Related by context. All words. (Click for frequent words.) 71 chromosomal instability 70 chromosomal abnormalities 69 mosaicism 67 MSH2 67 chromosomal aberrations 67 chromosome abnormalities 66 genetic abnormalities 66 transgene expression 66 microdeletion 66 PTPN# 66 mtDNA mutations 65 DNA methylation patterns 65 aneuploidies 65 HbF 65 hypermethylation 65 malignant transformation 64 aneuploid 64 HMGA2 64 mitochondrial dysfunction 64 IGF2 64 telomere dysfunction 64 PTEN protein 64 haematopoietic 64 pre eclamptic 64 chromosomal rearrangement 64 gonadotropins 64 tumor suppressor gene 64 somatic mutations 64 STAT4 64 de novo mutations 64 homozygosity 64 fetal malformations 63 gene amplification 63 monozygotic twins 63 allelic 63 epigenetic changes 63 p# mutations 63 PDGFR 63 APOE e4 63 somatic mutation 63 heterozygosity 63 WT1 63 CHD7 63 genomic instability 63 methylation 63 MLH1 63 ERCC1 63 TGF β 63 BRCA2 mutation carriers 63 inherited mutations 63 TSC1 63 proto oncogene 63 genotoxic stress 63 LKB1 63 chimerism 62 MECP2 gene 62 PALB2 62 p#INK#a 62 breast cancer metastasis 62 chromosomal 62 mutant alleles 62 RUNX3 62 Jhdm2a 62 CFTR gene 62 mitochondrial mutations 62 cyclin E 62 mutations 62 intestinal epithelium 62 IgA deficiency 62 FGFR2 62 BRCA1 mutations 62 H#K#me# 62 NF1 62 PTEN gene 62 mammographic density 62 Leydig cell 62 #q#.# [001] 62 BRCA2 62 IDH1 62 epigenetic silencing 62 microsatellite instability 62 trisomy 61 TP# gene 61 IKZF1 61 cystatin C 61 p# mutation 61 mammary cancers 61 tyrosine phosphorylation 61 Notch signaling 61 chromosome abnormality 61 BRCA1 61 IUGR 61 thyroglobulin 61 germline 61 sFlt 1 61 GNAQ 61 spontaneous mutations 61 TAp# 61 overexpression 61 Cyclin D1 61 GSTP1 61 epigenetic markers 61 ectopic expression 61 follicle stimulating hormone FSH 61 micro RNAs 61 heterozygotes 61 HNPCC 61 atypical hyperplasia 61 beta1 integrin 61 genomic imprinting 61 ovarian hormones 61 chromosomal anomalies 61 aneuploidy screening 61 APOE gene 61 Prox1 61 factor PlGF 61 induce pluripotency 61 EZH2 61 hereditary breast cancer 61 mutation 61 uPAR 61 LRP5 61 BARD1 61 p# MAPK 61 carcinoembryonic antigen 61 telomere length 61 p# activation 61 Cytogenetic 61 KLF4 61 fetal chromosomal 61 mRNA expression 61 microglial 61 TGF ß 61 nucleotide substitutions 61 heritable 61 spontaneous mutation 61 CDH1 61 imprinted genes 61 autosomal recessive 61 transthyretin 61 BRCA1 gene 61 precursor lesions 61 basal cell nevus syndrome 61 tumorigenesis 61 suppressor gene 61 Pten 61 sporadic ALS 61 PARP inhibition 61 polycystic ovary syndrome 61 familial ALS 61 motor neuron degeneration 60 virulence genes 60 susceptibility gene 60 miR #a [001] 60 BCL#A 60 kidney allograft 60 APOL1 60 PON1 60 miRNA expression 60 GSTT1 60 UGT#A# * 60 tumor suppressor protein 60 X chromosome inactivation 60 melanocyte 60 Stat5 60 cyclin D1 60 K ras mutations 60 trophoblast cells 60 TOP2A 60 chlamydial infection 60 Foxp3 60 DNA methylation 60 etiologic 60 germline mutations 60 FGF# 60 mRNA transcripts 60 BRAF gene 60 Clusterin 60 FMR1 gene 60 lung adenocarcinoma 60 genes BRCA1 60 karyotype 60 blastomeres 60 HER2 overexpression 60 growth restriction IUGR 60 gene mutations 60 Heterozygous 60 epigenetic modification 60 FGFR3 60 renal fibrosis 60 chromosomal translocations 60 APOC3 60 DNMT1 60 CHEK2 60 E#F# 60 caveolin 1 60 karyotypes 60 activin 60 telomere shortening 60 leiomyomas 60 dizygotic 60 LQTS 60 mitochondrial fusion 60 penetrance 60 breast cancer genes BRCA1 60 axonal degeneration 60 abnormal chromosomes 60 missense mutations 60 Notch1 60 APOE ε4 59 activating mutations 59 X inactivation 59 IVF ICSI 59 chromosomal rearrangements 59 neural tube defect 59 varicoceles 59 transdifferentiation 59 prostate carcinogenesis 59 MLL gene 59 Chromosomal 59 polyadenylation 59 corpus luteum 59 MC1R 59 NRG1 59 BRIP1 59 epistasis 59 medulloblastomas 59 sCJD 59 spermatogenesis 59 prognostic indicator 59 prognostic factor 59 colorectal carcinoma 59 rs# [002] 59 APOE4 59 mutant huntingtin protein 59 thyrotropin levels 59 CCR3 59 HOTAIR 59 Genetic predisposition 59 TMEM#B 59 connexin 59 recurrent miscarriages 59 hamartomas 59 maternally inherited 59 Methylation 59 Immunohistochemical analysis 59 mtDNA 59 hepatic lipase 59 #q#.# [002] 59 holoprosencephaly 59 mRNA decay 59 #q# deletion 59 protein encoded 59 microRNAs miRNAs 59 recurrent miscarriage 59 endoplasmic reticulum stress 59 clusterin 59 Hashimoto thyroiditis 59 FLT3 59 glycosylation 59 PECAM 1 59 mammary cells 59 tumorigenicity 59 epigenetic alterations 59 promoter hypermethylation 59 KIT mutations 59 telomerase activation 59 fatty acid synthase 59 adrenal function 59 Rb gene 59 promoter methylation 59 mutated BRCA1 59 breast carcinomas 59 MDM2 59 homodimers 59 shortened telomeres 59 phenotypic expression 59 preterm deliveries 59 HER2 gene 59 cybrid 59 immunohistochemical 59 Smad3 59 BRCA2 gene 59 clinically insignificant 59 genetic mutations 59 genetic polymorphism 59 SOD1 gene 59 Genetic variation 59 prostate cancer CaP 59 claudin 59 colocalization 59 linkage disequilibrium 59 methylation patterns 59 methylated DNA 59 COX2 59 CagA 59 neoplastic 59 Aβ 59 Amino acid 59 histone modifications 59 RBP4 59 hTERT 59 cisplatin resistant 59 neuroligins 59 endometrial hyperplasia 59 coexpression 59 NNRTI resistance 59 myelination 59 chromosomal deletions 59 microchimerism 59 alleles 59 DNA hypermethylation 59 ABCB1 59 microdeletions 59 Treg cell 59 Fas ligand 59 adiponectin levels 59 amyloid peptide 59 leukemic cell 59 varicocele 59 OGG1 59 ependymoma 59 Leydig cells 59 progranulin 59 ADAM# 59 aneuploid cells 59 MLL2 59 TOP2A gene 59 microRNA expression 59 hyperplasia 59 FGF2 59 monocyte chemoattractant protein 59 missense mutation 59 c MYC 59 ERBB2 59 ovarian function 59 polygenic 59 bone resorption 59 transcriptional repression 59 Rh factor 59 gastric carcinoma 59 V Leiden 59 premature ovarian 59 BRCA mutations 59 KCNE2 59 Oxidative stress 59 alpha synuclein gene 59 familial aggregation 59 CYP#C# [002] 59 RhD 59 TP# mutations 59 deacetylation 59 leiomyoma 59 tryptase 59 LIS1 59 FGFR4 59 monozygotic 59 HER2 neu 59 NKX2 59 Metastases 59 BRCA2 carriers 58 endostatin 58 PIK3CA 58 epigenetic modifications 58 estrogen receptor alpha 58 adenoma 58 multiple gestations 58 causative genes 58 vascular endothelial cells 58 lymph node metastasis 58 chromosomal imbalance 58 miRNA genes 58 FISH fluorescence 58 KRAS oncogene 58 Folic acid deficiency 58 SIRT3 58 sarcosine 58 Wwox 58 melatonin receptor 58 CYP#B# 58 TNFa 58 anovulation 58 BMP4 58 BRAF protein 58 TGFBR1 * 6A 58 Inhibin B 58 genetic defects 58 FMRP protein 58 HGPS 58 EGFR gene 58 FGFR2 gene 58 thrombophilia 58 chromosomal disorders 58 micronuclei 58 UVB induced 58 #beta HSD1 58 prion infection 58 E cadherin 58 inhibin 58 androgen receptor AR 58 Sox9 58 LDLR 58 vimentin 58 demethylation 58 β catenin 58 MAPK pathway 58 p#NTR 58 genetic alteration 58 alternatively spliced 58 methylenetetrahydrofolate reductase 58 ADPKD 58 germline mutation 58 mutant genes 58 klotho 58 G#S mutation 58 CDK4 58 ovarian hyperstimulation 58 p# gene 58 embryo biopsy 58 piRNAs 58 rs# [001] 58 transgenic rats 58 medulloblastoma 58 single nucleotide polymorphism 58 constitutively active 58 pathogenic mutations 58 beta subunit 58 endometrial cancers 58 BRCA mutation 58 BRAF mutation 58 Bcl xL 58 overactivation 58 NGAL 58 multivariable analysis 58 Aneuploidy 58 renal cell carcinomas 58 filaggrin 58 familial clustering 58 impair fertility 58 hematopoetic stem cells 58 downregulation 58 folate deficiency 58 lobular carcinoma 58 chromosome segregation 58 GSTM1 58 autosomal 58 transcriptional repressor 58 AGTR1 58 Karlseder 58 GAPDH 58 CD8 + 58 PTEN mutations 58 NFKBIA 58 Activating mutations 58 SMN protein 58 phosphorylated tau 58 BMP signaling 58 TGF ß1 58 dedifferentiation 58 gene rearrangements 58 colorectal cancer CRC 58 chromosomal defect 58 premature menopause 58 CNTNAP2 58 overexpress 58 CMV infection 58 CNTNAP2 gene 58 MTHFR gene 58 JAK2 58 multidrug resistance 58 leptin receptor 58 prognostic marker 58 retinol binding protein 58 NFkB 58 cytological 58 molecular pathway 58 transcriptional regulation 58 TTR gene 58 ectopic 58 BMP2 58 hydroxyvitamin D levels 58 LDL receptor 58 sphingolipid 58 mitochondrial function 58 p tau 58 methylation markers 58 endometrial 58 IFRD1 58 MTHFR 58 STAT3 signaling 58 premalignant lesions 58 JAK mutations 58 bronchopulmonary dysplasia 58 HLA G 58 indels 58 CXCL5 58 arterial calcification 58 metabolomic profiles 58 immunoreactivity 58 genetic alterations 58 proteoglycan 58 autophagic 58 SGK1 58 spermidine 58 pancreatic endocrine 58 MC4R gene 58 Endometrial 58 tau mutation 58 synaptic function 58 5 methylcytosine 58 eNOS 58 testicular germ cell 58 HER2 expression 58 fetal microchimerism 58 FOXP3 58 MeCP2 gene 58 NF2 58 cyclophilin D 58 thyroid hormone levels 58 ß amyloid 58 nonmelanoma skin cancers 58 GPx 58 mitochondrial enzyme 58 germline cells 58 p# INK4a 58 pituitary hormone 58 aromatase 58 SOX9 58 NFκB 58 follicle stimulating hormone 58 pRb 58 invasive ductal 58 Rh incompatibility 58 Cyclin E 58 DFMO 58 estrogen receptor 58 epigenetic inheritance 58 eotaxin 58 myo inositol 58 Akt 58 GISTs 58 V#F mutation 58 ADAMTS# 58 postmenopausal breast cancer 58 microRNA molecules 58 antibody mediated 58 DLC1 58 pDCs 58 PB1 F2 58 lobular breast cancer 58 apoE4 57 myocyte 57 childhood leukemias 57 oncogenesis 57 TMPRSS2 ERG fusion 57 intact parathyroid hormone 57 thyrotropin 57 FGFR1 57 constitutively 57 dizygotic twins 57 humoral immunity 57 monozygotic twin 57 caveolin 57 FOXO1a 57 APOE allele 57 nAChR 57 TGF b 57 synapse formation 57 Akt1 57 HepG2 cells 57 colorectal neoplasia 57 CYP#D# 57 lipoprotein 57 Wnt signaling 57 Kabuki syndrome 57 metaplasia 57 epithelial tissues 57 Upregulation 57 amino acid substitution 57 resistin 57 folate intake 57 developmental abnormalities 57 plasma lipid 57 neurotrophin 57 estrogen metabolism 57 neurofibromas 57 TYMS 57 SNP rs# [002] 57 SHBG 57 mutant p# 57 differential gene expression 57 gestational diabetes mellitus 57 tumor suppressor genes 57 noncoding RNA 57 regulated kinase ERK 57 CDKN2A 57 folate metabolism 57 Sertoli cells 57 germ cells 57 chemosensitivity 57 autosomal dominant disorder 57 liver metastasis 57 chromosomal anomaly 57 androgen deprivation 57 parkin gene 57 KRAS mutations 57 insulin resistance 57 BRCA2 mutation 57 inherited predisposition 57 paraneoplastic 57 filaggrin gene 57 incidentalomas 57 VHL gene 57 S#K# 57 RIP1 57 CGG repeats 57 IGFBP 57 IDH1 mutation 57 Akt signaling 57 VEGFR1 57 superinfection 57 gene expression patterns 57 mitochondrial DNA mtDNA 57 CIN2 + 57 FTLD 57 mutated gene 57 anovulatory 57 splice junctions 57 nucleotide sequence 57 histone acetylation 57 monogenic 57 MSH6 57 Pin1 57 protein tyrosine phosphatase 57 telomere DNA 57 alpha synuclein protein 57 receptor activation 57 #ß 57 MnSOD 57 NKT cell 57 radial glia 57 chromosomal alterations 57 neurite outgrowth 57 CYP#D# gene 57 #p#.# [002] 57 P cadherin 57 molecular abnormalities 57 sequence homology 57 ataxin 57 hyperactivated 57 Skp2 57 DQB1 * 57 CD4 + CD8 + 57 proteolysis 57 clonogenic 57 Male infertility 57 colorectal tumor 57 epithelial tumors 57 TCF#L# gene 57 ovulatory cycles 57 EphA2 57 succinate dehydrogenase 57 Srcasm 57 LRAT 57 residual confounding 57 adenomatous polyps 57 neural crest 57 ductal cancer 57 male infertility 57 familial pancreatic cancer 57 GRP# 57 chromosomal defects 57 Genetic variants 57 histological subtype 57 calcineurin 57 mesenchymal cell 57 pancreatic adenocarcinoma 57 APOE genotype 57 BRCA1 BRCA2 57 sortilin 57 VNTR 57 STAT3 57 HGPIN 57 homozygotes 57 genomic rearrangements 57 maternal serum 57 gene loci 57 apoE 57 Wnt#b 57 Kufs disease 57 NR#A# gene 57 teratoma 57 familial adenomatous polyposis 57 ovarian tumors 57 suppresses tumor 57 copper zinc superoxide 57 DEAR1 57 congenital malformations 57 BRCA2 mutations 57 autosomal dominant 57 SLNB 57 mesothelin 57 CALHM1 57 dopamine transporter gene 57 SHANK3 57 neurofibrillary 57 Gestational 57 PGE2 57 MGUS 57 valine 57 hepatoma 57 amyloid deposition 57 C EBP alpha 57 anal cancers 57 apolipoprotein E 57 cAMP pathway 57 DNA demethylation 57 amyloid cascade 57 TNFalpha 57 embryonal 57 genes BRCA 57 amenorrhoea 57 telomerase activity 57 dysbindin 57 evolutionarily conserved 57 autoregulation 57 ERK2 57 HSCs 57 nonsense mutations 57 H#K# [002] 57 SLC#A# [002] 57 iNOS 57 cardiac fibroblasts 57 placenta praevia 57 pyloric stenosis 57 cohesin 57 cryptorchidism 57 HBeAg 57 subfertility 57 LRRK2 gene 57 intrauterine infection 57 hepatic stellate cells 57 CEACAM1 57 nitrotyrosine 57 prostate adenocarcinoma 57 PCa 57 homologous recombination 57 beta globin 57 subcellular localization 57 diagnostic biomarker 57 podocytes 57 nongenetic 57 TGFß 57 adipocyte 57 nestin 57 apolipoprotein E gene 57 lactate dehydrogenase 57 preeclamptic 57 atherosclerotic lesions 57 totipotent 57 estrogen deficiency 57 chlamydial 57 intracytoplasmic sperm injection 57 neovascularization 57 genotypic 57 ERK signaling 57 nucleotide substitution 57 dopamine receptor gene 57 eosinophil count 57 estrogen receptor beta 57 polyploidy 57 RASSF1A 57 carcinogenesis 57 H#K# [001] 57 androgens 57 TSLP 57 FXTAS 57 familial hypercholesterolemia 57 Dysregulation 57 hyperactivation 57 palladin 57 breast epithelial cells 57 osteocalcin 57 cardiac fibrosis 57 adipogenic 57 epigenetic reprogramming 57 genetic polymorphisms 57 gene mutation 57 IFN gamma 57 androgen receptor gene 56 pCR 56 catenin 56 frameshift mutation 56 Chlamydia pneumoniae 56 BRAF V#E 56 hepatocyte 56 microRNA miR 56 ectoderm 56 DNA rearrangements 56 syngeneic 56 prostate specific 56 apoptotic pathway 56 epigenetic regulation 56 3'UTR 56 qRT PCR 56 fertilized egg splits 56 subclinical hyperthyroidism 56 heterozygosity LOH 56 chromosomal abnormality 56 chorioamnionitis 56 genetic imprinting 56 cell adhesion molecule 56 polycystic ovary syndrome PCOS 56 N. gonorrhoeae 56 osteosarcomas 56 HPV# 56 gene locus 56 EUS FNA 56 endoxifen 56 pathophysiologic 56 HFE gene 56 MGMT gene 56 phenotype 56 Peutz Jeghers syndrome 56 gene polymorphisms 56 EGFR signaling 56 phthalate exposure 56 K#N 56 HDAC2 56 protein kinase C 56 breast carcinoma 56 nicotinamide 56 preterm delivery 56 #q# [001] 56 acinar 56 sonographic diagnosis 56 TEL AML1 56 BRAF mutations 56 TGF beta 56 EphB2 56 #q#.# deletion syndrome 56 ZNF# 56 MetAP2 56 IRF6 56 ductal breast cancer 56 neurofibromin 56 severe congenital neutropenia 56 JAK2 mutation 56 variant allele 56 steroidogenic 56 occludin 56 BMPR2 56 matriptase 56 spinocerebellar ataxia 56 Hcrt 56 premalignant 56 JAK2 enzyme 56 benign lesions 56 inducible nitric oxide synthase 56 DHEA supplementation 56 polycystin 56 Telomere length 56 multivariate Cox 56 atypia 56 Hh pathway 56 PEDF 56 chorionic villi 56 radiosensitivity 56 pyruvate kinase 56 NKG2D 56 microglial activation 56 calcium excretion 56 androgenic alopecia 56 FMR1 56 5 hydroxymethylcytosine 56 transgenic mice expressing 56 CYP#C# [001] 56 BubR1 56 TIMP 56 gamma globin gene 56 miRs 56 synthetic lethality 56 oncogenes 56 miR #b [001] 56 Hsp# [001] 56 NR#A# 56 Induced pluripotent stem cells 56 causative gene 56 tumoral 56 antioxidant enzyme 56 nephrogenic 56 hematopoietic cancers 56 grade cervical intraepithelial 56 splice variants 56 mitochondrial toxicity 56 ADRB2 56 PSA velocity 56 UCP2 56 insulin secreting cells 56 fatty acid oxidation 56 #p# [003] 56 trophoblast 56 uveal melanoma 56 RAR beta 56 nonmelanoma skin cancer 56 untreated celiac disease 56 pathophysiological 56 bcl 2 56 VEGF receptor 56 fetal aneuploidy 56 p# Shc 56 hydrops 56 microcephalin 56 endothelial dysfunction 56 normal karyotype 56 FGFs 56 C#Y 56 #q deletion 56 ABCA1 56 ribosomal proteins 56 enzymatic activity 56 5q 56 overt hypothyroidism 56 miRNA 56 BRCA2 gene mutations 56 Overexpression 56 PAX5 56 ApoE 56 pyrimidines 56 heterodimers 56 ApoE4 56 phosphorylate 56 neuronal migration 56 advanced adenoma 56 ApoE gene 56 T1DM 56 desmosomes 56 HSF1 56 phenotypic variation 56 extramedullary 56 DHFR 56 G6PD 56 urine cytology 56 chromosomal mutations 56 choriocarcinoma 56 mutant protein 56 cytokine interleukin 56 S nitrosylation 56 acetylation 56 MCADD 56 hedgehog signaling 56 G6PD deficiency 56 herpesviruses 56 P. gingivalis 56 HER2/neu 56 protein tau 56 antigen PSA 56 histone modification 56 keratinocyte 56 DISC1 56 MeCP2 protein 56 osteoblast 56 CDK8 56 Multivariate analysis 56 biochemical abnormalities 56 Prenatal diagnosis 56 transfusion syndrome 56 BRCA genes 56 unexplained infertility 56 mammary tumors 56 situ LCIS 56 prolactin 56 hippocampal function 56 thiopurine 56 NKX#.# 56 leptin receptors 56 pro angiogenic 56 Frizzled 56 receptor kinase 56 MYH9 gene 56 oncogenic 56 genetic recombination 56 metabolic abnormalities 56 hepatic glucose production 56 granzyme B 56 polymorphism 56 hypermethylated 56 p# protein 56 c myc 56 genetic abnormality 56 NF kappaB activation 56 serum biomarkers 56 bFGF 56 Thyroid hormone 56 epigenetic 56 #BP# 56 CTGF 56 triiodothyronine 56 BRCA1 mutation carriers