Related by context. All words. (Click for frequent words.) 77 sporadic ALS 71 ADPKD 70 familial pancreatic cancer 70 SOD1 gene 69 familial adenomatous polyposis 69 Epstein Barr virus EBV 69 FTLD 69 medulloblastomas 69 GBM tumors 69 mesotheliomas 69 MLH1 68 HER2 overexpression 68 progressive neurodegenerative disorder 68 dyskeratosis congenita 68 breast carcinomas 68 HNPCC 68 HbF 68 IgA deficiency 68 APOE e4 68 colorectal carcinoma 68 MGUS 68 autosomal dominant disorder 68 monogenic 67 missense mutations 67 Hashimoto thyroiditis 67 brain lesions 67 missense mutation 67 nonsense mutations 67 renal cell carcinomas 67 autosomal dominant 67 neurodegenerative disorder 67 basal cell nevus syndrome 67 BRAF gene 67 pathogenic mutations 67 osteosarcomas 67 NF1 67 K ras mutations 67 essential thrombocythemia 67 sCJD 67 herpesviruses 67 mutated K ras 66 LRP5 66 LQTS 66 nonmelanoma skin cancers 66 inherited mutations 66 inherited retinal degeneration 66 PTPN# 66 carcinoid 66 Li Fraumeni syndrome 66 EBV infection 66 T#I [002] 66 Leukemias 66 BRAF V#E 66 chronic myeloid 66 mosaicism 66 CMV infection 66 childhood leukemias 66 BRAF protein 66 neuroblastoma tumors 65 TTR gene 65 germline mutation 65 GBA mutations 65 MALT lymphoma 65 JAK2 enzyme 65 NNRTI resistance 65 mitochondrial dysfunction 65 squamous cell lung cancer 65 GNAQ 65 MSH2 65 germline mutations 65 alpha synuclein gene 65 paraganglioma 65 ataxias 65 LRAT 65 MECP2 gene 65 EGFR mutations 65 G#S mutation 65 progranulin gene 65 LHON 65 tumor suppressor protein 65 systemic lupus erythematosus SLE 65 idiopathic PAH 65 familial hypercholesterolemia 65 leukemia AML 65 leukaemias 65 pilocytic astrocytomas 65 mtDNA mutations 65 Gleevec resistant 65 FSGS 65 heterozygotes 65 ABCB1 65 motor neuron degeneration 65 elevated triglyceride levels 65 basal cell carcinoma BCC 65 GISTs 65 Relapsing remitting MS 64 carcinoid tumor 64 parkin gene 64 fatal neuromuscular disorder 64 PTLD 64 euthymic patients 64 prostate adenocarcinoma 64 TCF#L# gene 64 SSc 64 chromosomal instability 64 Leydig cell 64 GSTP1 64 apoE4 64 T2DM 64 myelofibrosis polycythemia vera 64 Clusterin 64 Haptoglobin 64 spontaneous mutation 64 C#Y 64 demyelination 64 CDH1 64 p# mutations 64 pancreatic adenocarcinoma 64 hepatocellular carcinomas 64 monocytic 64 VHL gene 64 imatinib resistance 64 serous ovarian cancer 64 HLA B# 64 myeloproliferative 64 subclinical hyperthyroidism 64 parkinsonism 64 medulloblastoma tumors 64 AAT deficiency 64 neuro degenerative disease 64 chromosome abnormality 64 MYH9 gene 64 spinocerebellar ataxia 64 GIST tumors 64 microcephalin 64 autosomal dominant inheritance 64 leukoencephalopathy 64 IDH1 mutation 64 Kufs disease 64 alpha synuclein protein 64 NKX2 64 endometrial hyperplasia 64 prostate cancer CaP 64 somatic mutation 64 pheochromocytoma 64 FASPS 64 fronto temporal dementia 64 PCNSL 64 atypical hyperplasia 64 HLA DRB1 64 myotonic dystrophy 64 hamartomas 64 ZNF# 64 epigenetic silencing 64 gastric carcinoma 64 immunodeficiency 64 amyloid deposition 64 Brugada syndrome 64 LRRK2 mutations 64 #q# deletion 64 pheochromocytomas 63 p# activation 63 fibrous tangles 63 autoimmune hemolytic anemia 63 Gorlin syndrome 63 untreated celiac disease 63 leukemia ALL 63 TEAEs 63 hypermethylated 63 neuroendocrine cancers 63 PARP inhibition 63 SOD1 mutations 63 TMEM#B 63 adenocarcinomas 63 FXTAS 63 microdeletions 63 neurofibromas 63 PAOD 63 Li Fraumeni 63 lung adenocarcinoma 63 APOL1 63 hereditary predisposition 63 airway hyperresponsiveness 63 KRAS oncogene 63 spontaneous mutations 63 de novo mutations 63 SCN5A 63 BRAF mutation 63 uveal melanoma 63 APOE ε4 63 IDH1 63 lobular breast cancer 63 colonic mucosa 63 beta thalassemia 63 juvenile myelomonocytic leukemia 63 BRCA1 mutations 63 acute promyelocytic leukemia 63 Acute myeloid leukemia 63 ependymomas 63 vWF 63 diabetic kidney 63 Lafora disease 63 telomere dysfunction 63 TP# mutation 63 inherited genetic mutations 63 endostatin 63 NOMID 63 EoE 63 chronic lymphocytic leukemia CLL 63 KRAS mutations 63 autosomal recessive 63 Alzheimers disease 63 GPC5 63 Wegener granulomatosis 63 neuroblastomas 63 smoldering myeloma 63 GSTT1 63 pCR 63 tumoral 63 APOE4 63 DFMO 63 micrometastases 63 Chronic lymphocytic leukemia 63 amyloid deposits 63 nutlin 3a 63 SOD1 mutation 63 aneuploidies 63 Sporadic CJD 63 Alzheimer Disease AD 63 FGFR2 63 Sjögren syndrome 63 motor neuron diseases 62 systemic scleroderma 62 normal karyotype 62 premalignant lesions 62 chronic granulomatous disease 62 nonhereditary 62 MLL2 62 Leber Congenital Amaurosis LCA 62 SOD1 62 WT1 62 Peutz Jeghers syndrome 62 thyrotoxicosis 62 microdeletion 62 Glioblastoma Multiforme GBM 62 chromosomal aberrations 62 myeloproliferative diseases 62 LIS1 62 nonsense mutation 62 primary biliary cirrhosis 62 Cryptococcus neoformans 62 glioblastoma tumors 62 heterotaxy 62 mutant protein 62 vimentin 62 severe congenital neutropenia 62 Neurofibromatosis type 62 HSV1 62 mutations 62 transfusion syndrome 62 KIF6 gene 62 GSTM1 62 mutation 62 facioscapulohumeral muscular dystrophy 62 pleural mesothelioma 62 PALB2 62 BMPR2 62 narcolepsy cataplexy 62 frontotemporal dementia 62 cyclin E 62 JAK2 mutation 62 complement inhibitor eculizumab 62 leukemias lymphomas 62 ApoE gene 62 clusterin 62 CDKN2A 62 supratentorial 62 p# mutation 62 KCNH2 62 SMAD4 62 neuron degeneration 62 anterior uveitis 62 CFTR gene 62 Diabetic nephropathy 62 somatic mutations 62 deletion 5q 62 JMML 62 mitochondrial disorders 62 mutated KRAS 62 BRCA1 BRCA2 62 paragangliomas 62 CHD7 62 postoperative delirium 62 Cholangiocarcinoma 62 ARVD 62 LRRK2 mutation 62 lysosomal storage disease 62 lysosomal storage diseases 62 spontaneous remission 62 geographic atrophy 62 NOTCH1 62 mitochondrial mutations 62 FUS1 62 Cytogenetic 62 epilepsies 62 progranulin protein 62 LRRK2 gene 62 #p#.# [002] 62 CYP#B# 62 rs# [002] 62 HeFH 62 neuronal dysfunction 62 infarcts 62 virus XMRV 62 ductal cancer 62 #q#.# [001] 62 IDH2 62 autoinflammatory diseases 62 A. fumigatus 62 inherited neurological disorder 62 ApoE4 62 OGG1 62 octreotide LAR 62 myeloproliferative neoplasms 62 NF1 gene 62 JAK mutations 62 Chronic pancreatitis 62 Systemic lupus erythematosus SLE 62 NKX#.# 62 advanced adenoma 62 acute myelogenous leukemia AML 62 bacteriuria 62 HCV infections 62 IL#R 62 TP# mutations 62 HCV infection 62 neurofibrillary tangles 62 severe neutropenia 62 gene rearrangements 62 causal variants 62 Upregulation 62 CC genotype 62 genetic abnormality 62 DQB1 * 62 homozygosity 62 MELAS 62 mutated genes 62 Prostatitis 62 Endometrial cancer 62 methylation patterns 62 pneumococci 62 glutamic acid decarboxylase 62 lymphocytosis 62 progranulin 62 QTc prolongation 62 UGT#A# * 62 neuropsychiatric disorder 62 Treg cell 62 epigenetic alterations 62 testicular tumors 62 chromosomal abnormalities 62 relapsed ALL 62 atrophic gastritis 62 muscular dystrophies 62 huntingtin gene 62 recurrent glioblastoma multiforme 62 Brugada Syndrome 62 CCR5 delta# 62 neurologic complications 62 hematologic disorders 62 neoplastic 62 arterial calcification 62 chromosomal alterations 62 HBeAg negative 62 subclinical 62 atypical hemolytic uremic syndrome 62 Squamous 62 thyroglobulin 62 Leber congenital amaurosis LCA 62 Hutchinson Gilford progeria 62 chromosome #q#.# [001] 62 lung adenocarcinomas 62 achromatopsia 62 JAK2 gene 62 Hurthle cell 62 transgene expression 62 proband 61 circulating EPCs 61 epithelial tumors 61 astrocytomas 61 abnormal proteins 61 mTOR inhibitors 61 neurofibromatosis type 61 renal fibrosis 61 NFkB 61 MTHFR 61 chromosomal defect 61 Aortic stenosis 61 post transplant lymphoproliferative 61 cytopathic 61 sortilin 61 sarcomatoid 61 testicular germ cell 61 T1DM 61 vWD 61 hyperplastic 61 Hemophilia B 61 adenomatous polyps 61 hepatoma 61 Vitamin B# deficiency 61 genetic loci 61 underlying pathophysiology 61 HNSCC 61 genetic variants associated 61 ADAM# 61 inactive X chromosome 61 cellular prion protein 61 SORL1 61 gastrointestinal stromal tumors GISTs 61 hypermethylation 61 PrPSc 61 AAV2 61 epigenetic inheritance 61 apolipoprotein E gene 61 CP CPPS 61 malignant pleural mesothelioma 61 H. pylori infections 61 NSCLC tumors 61 autoantibody positive 61 proto oncogene 61 meningiomas 61 Mycoplasma pneumoniae 61 cytogenetic abnormalities 61 medulloblastoma 61 ALK mutations 61 thyroid carcinoma 61 Myelodysplastic syndromes 61 synovial cells 61 heterozygous 61 fatal neurodegenerative 61 frataxin gene 61 cisplatin resistant 61 bexarotene 61 FLT3 mutations 61 genetic mutations 61 metachronous 61 CYP#C# [002] 61 gastric adenocarcinoma 61 hyperprolactinemia 61 neuroligins 61 E#F# 61 genes BRCA1 61 BRCA2 gene 61 XMRV infection 61 myeloproliferative disorders 61 Ribavirin causes 61 transgenic mouse models 61 IL 1ß 61 progressive multifocal PML 61 Legg Calvé Perthes disease 61 LKB1 61 chromosomal rearrangement 61 monoclonal gammopathy 61 oesophageal adenocarcinoma 61 Parkinson Disease PD 61 systemic amyloidosis 61 ORMDL3 61 cause cardiac channelopathies 61 ERBB2 61 myeloid 61 nonsmall cell lung cancer 61 familial adenomatous polyposis FAP 61 gene MECP2 61 cytopenias 61 cytomegalovirus CMV 61 NF2 61 inherited genetic mutation 61 activating mutations 61 Pancreatic neuroendocrine tumors 61 gene APOE4 61 mutated BRCA1 61 COX2 61 oncoprotein 61 ANCA associated 61 mutant allele 61 FMR1 gene 61 apolipoprotein E4 61 primary immunodeficiencies 61 M. pneumoniae 61 Chlamydia pneumoniae 61 TTR amyloidosis 61 Arrhythmogenic Right Ventricular Cardiomyopathy 61 BCR ABL mutations 61 colorectal adenocarcinoma 61 homozygous FH 61 bronchogenic carcinoma 61 familial aggregation 61 Papillary 61 ADAMTS# 61 neovascular AMD 61 atherosclerotic lesions 61 STAT4 61 TACI mutations 61 HMGA2 61 Myelodysplastic syndromes MDS 61 acute leukemias 61 S#A# [002] 61 lateral sclerosis ALS 61 bone metastasis 61 susceptibility gene 61 hypereosinophilic syndrome 61 DNMT1 61 recurrent VTE 61 protein encoded 61 liver metastasis 61 enzymatic activity 61 homozygous familial hypercholesterolemia 61 chromosome #p# [001] 61 Aß 61 Cowden syndrome 61 BRAF mutations 61 CYP#C# [001] 61 pulmonary hypertension PH 61 Cyclin D1 61 Amyloid beta protein 61 LV dysfunction 61 KLF# 61 Von Willebrand disease 61 pancreatic endocrine 61 diabetes mellitus DM 61 colorectal adenoma 61 HER2 positivity 61 Becker muscular dystrophy 61 KIBRA 61 amyloid peptide 61 Sezary syndrome 61 incurable neurodegenerative disease 61 malignant neoplasm 61 gene mutations 61 autosomal 61 glucocorticoid receptors 61 squamous cell carcinoma SCC 61 commonly mutated genes 61 ductal adenocarcinoma 61 TOP2A 61 neurological manifestations 61 dopaminergic therapy 61 chronic inflammatory bowel 61 malignant pleural effusion 61 intestinal polyps 61 SGPT 61 endoplasmic reticulum stress 61 herpes zoster shingles 61 dysglycemia 61 mutated gene 61 Foxp3 61 Neutrophil 61 phenotypic expression 61 CD#c 61 optica 61 immunopathology 61 Autoimmune disorders 61 thrombotic complications 61 Bardet Biedl syndrome 61 cardiac dysfunction 61 haematopoietic 61 interferon beta therapy 61 epigenetic modification 61 CHEK2 61 extramedullary 61 benign proliferative breast 61 Vitamin D insufficiency 61 Diabetic neuropathy 61 #q# [001] 61 EXJADE 61 #beta HSD1 61 inducible nitric oxide synthase 61 chronic HBV infection 61 genomic instability 61 G#S [002] 61 senile plaques 61 aneuploidy 61 T1D 61 ApoE4 gene 61 MIF gene 61 medullary thyroid cancer 61 underlying vasculopathy 61 autosomal recessive disease 61 presymptomatic 61 neurological abnormalities 60 PDGFR 60 troponin T 60 Irritable bowel syndrome IBS 60 epigenetic changes 60 syngeneic 60 bcl 2 60 epigenetic markers 60 respiratory viral infections 60 tau pathology 60 cerebral infarction 60 bronchopulmonary dysplasia 60 MEF2A 60 cell adhesion molecule 60 cardioembolic stroke 60 monozygotic twin 60 miRNA genes 60 β amyloid 60 chromosomal rearrangements 60 histone acetylation 60 NAFLD 60 homozygotes 60 IL#B 60 neuroblastoma tumor 60 circadian genes 60 ependymoma 60 axonal damage 60 premalignant 60 mutant proteins 60 chronic eosinophilic leukemia 60 palladin 60 benign polyps 60 degenerative disorder 60 malignant lymphomas 60 immunocompetent 60 Staphylococcus aureus infections 60 vaso occlusive crisis 60 glioma tumors 60 developmental abnormalities 60 genetic alteration 60 Helicobacter 60 prostate carcinoma 60 BCR ABL protein 60 sporadic Creutzfeldt Jakob 60 hippocampal atrophy 60 relapsing remitting 60 GSTM1 gene 60 maternally inherited 60 PTEN mutations 60 Parkinson disease PD 60 generalized epilepsy 60 Hereditary angioedema HAE 60 genes predisposing 60 embryonal 60 apoE 60 VIPR2 60 Retinitis pigmentosa 60 Epidermal Growth Factor Receptor 60 Immunohistochemical analysis 60 von Hippel Lindau 60 Meckel Gruber 60 SHANK3 60 BCL#A 60 Genetic variants 60 eosinophilic esophagitis 60 autoantibodies 60 carcinoembryonic antigen 60 enteroviruses 60 malignant transformation 60 autoimmune thyroid 60 BRCA mutation 60 Irritable bowel syndrome 60 Niemann Pick disease 60 TNF blocker therapy 60 parainfluenza virus 60 diffuse gastric 60 IGFBP2 60 #p#.# [001] 60 HGPS 60 inherited predisposition 60 amyloid ß 60 T2D 60 BARD1 60 myopathies 60 Renal cell carcinoma 60 autosomal recessive disorder 60 CYT# potent vascular disrupting 60 idiopathic myelofibrosis 60 TGF b 60 variable immunodeficiency 60 Cushing syndrome 60 osteopontin 60 herpes zoster virus 60 varicella infection 60 lymphocytic 60 FGFR1 60 OSAHS 60 mitochondrial toxicity 60 de ath 60 hyper IgE syndrome 60 Fas ligand 60 Lupus nephritis 60 epithelioid 60 FLT3 60 NQO1 60 Male pattern baldness 60 GBMs 60 variant allele 60 complete cytogenetic response 60 atypical ductal hyperplasia 60 Genetic variation 60 seminoma 60 PTEN gene 60 neurodegenerative disease 60 cystatin C 60 pituitary adenomas 60 metastatic lung cancer 60 lobular cancer 60 TLR3 60 ankyrin B 60 V#F mutation 60 MYCN amplification 60 oligodendrogliomas 60 prolonged QT interval 60 methylation markers 60 LPA gene 60 EGFR gene 60 AML MDS 60 acute aortic dissection 60 polycystic ovary syndrome PCOS 60 microRNA expression 60 isolated systolic hypertension 60 tuberous sclerosis complex 60 lichen planus 60 protein alpha synuclein 60 myotonic muscular dystrophy 60 genetic abnormalities 60 transthyretin 60 Uterine cancer 60 immunodeficiencies 60 carcinoid tumors 60 olfactory dysfunction 60 rifamycins 60 TRAIL induced apoptosis 60 EAAT2 60 GG genotype 60 CNTNAP2 60 gene p# 60 dominantly inherited 60 K#N 60 MC4R gene 60 hemorrhagic strokes 60 genetic polymorphisms 60 glycated hemoglobin levels 60 spinocerebellar ataxia type 60 ETV1 60 allogeneic HSCT 60 grade cervical intraepithelial 60 endogenous retroviruses 60 bacteraemia 60 uPAR 60 steatohepatitis 60 metastatic gastric 60 tubercle bacillus 60 Waldenstrom macroglobulinemia 60 Wwox 60 CXCL# 60 poorer prognosis 60 polyomavirus 60 IKZF1 60 POAG 60 Glioblastoma multiforme GBM 60 NMIBC 60 deacetylation 60 miRNA expression 60 Six3 60 cytogenetic responses 60 leptin deficiency 60 BRIP1 60 splice junctions 60 flavopiridol 60 Major depressive disorder 60 nonalcoholic steatohepatitis NASH 60 polymorphic ventricular tachycardia 60 type 1diabetes 60 5q 60 transthyretin amyloidosis 60 microglial activation 60 proliferative disorders 60 proliferative diabetic retinopathy 60 synuclein 60 genetic syndromes 60 Kabuki syndrome 60 thyrotropin 60 hyperalgesia 60 PNET 60 FVIII inhibitors 60 metastatic neuroendocrine tumors 60 hypoperfusion 60 liver scarring 60 mucinous 60 HepG2 cells 60 distant metastasis 60 nerve degeneration 60 neurofibrillary 60 neoplastic cells 60 holoprosencephaly 60 hereditary spastic paraplegia 60 amnestic mild cognitive impairment 60 spinal muscle atrophy 60 BRAF V#E mutation 60 mutant genes 60 Chronic Myelogenous Leukemia 60 thyrotropin levels 60 HIV HCV coinfected 60 CMV infections 60 ARVC 60 hypogonadotropic hypogonadism 60 clinically insignificant 60 protein misfolding 60 latent TB infection 60 demyelinating 60 gliosis 60 chromosome #q# [001] 60 advanced adenomas 60 microbleeds 60 HPV# 60 lymphoproliferative disorders 60 von Willebrand 60 Epstein Barr Virus EBV 60 carcinoid cancer 60 Leber hereditary optic neuropathy 60 probands 60 sphingolipid 60 #q#.# [002] 60 Pulmonary hypertension 60 oligodendrocyte progenitor cells 60 histological subtype 60 NR#A# 60 TRAF1 C5 60 Dystrophin 60 neuropilin 60 nNOS 60 chromosome #q# [002] 60 affective psychoses 60 Asymptomatic 60 androgen receptor gene 60 Acute lymphoblastic leukemia 60 DLX5 60 TGF ß1 60 herpes viruses 60 tyrosine phosphorylation 60 bowel polyps 60 EGFR protein 60 neoplasm 60 amnestic MCI 60 Leber Hereditary Optic Neuropathy 60 Hsp# [001] 60 Dysregulation 60 NPHP 60 metaplasia 60 ductal lobular 60 T#I mutation 60 overt nephropathy 60 C1q 60 BRCA1 mutation carriers 59 microalbuminuria 59 Medulloblastoma 59 tau protein tangles 59 overt hypothyroidism 59 lacunar 59 operable breast cancer 59 multidrug resistance 59 breast cancer metastasis 59 penetrance 59 Chronic sinusitis 59 ptau 59 SMN protein 59 diabetic nephropathy 59 Tumor shrinkage 59 genetic polymorphism 59 molecular abnormalities 59 Helicobacter pylori infection 59 nonischemic 59 microsatellite instability 59 neurosyphilis 59 constitutively 59 Janus kinase 59 telomere shortening 59 C. difficile colitis 59 murine leukemia virus 59 Ischemic 59 pathological hallmark 59 peritoneal carcinomatosis 59 susceptibility genes 59 Prion proteins 59 myocardial fibrosis 59 thymoma 59 histologic subtype 59 chromosomal translocations 59 Coeliac disease 59 lung metastases 59 autism susceptibility genes 59 chronic prostatitis 59 LHRH agonists 59 latently infected 59 nucleoside analogues 59 carcinoids 59 Chronic Lymphocytic Leukemia CLL 59 chlamydial infections 59 Borrelia 59 Genetic mutations 59 seminomas 59 urethritis 59 degenerative retinal diseases 59 functional polymorphism 59 fatal neurodegenerative disorder 59 TP# gene 59 virulence genes 59 crystallin 59 mitogen activated protein kinase 59 precancerous cervical 59 transgenic mouse model 59 degenerative neurological disorder 59 neurofibromin 59 SOD1 protein 59 exfoliation glaucoma 59 caveolin 59 IFN γ 59 G6PD deficiency 59 ApoE 59 colon tumors 59 lymphoid 59 B7 H3 59 apoC III 59 APOE gene 59 plasma kallikrein 59 anaplastic lymphoma kinase 59 Amyloid plaques 59 colorectal tumors 59 hemolytic uremic syndrome HUS 59 recurrent miscarriages 59 EGFRvIII 59 ERK1 2 59 promoter methylation 59 ovarian tumors 59 neural cells 59 node metastases 59 LVNC 59 M. genitalium 59 Polycystic ovary syndrome PCOS 59 Helicobacter pylori H. pylori 59 microvascular disease 59 Myelosuppression 59 Myotonic dystrophy 59 incidentalomas 59 catechol O methyltransferase 59 Myocardial infarction 59 TGFBR1 * 6A 59 ras gene 59 neuroinflammation 59 micro RNA 59 shorter telomeres 59 ovale 59 RIP1 59 vivax 59 CNVs 59 hemolytic anemia 59 EHEC infections 59 Wiskott Aldrich syndrome 59 retinitis pigmentosa RP 59 atypical parkinsonism 59 cranial irradiation 59 mesothelin 59 chronic hepatitis cirrhosis 59 synovial sarcoma 59 white matter hyperintensities 59 subependymal giant cell 59 chemoresistant 59 serum urate levels 59 Carcinoid tumors 59 Pulmonary arterial hypertension 59 dopamine signaling 59 CLL cells 59 Enlarged prostate 59 connexin 59 VaD 59 Obstructive sleep apnea 59 histiocytosis 59 interleukin IL -# 59 basal cell carcinomas 59 gene amplification 59 CNTNAP2 gene 59 bowel cancers 59 intravenous bisphosphonates 59 neoplasias 59 relapsed MM 59 breast cancer genes BRCA1 59 engineered RAP peptides 59 HAAH 59 hypomethylation 59 AGTR1 59 Basal cell carcinoma 59 sequence homology 59 mutant SOD1 59 chlamydial infection 59 intracranial hemorrhage ICH 59 Cathepsin B 59 leukemia CLL 59 ccRCC