Related by context. All words. (Click for frequent words.) 74 FMR1 gene 71 premutation 68 FXTAS 68 LRAT 67 PTPN# 67 missense mutations 67 MLH1 67 associated tremor ataxia 67 CGG repeats 66 MSH2 66 SHANK3 66 chromosome #q#.# [001] 66 heterozygotes 65 FUS1 65 de novo mutations 65 Prox1 65 #p#.# [001] 65 triplet repeats 65 ABCB1 65 Fragile X mental retardation 65 CFTR gene 64 #q#.# [001] 64 CHD7 64 chromosomal aberrations 64 MTHFR 64 NFKBIA 64 FMRP protein 64 MLL2 64 HbF 64 mosaicism 64 maternally inherited 64 CYP#C# [002] 64 transmembrane protein 63 karyotype 63 IgA deficiency 63 aneuploidies 63 mutant alleles 63 allelic variants 63 filaggrin 63 haematopoietic 63 #q# [001] 63 microdeletion 63 cystic fibrosis transmembrane conductance 63 heterozygous 63 HepG2 cells 63 orthologs 63 neuroligins 63 microdeletions 63 C#Y 63 PTEN gene 63 Clusterin 63 alleles 63 atherosclerotic lesions 63 coding genes 63 SOD1 protein 63 mRNA transcripts 62 KCNE2 62 K ras mutations 62 Alu elements 62 transgenic mice expressing 62 Jhdm2a 62 apoE 62 allelic 62 catechol O methyltransferase 62 germline mutations 62 chromosome #q# [001] 62 PALB2 62 SOCS3 62 hippocampal neurons 62 Leydig cells 62 COL#A# 62 NR#A# 62 syndrome FXTAS 62 #q#.# [002] 62 chromosome #q# [002] 62 OGG1 62 KRAS oncogene 62 apoE4 62 alternatively spliced 62 CCR5 delta# 62 chromosome #q#.# [002] 62 IGF1 62 p# mutations 62 mice lacking 62 IFN γ 61 mRNA encoding 61 caveolin 61 methylation patterns 61 MECP2 gene 61 enzymatic activity 61 chromosomal deletions 61 monogenic 61 null mice 61 inherited mutations 61 pDC 61 Nf1 61 ERK signaling 61 microsatellite instability 61 IGF2 61 Fc receptor 61 thyrotropin 61 TSC1 61 KCNH2 61 inhibin 61 beta globin gene 61 β catenin 61 functional polymorphism 61 H#K# [002] 61 splice variants 61 penetrance 61 G6PD 61 Chromosomal 61 Homozygous 61 APOE e4 61 p# activation 61 MTHFR gene 61 missense mutation 61 Polymorphisms 61 CEACAM1 61 mesangial 61 RPE# 61 sporadic ALS 61 ß amyloid 61 cell adhesion molecule 61 microglial 61 #p#.# [002] 61 circadian genes 61 differential gene expression 61 Pten 61 pathogenic mutations 61 RCAN1 61 mRNA expression 61 epigenetic alterations 61 SMAD4 61 microglial activation 61 TGF ß 61 variant allele 61 SMN1 61 proto oncogene 61 CNTNAP2 gene 61 GSTM1 61 APOE4 61 C1q 61 synuclein 61 intronic 61 trophoblast cells 61 MLL gene 61 homozygotes 61 tyrosine phosphorylation 61 chromosomal rearrangements 61 von Hippel Lindau 61 Heterozygous 61 TMPRSS2 ERG 61 circulating endothelial cells 61 TMEM#B 61 ZNF# 60 PBMCs 60 hypermethylated 60 KLF4 60 MECP2 60 CD8 + 60 hypoperfusion 60 transgene expression 60 vimentin 60 BCL#A 60 globin genes 60 microcephalin 60 autosomal dominant disorder 60 gene MECP2 60 gene encoding 60 homozygous 60 somatic mutations 60 PKD1 60 ERK1 2 60 CagA 60 FGFR2 60 BRAF V#E 60 germline mutation 60 promoter methylation 60 dysbindin 60 matrix metalloproteinase 60 autosomal 60 p# biomarker 60 substrate specificity 60 SMN2 60 lysosomal 60 neurofibrillary 60 variant alleles 60 polyglutamine 60 immunoreactivity 60 TrkB 60 somatic mutation 60 Inactivation 60 nNOS 60 HFE gene 60 JAK2 enzyme 60 transthyretin 60 rs# [004] 60 GSTT1 60 folate metabolism 60 miR #a [001] 60 short hairpin RNA 60 HMGA2 60 ectopic expression 60 gene rearrangements 60 effector functions 60 breast carcinomas 60 SMN2 gene 60 Aß 60 GSTP1 60 E#F# 60 ERK2 60 LIS1 60 SMN protein 60 CDH# 60 hTERT 60 p#NTR 60 CYP#D# 60 Immunohistochemical analysis 60 synaptic function 60 SCN5A 60 ADAMTS# 60 mitochondrial dysfunction 60 methyltransferase 60 mitochondrial DNA mtDNA 60 bronchopulmonary dysplasia BPD 60 Treg cell 60 Phosphorylation 60 inactive X chromosome 60 PDGFR 60 PDGFRA 60 HOTAIR 60 isoform 60 Cyclin D1 60 neurite outgrowth 60 MnSOD 60 autosomal recessive disorder 60 CYP#B# 60 p# mutation 60 TNFalpha 60 nonsense mutation 60 Cytogenetic 60 apolipoprotein E4 60 normal karyotype 59 GABAergic interneurons 59 Htt 59 R#W [002] 59 genomic deletions 59 β amyloid 59 homozygosity 59 VNTR 59 TPMT 59 ADPKD 59 MYH9 gene 59 DNA methyltransferase 59 activin 59 FGF2 59 corpus luteum 59 neuroblastoma tumors 59 periventricular 59 NKT cell 59 CAG repeats 59 virulence genes 59 IUGR 59 BMPR2 59 CYP #D# 59 KRAS mutations 59 TACI 59 superoxide dismutase 59 monozygotic twins 59 DNA methylation patterns 59 p# Shc 59 segmental duplications 59 chromosomal anomalies 59 SLC#A# gene [001] 59 chronic granulomatous disease 59 CYP# [002] 59 receptor gene 59 PON1 59 #p# [001] 59 inducible nitric oxide synthase 59 decarboxylase 59 methylenetetrahydrofolate reductase 59 adipogenic 59 TP# mutations 59 mutated K ras 59 UGT#A# * 59 nucleotide substitutions 59 DQB1 * 59 GAPDH 59 replicon 59 aneuploid 59 miRNA expression 59 lysine residues 59 MAPK pathway 59 tetramer 59 glycosylation 59 SOX3 gene 59 transgenic mouse models 59 huntingtin gene 59 mtDNA mutations 59 constitutively 59 SOD1 gene 59 microRNAs miRNAs 59 AGTR1 59 tropomyosin 59 pituitary hormone 59 Leydig cell 59 unmethylated 59 genes encoding 59 histone acetylation 59 hepatoma 59 thioredoxin 59 NF1 gene 59 phenotype 59 Dpp 59 micronuclei 59 non coding RNA 59 blastomeres 59 allele 59 CDH1 59 transcriptionally active 59 MeCP2 gene 59 upregulates 59 ERalpha 59 epigenetic silencing 59 paternally inherited 59 HER2 expression 59 HLA DRB1 * 59 IgG4 59 hypomethylation 59 autophagic 59 GH deficiency 59 phthalate syndrome 59 dystrophin gene 59 immunoreactive 59 peripheral blood mononuclear 59 erythrocytes 59 GABAergic neurons 59 tumorigenicity 59 hyperactivation 59 CHEK2 59 granzyme B 59 MMP9 59 ultrastructural 59 SMN1 gene 59 FasL 59 G#S [002] 59 hypermethylation 59 PIK3CA 59 Apolipoprotein E 59 estrogen receptor alpha 59 c Myb 59 ribosomal proteins 59 brain lesions 59 CD#c 59 colorectal tumor 59 haplotypes 59 EGFR gene 59 #q# [002] 59 catenin 59 coexpression 59 CNTNAP2 59 holoprosencephaly 59 TET2 59 Fibroblasts 59 Fragile X gene 59 bile acid metabolism 59 mitochondrial gene 59 polymorphisms 59 IGFBP 3 59 calcium homeostasis 59 LRP5 59 constitutively expressed 59 neuronal dysfunction 59 isoenzyme 59 ENaC 59 GPx 59 Macrophage 59 amyloid peptide 58 transcriptional repressor 58 apolipoprotein E gene 58 alveolar epithelial cells 58 chromosomal rearrangement 58 TOP2A gene 58 cellularity 58 KCNQ1 58 GNAQ 58 homozygote 58 hydroxylase 58 cardiolipin 58 leukemic stem cells 58 VIPR2 58 intergenic 58 transgenic rats 58 Alleles 58 synaptogenesis 58 plasma pharmacokinetics 58 rRNA 58 cultured neurons 58 mtDNA 58 coinfection 58 GluR1 58 presenilin 58 clefting 58 Tie2 58 prostaglandin E 58 progranulin 58 autosomes 58 ApoE4 58 Transcriptome 58 myocyte 58 HIF 1alpha 58 OPRM1 gene 58 COMT gene 58 adrenal function 58 autosomal recessive 58 endonuclease 58 Fas ligand 58 cDNA libraries 58 mutant allele 58 BRIP1 58 tumor suppressor gene 58 APOL1 58 BDNF gene 58 chromosome rearrangements 58 tau protein 58 SLC#A# [002] 58 proteoglycan 58 Abeta# 58 binding affinities 58 APOC3 58 CALHM1 58 phosphoprotein 58 IKZF1 58 dysgenesis 58 MELAS 58 exon 58 p tau 58 genes predisposing 58 CYP#C# gene 58 subcellular compartments 58 p#INK#a 58 androgen receptor AR 58 Akt1 58 rs# [001] 58 MC4R gene 58 NF1 58 plasminogen 58 H#K#me# 58 VE cadherin 58 cytochrome b 58 ß catenin 58 genetic polymorphism 58 Prolactin 58 podocytes 58 glycogen synthase kinase 58 Sp1 58 Lymphocyte 58 sequence homology 58 TGF ß1 58 Klinefelter syndrome 58 EAAT2 58 homolog 58 PDE1 58 hyperoxia 58 DISC1 gene 58 neuroligin 58 syngeneic 58 fibrillin 1 58 CatB 58 G#D 58 TMPRSS2 ERG fusion 58 MMP# 58 regulator CFTR gene 58 beta globin 58 NFκB 58 prostate epithelial cells 58 DISC1 58 KIAA# 58 MMP2 58 BDNF protein 58 karyotypes 58 paraneoplastic 58 SNP rs# [001] 58 carcinoembryonic antigen 58 β cells 58 COMT 58 gene polymorphisms 58 progressive neurodegenerative disorder 58 VKORC1 58 cAMP signaling 58 osteoblastic 58 SORL1 58 ALK mutations 58 leptin receptor 58 β1 58 dopamine D4 receptor 58 gene amplification 58 allele frequencies 58 chromosomal instability 58 DNA rearrangements 58 TTR gene 58 epithelia 58 transgenic mouse model 58 inhibin B 58 Genotypes 58 X chromosome 58 protein tau 58 pancreatic endocrine 58 ribosomal protein 58 congenital adrenal hyperplasia CAH 58 telomerase activity 58 heterodimers 58 vascular endothelial cells 58 Germline 58 PGC 1α 58 endogenous retroviruses 58 breast epithelial cells 58 germline 58 dinucleotide 58 STAT4 58 TCF#L# gene 58 HGPIN 58 cytochrome c oxidase 58 TAp# 58 TYMS 58 evolutionarily conserved 58 microRNA molecules 58 5 HTTLPR 58 miRNA genes 58 DNMT1 58 FLT3 58 splice junctions 58 RRM1 58 untranslated regions 58 ribosomal DNA 58 chromosome #q 58 APOE allele 58 motor neuron degeneration 58 leptin receptors 58 metaplasia 58 IL 1ß 58 IFN gamma 58 APOE ε4 58 Overexpression 58 RNA transcripts 58 dopamine transporter 58 striated muscle 58 colocalization 58 gene locus 58 TGF β1 58 transfected cells 57 D. melanogaster 57 anterior pituitary 57 GPR# [002] 57 granulocyte 57 epithelial barrier 57 mRNAs 57 cDNAs 57 pseudogenes 57 Placental 57 RBP4 57 congenital anomalies 57 LRP6 57 DEAR1 57 frataxin 57 ERCC1 57 HLA DQ2 57 CD1d 57 overexpress 57 caveolin 1 57 MSMB 57 myostatin gene 57 G6PD deficiency 57 hypothalamic pituitary adrenal axis 57 TP# gene 57 hypogonadotropic hypogonadism 57 transcriptional activation 57 aminotransferase 57 dentate gyrus 57 DNA methylation 57 bFGF 57 myelination 57 ApoE gene 57 erythropoiesis 57 BMP2 57 lymphoid cells 57 S#A# [002] 57 mutations 57 SRY gene 57 BMP signaling 57 apolipoprotein E 57 BMP4 57 Wwox 57 E cadherin expression 57 neurotrophic factor 57 periodontal tissues 57 tumor suppressor protein 57 TGF b 57 phosphatases 57 serum BDNF 57 K#N 57 RPE# gene 57 T1DM 57 TCF#L# 57 eNOS 57 annexin V 57 BRCA1 mutations 57 neuregulin 57 epithelial tissues 57 CDKN2A 57 intestinal mucosa 57 encodes protein 57 quantitative trait loci 57 Notch receptor 57 neovascular 57 plasminogen activator inhibitor 57 chromosome #p# [001] 57 autosomal recessive disease 57 trinucleotide 57 trinucleotide repeat 57 parkin gene 57 missense 57 A. thaliana 57 homodimer 57 IL #R 57 GLI1 57 JAK2 mutation 57 autosomal dominant 57 #beta HSD1 57 nitrotyrosine 57 rDNA 57 myocardial tissue 57 intestinal microflora 57 klotho 57 CCR5 gene 57 glycosylated 57 hepatocellular carcinomas 57 sphingolipid 57 Akt activation 57 noncoding 57 testosterone secretion 57 cerebellar 57 intestinal epithelium 57 thyroglobulin 57 factor PlGF 57 C EBP alpha 57 CFTR protein 57 ciliated 57 transfusion syndrome 57 Wnt signaling 57 SGPT 57 GBM tumors 57 ERBB2 57 ß1 57 cardiac myocytes 57 Smad7 57 CYP#D# gene 57 isoenzymes 57 adrenal cortex 57 FANCD2 57 Arabidopsis genome 57 Secretase 57 alpha synuclein gene 57 cytokeratin 57 umbilical vein 57 Single Nucleotide Polymorphisms SNPs 57 short hairpin RNAs 57 tryptase 57 renal fibrosis 57 spontaneous mutations 57 succinate dehydrogenase 57 mutant gene 57 Western blotting 57 structural rearrangements 57 uPAR 57 histone modification 57 apolipoprotein 57 IRS1 57 mediated inhibition 57 genotoxic stress 57 neurodevelopmental outcome 57 exons 57 liver histology 57 CXCL# 57 ACh 57 heterochromatic 57 ubiquitylation 57 triacylglycerol 57 chromosomal DNA 57 indels 57 GSTM1 gene 57 HLA antigens 57 CD4 + CD# 57 dystrophin 57 genes differentially expressed 57 herpesviruses 57 gene deletions 57 developmental abnormalities 57 FHIT 57 autoregulation 57 mRNA 57 HER2 receptor 57 overexpressing 57 airway hyperresponsiveness 57 transmembrane 57 cytoplasmic domain 57 Histologic 57 Polymorphism 57 midgut 57 chromosomal 57 LVNC 57 wildtype 57 Haptoglobin 57 protein tyrosine kinase 57 Math1 57 IDH2 57 dominantly inherited 57 TRAF1 C5 57 hereditary hemochromatosis 57 mutated gene 57 immunocompetent 57 chromosome abnormality 57 amyloid deposition 57 WNK1 57 isoforms 57 pro angiogenic 57 NPM1 mutations 57 glomerular 57 downregulation 57 piRNAs 57 familial ALS 57 Ki# 57 deleterious mutations 57 pDCs 57 DLC1 57 claudin 57 Runx1 57 DGAT1 57 DRB1 * 57 H#K# methylation 57 S. cerevisiae 57 homologues 57 amyloidogenic 57 homodimers 57 albumin excretion 57 lymphangioleiomyomatosis LAM 57 glucose transporter 57 aneuploidy screening 57 serine threonine kinase 57 copper zinc superoxide 57 SNPs pronounced snips 57 VEGF expression 57 heterozygosity 57 X inactivation 57 ataxin 57 HER2 neu 57 dystrophin protein 57 palladin 57 PTP1B 57 spermidine 57 intracytoplasmic 57 BARD1 57 Rap1 57 immunoblotting 57 siRNA knockdown 57 mitochondrial metabolism 57 malignant transformation 56 placental function 56 remyelination 56 primordial germ cells 56 Hutchinson Gilford progeria 56 crystallin 56 left ventricular systolic 56 chromosomal regions 56 colorectal carcinoma 56 noncoding RNAs 56 GPC5 56 epigenetic changes 56 LTB4 56 nucleoli 56 lymph node metastasis 56 pancreatic islet 56 HBsAg 56 LQTS 56 Igf2 56 perilipin 56 trisomy 56 thyroid hormone levels 56 postnatally 56 #q# deletion 56 proteolytic cleavage 56 frameshift mutation 56 phenotypic expression 56 At#g# 56 mutation 56 epigenetically 56 CCL#L# 56 genes BRCA1 56 PrPSc 56 colorectal neoplasms 56 TIMP 1 56 OCT4 56 gene polymorphism 56 myofibroblasts 56 outer membrane proteins 56 N. gonorrhoeae 56 UGT#B# 56 HSF1 56 mitochondrial mutations 56 pRb 56 Kupffer cells 56 LMNA 56 #S rRNA 56 UCP2 56 FOXP3 56 progranulin gene 56 nicotinic receptor 56 mitochondrial enzyme 56 C. neoformans 56 dizygotic twins 56 cysteines 56 heterochromatin 56 lung adenocarcinomas 56 primary ovarian insufficiency 56 rs# [003] 56 Rb gene 56 autosomal recessive genetic 56 N Myc 56 HLA B# 56 aggrecan 56 circadian clock genes 56 CCR7 56 thrombophilia 56 acinar 56 transcriptional machinery 56 polycystic ovary syndrome PCOS 56 subcellular localization 56 airway responsiveness 56 SCN1A 56 Sonic Hedgehog 56 amyloid deposits 56 neurodevelopmental disorders 56 ventricular myocardium 56 eosinophil count 56 p# gene 56 pulmonary hypoplasia 56 epididymal 56 Rab5 56 SOD2 gene 56 replicase 56 mutant mouse 56 HLA DR 56 neurofibrillary tangles 56 osteoblast 56 radial glia 56 contractile function 56 lactate dehydrogenase LDH 56 persistent pulmonary hypertension 56 POMC neurons 56 COX2 56 major histocompatibility complex 56 epigenetic modification 56 protein tyrosine phosphatase 56 congenital toxoplasmosis 56 chromosome abnormalities 56 epithelial tumors 56 IgG1 56 huntingtin protein 56 hepatic glucose production 56 aneuploidy 56 nestin 56 polyploid 56 presynaptic 56 WT1 56 TIMP 56 immunohistochemical 56 gliosis 56 LDL receptor 56 prion protein gene 56 affective psychosis 56 tumor suppressor genes 56 endothelial activation 56 chromosome #p# [002] 56 telomeric 56 causative mutations 56 thyroid hormones 56 gonadotropins 56 ubiquitinated 56 CpG 56 gene loci 56 metalloprotease 56 RT qPCR 56 TGF beta1 56 AAT deficiency 56 podocyte 56 WAGR syndrome 56 N cadherin 56 connexin 56 TACI mutations 56 HGPS 56 Androgen 56 B. cereus 56 dyskeratosis congenita 56 MYCN 56 Nedd4 56 RNA splicing 56 Li Fraumeni 56 Cx# [001] 56 lacZ 56 glutamyl 56 phenotypes 56 CC genotype 56 constitutively active 56 fetal hemoglobin 56 activating mutations 56 neurotrophic factors 56 chromosomal abnormalities 56 proapoptotic 56 costimulatory 56 pyrimidine 56 fibulin 56 cellular prion protein 56 Neuregulin 1 56 miRNAs 56 TGF β 56 striatal neurons 56 lymphoblastoid cell lines 56 genetic loci 56 agonist induced 56 Smad3 56 alkaline phosphatase 56 SNCA 56 leiomyoma 56 EGFP 56 bone resorption 56 diagnostic biomarker 56 glioblastoma tumors 56 Foxp3 56 CD4 + CD8 + 56 BRAF V#E mutation 56 HER2/neu 56 4E BP1 56 neuronal function 56 ataxias 56 hamartomas 56 Peutz Jeghers syndrome 56 chromatin structure 56 adrenocortical 56 breast carcinoma 56 hypoplasia 56 fetal chromosomal 56 chitinase 56 LKB1 56 serine protease 56 mutant protein 56 cyclin E 56 aromatase 56 TLR3 56 Corynebacterium 56 BMAL1 56 motoneurons 56 Neural stem cells 56 synthases 56 homeobox gene 56 vWF 56 micro RNAs 56 factor HGF 56 secretase 56 SHANK3 gene 56 posttranslational modification 56 F#del mutation 56 IKK beta 56 isotypes 56 dopamine signaling 56 db db mice 56 CpG island 56 chromosomal alterations 56 microvessel density 56 gene mutations 56 hydrops 56 vitamin B# folic acid 56 serum TSH 56 toxic beta amyloid 56 APOE gene 56 murine 56 deacetylation 56 EF Tu 56 amino acid substitutions 56 Smad4 56 regulated kinase ERK 56 isoprostane 56 nonsense mutations 56 sortilin 56 Mitochondrial 56 protein phosphorylation 56 mutant mice 56 GISTs