Related by context. All words. (Click for frequent words.) 71 SOD1 gene 70 nonsense mutation 70 dystrophin gene 69 missense mutation 69 CFTR gene 67 BCR ABL protein 67 LRAT 67 familial ALS 67 mtDNA mutations 67 MECP2 gene 67 PTPN# 67 K ras mutations 66 CHD7 66 TTR gene 66 chromosomal rearrangement 65 monogenic 65 BRAF gene 65 MYH9 gene 65 progressive neurodegenerative disorder 64 huntingtin gene 64 SHANK3 64 NFKBIA 64 somatic mutations 64 motor neuron degeneration 64 renal fibrosis 64 sporadic ALS 64 RPE# 64 inherited mutations 64 KIT mutations 64 SMAD4 64 MTHFR 63 E#F# 63 mutant protein 63 cytomegalovirus CMV 63 aneuploidies 63 MSH2 63 gastrointestinal stromal tumors GISTs 63 C#Y 63 VHL gene 63 LRRK2 gene 63 Gorlin syndrome 63 autosomal dominant disorder 63 neuroblastoma tumors 63 MeCP2 protein 62 IgA deficiency 62 activating mutations 62 chemoresistant 62 de novo mutations 62 APOL1 62 NOTCH1 62 NF1 62 KRAS oncogene 62 Notch1 62 SMN1 62 microdeletion 62 chromosomal instability 62 JAK2 enzyme 62 c myc 62 mesotheliomas 62 abnormal p# 62 Foxp3 62 mutated K ras 62 FGFR2 62 BRAF V#E 62 gene MECP2 62 mutations 62 CDH1 62 mRNA transcripts 62 TSC1 62 CFTR protein 62 LMNA 62 autosomal recessive 62 WT1 62 GBM tumors 62 herpesviruses 62 CYP#C# [002] 62 susceptibility gene 62 BRAF mutation 61 somatic mutation 61 HbF 61 chronic granulomatous disease 61 p# mutation 61 normal karyotype 61 telomere dysfunction 61 missense mutations 61 protein encoded 61 epigenetic alterations 61 ADPKD 61 lysosomal storage diseases 61 Clusterin 61 protein misfolding 61 LDL receptor 61 BMP2 61 microdeletions 61 lung adenocarcinoma 61 FUS1 61 inactivating mutations 61 JAK2 mutation 61 genetic defect 61 FLT3 61 progranulin gene 61 Bcr Abl 61 ABCB1 61 NFkB 61 Gleevec resistant 61 gene rearrangements 61 ZNF# 61 dyskeratosis congenita 61 tumor suppressor protein 61 basal cell carcinoma BCC 61 SMN protein 61 iNOS 61 lysosomal 61 cyclin E 61 transcriptional repression 60 MAP#K# 60 causal variants 60 myeloid 60 Duchenne muscular dystrophy DMD 60 Brugada syndrome 60 OGG1 60 breast carcinomas 60 autosomal dominant 60 MLH1 60 Hashimoto thyroiditis 60 SMN1 gene 60 hypermethylation 60 neurodegenerative disorder 60 neuronal dysfunction 60 inherited retinal degeneration 60 filaggrin 60 leptin deficiency 60 FMR1 gene 60 genetic defects 60 NF2 60 MLL2 60 adenocarcinomas 60 molecular abnormalities 60 multidrug resistance 60 filaggrin gene 60 splice variants 60 PDGFR 60 Peutz Jeghers syndrome 60 dopaminergic neurons 60 LKB1 60 Epstein Barr virus EBV 60 hypermethylated 60 EGFR gene 60 muscular dystrophies 60 #q#.# [001] 60 causative gene 60 HER2 overexpression 60 sortilin 60 pathogenic mutations 60 breast cancer genes BRCA1 60 GISTs 60 TP# gene 60 heterotaxy 60 lung cancer NSCLC 60 #beta HSD1 60 SSc 60 p# gene 60 axonal degeneration 60 proto oncogene 60 syngeneic 60 JAK2 gene 60 SMN2 60 genetic alteration 60 chromosome abnormality 60 TAp# 60 p# mutations 60 familial hypercholesterolemia 60 EGFRvIII 60 mutated gene 60 GABAergic neurons 60 tyrosine phosphorylation 60 transgene expression 60 FOXP3 60 glial derived neurotrophic 60 genetic mutations 60 mutant genes 60 demyelination 60 TMEM#B 60 pancreatic endocrine 59 synovial cells 59 pilocytic astrocytomas 59 Cyclin D1 59 frataxin gene 59 chromosomal aberrations 59 medulloblastomas 59 Skp2 59 motor neuron diseases 59 subependymal giant cell 59 epigenetic modifications 59 lysosomal enzyme 59 DLC1 59 Leber congenital amaurosis LCA 59 NKX#.# 59 HNPCC 59 osteosarcomas 59 MeCP2 gene 59 lymphoid 59 chimeric mice 59 IDH1 mutation 59 ADAMTS# 59 VEGF receptor 59 chromosome #q# [002] 59 EGFR mutations 59 causative mutations 59 genetic abnormalities 59 inactive X chromosome 59 FTLD 59 synaptogenesis 59 immunopathology 59 lymphocytic 59 nNOS 59 Fas ligand 59 cystic fibrosis transmembrane conductance 59 pDC 59 pheochromocytoma 59 myeloproliferative neoplasms 59 T#I [002] 59 #q#.# [002] 59 mitochondrial dysfunction 59 germline mutation 59 epigenetic mechanisms 59 IKZF1 59 tumor suppressor gene 59 PTP1B 59 Hemophilia B 59 myeloproliferative diseases 59 KIF6 gene 59 ERK1 2 59 heterozygotes 59 PTEN gene 59 chemoresistance 59 NF kB pathway 59 IRAK1 59 prostate adenocarcinoma 59 DNMT1 59 myeloproliferative 59 epigenetic silencing 59 Epidermal Growth Factor Receptor 59 cell adhesion molecule 59 BRAF protein 59 genomic instability 59 adenoviral 59 interferon pathway 59 fatal neurodegenerative 59 CYP# [002] 59 genetic alterations 59 paralogs 59 CDK4 59 spinocerebellar ataxia 59 neuroendocrine cancers 59 endostatin 59 hedgehog pathway 59 gene mutations 59 genetic polymorphisms 59 androgen receptor AR 59 fibrotic disease 59 maternally inherited 59 gastric carcinoma 59 micro RNAs 59 Janus kinase 59 PTEN mutations 59 VIPR2 59 genotoxic stress 59 mutated genes 59 Staphylococcus aureus infections 59 NF1 gene 59 tumor antigen 59 autosomal recessive disorder 59 Lymphocytic 59 vWD 59 SCN5A 59 mosaicism 59 epigenetic markers 59 COL#A# 59 NPHP 59 epigenetic changes 59 TOP2A 59 beta catenin protein 59 BRCA2 gene 59 Trypanosoma brucei 59 myelofibrosis polycythemia vera 59 neuroblastoma cells 59 cystic fibrosis chronic pancreatitis 59 Treg cell 59 PARP inhibition 59 prostate cancer CaP 59 myeloma cells 59 Lupus nephritis 59 leukaemic stem cells 59 PALB2 59 gene amplification 59 transthyretin amyloidosis 59 genetic abnormality 59 EGFR protein 59 mutant proteins 59 HGPS 59 caveolin 1 59 fusion protein 59 Autoimmune disorders 59 intracranial hemorrhage ICH 59 retinitis pigmentosa RP 59 caveolin 59 airway hyperresponsiveness 59 Friedreich ataxia 58 familial adenomatous polyposis 58 Chemokine Receptor 58 RUNX3 58 hepatic lipase 58 miRs 58 PAOD 58 SOCS1 58 lymphocyte activation 58 fronto temporal dementia 58 Ets2 58 immunodeficiency 58 gene loci 58 TTR amyloidosis 58 FGFR1 58 Kufs disease 58 BCL#A 58 neural cells 58 TP# mutations 58 ataxias 58 miR #a [002] 58 GNAQ 58 5q chromosome 58 kidney urologic 58 lymphoid organs 58 NEIL1 58 basal cell nevus syndrome 58 progranulin 58 V#F mutation 58 nerve degeneration 58 MELAS 58 alpha synuclein gene 58 apoE4 58 CYP #D# 58 histologic subtype 58 c KIT 58 mutant huntingtin 58 PDGFRA 58 CEACAM1 58 uPA 58 splice junctions 58 tumor suppressor genes 58 SMN2 gene 58 nonmelanoma skin cancers 58 Immunohistochemical analysis 58 B lymphocytes 58 mutant gene 58 mutant alleles 58 TGF β 58 chromosomal defect 58 biologic pathway 58 Smad7 58 Tuberous sclerosis 58 granzyme B 58 autophagic 58 neuroinflammation 58 humanized monoclonal antibodies 58 E1A 58 CYP#D# gene 58 FSGS 58 HBx 58 modifier genes 58 transgenic mouse model 58 hypomethylation 58 PKM2 58 microglial cells 58 MDM2 58 proapoptotic 58 secretory pathway 58 gamma globin gene 58 methylenetetrahydrofolate reductase 58 retinal degeneration 58 retinal dystrophy 58 ependymoma 58 DLX5 58 MAPK pathway 58 HMGA2 58 transgenic rats 58 facioscapulohumeral muscular dystrophy 58 JMML 58 MMP9 58 germline mutations 58 STAT4 58 Epstein Barr Virus EBV 58 RNAi therapeutic targeting 58 virulence determinants 58 IFN gamma 58 Wnt signaling pathway 58 C1q 58 TCF#L# 58 Sezary syndrome 58 CD8 + 58 VKORC1 58 HLA alleles 58 parainfluenza virus 58 SGLT2 58 enteroviruses 58 RPE# gene 58 SOD1 58 Prox1 58 chitinase 58 hyperprolactinemia 58 amyloid deposits 58 dystrophin 58 beta1 integrin 58 aldehyde dehydrogenase 58 cardiac fibrosis 58 G6PD deficiency 58 dystrophin protein 58 RANKL 58 protein kinase C 58 beta thalassemia 58 receptor tyrosine kinase 58 G6PD 58 AAV2 58 overactivation 58 defective gene 58 TCF#L# gene 58 gene encoding 58 chromosome #q#.# [001] 58 genomic deletions 58 CCR1 58 autoimmunity 58 promoter hypermethylation 58 herpes zoster virus 58 histone deacetylase inhibitors 58 atherosclerotic lesions 58 systemic amyloidosis 58 Jhdm2a 58 myasthenia gravis MG 58 miRNA genes 58 susceptibility genes 58 virulence genes 58 NQO1 58 androgen receptor gene 58 APOC3 58 NOD2 58 Smad3 58 murine leukemia virus 58 beta globin gene 58 mitochondrial disorders 58 hyperplastic 58 cerebral vasospasm 58 genetic loci 58 IDH1 58 Th# cells 58 GRNOPC1 contains 58 shortened telomeres 58 MGUS 58 H#K#me# 58 choroidal neovascularization CNV 58 EBNA1 58 BRCA1 gene 58 myopathies 58 receptor kinase 58 IL#B 58 Treg cells 58 MECP2 58 neoplastic 58 p# activation 58 inherited genetic mutations 58 T#M 58 Upregulation 58 autoimmune encephalitis 58 CCR5 delta# 58 IFN γ 58 FTIs 58 CDKN2A 58 Meckel Gruber 58 colorectal carcinoma 58 HFE gene 58 papillomas 57 TH# cells 57 tyrosine kinases 57 underlying vasculopathy 57 miR #a [001] 57 DISC1 gene 57 ERK pathway 57 familial adenomatous polyposis FAP 57 precursor lesions 57 AT1R 57 peroxisomal 57 genetic polymorphism 57 imatinib resistance 57 microcephalin 57 DNA methyltransferase 57 downstream effectors 57 leukaemias 57 GIST tumors 57 S#A# [002] 57 microglial activation 57 protein tyrosine phosphatase 1B 57 MIF protein 57 Activating mutations 57 Neurofibromatosis type 57 cyclin D1 57 T1DM 57 WNK1 57 progerin 57 Leber congenital amaurosis 57 Dystrophin 57 Li Fraumeni 57 fatal neuromuscular disorder 57 channelopathies 57 chromosome #q 57 antibody mediated 57 LRP5 57 holoprosencephaly 57 micro RNA 57 EBV infection 57 PIK3CA 57 defective cilia 57 Six3 57 BRCA1 BRCA2 57 genes encoding 57 neurological manifestations 57 NOMID 57 hypereosinophilic syndrome 57 gastric carcinomas 57 eotaxin 57 Leber Congenital Amaurosis LCA 57 selective inhibition 57 amino acid substitutions 57 genus Plasmodium 57 mitochondrial DNA mutations 57 tumorigenicity 57 gene APOE4 57 metastatic neuroendocrine tumors 57 ano genital warts 57 neurite outgrowth 57 TET2 57 M. genitalium 57 MYH9 57 uPAR 57 CHEK2 57 elevated triglyceride levels 57 colon carcinoma 57 #q# [001] 57 Genetic variation 57 childhood leukemias 57 connexin 57 HBeAg negative 57 unknown etiology 57 tumor metastases 57 Muscular dystrophies 57 ubiquitinated 57 SOD1 protein 57 unmutated 57 downregulation 57 homologous recombination 57 prion infection 57 genes BRCA1 57 lung fibrosis 57 constitutively 57 TACI 57 vasculopathy 57 oncogenic 57 inherited retinal 57 asymptomatic carriers 57 Cx# [001] 57 genomic variants 57 neurofibromas 57 ubiquitylation 57 coding exons 57 CNTNAP2 gene 57 leukoencephalopathy 57 ubiquitin ligases 57 DNA demethylation 57 CXCL# 57 deacetylation 57 HepG2 cells 57 apoptotic pathway 57 dominantly inherited 57 NF kappaB activation 57 matrix metalloproteinases 57 Sjögren syndrome 57 AAV vectors 57 microRNA molecules 57 abnormal proteins 57 congenital disorders 57 liver scarring 57 PTEN protein 57 Raf MEK ERK 57 paraganglioma 57 podocytes 57 biochemical abnormalities 57 genetic syndromes 57 Hsp# [001] 57 pleiotropic 57 CHD5 57 Systemic lupus erythematosus SLE 57 Hutchinson Gilford progeria 57 rs# [004] 57 achromatopsia 57 CD#b 57 medulloblastoma 57 periodontal tissues 57 mutated protein 57 endocrine tumors 57 HLA B# 57 transthyretin 57 myotonia 57 heterozygous 57 Trichophyton rubrum 57 multi factorial disease 57 insertional mutagenesis 57 sCD# 57 β catenin 57 neuroblastomas 57 G#S mutation 57 Prion diseases 57 β cells 57 deletion 5q 57 Beta thalassemia 57 underlying pathophysiology 57 F#del mutation 57 p# MAPK 57 abnormal chromosome 57 EGF receptor 57 crystallin 57 H#Y 57 alpha synuclein protein 57 immunodeficiencies 57 etiologic 57 breast cancer metastasis 57 Pten 57 cytopathic 57 C. pneumoniae 57 aneuploidy 57 undergo apoptosis 57 BMPR2 57 primary cilia 57 MIF gene 57 mice lacking 57 CCR3 57 shRNAs 57 C1 INH deficiency 57 GPC5 57 mutation 57 malignant transformation 57 p#NTR 57 sCJD 57 narcolepsy cataplexy 57 HDAC6 57 BCR ABL 57 Bardet Biedl syndrome 57 #p#.# [002] 57 inducible nitric oxide synthase 57 SCD1 57 plasma kallikrein 57 EZH2 57 SIRT1 gene 57 DFMO 57 hyperphosphorylation 57 KLF# 57 Leukemias 57 testicular tumors 57 cisplatin resistant 57 Chronic lymphocytic leukemia 57 senescent cells 57 gene deletions 57 developmental abnormalities 57 steatohepatitis 57 activated lymphocytes 57 HLA DRB1 57 immunocompetent 57 atypical hemolytic uremic syndrome 57 proteins encoded 57 squamous cell lung cancer 57 mutated BRCA1 57 TNFa 57 methylation patterns 57 FGFR3 57 promoter methylation 57 phosphorylate 57 Leydig cells 57 regulator CFTR gene 57 acute promyelocytic leukemia 57 misfolding 57 autosomal recessive disease 57 EphA2 56 proteoglycan 56 IDH2 56 interferon IFN 56 γ secretase 56 Kabuki syndrome 56 HER2 expression 56 costimulatory 56 Helicobacter 56 amino acid substitution 56 Pulmonary hypertension 56 excitotoxicity 56 chemokine receptor 56 endogenous ligands 56 drug metabolizing enzymes 56 EGFR inhibitors 56 axonal damage 56 skeletal metastases 56 variant allele 56 c MET 56 incurable neurodegenerative disease 56 leukemic cell 56 bacterium Mycobacterium tuberculosis 56 G#S [002] 56 LQTS 56 mitogen activated protein kinase 56 severe congenital neutropenia 56 GRK2 56 chromosome #q# [001] 56 autoinflammatory diseases 56 eIF4E 56 IL#R 56 DGAT1 56 Genetic variants 56 cellular prion protein 56 E cadherin 56 hypoperfusion 56 mammary cells 56 PC3 cells 56 AAT deficiency 56 CNTNAP2 56 BRIP1 56 Becker muscular dystrophy 56 ubiquitination 56 GLUT1 56 IKK2 56 FGFs 56 Akt3 56 N Myc 56 NKX2 56 short hairpin RNAs 56 inherited neurological disorder 56 LIS1 56 Niemann Pick disease 56 Dysregulation 56 aplasia 56 TOP2A gene 56 airway remodeling 56 activin 56 polymorphic ventricular tachycardia 56 replicon 56 IGF2 56 Helicobacter pylori H. pylori 56 Neurodegenerative diseases 56 genetic mutation 56 thioredoxin 56 NFκB 56 karyotypes 56 upregulating 56 Leydig cell 56 suppressor gene 56 leukocyte adhesion 56 human papilloma viruses 56 functional dystrophin protein 56 pRb 56 chromosomal deletions 56 HPVs 56 KRAS mutations 56 ectopic expression 56 Vidaza ® 56 gene locus 56 HER2 neu 56 phosphorylates 56 cystic fibrosis muscular dystrophy 56 anti apoptotic proteins 56 ApoE4 56 engineered RAP peptides 56 ovarian tumors 56 ChR2 56 Fibroblast Growth Factor Receptor 56 medulloblastoma tumors 56 PDE#A 56 non coding RNA 56 KCNE2 56 thymidylate synthase TS 56 CMV infections 56 basal cell carcinomas 56 EAAT2 56 gastroenteritis conjunctivitis 56 parasite Plasmodium falciparum 56 misregulation 56 Factor Receptor 56 RAF kinase VEGFR 56 ERK signaling 56 molecular mimicry 56 CYT# potent vascular disrupting 56 globin 56 p tau 56 Fanconi Anemia 56 Htt 56 BH4 deficiency 56 IGFBP2 56 MEK ERK 56 myeloproliferative disorders 56 hTERT 56 experimental autoimmune encephalomyelitis 56 p#INK#a 56 Pulmonary arterial hypertension 56 abnormal hemoglobin 56 anthracycline induced 56 chronic eosinophilic leukemia 56 Polymorphisms 56 HCV replication 56 defective CFTR 56 nephronophthisis 56 exons 56 BARD1 56 Squamous 56 clinically heterogeneous 56 sporadic Creutzfeldt Jakob 56 spontaneous mutation 56 neural crest stem cells 56 adrenocortical cancer 56 podocyte 56 CIN2 + 56 choroidal neovascularization 56 brain malformation 56 proliferative disorders 56 intestinal epithelium 56 Cryptococcus neoformans 56 mRNA molecules 56 aneuploid cells 56 GABAergic interneurons 56 Genetic mutations 56 JAK3 56 neuronal degeneration 56 pDCs 56 constitutively active 56 mitochondrial proteins 56 adipogenic 56 epithelial tumors 56 NF kB signaling 56 RAR beta 56 Tay Sachs thalassemia 56 PGE2 56 Hurthle cell 56 mitochondrial mutations 56 TGF beta signaling 56 lysosomal storage disease 56 #p#.# [001] 56 neuroligins 56 GSK3 56 Dpp 56 plasminogen 56 HCMV 56 IL 1β 56 gastric adenocarcinoma 56 TLR9 agonists 56 oncogenes 56 hematopoietic cells 56 TACI mutations 56 cysteines 56 tumor metastasis 56 peroxisome 56 Ras oncogene 56 meningiomas 56 survivin 56 HMGCR 56 pleiotropic effects 56 malignant prostate 56 clusterin 56 PARP inhibitor 56 vimentin 56 indels 56 pathogenic mechanisms 56 phenotypic variation 56 Aβ 56 glycogen synthase kinase 56 fatal neurodegenerative disorder 56 klotho gene 56 EGFR pathway 56 MEFs 56 diagnostic biomarker 56 multisystem disease 56 genomic alterations 56 FMR1 56 TGF alpha 56 TP# mutation 56 hepatotoxicity 56 acute lymphoid leukemia 56 hematologic disorders 56 NAGS deficiency 56 metastatic malignant 56 carcinoid 56 thyrotropin 56 fatty acid synthesis 56 pro angiogenic 56 K#N 56 vWF 56 granulosa cell 56 TGF ß 56 metaplasia 56 dilated cardiomyopathy DCM 56 T#I mutant 56 cerebral ischemia 56 EGFR tyrosine kinase inhibitors 56 Postoperative complications 56 WDR# 56 epithelial cancers 56 mutant allele 56 tumor specific antigen 56 osteoclast activity 56 CREBBP 56 cyclin dependent kinase 56 DEAR1 56 chronic HBV infection 56 beta amyloid peptide 56 pneumococci 56 pituitary adenomas 56 ALK gene 56 T2D 56 mutated KRAS gene 56 degenerative retinal diseases 56 protein isoforms 56 lichen planus 56 Cytotoxic T 56 demethylation 56 chromosomal translocations 56 methylated DNA 56 hypercalcaemia 56 cDNAs 56 BDNF gene 56 miRNA expression 56 diabetic nephropathy 56 tyrosine kinase receptor 56 MTDH 56 bacterium Neisseria meningitidis 56 IGFD 56 Parkinson disease neurodegenerative disorder 56 primary biliary cirrhosis 56 CENP E 56 miR #b [001] 56 chemokine receptors 56 dimerization 56 TRAIL induced apoptosis 56 Fragile X gene 56 hepatocellular carcinomas 56 ribosomal proteins 56 neuron degeneration 56 potent inhibitors 56 nonviral 56 Myasthenia gravis 56 polyomavirus 56 autoantibody 56 COX2 56 PAR1 56 histone deacetylases 56 PrPSc 56 epithelial tissues 56 hepatoma 56 anaplastic lymphoma kinase 56 protein tyrosine phosphatases 56 Eisenmenger syndrome 56 TNF antagonist 56 SORL1 56 anemias 56 Plasmodium falciparum 56 antisense oligonucleotides 56 SGK1 56 Metastases 56 HERV 56 glioblastoma tumors 56 allelic variants 55 bcl 2 55 breast carcinoma 55 prostate epithelial cells 55 acute humoral rejection 55 MTHFR gene 55 causative genes 55 PKC beta 55 CYP#C# gene 55 NSCLC tumors 55 MyD# 55 microglial 55 hereditary hemochromatosis 55 CFTR 55 glycosylated 55 colorectal tumor 55 Neutrophil 55 MLL gene 55 gene mutation 55 nicotinic receptor 55 hamartomas 55 cystic fibrosis CF 55 adenylate cyclase 55 Familial Adenomatous Polyposis FAP 55 Vitamin B# deficiency 55 autosomal recessive genetic 55 DSBs 55 Malignant mesothelioma 55 Brugada Syndrome