Related by context. All words. (Click for frequent words.) 80 mutated gene 73 defective gene 72 genetic mutation 71 mutation 71 gene mutation 71 gene 67 mutations 67 genetic defect 67 recessive gene 67 genes 66 genetic variant 66 p# gene 65 mutant genes 65 BRCA1 gene 64 genetic mutations 64 mutated genes 64 CFTR gene 64 gene variant 64 myostatin gene 64 MECP2 gene 64 tumor suppressor gene 64 heterozygous 64 genetic abnormality 63 RPE# gene 63 APOE4 63 FMR1 gene 63 VHL gene 63 mutant protein 63 X chromosome 62 allele 62 gene mutations 62 recessive genes 62 apoE4 62 alpha synuclein gene 62 SMN1 62 G#S mutation 62 LRRK2 gene 62 genetic defects 62 recessive trait 62 homozygous 61 alleles 61 HFE gene 61 LIS1 61 genes predisposing 61 huntingtin gene 61 SMN1 gene 61 NF1 gene 61 protein encoded 61 PTPN# 61 genetic alteration 61 missense mutation 61 epigenetic silencing 61 recessive mutation 61 SMN2 gene 61 RUNX3 61 progranulin gene 61 gene p# 60 SMN2 60 tumor suppressor protein 60 mutated protein 60 autosomal recessive 60 BRCA2 gene 60 mice lacking 60 IGF2 60 Wwox 60 parkin gene 60 receptor gene 60 MLL gene 60 progerin 60 recessive mutations 60 PTEN gene 60 genetic trait 60 LRAT 60 PALB2 60 MSH2 60 transgene 59 RPE# 59 APOE gene 59 mutant allele 59 ApoE4 59 TP# mutation 59 C#Y 59 Foxp3 59 ApoE4 gene 59 gene encoding 59 KLF# 59 CHD7 59 trypanosome 59 COMT gene 59 alternatively spliced 59 genetic variation 59 apoE 59 phenotype 59 SHANK3 59 PrP 59 MC4R gene 59 familial ALS 59 MECP2 59 imprinted genes 59 SOD1 gene 59 microcephalin 59 PTP1B 58 abnormal hemoglobin 58 SOD1 protein 58 autosomal dominant 58 nonsense mutations 58 Skp2 58 APOE e4 58 dystrophin gene 58 LKB1 58 mutant worms 58 susceptibility gene 58 haplotype 58 protein p# 58 homolog 58 Vpu 58 pRb 58 Sonic Hedgehog 58 mitochondrial genes 58 BRAF gene 58 Pdx1 58 APOE4 gene 58 RCAN1 58 IGF1 58 p# protein 58 FTO gene 58 huntingtin protein 57 tumor suppressor genes 57 enzymatic activity 57 G#S [002] 57 maternally inherited 57 apolipoprotein E gene 57 laforin 57 TP# gene 57 CYP#E# gene 57 HMGA2 57 epigenetically 57 MC1R gene 57 Ets2 57 MDM2 57 genes encoding 57 Cyclin D1 57 signaling molecule 57 chromosome abnormality 57 mitochondria 57 DICER1 57 retrovirus 57 chromosome 57 endogenous retroviruses 57 Fragile X gene 57 TAp# 57 FMR1 57 mutant proteins 57 MC1R 57 GSTM1 gene 57 MYH9 gene 57 C EBP alpha 57 activating mutations 57 breast epithelial cells 57 Htt 57 histone modification 57 LMNA 57 SIR2 gene 57 inherited mutations 57 BARD1 57 mRNA transcripts 57 mutant alleles 57 receptor protein 57 Pten 57 cystic fibrosis transmembrane conductance 57 EGFR gene 57 MTHFR gene 57 estrogen receptor alpha 57 genetically engineered mice 56 FOXP3 gene 56 HLA B# 56 gene variation 56 Meckel Gruber 56 genetic variations 56 chromosomal translocations 56 CDH1 56 MnSOD 56 androgen receptor gene 56 gene variants 56 DISC1 gene 56 klotho 56 MEF2A 56 KRAS gene 56 genetic abnormalities 56 spontaneous mutations 56 STAT4 56 mosaicism 56 polymorphism 56 activin 56 DICER1 gene 56 epigenetic changes 56 protein fragment 56 FXTAS 56 TRIM5 56 GFP gene 56 FLT3 56 mutated 56 Notch signaling 56 APOE ε4 56 MTHFR 56 E1A 56 endostatin 56 chitinase 56 MeCP2 gene 56 GABAergic neurons 56 mtDNA mutations 56 primordial germ cells 56 NFKBIA 56 retinoblastoma protein 56 tumor suppressor 56 SGK1 56 mitochondrial mutations 56 suppressor gene 56 genomic instability 56 homozygosity 56 fetal hemoglobin 56 MDMX 56 presenilin 56 mutated BRCA1 56 filaggrin gene 55 Nf1 55 caveolin 55 mammary cells 55 lamin 55 prion gene 55 autosomal recessive disease 55 NFkB 55 genetic variants 55 NOTCH1 55 CCR5 gene 55 Alu elements 55 EZH2 55 mice genetically engineered 55 Id1 55 Sox9 55 SATB1 55 micro RNAs 55 vesicular stomatitis virus 55 abnormal chromosome 55 SORL1 55 breast cancer genes BRCA1 55 Pin1 55 ZNF# 55 PINK1 55 ChR2 55 constitutively 55 IL# [001] 55 placental function 55 CXCL# 55 causative genes 55 STAT1 55 IKZF1 55 NF1 55 mutant mouse 55 chromosomal abnormality 55 APOE 55 tumor suppressing 55 TGFBR1 55 Hox gene 55 MIF gene 55 Klotho gene 55 mutant mice 55 mRNAs 55 TRPA1 gene 55 MLH1 55 CNTNAP2 gene 55 DLX5 55 prion proteins 55 IL#R 55 BRAF protein 55 tumor suppressor p# 55 ApoE gene 55 DISC1 55 Dpp 55 transcriptional repressor 55 de novo mutations 55 Rhes 55 TRIM5 alpha 55 prion protein 55 HGPS 55 TSC1 55 epigenetic 55 sporadic ALS 55 Six3 55 abnormal prions 55 CAG repeats 55 chromosomes 55 BDNF gene 55 receptor molecule 55 TRAF6 55 KLF4 55 Myb 55 HLA molecules 55 Angelman syndrome 55 p# mutation 55 APOE allele 55 PKD1 55 FOXP2 gene 55 telomerase gene 55 spontaneous mutation 55 C1q 55 epigenetic alterations 55 myotonic dystrophy 55 agouti gene 55 tyrosine phosphorylation 55 dynamin 55 Epstein Barr virus EBV 55 5 HTT gene 54 Notch1 54 genetic 54 proto oncogene 54 MAOA gene 54 proteins 54 heterozygotes 54 CDKN2A 54 beta globin 54 BRCA1 54 cyclin D1 54 Nrf2 54 Pax6 54 beta globin gene 54 mutated K ras 54 Prox1 54 NF kB 54 Sox2 54 neural cells 54 rDNA 54 WT1 54 globin 54 SRY gene 54 familial adenomatous polyposis 54 IDH2 54 virulence genes 54 GATA4 54 aldehyde dehydrogenase 54 CFTR protein 54 Helicobacter 54 chromosomal translocation 54 MLL2 54 genetic alterations 54 Bcr Abl 54 p# mutations 54 KSHV 54 Nanog 54 gene locus 54 BRIP1 54 SIRT1 gene 54 germline 54 JAK STAT 54 S#K# 54 chimeric mice 54 Hsp# [001] 54 CIB1 54 TACI 54 enzyme 54 lacZ 54 ApoE 54 transgenic mice 54 ubiquitination 54 globin genes 54 Homozygous 54 germline mutation 54 hypermethylated 54 Argonaute 54 GSTT1 54 encodes protein 54 protein 54 D. melanogaster 54 CCL#L# 54 SOD1 54 Neuregulin 1 54 chimeric 54 BMP2 54 polymorphisms 54 retinoblastoma Rb 54 Mdm2 54 transposon 54 Runx1 54 clusterin 54 misfolded protein 54 germline mutations 54 apoC III 54 IRAK1 54 melanocyte 54 prion protein gene 54 herpes virus 54 mitochondrial dysfunction 54 apolipoprotein E 54 blastomeres 54 genotype 54 overexpressing 54 mammalian embryos 54 mutant 54 Nkx#.# 54 neural crest cells 54 messenger RNA 54 Ras oncogene 54 homologous recombination 54 achromatopsia 54 SOCS1 54 HLA DQ2 54 miRNA genes 54 AAV2 54 filaggrin 54 diploid 54 CCR5 mutation 54 GPR# [002] 54 chromosome #q# [001] 54 Arf gene 54 ABCB1 54 constitutively active 54 transcriptionally active 54 hypermethylation 54 gene expression 54 missense mutations 54 HSF1 54 SCD1 54 Li Fraumeni syndrome 54 H#K# methylation 54 SIRT6 54 COMT 54 transmembrane receptor 54 PGC 1alpha 54 Bcl2 54 interferon pathway 53 BCL#A 53 aneuploidy 53 fusion protein 53 mtDNA 53 holoprosencephaly 53 overexpress 53 kinase gene 53 NEIL1 53 uPAR 53 Pten gene 53 selfing 53 signaling pathway 53 PrPSc 53 MIF protein 53 autoantibodies 53 E cadherin 53 X inactivation 53 serotonin transporter gene 53 Src 53 palmitoylation 53 FOXO1 53 TGF ß 53 gene encodes protein 53 R#W [002] 53 IKK beta 53 normal prion proteins 53 Fanconi anemia 53 CTCF 53 SLC#A# [002] 53 ADAM# 53 TCF#L# gene 53 SCN5A 53 LRRK2 53 tRNAs 53 leptin receptors 53 metabolic enzymes 53 transactivation 53 catenin 53 p# [001] 53 chromosomal aberrations 53 cryptochrome 53 NKX#.# 53 synuclein 53 LDL receptor 53 Mutation 53 H#Y 53 A. thaliana 53 mitochondrial gene 53 dystrophin 53 BRCA2 53 HCMV 53 Wnt signaling 53 BMAL1 53 recessive genetic 53 tyrosine kinases 53 genetically 53 BCR ABL 53 neuroblasts 53 cyclophilin D 53 phenotypes 53 Wolbachia 53 malignant transformation 53 neurodegenerative disorder 53 mutant huntingtin protein 53 transmembrane protein 53 homologs 53 X chromosomes 53 RNA molecule 53 autosomal dominant disorder 53 mutant flies 53 SIRT3 53 neuroD2 53 transgenic mouse model 53 centrioles 53 TSLP 53 RANKL 53 alpha synuclein toxicity 53 HNPCC 53 PKM2 53 Sonic hedgehog 53 KEAP1 53 CHD5 53 uncoupling protein 53 CFTR 53 GSTM1 53 biochemical pathway 53 PTEN protein 53 PP2A 53 c myc 53 haplotypes 53 neurotrophin 53 FGFR2 53 SLC#A# gene [001] 53 SOX3 gene 53 chromosomal 53 JAK2 enzyme 53 lectin 53 hormone glucagon 53 ubiquitylation 53 DUX4 53 cyclopamine 53 C. neoformans 53 DNMT1 53 histone deacetylases 53 lysosomal enzyme 53 mRNA 53 Rad# 53 CYP#C# * 53 glucocerebrosidase 53 chromosome rearrangements 53 dopaminergic neurons 53 ALK gene 53 Apobec3 53 Myc 53 E#F# 53 nonsense mutation 53 paralogs 53 H#K# [001] 53 H#K# [002] 53 BRCA gene 53 cyclin E 53 Niemann Pick disease 53 APOL1 53 FUS1 53 Kv#.# 53 miRNAs 53 C#Y mutation 53 retroviruses 53 SORL1 gene 53 genetically engineered mouse 53 Akt1 53 small RNAs 53 Mcl 1 53 allelic variants 53 DHFR 53 DEC2 53 CatB 53 TGF β 53 germline cells 52 LRP5 52 progranulin 52 nematode worm 52 androgen receptor AR 52 protein misfolding 52 OCT4 52 CETP VV 52 PGE2 52 SMN protein 52 Ras pathway 52 p# deficient 52 insulin secreting cells 52 Mitochondrial 52 epigenetic mechanisms 52 calcineurin 52 SRY 52 viral genome 52 RNA molecules 52 chromosomal defect 52 gut microbes 52 micro RNA 52 Lafora disease 52 K ras gene 52 herpesviruses 52 GNAQ 52 regulated kinase ERK 52 FANCD2 52 serotonin receptor 52 Kufs disease 52 plasminogen 52 mutated BRCA 52 TGF beta 52 genomic imprinting 52 PAK1 52 trypanosomes 52 molecular pathway 52 mitochondrial DNA mtDNA 52 lipin 52 FMRP protein 52 NF κB activation 52 myelination 52 interferon gamma 52 transgenic mouse models 52 chaperone proteins 52 mitochondrial genome 52 primary cilia 52 glutamate signaling 52 KCNQ1 52 pDCs 52 Dystrophin 52 TGF beta pathway 52 APOE e4 gene 52 motor neuron 52 germ cells 52 progressive neurodegenerative disorder 52 palladin 52 CYP#C# gene 52 ribosomal protein 52 leptin receptor 52 cybrids 52 medulloblastomas 52 organism genome 52 APOC3 52 breast cancer metastasis 52 OCA2 gene 52 CD#L 52 multidrug resistance 52 HLA DRB1 * 52 heritable 52 inherited neurological disorder 52 HLA genes 52 Th2 52 inactive X chromosome 52 defective mitochondria 52 amyloid precursor protein 52 DQB1 * 52 unmutated 52 severe congenital neutropenia 52 defensin 52 methylation patterns 52 RhoA 52 BRCA1 mutation 52 receptor tyrosine kinase 52 IKKa 52 GAB2 52 piRNAs 52 SHANK3 gene 52 maternally transmitted 52 isoform 52 TOMM# 52 olfactory receptor 52 GRK2 52 heterozygote 52 ErbB4 52 sphingolipid 52 IgA deficiency 52 RNA splicing 52 cysteines 52 CaMKII 52 RNAs 52 V#F mutation 52 DRD2 gene 52 ERK2 52 JAK2 mutation 52 p# activation 52 Math1 52 TTR gene 52 chromosome #q# [002] 52 short hairpin RNA 52 oncoprotein 52 monogenic 52 herpes viruses 52 mitochondrial proteins 52 budding yeast 52 orthologs 52 EGFR protein 52 PIP2 52 NR#A# 52 mouse embryos 52 PTEN tumor suppressor 52 JAK2 52 CNVs 52 ubiquitin ligase 52 genetic polymorphism 52 LQTS 52 homeobox gene 52 leukemic cells 52 MyoD 52 c Myc 52 androgen receptor 52 miR# 52 IDH1 52 sortilin 52 GBM tumors 52 alpha synuclein 52 downregulated 52 #p#.# [001] 52 Smad3 52 ALDH2 52 EGFRvIII 52 number variations CNVs 52 single nucleotide polymorphism 52 Mutations 52 ankyrin 52 dopamine D4 receptor 52 ALDH2 enzyme 52 TACI mutations 52 Or#b 52 Entamoeba 52 frameshift mutation 52 microdeletion 52 sirtuin 52 huntingtin 52 BRAF mutation 52 parthenogenetic 52 gamma globin gene 52 SIRT1 52 Toxoplasma 52 abnormal chromosomes 52 genetic traits 52 genes BRCA 52 TH# cells 52 PDGFR 52 gene APOE4 52 anaplastic lymphoma kinase 52 DEAR1 52 IRS1 52 TGFBR1 * 6A 52 CYP#D# gene 52 Pol IV 52 beta1 integrin 52 CYP#B# 52 IL #R 52 nNOS 52 amyloid peptide 52 mutant strain 52 oncogene 52 serotonin transporter 52 CYP#C# [001] 52 genotypes 52 evolutionarily conserved 52 factor GDNF 52 normal prion protein 51 BACE1 51 NPC1 51 collagen VII 51 glycoproteins 51 vimentin 51 dopamine transporter gene 51 germline stem cells 51 RAR beta 51 HOTAIR 51 neuropeptide 51 transthyretin 51 copper zinc superoxide 51 noncoding RNAs 51 transcription factors 51 tRNA synthetase 51 polymerase 51 medulloblastoma 51 Trypanosoma brucei 51 wildtype 51 Th# cells 51 KRAS oncogene 51 XBP1 51 TERT 51 ADPKD 51 heterochromatin 51 chromosome #q 51 Genetic mutations 51 regulates gene expression 51 CNTNAP2 51 MeCP2 protein 51 gene deletions 51 hypocretin 51 cohesin 51 N Myc 51 microRNA molecules 51 LRP6 51 epigenetic modifications 51 insulin receptors 51 ribosomal proteins 51 beta thalassemia 51 GAPDH 51 Igf2 51 retinal degeneration 51 chromosomal instability 51 IGFBP7 51 IKK2 51 X chromosome genes 51 susceptibility genes 51 GSTP1 51 genes BRCA1 51 ENaC 51 Fragile X syndrome 51 arrestin 51 misfolded 51 peroxisome 51 incomplete penetrance 51 NKCC1 51 mutant huntingtin 51 KCNE2 51 IDH1 gene 51 Genes 51 Overexpression 51 retroviral infection 51 gene rearrangements 51 Irs2 51 cell adhesion molecule 51 mutant BRAF 51 OPRM1 gene 51 oncogenic 51 genetically identical 51 chromosome #q#.# [001] 51 TGF β1 51 klotho gene 51 rRNA 51 EBV infection 51 cardiolipin 51 transplanted bone marrow 51 transcription factor 51 TEL AML1 51 CDK4 51 globin gene 51 Sandhoff disease 51 dopamine receptor 51 PDGFRA 51 syngeneic 51 cell signaling pathway 51 amino acid substitution 51 lysosomal 51 progranulin protein 51 GLUT1 51 unmethylated 51 transposons 51 lactase gene 51 genetic makeup 51 RNA silencing 51 gene MECP2 51 WNK1 51 murine leukemia virus 51 DLC1 51 SIR2 51 Aβ 51 fronto temporal dementia 51 neuroblastoma cells 51 TET2 51 protein CETP 51 Chromosome 51 nucleotide sequence 51 viral proteins 51 Akt 51 cardiac channelopathies 51 dyskeratosis congenita 51 c Abl 51 COX2 51 chromosomal abnormalities 51 kisspeptin 51 sickle hemoglobin 51 bacterial pathogen 51 chromatin structure 51 molecular pathways 51 ADDLs 51 simian immunodeficiency virus 51 faulty BRCA1 gene 51 KIF6 gene 51 Cdc# 51 polyploid 51 CYP# [002] 51 retinoic acid 51 ABCA1 51 homozygotes 51 caveolin 1 51 Sup# 51 autosomal recessive disorder 51 protozoan parasite 51 fatty acid synthase 51 messenger RNAs 51 HbF 51 gag pol 51 aneuploidies 51 deleterious mutations 51 regulator CFTR gene 51 NKX2 51 transgenes 51 naturally occurring enzyme 51 telomerase reverse transcriptase 51 neuroligins 51 #q# [002] 51 TCF#L# 51 CagA 51 CFH gene 51 genetically inherited 51 JAK2 gene 51 P. falciparum 51 aY chromosome 51 ataxia telangiectasia 51 SMAD4 51 chaperone protein 51 genotoxic stress 51 Rb protein 51 hereditary deafness 51 cyclin 51 MHC molecules 51 neurofibromin 51 deficient mice 51 MeCP2 51 connexin 51 incurable neurodegenerative disease 51 stathmin 51 UGT#B# 51 recessive traits 51 SERT gene 51 tumorigenesis 51 apolipoprotein E4 51 PTEN mutations 51 HOX genes 51 neuroendocrine 51 neural crest 51 CCR5 delta# 51 chromosome segregation 51 tau mutation 51 MSH6 51 serine threonine kinase 51 P. infestans 51 measles virus 51 HTLV 51 HDAC3 51 NFAT 51 mRNA decay 51 PAX5 51 defensins 51 myeloma cells 51 SOD2 gene 51 CCR3 51 GTPase 51 TIR1 51 FGFR1 51 Akt3 51 arginase 51 NF2 51 SAPAP3 51 senescent cells 51 amino acid sequence 51 bcl 2 51 nematode worms 51 hTERT 51 transcriptional regulators 51 HDACs 51 Mycoplasma pneumoniae 51 Notch receptor 51 COL#A# 51 Th2 cells 51 transcriptionally 51 artificial chromosomes 51 TRF1 51 FASPS 51 CRTC3 51 DRD2 51 NKT cells 51 segmental duplications 51 causative gene 51 Heterozygous 51 intronic 51 PRDM# 51 morphogen 51 prion protein PrP 51 disulfide bond 51 Vif 51 tau gene 51 TrkB 51 CPEB 51 pyruvate kinase 51 synaptogenesis 51 proband 51 PHLPP 51 fibroblast cells 51 motor neuron degeneration 51 cofilin 51 endogenous retrovirus 51 thymocytes 51 WAGR syndrome 51 iNOS 51 centromeres 51 pseudogenes 51 cerevisiae 51 5 HTTLPR 51 MAP#K# 51 hair follicle stem cells 51 tumor suppressors