Related by context. All words. (Click for frequent words.) 69 sporadic ALS 68 NF2 68 neurofibromatosis type 67 autosomal dominant 67 familial ALS 67 Hashimoto thyroiditis 66 neuroblastomas 66 FTLD 66 Angelman syndrome 66 medulloblastomas 66 PDGFR 66 HGPS 66 ADPKD 66 inherited mutations 66 GISTs 65 osteosarcomas 65 HbF 65 FLT3 65 medulloblastoma 65 LRAT 65 dyskeratosis congenita 65 MSH2 64 basal cell nevus syndrome 64 NFkB 64 progressive neurodegenerative disorder 64 mosaicism 64 RPE# 64 FXTAS 64 familial hypercholesterolemia 64 neurofibromas 64 CDH1 64 autosomal recessive 64 de novo mutations 64 germline mutations 64 MLH1 64 frontotemporal dementia 64 ependymoma 64 Peutz Jeghers syndrome 64 PTPN# 64 podocytes 64 MECP2 gene 63 missense mutations 63 monogenic 63 WT1 63 heterozygous 63 paraganglioma 63 CHD7 63 mitochondrial dysfunction 63 microcephalin 63 GBM tumors 63 CYP#C# [002] 63 Leydig cell 63 synaptogenesis 63 T1DM 63 mtDNA mutations 63 astrocytomas 63 T1D 63 neurodegenerative disorder 63 neuroendocrine 63 Heterozygous 63 motor neuron degeneration 63 CNVs 63 TGF β 63 Lafora disease 62 myotonic dystrophy 62 MYCN amplification 62 CFTR gene 62 STAT4 62 FGFR1 62 colorectal carcinoma 62 pheochromocytoma 62 cardiac hypertrophy 62 nonsense mutations 62 holoprosencephaly 62 leptin receptor 62 PARP inhibition 62 germline mutation 62 chromosomal defect 62 Severe Primary IGFD 62 BCL#A 62 Smad3 62 inherited retinal degeneration 62 #q# [001] 62 ABCB1 62 activating mutations 62 MTHFR 62 ADAM# 62 essential thrombocythemia 62 TMEM#B 62 malignant transformation 62 uveal melanoma 62 Sjögren syndrome 62 aneuploidy 62 BRAF gene 62 IgA deficiency 62 renal fibrosis 62 proto oncogene 62 Friedreich ataxia 62 immunocompetent 62 cAMP signaling 62 Fanconi anemia 62 chromosomal aberrations 62 vWD 62 Hurler syndrome 61 ataxias 61 gastric carcinoma 61 tumor suppressor protein 61 airway hyperresponsiveness 61 calcineurin 61 VHL gene 61 heterozygotes 61 Li Fraumeni syndrome 61 p# mutations 61 chromosomal abnormalities 61 breast carcinomas 61 FMR1 gene 61 interferon pathway 61 CNTNAP2 61 LQTS 61 JAK2 enzyme 61 LHON 61 VEGF receptor 61 breast carcinoma 61 cyclin E 61 mammary tumors 61 synuclein 61 diabetes mellitus DM 61 Neurofibromatosis type 61 familial pancreatic cancer 61 haematopoietic 61 G6PD deficiency 61 mutated gene 61 retinal degeneration 61 Niemann Pick disease 61 Six3 61 ependymomas 61 achromatopsia 61 ALK mutations 61 acute myelogenous leukemia AML 61 Leber congenital amaurosis LCA 61 amyloid deposition 61 PDGFRA 61 MAPK pathway 61 Alzheimer Disease AD 61 lung adenocarcinoma 61 MALT lymphoma 61 LKB1 61 COX2 61 Glioma 61 Leber Hereditary Optic Neuropathy 61 microdeletion 61 beta1 integrin 61 chromosome abnormality 61 p# mutation 61 GIST tumors 61 autosomal dominant disorder 61 GBA mutations 61 PTEN mutations 61 leukemia ALL 61 Hh 61 chromosomal rearrangement 61 genetic abnormalities 61 atypical hemolytic uremic syndrome 61 neural cells 61 carcinoid 61 aneuploidies 61 leukemia AML 61 IGF1 61 SHANK3 61 APOE e4 61 inherited neurological disorder 61 ApoE gene 61 SCN5A 61 Hurthle cell 61 MDM2 61 Clusterin 61 basal cell carcinoma BCC 61 prostate adenocarcinoma 61 SOD1 gene 61 somatic mutations 61 IDH1 mutation 61 basal cell carcinomas 61 Immunohistochemical analysis 61 degenerative disorder 61 nonsense mutation 61 AAT deficiency 61 TACI mutations 61 MC1R 61 beta thalassemia 61 myeloproliferative disorders 61 developmental abnormalities 61 MELAS 61 uPA 60 spinocerebellar ataxia 60 thrombophilia 60 KRAS oncogene 60 MeCP2 gene 60 neurodegenerative disease 60 acute lymphoid leukemia 60 narcolepsy cataplexy 60 ADAMTS# 60 hyperactivation 60 LRRK2 60 mitochondrial disorders 60 GNAQ 60 GSTP1 60 mitochondrial mutations 60 demyelination 60 heterotaxy 60 Medulloblastoma 60 carcinoid tumors 60 tyrosine phosphorylation 60 V#F mutation 60 neuronal differentiation 60 paraneoplastic 60 Leukemias 60 phenotype 60 BRAF mutation 60 hyperplastic 60 transgenic mouse model 60 protein kinase C 60 pancreatic adenocarcinoma 60 micro RNAs 60 Fas ligand 60 pyloric stenosis 60 apoE4 60 euthymic patients 60 cerebellar 60 susceptibility gene 60 plasma kallikrein 60 EGFR mutations 60 subependymal giant cell 60 familial adenomatous polyposis 60 Prox1 60 autosomal dominant polycystic kidney 60 galactosemia 60 FGFR2 60 recessive genetic 60 CagA 60 FGFR3 60 neuropsychiatric disorder 60 APOE4 60 primary biliary cirrhosis 60 pRb 60 PAOD 60 presenilin 60 5q 60 atherosclerotic lesions 60 Wwox 60 bexarotene 60 Epstein Barr virus EBV 60 retinitis pigmentosa RP 60 C#Y 60 autosomal recessive disease 60 pancreatic endocrine 60 S#A# [002] 60 TACI 60 genetic abnormality 60 APOE gene 60 TP# mutation 60 phenylketonuria 60 Myotonic dystrophy 60 CEACAM1 60 neurofibromatosis 60 T2DM 60 Pten 60 Wiskott Aldrich syndrome 60 neuropsychiatric disorders 60 hypothalamic pituitary adrenal axis 60 MMP9 60 #q#.# [001] 60 Notch1 60 sortilin 60 lung metastasis 60 APOL1 60 Hutchinson Gilford progeria 60 tumor suppressor gene 60 gene MECP2 60 p# MAPK 60 NKX2 60 Leber congenital amaurosis 60 cell adhesion molecule 60 neoplastic 60 neuroendocrine tumors 60 epithelial tissues 60 ERK signaling 60 IGFBP2 60 mammary cancers 60 brain malformation 60 caveolin 60 vWF 60 CYP#D# gene 60 neurological abnormalities 60 estrogen receptor alpha 60 brain lesions 60 hamartomas 60 mutations 60 activating mutation 60 microdeletions 60 PNET 60 Cushing syndrome 60 experimental autoimmune encephalomyelitis 60 immunodeficiencies 60 FGFR4 60 von Hippel Lindau 60 subclinical hypothyroidism 59 genetic syndromes 59 Transgenic Mice 59 malignant lymphoma 59 Neuregulin 1 59 biochemical abnormalities 59 syngeneic 59 metaplasia 59 VCFS 59 myelofibrosis polycythemia vera 59 lymphangiogenesis 59 epigenetic changes 59 circadian genes 59 renal carcinoma 59 NOTCH1 59 Aß 59 Cyclin D1 59 C1q 59 hepatocellular carcinomas 59 EGFR inhibitors 59 #p#.# [002] 59 BMP4 59 mice lacking 59 adenocarcinomas 59 transgene expression 59 COMT 59 atypical hyperplasia 59 hematologic disorders 59 Rett syndrome 59 neoplasm 59 HNPCC 59 Klinefelter syndrome 59 mastocytosis 59 leukaemias 59 neurofibromin 59 grade cervical intraepithelial 59 IGFBP 3 59 JAK mutations 59 amyloid deposits 59 Joubert syndrome 59 K ras mutations 59 mutant alleles 59 Gleevec resistant 59 neural crest 59 genetic alteration 59 VIPR2 59 nonmelanoma skin cancers 59 neurofibroma 59 Bardet Biedl syndrome 59 infarcts 59 BMP2 59 homozygotes 59 TSLP 59 homozygous 59 missense mutation 59 gastrointestinal stromal tumors GISTs 59 huntingtin gene 59 dopaminergic neurons 59 neurological disorder affecting 59 KIT mutations 59 osteopetrosis 59 Cholangiocarcinoma 59 EoE 59 primitive neuroectodermal tumors 59 CCR5 delta# 59 Aortic stenosis 59 myeloma cells 59 Kv#.# 59 homozygous FH 59 demyelinating 59 molecular abnormalities 59 serous ovarian cancer 59 monozygotic twins 59 BRCA1 gene 59 mutated K ras 59 sCJD 59 systemic lupus erythematosus SLE 59 mental retardation epilepsy 59 TNF α 59 IFN gamma 59 T#I [002] 59 epigenetic alterations 59 MTHFR gene 59 dominantly inherited 59 IGF2 59 acute leukemias 59 HMGA2 59 DNA methylation patterns 59 Becker muscular dystrophy 59 BRAF mutations 59 chronic eosinophilic leukemia 59 TCF#L# 59 JAK2 59 TTR gene 59 CYP#D# 59 SMN1 59 claudin 59 von Willebrand disease 59 MCAD deficiency 59 androgen receptor AR 59 TGF ß 59 polycystic ovary syndrome PCOS 59 premalignant 59 causative gene 59 glucocorticoid receptors 59 costimulatory 59 cyclin dependent kinase 59 hyperinsulinemia 59 cystic fibrosis transmembrane conductance 59 IRS1 59 CALHM1 59 catenin 59 lysosomal 59 hypereosinophilic syndrome 59 B7 H3 59 NF kB signaling 59 TP# mutations 59 immunodeficiency 59 NF kB pathway 59 chromosome #q#.# [001] 59 NAFLD 59 androgen receptor gene 59 apoE 59 sarcomas 59 dysbindin 59 sarcomatoid 59 mutant protein 59 1 diabetes T1D 59 JMML 59 Foxp3 59 homozygosity 59 DiGeorge syndrome 59 myelomeningocele 59 elevated triglyceride levels 59 DQB1 * 59 #q#.# [002] 59 tyrosine kinases 59 Wilms tumor 59 meningiomas 59 xenograft tumors 59 clusterin 59 neovascularization 59 enzymatic activity 59 p#INK#a 59 leukemias lymphomas 59 extramedullary 59 CD8 + 59 interferon IFN 59 MLL gene 59 penetrance 59 PsA 59 hyperplasia 59 Fanconi Anemia 59 Parkinson disease PD 59 oligodendrogliomas 59 TTR amyloidosis 59 NF1 gene 59 systemic amyloidosis 59 lymphoid 59 SSc 59 tumoral 59 P cadherin 59 N myc 59 Wnt signaling pathway 59 chronic granulomatous disease 59 APOE ε4 59 medium chain acyl 59 CDKN2A 59 filaggrin 59 prosopagnosia 59 MGUS 59 hepatocellular carcinoma HCC 59 proband 59 Cryptococcus neoformans 59 CDK4 59 neuronal dysfunction 58 MEK1 58 MC4R gene 58 CYP#C# gene 58 IKZF1 58 KRAS mutations 58 mitogen activated protein kinase 58 hypermethylation 58 mutated genes 58 genetic defect 58 Nf1 58 idiopathic myelofibrosis 58 bladder cancers 58 steatohepatitis 58 microRNA miR 58 RIP1 58 BMP signaling 58 Alzheimers disease 58 ANCA associated 58 pseudotumor cerebri 58 spontaneous mutations 58 serine protease 58 PAR1 58 Retinitis pigmentosa 58 IGFBP 58 Fibroblasts 58 LRP5 58 Carcinoid tumors 58 ectodermal dysplasia 58 diabetes mellitus T2DM 58 leiomyoma 58 TSC1 58 CMV infection 58 cortical dysplasia 58 PTEN gene 58 lymphocyte activation 58 lymphoblasts 58 myeloproliferative neoplasms 58 MECP2 58 nucleoside analogues 58 TEL AML1 58 miR #a [001] 58 CAG repeats 58 hydrops 58 β thalassemia 58 muscarinic receptors 58 genetic mutations 58 activin 58 urothelial carcinoma 58 LIS1 58 herpesviruses 58 imatinib resistance 58 vascular endothelial 58 nonalcoholic steatohepatitis NASH 58 radial glia 58 PC# cells 58 lysosomal storage diseases 58 p# gene 58 MLL2 58 tuberous sclerosis complex 58 IDH1 58 DISC1 58 N Myc 58 epilepsies 58 rheumatic disease 58 BRCA1 mutations 58 BRAF V#E 58 melanocyte 58 IDDM 58 pancreatic neuroendocrine tumors 58 lysosomal storage disease 58 PDGF receptor 58 Aβ 58 mRNA expression 58 untreated celiac disease 58 TrkB 58 virulence genes 58 lymphocytic 58 behavioral abnormalities 58 Skp2 58 SIRT6 58 FMR1 58 polycystic kidneys 58 GPC5 58 Cockayne syndrome 58 Bcl 58 prostate cancer CaP 58 Dysregulation 58 transgenic mouse models 58 hypoperfusion 58 β catenin 58 BRAF protein 58 NFKBIA 58 hypogonadotropic hypogonadism 58 transgenic mice 58 E#F# 58 spinocerebellar ataxia type 58 beta amyloid peptides 58 ZNF# 58 normal karyotype 58 synovial sarcoma 58 motoneurons 58 neuroblastoma tumors 58 Haptoglobin 58 TNFalpha 58 adhesion molecule 58 chromosomal disorder 58 LHRH receptor positive 58 HLA B# 58 oncoprotein 58 endostatin 58 DICER1 58 ASDs 58 angiosarcoma 58 FOXP3 58 Neurofibromatosis Type 58 Papillary 58 autosomal dominant inheritance 58 PIK3CA 58 ApoE 58 underlying pathophysiology 58 bcl 2 58 protein tyrosine phosphatase 58 telomere dysfunction 58 β cells 58 BRCA1 BRCA2 58 microRNA expression 58 leiomyomas 58 chromosomal translocations 58 hypophosphatasia 58 PON1 58 mild cognitive 58 aldehyde dehydrogenase 58 alleles 58 Leber hereditary optic neuropathy 58 autosomal 58 FSGS 58 ERK1 2 58 Polymorphic Ventricular Tachycardia CPVT 58 mito 58 p# activation 58 myeloid 58 IDH2 58 PALB2 58 epigenetic silencing 58 type 1diabetes 58 colorectal tumors 58 TLR3 58 Brugada Syndrome 58 Duchenne muscular dystrophy DMD 58 chemokine receptor 58 neuritic 58 urothelium 58 HER2 positivity 58 recessive inheritance 58 intestinal epithelium 58 breast cancer metastasis 58 neovascular 58 Philadelphia Chromosome Positive 58 bronchopulmonary dysplasia 58 DIPG 58 ductal adenocarcinoma 58 neuroinflammation 58 WDR# 58 ectopic expression 58 cutaneous lesions 58 choroidal neovascularization 58 M. pneumoniae 58 pDCs 58 neurological dysfunction 58 MYH9 gene 58 Treg cell 58 achondroplasia 58 alpha synuclein 58 CD4 + CD# 58 Apert syndrome 58 carcinoid tumor 58 neurofibrillary 58 epithelial tumors 58 NKT cells 58 juvenile idiopathic arthritis 58 glomerulonephritis 58 HBeAg negative 58 complement inhibitor eculizumab 58 pDC 58 chromosomal instability 58 lymphoblastic leukemia 58 plexiform neurofibromas 58 COMT gene 58 congenita 58 N. gonorrhoeae 58 TGF beta 58 SOD1 58 HFE gene 58 lymphocytic leukemia 58 G#S mutation 58 tumorigenesis 58 genes predisposing 58 ß1 58 nondemented 58 papillary RCC 58 motor neuron diseases 58 mucinous 58 hepatoma 58 KCNH2 58 CYP# [002] 58 mutant huntingtin protein 58 Meningiomas 58 Meckel Gruber 58 EGF receptor 58 neurodevelopmental 58 congenital adrenal hyperplasia CAH 58 PKU genetic 58 leukoencephalopathy 58 Kufs disease 58 COL#A# 58 autoimmune thyroid 58 apoptotic pathway 58 prostate carcinoma 58 CYP#B# 58 mutation 58 demyelinating diseases 58 hippocampal neurons 58 HER2 overexpression 58 dysregulated 58 hypopituitarism 58 cellular prion protein 58 transgenic rats 58 invasive carcinoma 58 CD#c 57 GRP# 57 autosomal recessive genetic 57 cisplatin resistant 57 neoplasia 57 Notch signaling 57 Purkinje cells 57 serotonin receptor 57 myeloproliferative 57 Wnt signaling 57 KCNE2 57 PKC beta 57 ORMDL3 57 GH deficiency 57 nNOS 57 adaptive immunity 57 Aurora kinase 57 Cowden syndrome 57 gene mutations 57 trophoblast cells 57 EGFr 57 diabetic nephropathy 57 PTHrP 57 miR #a [002] 57 supratentorial 57 mitochondrial diseases 57 lymphoid cells 57 cerebellar hypoplasia 57 interleukins 57 hyperparathyroidism 57 Beta thalassemia 57 dystrophies 57 mGluR5 antagonist 57 TRIM5 57 genes BRCA1 57 MAP kinase 57 gene polymorphisms 57 parainfluenza virus 57 iNOS 57 basal forebrain 57 colorectal tumor 57 Glioblastoma Multiforme GBM 57 metastatic lesions 57 adrenal function 57 CLL cells 57 genetic polymorphism 57 remyelination 57 embryonal rhabdomyosarcoma 57 isoenzymes 57 autophagic 57 T2D 57 LRP6 57 Li Fraumeni 57 nicotinic receptors 57 IL#R 57 thymosin 57 epigenetically 57 receptor tyrosine kinase 57 neurodevelopmental disorder 57 fibrotic disease 57 Abl 57 chromosomal anomaly 57 OGG1 57 melanocytic nevi 57 neurofibrillary tangles 57 PCa 57 histone deacetylases 57 C#BL/#J 57 cytogenetic abnormalities 57 abnormal chromosome 57 pancreatic ductal adenocarcinoma 57 AAT Deficiency 57 recessive trait 57 hyper IgE syndrome 57 monocytic 57 chromosomal anomalies 57 defective gene 57 genotoxic stress 57 glycogen synthase kinase 57 polycystic ovarian syndrome PCOS 57 hamartoma 57 adenomatous 57 alveolar epithelial cells 57 Retinoblastoma 57 CXCL# 57 pilocytic astrocytomas 57 embryonal 57 NR2B 57 myelination 57 anaplastic lymphoma kinase 57 methylation patterns 57 precocious puberty 57 CD#L 57 transthyretin 57 enzyme deficiency 57 SMAD4 57 noncoding RNAs 57 liver metastasis 57 calcium homeostasis 57 neurotrophin 57 Hemophilia B 57 Mycoplasma pneumoniae 57 progranulin mutations 57 gene amplification 57 bleomycin 57 CIDP 57 pathogenic mutations 57 granzyme B 57 EBV infection 57 thyroid carcinoma 57 Wnt1 57 hereditary deafness 57 enterocolitis 57 transcriptional regulation 57 neuronal plasticity 57 miRNA expression 57 Hedgehog pathway 57 HLA B 57 muscular dystrophies 57 hereditary disorder 57 seminomas 57 childhood leukemias 57 myeloproliferative diseases 57 meningioma 57 EGFRvIII 57 Retinitis Pigmentosa RP 57 endometrial hyperplasia 57 neuro degenerative disease 57 ErbB1 57 homozygous familial hypercholesterolemia 57 gastric cancers 57 imatinib Gleevec 57 arrhythmogenic right 57 vimentin 57 Chronic lymphocytic leukemia 57 NOMID 57 KLF# 57 alveolar rhabdomyosarcoma 57 FMRP protein 57 generalized epilepsy 57 fronto temporal dementia 57 Glucocorticoids 57 chronic autoimmune disorder 57 pathophysiological 57 Janus kinase 57 downregulation 57 β amyloid 57 causative genes 57 Alport syndrome 57 microglial 57 deacetylation 57 KIBRA 57 CYP #D# 57 c KIT 57 vestibular schwannomas 57 metastatic cancer 57 Acute Myelogenous Leukemia 57 adrenal cortex 57 cadherin 57 Ribavirin causes 57 gastric carcinomas 57 CHEK2 57 HER2 neu 57 unmutated 57 Fragile X gene 57 Spinal muscular atrophy 57 overactivity 57 CNTNAP2 gene 57 VUR 57 dopamine transporter gene 57 metastatic neuroendocrine tumors 57 Klotho gene 57 hedgehog signaling 57 myasthenia gravis MG 57 IL 1beta 57 metabolic abnormalities 57 perilipin 57 deletion 5q 57 paragangliomas 57 ovarian tumors 57 Alzheimer pathology 57 WAGR syndrome 57 lichen planus 57 induce apoptosis 57 lacunar 57 tumors 57 G#S [002] 57 atrophic gastritis 57 ARVD 57 lymphangioleiomyomatosis LAM 57 GABAergic interneurons 57 colorectal adenocarcinoma 57 fibrogenesis 57 homeobox gene 57 neoplastic lesions 57 estrogen receptor beta 57 chronic HCV infection 57 c MET 57 nevi 57 PDE#A 57 renal cell carcinomas 57 gastrointestinal stromal tumor 57 thyrotropin levels 57 chromosome #q 57 APOE 57 striatal neurons 57 gene locus 57 rs# [002] 57 papillomas 57 hereditary spastic paraplegia 57 knockout mice 57 SGS# 57 gene APOE4 57 infantile onset 57 TOP2A 57 proteolysis 57 apolipoprotein E gene 57 discoid lupus 57 PANDAS 57 cytokine IL 57 RBP4 57 gene expression patterns 57 cerebral vasospasm 57 endoplasmic reticulum stress 57 ERBB2 57 KIF6 gene 57 granule cells 57 JAK STAT signaling 57 incurable neurodegenerative disease 57 dystrophin gene 57 UGT#A# * 57 NSCLC tumors 57 parkin gene 57 ApoE4 gene 57 gene mutation 57 squamous cell lung cancer 57 tau aggregates 57 oncogenesis 57 liver metastases 57 colon tumors 57 Glioblastoma multiforme GBM 57 hypoplasia 57 E cadherin 57 gastric carcinogenesis 57 tau protein 57 postoperative delirium 57 cellular pathways 57 autoantibody 57 Leydig cells 57 CYP#C# * 57 inherited neurodegenerative 57 BMPR2 57 BARD1 57 polycystic ovary syndrome 57 ERK2 57 prefrontal cortical 57 ovarian carcinoma 57 pathogenic mechanisms 57 transmembrane protein 57 atopic 57 spinal muscular atrophy SMA 57 chronic myeloid 57 eNOS 57 Primary IGFD 57 sphingolipid 57 GBMs 57 Squamous 57 Src 57 #beta HSD1 57 pre malignant lesions 57 hereditary blindness 57 G6PD 57 colorectal polyps 57 HCV infected 57 tyrosine kinase inhibitors 57 tuberous sclerosis 57 spontaneous mutation 57 aniridia 57 alpha synuclein gene 57 NFAT 57 FASPS 57 constitutively active 57 JAK inhibitors 57 paralogs 57 non coding RNA 57 ApoE4 57 antisense inhibition 57 neuroligins 57 genetic polymorphisms 57 Irs2