 genetically reprogrammed 49 transcriptional profiles 49 FANCD2 49 PAK1 49 NOD2 49 null mice 49 antigenic epitopes 49 JAK mutations 49 radioiodine therapy