Related by context. All words. (Click for frequent words.) 67 motor neuron degeneration 67 dyskeratosis congenita 66 ADPKD 65 HbF 65 LKB1 65 inherited mutations 65 PTPN# 65 TMEM#B 65 CEACAM1 64 HGPS 64 atherosclerotic lesions 64 SMN protein 64 BRAF V#E 64 autoimmune encephalitis 64 ERK signaling 64 CHD7 64 LRAT 64 monogenic 64 Sjögren syndrome 64 progressive neurodegenerative disorder 64 SCN5A 64 p# mutations 64 Leydig cell 64 basal cell nevus syndrome 64 gene rearrangements 64 NF1 64 KRAS oncogene 64 Upregulation 63 muscular dystrophies 63 adipogenic 63 Six3 63 chromosomal rearrangement 63 gene MECP2 63 BCL#A 63 tumor suppressor protein 63 neurofibrillary 63 kidney urologic 63 CDH1 63 paraneoplastic 63 renal fibrosis 63 neurofibromas 63 de novo mutations 63 synaptogenesis 63 molecular abnormalities 63 pancreatic endocrine 63 MMP2 63 ADAMTS# 63 C1q 63 aneuploidies 63 G6PD 63 chronic granulomatous disease 63 chromosomal instability 63 Hashimoto thyroiditis 63 osteosarcomas 63 germline mutations 63 mtDNA mutations 63 airway hyperresponsiveness 63 podocytes 63 Clusterin 63 MMP# 62 lymphangiogenesis 62 familial ALS 62 myopathies 62 malignant transformation 62 Gorlin syndrome 62 oncogenic transformation 62 mitochondrial metabolism 62 folate metabolism 62 epithelial tissues 62 microdeletion 62 Aortic stenosis 62 EBV infection 62 anemias 62 PIK3CA 62 shortened telomeres 62 mitochondrial fusion 62 CP CPPS 62 somatic mutations 62 MTHFR 62 colorectal carcinoma 62 beta1 integrin 62 costimulatory 62 FMRP protein 62 mitochondrial function 62 nonsense mutation 62 JAK2 enzyme 62 p#INK#a 62 proto oncogene 62 neurite outgrowth 62 erythropoiesis 62 hyperplastic 62 WAGR syndrome 62 NF2 62 amyloid deposition 62 interferon pathway 62 β catenin 62 P cadherin 62 carcinoids 62 DNA methylation patterns 62 Becker muscular dystrophy 62 Fas ligand 62 B7 H3 62 activating mutation 62 LQTS 62 chromosomal aberrations 62 epigenetically 62 TPMT 61 prostate cancer CaP 61 TRPV4 61 ZNF# 61 promoter methylation 61 colorectal adenoma 61 ABCB1 61 COX2 61 FASPS 61 Beta thalassemia 61 GLI1 61 paraganglioma 61 LRP5 61 gastric carcinoma 61 nondemented 61 Treg cell 61 Activating mutations 61 SHANK3 61 MMP9 61 premalignant 61 epigenetic modification 61 hyperactivation 61 non coding RNA 61 TTR amyloidosis 61 Wnt1 61 Genetic variants 61 filaggrin 61 breast carcinomas 61 tyrosine phosphorylation 61 syngeneic 61 Cockayne syndrome 61 MSH2 61 autosomal dominant inheritance 61 Epstein Barr virus EBV 61 hypomethylation 61 PTEN gene 61 hypothalamic pituitary 61 p#NTR 61 WT1 61 BRAF gene 61 modulate gene expression 61 AT1R 61 transgene expression 61 germline mutation 61 Alzheimer pathology 61 autoimmune thyroiditis 61 cystic fibrosis transmembrane conductance 61 systemic amyloidosis 61 prostate carcinoma 61 SMAD4 61 familial adenomatous polyposis 61 STAT3 signaling 61 chromosomal anomalies 61 cardiac hypertrophy 61 dominantly inherited 61 upregulating 61 mitochondrial enzyme 61 NOTCH1 61 Brugada syndrome 61 microsatellite instability 61 aldehyde dehydrogenase 61 PDGFR 61 vascular endothelial 61 Prostatitis 61 BRCA1 BRCA2 61 Klinefelter syndrome 61 antibody mediated 61 SCD1 61 gastrointestinal stromal tumors GISTs 61 Myasthenia gravis 61 Diabetic neuropathy 61 Dystrophin 61 #beta HSD1 61 ANCA associated 61 MLH1 61 clefting 61 dystrophies 61 CAG repeats 61 apoptotic pathway 60 motor neuron diseases 60 hereditary deafness 60 autosomal dominant 60 penetrance 60 MECP2 gene 60 FGFR2 60 BCR ABL protein 60 beta globin gene 60 PDE#A 60 choroidal neovascularization 60 genomic instability 60 haematopoietic 60 connexin 60 breast cancer metastasis 60 vascular dysfunction 60 pro angiogenic 60 oncoprotein 60 GBM tumors 60 NPHP 60 GH deficiency 60 hedgehog pathway 60 transgenic rats 60 ovarian pancreatic 60 Hurler syndrome 60 Pulmonary hypertension 60 HNPCC 60 beta subunit 60 tumorigenicity 60 chronic periodontitis 60 oncogenic mutations 60 electrophysiologic 60 androgen receptor AR 60 mitochondrial dysfunction 60 hamartomas 60 microRNA expression 60 GBA mutations 60 GRP# 60 PsA 60 ectopic expression 60 nonsense mutations 60 autosomal recessive 60 immunopathology 60 huntingtin gene 60 cortical dysplasia 60 myotonic dystrophy 60 GSTP1 60 hypermethylation 60 GPx 60 neuro degenerative disease 60 Carcinoid tumors 60 costimulation 60 MELAS syndrome 60 transthyretin 60 trophoblast cells 60 Cyclin D1 60 seminomas 60 1 diabetes T1D 60 inherited retinal degeneration 60 Fragile X gene 60 IL 1ß 60 ataxias 60 Prion diseases 60 normal karyotype 60 Li Fraumeni 60 overactivity 60 KIBRA 60 HER2 neu 60 PDGF receptor 60 achromatopsia 60 Genetic variations 60 miRNA expression 60 CFTR gene 60 LMNA 60 infantile hemangioma 60 FGFR1 60 lysophosphatidic acid 60 Atopic eczema 60 lymphatic vasculature 60 chronic eosinophilic leukemia 60 leukemias lymphomas 60 TGF ß 60 Wnt signaling pathway 60 Chronic pancreatitis 60 congenital deficiency 60 neurofibromin 60 intestinal polyps 60 TGF b 60 androgen receptor gene 60 mitochondrial mutations 60 autoinflammatory diseases 60 nonmelanoma skin cancers 60 MALT lymphoma 60 NF kB pathway 60 cone photoreceptors 60 BMP signaling 60 fatal neurodegenerative disorder 60 heterotaxy 60 desmosomes 60 cardiac fibroblasts 60 sporadic ALS 60 DNA rearrangements 60 FOXP3 60 mitogen activated protein kinases 60 beta thalassemia 60 SMN1 60 acinar 60 RAS mutations 60 p# activation 60 IGFBP2 60 T1DM 60 SMN2 60 hypophosphatasia 60 beta amyloid peptides 60 transgenic mouse models 60 GATA3 60 Genetic predisposition 60 poorer prognosis 60 enzymatic activity 60 γ secretase 60 Kufs disease 60 BMP4 60 mesenchymal cell 60 Drosha 60 mTOR mammalian target 60 remyelination 60 thoracic aortic aneurysm 60 Polymorphisms 60 NOD2 60 neuronal plasticity 60 PPAR γ 60 retinal degeneration 60 GSTT1 60 mutated K ras 60 Atopic dermatitis 60 familial pancreatic cancer 60 neurodegenerative disorder 60 mitochondrial respiration 60 Hutchinson Gilford progeria 59 pulmonary hypertension PH 59 Hedgehog signaling 59 cell signaling pathways 59 hypermethylated 59 metaplasia 59 parathyroid carcinoma 59 epithelial tumors 59 mGluR5 antagonist 59 SERCA2a 59 MYH9 gene 59 NR#A# 59 MAP#K# 59 embryonic tissues 59 sortilin 59 lymphoblasts 59 nonalcoholic steatohepatitis NASH 59 lymphomas leukemias 59 neuroligins 59 proapoptotic 59 TXNIP 59 eIF 4E 59 secretory pathway 59 oesophageal adenocarcinoma 59 FGFR3 59 cause cardiac channelopathies 59 metastatic neuroendocrine tumors 59 lymphocyte activation 59 PDE7B 59 transgenic mouse model 59 severe congenital neutropenia 59 hypoxia inducible factor 59 dysplasias 59 atherosclerotic disease 59 E selectin 59 fibrotic disease 59 CCR5 delta# 59 hormone secretion 59 Cowden syndrome 59 prefrontal regions 59 pheochromocytomas 59 choroidal neovascularization CNV 59 vesicoureteral reflux VUR 59 inherited neurological disorder 59 COL#A# 59 embryonal 59 SIRT1 gene 59 histone methylation 59 lactose malabsorption 59 STAT4 59 HDAC2 59 transcriptional repressor 59 FTLD 59 hedgehog signaling 59 basal cell carcinoma BCC 59 intracellular bacteria 59 FGFR4 59 TGF β 59 Huntingtons disease 59 Mesenchymal 59 pituitary tumors 59 Pulmonary arterial hypertension 59 hereditary hemochromatosis 59 electrical conduction 59 gastric carcinomas 59 squamous cell lung cancer 59 genotoxic stress 59 Neurodegenerative diseases 59 SOD1 gene 59 leiomyomas 59 brain lesions 59 ubiquitylation 59 Irritable bowel syndrome IBS 59 Alzheimer Disease AD 59 leptin deficiency 59 FANCD2 59 NF kappaB activation 59 mesothelial cells 59 prostanoid 59 UCP2 59 Gleevec resistant 59 #ß HSD1 59 GPC5 59 immunodeficiency disorders 59 K ras mutations 59 ependymoma 59 metastatic lymph nodes 59 FGFs 59 PARP inhibition 59 thyroid hormone deficiency 59 alpha1 antitrypsin deficiency 59 osteoclast activity 59 FMR1 gene 59 acute myelogenous leukemia AML 59 lysosomal storage disease 59 Elevated serum 59 H#K# methylation 59 myogenesis 59 MC1R 59 cisplatin resistant 59 activin 59 muscular dystrophy cystic fibrosis 59 pathophysiological effects 59 spinocerebellar ataxia 59 telomere maintenance 59 Wnts 59 neuropsychiatric diseases 59 IL#R 59 myelination 59 neuromuscular junction 59 Skp2 59 BRCA2 gene 59 CCR3 59 hypereosinophilic syndrome 59 astrocytic 59 GATA4 59 HER2 overexpression 59 NKX#.# 59 Hypophosphatasia 59 PKCi 59 nerve degeneration 59 neovascular 59 microcephalin 59 glial tumors 59 Lafora disease 59 microRNA molecules 59 osteolytic 59 discoid lupus 59 pituitary adenomas 59 neurosensory 59 clinicopathological 59 Li Fraumeni syndrome 59 telomere DNA 59 axonal damage 59 lung fibrosis 59 spontaneous mutations 59 BMP2 59 Alport syndrome 59 Systemic lupus erythematosus SLE 59 prefrontal cortical 59 osteoclast 59 epigenetic alterations 59 SSc 59 nonhereditary 59 cystic fibrosis chronic pancreatitis 59 gastric adenocarcinoma 59 chronic myeloid 59 chromosomal translocation 59 oncogenesis 59 galactosemia 59 IgG4 59 TMPRSS6 59 Severe Primary IGFD 59 Foxp3 59 chronic autoimmune disorder 59 pathogenic mutations 59 neural cells 59 homozygous FH 59 VEGF expression 59 malignant prostate 59 BMPR2 59 PTEN protein 59 exocrine glands 59 adrenocortical 59 myeloproliferative diseases 59 PALB2 59 heterozygotes 59 neurofibroma 59 Cholangiocarcinoma 59 hepatic steatosis 59 sarcomatoid 59 severe malignant osteopetrosis 59 myelofibrosis polycythemia vera 59 Notch signaling 59 lysosomal storage diseases 59 hepatocellular 59 calcium homeostasis 59 uricase 59 idiopathic pulmonary 59 Papillary 59 intestinal epithelium 59 G6PD deficiency 59 malignant pancreatic 59 SLC#A# gene [001] 59 HBeAg negative 59 breast endometrial 59 hedgehog signaling pathway 59 histologic subtype 59 PCNSL 59 neurological manifestations 59 Akt1 59 tumorigenesis 59 fibrous dysplasia 59 epigenetic mechanisms 59 coronary microvascular 59 CHEK2 59 Raf MEK ERK 58 p# MAPK 58 JAK2 mutation 58 amyloidogenic 58 methylation patterns 58 KCNH2 58 LDL receptor 58 levodopa therapy 58 iPS derived 58 progressive degeneration 58 thyrotropin 58 myelomeningocele 58 pDC 58 Aß 58 gastric cardia 58 leptin receptor 58 CC genotype 58 GnT 4a 58 Ribavirin causes 58 apoE 58 peroxisomal 58 podocyte 58 neuroinflammation 58 myasthenia gravis MG 58 carcinoid tumors 58 HNSCC 58 neoplastic diseases 58 endocrine tumors 58 autosomal recessive disease 58 BRAF protein 58 Pin1 58 neoplasias 58 Prox1 58 immunodeficiencies 58 maturational 58 dermatomyositis 58 JAK2 gene 58 allelic variants 58 paxillin 58 UVB induced 58 AAT deficiency 58 Chronic lymphocytic leukemia CLL 58 fronto temporal dementia 58 Phosphorylation 58 lactase deficiency 58 fungoides 58 protein alpha synuclein 58 progranulin 58 lymphoid cells 58 TNFR 58 IL #R 58 dermopathy 58 radiosensitivity 58 Symadex 58 NADPH oxidase 58 adenomatous 58 antitumor efficacy 58 membranous nephropathy 58 neuronal dysfunction 58 airway remodeling 58 Akt phosphorylation 58 methylenetetrahydrofolate reductase 58 Thyroid disorders 58 VHL gene 58 thyroid dysfunction 58 TCF#L# 58 hypothalamic amenorrhea 58 axonal degeneration 58 RIP1 58 ADAM# 58 cypin 58 urothelial cancer 58 epithelia 58 glucocorticoid receptors 58 homozygosity 58 neuritic 58 proteolysis 58 Prolactin 58 antiphospholipid syndrome 58 histone deacetylases 58 neuropathologic 58 neuronal signaling 58 synovial cells 58 prostate carcinomas 58 Joubert syndrome 58 retinitis pigmentosa RP 58 splice variants 58 tissue fibrosis 58 liver metastasis 58 Progenitor cells 58 CCR7 58 hepatic fibrosis 58 RPE# 58 promoter hypermethylation 58 VSMCs 58 gene locus 58 nitric oxide synthase 58 Chronic lymphocytic leukemia 58 embryonic lethality 58 ERBB2 58 pancreatic islet 58 Bardet Biedl syndrome 58 Prognostic factors 58 COMT 58 microdeletions 58 homocystinuria 58 Autoimmune disorders 58 vascular reactivity 58 CHD5 58 gamma globin gene 58 neuropsychiatric disorder 58 MSMB 58 CagA 58 Basal cell 58 TCF#L# gene 58 CNTNAP2 58 immunocompetent 58 SLC#A# [002] 58 monocytic 58 Brd4 58 JAK STAT 58 TNFalpha 58 skeletal muscle cells 58 Synovial sarcoma 58 leukaemic stem cells 58 fatty acid metabolism 58 Maroteaux Lamy Syndrome 58 antisense oligonucleotides 58 ENPP1 58 IFN γ 58 gastrointestinal stromal tumor 58 Hsp# [001] 58 fatty acid oxidation 58 missense mutations 58 Parkinson Disease PD 58 RUNX3 58 hematopoietic malignancies 58 cellular prion protein 58 microglial activation 58 steroidogenic 58 Her-2/neu 58 osteoblastic 58 mineralocorticoid 58 lymphangioleiomyomatosis LAM 58 tenascin C 58 autosomal dominant polycystic kidney 58 PTEN mutations 58 miR #a [002] 58 subclinical atherosclerosis 58 osteoblast 58 Acute myeloid leukemia 58 vascularisation 58 overexpress 58 neoplastic transformation 58 congenital disorders 58 schwannomas 58 hereditary spastic paraplegia 58 hyperammonemia 58 neovascularization 58 ENaC 58 metabolic abnormality 58 Spinal muscular atrophy 58 osteogenic differentiation 58 Akt3 58 MYCN amplification 58 primary biliary cirrhosis 58 Leukemias 58 PAOD 58 Wiskott Aldrich syndrome 58 HIF 1a 58 TNFa 58 pituitary adenoma 58 granzyme B 58 Smad7 58 pancreatic prostate 58 LPA gene 58 PAR1 58 circadian genes 58 histological subtype 58 Systemic lupus erythematosus 58 Adenomas 58 Eisenmenger syndrome 58 CYP#C# gene 58 G#S mutation 58 p# gene 58 chromatin structure 58 prostate carcinogenesis 58 ectodermal dysplasia 58 copper zinc superoxide 58 V#F mutation 58 proliferative diabetic retinopathy 58 ductal adenocarcinoma 58 CD8 + 58 Cyclin E 58 CYP#D# gene 58 BCR ABL 58 aberrant activation 58 Myotonic dystrophy 58 epigenetic changes 58 Leber hereditary optic neuropathy 58 somatic mutation 58 contractile function 58 synaptic function 58 alpha synuclein protein 58 anaplastic lymphoma kinase 58 gene polymorphisms 58 mice lacking 58 PDE1 58 HLA B# 58 mucosal immune responses 58 neuroblastomas 58 incurable neurological disorder 58 urothelial carcinoma 58 autosomal dominant disorder 58 CYT# potent vascular disrupting 58 Magnesium deficiency 58 protein misfolding 58 MELAS 58 Th2 cytokines 58 polymyalgia rheumatica 58 c MYC 58 c myc 58 MTHFR gene 58 mastocytosis 58 Acute lymphoblastic leukemia 58 telomere lengths 58 atrophic gastritis 58 alveolar rhabdomyosarcoma 58 familial clustering 58 dopaminergic therapy 58 IL6 58 dysgenesis 58 HER2 expression 58 aplasia 58 Epstein Barr Virus EBV 58 Smad3 58 cyclin E 58 dysplastic 58 pseudotumor cerebri 58 ORMDL3 58 nNOS 58 solar keratosis 58 β amyloid 58 congenital adrenal hyperplasia CAH 58 mitochondrial disorders 58 abnormal cytology 58 CD#c 58 atopic dermatitis AD 58 APOE ε4 58 MEF2A 58 Hurthle cell 58 intermittent hypoxia 58 inhibitory neurotransmitters 58 CYP#B# 58 Leydig cells 58 EZH2 58 VEGF inhibitors 58 Von Willebrand disease 58 selective inhibition 58 Hypertrophy 58 hyperprolactinemia 58 immunodeficiency 58 ERK1 2 58 lesional 58 repolarization 58 melanocyte stimulating hormone 58 Hh pathway 58 estrogen receptor alpha 58 IRS1 58 constitutively expressed 58 beta adrenergic receptor 58 intracellular accumulation 58 essential thrombocythemia 58 holoprosencephaly 58 hepatic lipase 58 HLA DRB1 58 DNA demethylation 58 familial hypercholesterolemia 58 degenerative neurological diseases 58 mesangial 58 deacetylation 58 multigenic 58 FGF2 58 beta adrenergic receptors 58 differential gene expression 58 trophoblasts 58 H#K# [001] 58 atrioventricular 58 carbohydrate absorption 58 E3 ubiquitin ligase 58 cAMP signaling 58 torsade de pointes 58 downregulating 57 Haptoglobin 57 steroidogenesis 57 IDH1 mutation 57 lung carcinomas 57 cervical breast 57 Thyroid hormone 57 metastatic bladder 57 experimental autoimmune encephalomyelitis 57 MAP kinase 57 CD#b 57 inherited neurodegenerative disorder 57 prostate ovarian 57 causative genes 57 sequence homology 57 Endometrial cancer 57 H#K# [002] 57 Critical limb ischemia 57 hepatic encephalopathy HE 57 osteogenic 57 atypical hemolytic uremic syndrome 57 isoenzyme 57 striated muscle 57 FKBP# 57 OGG1 57 pRb 57 artery stenosis 57 MC4R gene 57 testicular germ cell 57 immunoreactivity 57 GIST tumors 57 mammary cancers 57 Peritoneal mesothelioma 57 Notch signaling pathway 57 Immunohistochemical analysis 57 acadesine 57 retinal dystrophy 57 interleukin IL -# 57 upregulates 57 gene amplification 57 Meckel Gruber 57 chronic venous insufficiency 57 c myc gene 57 ApoE gene 57 sCJD 57 genetic abnormalities 57 craniofacial defects 57 utrophin 57 LHRH receptor positive 57 genomic alterations 57 neuronal degeneration 57 Cathepsin B 57 valvular heart disease 57 lichen planus 57 humoral immunity 57 heritable disorders 57 inducible nitric oxide synthase 57 lung metastasis 57 kinase gene 57 NFKBIA 57 acetylcholine receptor 57 interstitial cystitis IC 57 arterial calcification 57 epithelial cancers 57 fibrin deposition 57 Duchenne muscular dystrophy DMD 57 Sezary syndrome 57 allergic inflammation 57 noncoding RNAs 57 amyloid β 57 cardiac channelopathies 57 erythropoietic 57 proteoglycan 57 mental retardation epilepsy 57 Polymorphic Ventricular Tachycardia CPVT 57 underlying pathophysiology 57 genes predisposing 57 channelopathies 57 S#A# [002] 57 nasopharyngeal carcinoma NPC 57 renal allograft 57 hyperparathyroidism 57 colorectal adenocarcinoma 57 orchitis 57 tryptase 57 cell adhesion molecule 57 DISC1 gene 57 rs# [002] 57 Brugada Syndrome 57 neurotrophic 57 neurologic disorder 57 NAGS deficiency 57 NFkB 57 mice genetically engineered 57 lactate dehydrogenase LDH 57 airway hyper responsiveness 57 imatinib resistance 57 adrenal function 57 XLHED 57 #q#.# [002] 57 malignant phenotype 57 neuroendocrine 57 developmental abnormalities 57 spermidine 57 Htt 57 lupus nephritis 57 cellular metabolism 57 protein phosphorylation 57 beta amyloid peptide 57 epididymal 57 Rap1 57 LDLR 57 coexpression 57 embryonal rhabdomyosarcoma 57 mGluR2 NAM 57 PON1 57 multipotent 57 Genetic variation 57 IL 1β 57 granule cells 57 Myelodysplastic syndromes MDS 57 progranulin protein 57 proliferative disorders 57 myotonic muscular dystrophy 57 Interstitial cystitis 57 Retinopathy 57 Apert syndrome 57 FasL 57 NF kB signaling 57 homodimers 57 ubiquitin ligases 57 neuropathological 57 LHON 57 colorectal carcinogenesis 57 LIS1 57 Kv#.# 57 Hedgehog pathway 57 neurocognitive deficits 57 OSAHS 57 MDM2 57 Hh 57 HDAC6 57 APOL1 57 phospholipase A2 57 telomerase activity 57 tumor suppressor genes 57 mosaicism 57 thyroid deficiency 57 tau pathology 57 IgA deficiency 57 chromosomal mutations 57 endocannabinoid signaling 57 hypoperfusion 57 γδ T cells 57 fusiform 57 Jhdm2a 57 atypical hyperplasia 57 chitinase 57 beta catenin protein 57 ubiquitination 57 BH4 deficiency 57 PKC beta 57 NQO1 57 untreated celiac disease 57 aP2 57 KCNE2 57 ACh 57 choroidal vasculopathy 57 supratentorial 57 PKM2 57 idiopathic PAH 57 pulmonary metastases 57 FLT3 57 chromosomal rearrangements 57 Flt3 57 Th# cells 57 telomere dysfunction 57 tumoral 57 flavopiridol 57 TGF ß1 57 Colon polyps 57 laforin 57 synthetase 57 pericytes 57 microglial 57 genetic syndromes 57 histone modification 57 Duchenne Muscular Dystrophy DMD 57 granulosa cell