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(Click for frequent words.) 75 Genetic variations 74 hereditary predisposition 73 Genetic mutation 73 Genetic predisposition 72 Genetic mutations 72 monogenic 71 APOE genotype 71 MTHFD1L gene 71 DNA methylation patterns 71 GBA mutations 71 TCF#L# gene 71 epigenetic changes 71 genetic loci 71 LRP5 71 familial clustering 71 breast endometrial 71 Thyroid disorders 70 Genetic variation 70 genetic polymorphisms 70 insulin resistance syndrome 70 prostate carcinogenesis 70 arterial calcification 70 narcolepsy cataplexy 70 neurocognitive impairment 70 leptin deficiency 70 testicular germ cell 70 ovarian hormones 70 Neurological disorders 70 diabetic kidney 70 obesity insulin resistance 70 predisposing factor 70 biologic pathways 69 familial pancreatic cancer 69 PTEN mutations 69 APOE ε4 69 Chronic pancreatitis 69 Magnesium deficiency 69 neuropsychiatric diseases 69 airway hyperresponsiveness 69 breast cancer metastasis 69 cardiovascular disease hypertension 69 de novo mutations 69 underlying pathophysiology 69 inherited mutations 69 BMPR2 69 bile acid metabolism 69 susceptibility locus 69 epigenetic alterations 69 ABCB1 69 chromosomal rearrangement 69 impaired glucose metabolism 68 Soy isoflavones 68 JAK2 enzyme 68 BRCA1 BRCA2 68 potentially modifiable 68 impair fertility 68 neuro degenerative disorders 68 vascular dysfunction 68 testicular tumors 68 CYP#D# gene 68 hypermethylated 68 pleiotropic effects 68 G6PD deficiency 68 thrombo embolic 68 susceptibility loci 68 genetic variants associated 68 MYH9 68 KRAS oncogene 68 thyrotropin 68 prostate cancer CaP 68 elevated triglyceride levels 68 GPC5 68 chromosome #p#.# 68 Fatty liver 68 FGFR2 gene 68 shorter telomere length 68 metabolic abnormality 68 Cognitive impairment 68 MC4R gene 68 myopathies 68 ApoE gene 67 intestinal permeability 67 airway remodeling 67 germline mutations 67 atherothrombotic 67 multifactorial disease 67 VEGF expression 67 genetic determinants 67 metabolic disturbances 67 Thyroid hormone 67 Heavy menstrual bleeding 67 squamous cell lung cancer 67 folate metabolism 67 KCNH2 67 ADPKD 67 oesophageal adenocarcinoma 67 PTPN# 67 APOE e4 67 abnormal lipids 67 type2 diabetes 67 apolipoprotein E4 67 Hormone pills 67 motor neuron degeneration 67 carotid plaques 67 Hashimoto thyroiditis 67 thyroid hormone levels 67 SMAD4 67 MYH9 gene 67 hypothalamic pituitary adrenal axis 67 nongenetic 67 HLA DRB1 67 hypovitaminosis D 67 chronic obstructive airway 67 Heavy snorers 67 mitochondrial mutations 67 miRNA expression 67 amyloid plaque formation 67 Clusterin 67 susceptibility genes 67 glucocorticoid hormones 67 FUS protein 67 PIK3CA 67 idiopathic pulmonary 67 differential gene expression 67 epigenetic mechanisms 67 tumor histology 67 Uncontrolled hypertension 67 genes CYP#C# 66 gastric cardia 66 molecular abnormalities 66 p# activation 66 gene rearrangements 66 tumor suppressor protein 66 hormonal abnormalities 66 JAK mutations 66 FGFs 66 invasive ductal breast cancer 66 colorectal carcinogenesis 66 BCL#A 66 carotid atherosclerosis 66 ERK signaling 66 Nonalcoholic fatty liver 66 thyrotropin levels 66 Zinc deficiency 66 SLC#A# [002] 66 nonhereditary 66 degenerative neurological diseases 66 genetic syndromes 66 metabolic abnormalities 66 antiphospholipid syndrome 66 microdeletions 66 neurodevelopmental outcome 66 rheumatic disorders 66 VSMCs 66 inflammatory biomarkers 66 neuro endocrine 66 K ras mutations 66 dysglycemia 66 causative genes 66 genomic alterations 66 unmeasured confounders 66 impaired insulin secretion 66 renal fibrosis 66 gastrointestinal dysfunction 66 nonalcoholic steatohepatitis NASH 66 sCJD 66 cystic fibrosis chronic pancreatitis 66 glial tumors 66 gene polymorphisms 66 STAT4 66 aetiological 66 aberrant methylation 66 GSTP1 66 somatic mutations 66 #q# deletion 66 Telomere length 66 fronto temporal dementia 66 HER2 expression 66 astrocytomas 66 genetic polymorphism 66 LRRK2 gene 66 TCF#L# 66 gastrointestinal stromal tumors GISTs 66 serum BDNF 66 brain lesions 66 clefting 66 Treg cell 66 synovial cells 66 Aortic stenosis 66 Untreated sleep apnea 66 valvular heart disease 66 nonalcoholic steatohepatitis 66 pathophysiological mechanisms 66 CETP gene 66 Colon polyps 66 neurosensory 66 nodal metastasis 66 Stress hormones 66 neuronal dysfunction 66 diabetic microvascular complications 66 neuroinflammation 66 untreated celiac disease 66 multi factorial disease 66 APOL1 66 shortened telomeres 66 neurocognitive dysfunction 66 periodontal infections 66 ABCB1 gene 66 environmental toxicants 66 fibrate drugs 66 LRRK2 mutations 65 genetic susceptibilities 65 mitochondrial disorders 65 subclinical hyperthyroidism 65 endocrine dysfunction 65 modifier genes 65 chromosomal alterations 65 infantile hemangioma 65 hormonally sensitive 65 kidney urologic 65 C. pneumoniae 65 cardiometabolic disorders 65 cortisol secretion 65 HGPS 65 obstructive coronary artery 65 intracellular signal transduction 65 promoter hypermethylation 65 cypin 65 NF kB pathway 65 neuropathologic 65 genes predisposing 65 MEF2A 65 circadian genes 65 podocyte 65 Secondhand smoke exposure 65 hyperhomocysteinemia 65 nonmelanoma skin cancers 65 lupus scleroderma 65 hepatocellular carcinoma liver 65 CALHM1 65 gene locus 65 p# mutations 65 male hormone androgen 65 disease NAFLD 65 Inflammatory bowel diseases 65 lung epithelium 65 GAB2 65 Leydig cell 65 IRF6 65 Alzheimer disease vascular dementia 65 Ischemic heart 65 lung fibrosis 65 DRD2 gene 65 comorbid depression 65 etiologic 65 Hp2 2 65 oxidized cysteine 65 dysbindin 65 ALK gene 65 Telomere shortening 65 Darapladib 65 KIBRA 65 orofacial clefts 65 overactivation 65 alexithymia 65 carotid plaque 65 fetal malformations 65 HIV HCV coinfected 65 apoC III 65 PI3K signaling 65 abnormal lipid levels 65 osteosarcomas 65 Short telomeres 65 arterial inflammation 65 subclinical atherosclerosis 65 ciliopathies 65 etiologic factors 65 methylation patterns 65 beta1 integrin 65 cerebral microbleeds 65 plasma lipid 65 atopic disorders 65 inherit predisposition 65 elevated fasting glucose 65 susceptibility gene 65 postoperative delirium 65 causal pathway 65 HbF 65 gastric carcinoma 65 Chronic lymphocytic leukemia 65 KLF4 65 Leukemias 65 CHEK2 65 lymphomas leukemias 65 familial adenomatous polyposis FAP 65 SCD1 65 telomere lengths 65 untreated OSA 65 epigenetic modification 65 hematopoietic cancers 65 EBV infection 65 PDE#A 65 chlamydial infection 65 SHANK3 65 missense mutations 65 chromosomal anomalies 65 hormone adiponectin 65 Folate deficiency 65 Rh incompatibility 65 cholinergic tone 65 causative mutations 65 NKX#.# 65 atherosclerosis narrowing 65 adiponectin levels 65 arterial stiffening 65 Polycystic ovary syndrome PCOS 65 FGF2 65 diagnostic biomarker 65 persistent pulmonary hypertension 65 lymphangiogenesis 65 pAkt 65 genomewide 65 DISC1 gene 65 LIS1 65 metabolic syndromes 65 mutant huntingtin protein 65 bone marrow mesenchymal stem 65 C1q 65 progressive neurodegenerative disorder 65 ORMDL3 65 MSMB 65 mtDNA mutations 65 CHD7 65 neuropsychological impairments 65 biochemical imbalances 65 hepatic liver 65 HER2 overexpression 65 molecular biomarkers 65 microangiopathy 65 melanocortin receptor 65 gene APOE 65 coagulation abnormalities 65 unmeasured factors 65 dopamine receptor gene 65 amino acid homocysteine 65 Erythropoietic therapies may 65 esophagus bladder 65 Shortened telomeres 65 Sjögren syndrome 65 CEACAM1 65 allergic sensitization 65 obstructive coronary 64 haematopoietic 64 HG PIN 64 autosomal dominant polycystic kidney 64 Li Fraumeni 64 circulating estrogens 64 Viral infections 64 childhood leukemias 64 Male infertility 64 Smad3 64 molecular determinants 64 mitochondrial dysfunction 64 Fibroblast 64 pressure natriuresis 64 CDH1 64 Sporadic CJD 64 tumorigenicity 64 hyperinsulinism 64 sortilin 64 histone acetylation 64 ADAMTS# 64 chromosomal aberrations 64 causal variants 64 Vitamin B# deficiency 64 Sleep disturbances 64 Huntingtons disease 64 causal pathways 64 recurrent miscarriage 64 intestinal polyps 64 eczema asthma 64 p#INK#a 64 Vitamin D insufficiency 64 Skeletal muscle 64 prostate abnormalities 64 aneuploidies 64 chromosome aberrations 64 bronchopulmonary dysplasia BPD 64 hormone aldosterone 64 nicotinic receptor 64 lipodystrophy syndrome 64 BRAF gene 64 insulin resistance precursor 64 mutated K ras 64 KIF6 gene 64 lichen planus 64 extramedullary 64 immune dysregulation 64 olfactory dysfunction 64 atherogenesis 64 seminomas 64 Avandia Actos 64 heterotaxy 64 MIF protein 64 amyloid deposition 64 lipid abnormalities 64 albumin excretion 64 pancreatic prostate 64 mitochondrial toxicity 64 autonomic dysfunction 64 Dr. Bezprozvanny 64 neuro developmental disorder 64 apolipoprotein E gene 64 undiagnosed celiac disease 64 chromosomal instability 64 NF kB signaling 64 PTEN protein 64 underlying molecular mechanisms 64 lipoprotein metabolism 64 monozygotic twin 64 incidentalomas 64 LPA gene 64 colorectal adenoma 64 hormones leptin 64 GATA4 64 p# mutation 64 diabetes mellitus DM 64 neuroblastomas 64 comorbid disorders 64 MGUS 64 endometrial hyperplasia 64 ATG#L# 64 nonmelanoma 64 herpesviruses 64 chorioamnionitis 64 Epidemiologic studies 64 T1DM 64 neurologic complications 64 apoE4 64 colonic motility 64 CNTNAP2 64 SSc 64 Autoimmune disorders 64 apoE 64 cardio vascular disease 64 phenotypic expression 64 pharmacologic intervention 64 TPMT 64 prenatal exposures 64 histological subtype 64 Severe Primary IGFD 64 SE alleles 64 Irritable bowel syndrome IBS 64 microvascular disease 64 autosomal dominant inheritance 64 Pseudomonas aeruginosa infections 64 IDH mutations 64 PARP inhibition 64 neurocognitive deficits 64 histone deacetylases 64 GABRA2 64 CMV infections 64 mammary cancers 64 LVNC 64 Oxidative damage 64 alpha synuclein protein 64 nerve degeneration 64 CP CPPS 64 thyroid deficiency 64 glutamate signaling 64 airway responsiveness 64 mammographic density 64 OGG1 64 Hypertrophic cardiomyopathy 64 thyroid carcinoma 64 Hurthle cell 64 Fas ligand 64 chromosomal regions 64 Ovary removal 64 neuropsychiatric disorder 64 dominantly inherited 64 Epstein Barr Virus EBV 64 impaired cognition 64 Diabetic nephropathy 64 Maternal obesity 64 S. maltophilia 64 coinfection 64 pathophysiological 64 serum PTH 64 thromboembolic disease 64 Opportunistic infections 64 basal cell nevus syndrome 64 Tasigna prolongs 64 muscular dystrophy cystic fibrosis 64 nondemented 64 polycystic ovarian syndrome PCOS 64 CYP#C# gene 64 hormone receptor negative 64 gallstone disease 64 mitochondrial oxidative 64 immunoregulation 64 Alpha synuclein 64 IgA deficiency 64 gastric carcinogenesis 64 developmental abnormalities 64 AAT deficiency 64 heritable diseases 64 murine models 64 dentinal hypersensitivity 64 penetrance 64 estrogen metabolism 64 androgen receptor gene 64 familial hypercholesterolaemia FH 64 COX2 64 neuronal plasticity 64 MTHFR 64 nonvascular 64 psychosocial variables 64 calcium homeostasis 64 CHI#L# 64 APOE e4 allele 64 hypomethylation 64 Premature menopause 64 pathogenic mechanisms 64 tic severity 64 neural progenitor 64 abnormal glucose metabolism 64 systemic amyloidosis 64 renal cysts 64 carbohydrate metabolism 64 FGFR2 64 ductal carcinomas 64 Human cl 64 biochemical abnormalities 64 gallstone formation 64 BARD1 64 cardioembolic stroke 64 autoantibody levels 64 salivary gland tumors 64 Angiotensin converting enzyme 63 MSH2 63 POAG 63 beta amyloid accumulation 63 tryptase 63 Excessive daytime sleepiness 63 cirrhosis liver failure 63 IKZF1 63 cranial irradiation 63 pathophysiologic 63 fat hormone leptin 63 ataxias 63 adipokines 63 IUGR 63 thyroid dysfunction 63 CSF biomarkers 63 Diabetic neuropathy 63 subclinical disease 63 #ß HSD1 63 obstructive lung 63 tau protein tangles 63 UCP2 63 TGFBR1 * 6A 63 neuroligins 63 neuroinflammatory 63 gene deletions 63 Chronic insomnia 63 comorbid anxiety 63 IPAH 63 mammary cells 63 amyloidogenic 63 imatinib resistance 63 Calorie restriction 63 cAMP signaling 63 abdominal adiposity 63 tumor subtypes 63 hyper IgE syndrome 63 Mitochondrial dysfunction 63 atherothrombosis 63 hyperparathyroidism 63 male hormones androgens 63 prognostic indicators 63 transgenic rats 63 HPA axis 63 glycogen metabolism 63 DQB1 * 63 APOE4 63 metabolic dysfunction 63 liver metastasis 63 Prostaglandins 63 microvessels 63 Chronic inflammation 63 androgen receptor AR 63 Hutchinson Gilford progeria 63 Calcium intake 63 adrenocortical cancer 63 JNK1 63 prefrontal cortical 63 hypothalamic pituitary 63 plasma kallikrein 63 cisplatin resistant 63 dopamine D2 receptor 63 membranous nephritis 63 myeloperoxidase 63 ovarian pancreatic 63 lipid homeostasis 63 inflammatory bowel syndrome 63 Peptide YY 63 Contraceptive pill 63 pathogenetic 63 syndrome OSAS 63 MAPK pathway 63 metabolizing enzymes 63 PPARg 63 PTEN gene 63 reproductive abnormalities 63 colonic mucosa 63 decompensated cirrhosis 63 potent inducer 63 #p#.# [001] 63 follicular adenoma 63 susceptibility alleles 63 muscarinic receptors 63 pancreatic islet 63 inhibiting COX 63 Cryptococcus neoformans 63 debilitating neurodegenerative disorder 63 systemic inflammation 63 Atopic dermatitis 63 lymphocyte activation 63 tau pathology 63 latent celiac disease 63 BRAF V#E 63 da mage 63 #q#.# [001] 63 postoperative pulmonary 63 Alzheimer Disease AD 63 MECP2 gene 63 vitamin B1 deficiency 63 TGF beta pathway 63 MAP kinases 63 serum parathyroid hormone 63 multiorgan 63 neurobiological underpinnings 63 intima media thickness 63 developmental neurotoxicity 63 Eisenmenger syndrome 63 monoclonal gammopathy 63 prodynorphin 63 fibroids endometriosis 63 adult neurogenesis 63 cancerdefine 63 chromosome #p# [002] 63 ductal breast cancer 63 Heritability 63 tumor subtype 63 hypoperfusion 63 microdeletion 63 arthritis lupus 63 chronic thromboembolic pulmonary 63 gonococcal infection 63 hepatic enzymes 63 Lafora disease 63 unstable detrusor muscle 63 Neurofibromatosis type 63 Logistic regression analysis 63 esophageal reflux 63 gonadal hormones 63 histone modifications 63 axonal degeneration 63 compensatory mechanisms 63 ADAM# 63 apoptotic pathway 63 renal carcinoma 63 hypokalemia hypomagnesemia 63 Wnt signaling pathway 63 Singh Manoux 63 activated microglia 63 Selenium supplements 63 chronic inflammations 63 GSTT1 63 microglial 63 eczema hay fever 63 myeloproliferative diseases 63 metabolic alterations 63 oxidized phospholipids 63 androgen hormone 63 caveolin 63 aP2 63 endogenous hormones 63 RIP1 63 amyloid beta plaques 63 multisystem disease 63 spongiform encephalopathies 63 endocrine tumors 63 ZNF# 63 paraneoplastic 63 autoimmune thyroid 63 PLX STROKE targeting 63 torsade de pointes 63 neovascularisation 63 ANGPTL4 63 inherited predisposition 63 epigenetically 63 Socioeconomic status 63 causative mutation 63 antimetabolites 63 proliferative disorders 63 biochemical imbalance 63 cardiac insufficiency 63 neuron degeneration 63 Cholinesterase inhibitors 63 Folic acid supplements 63 LXRs 63 neurocognitive function 63 HMGCR 63 hypocalcaemia 63 adiponectin hormone 63 prothrombotic 63 rhinovirus infection 63 metabolic syndrome MetS 63 CVD mortality 63 JAK2 mutation 63 nephrogenic 63 Parkinsonian Syndromes 63 pathological hallmark 63 cellular pathways 63 connexin 63 SORL1 63 Beta thalassemia 63 oncogenesis 63 MYCN amplification 63 myalgic encephalomyelitis ME 63 Comorbid 63 Th2 cytokines 63 levodopa induced 63 hormone imbalances 63 Ribavirin causes 63 Observational studies 63 BRCA2 carriers 63 VLDL cholesterol 63 PIGF 63 chromosome #q# [002] 63 hyperactivated 63 genetic biomarkers 63 Barrett mucosa 63 haematologic 63 bladder cervix 63 pilocytic astrocytomas 63 hippocampal function 63 Hormonal imbalances 63 nonfasting triglyceride levels 63 cervical lymph nodes 63 chromosomal mutations 63 Cardiac hypertrophy 63 fetuin 63 circadian clock genes 63 HFE gene 63 CFH gene 63 SCN5A 63 cardiac dysfunction 63 sirtuin activators 63 folate deficiency 63 vitamin B# deficiency 63 allograft rejection 63 androgen signaling 63 endocrine abnormalities 63 varicella infection 63 enterovirus infection 63 smoldering myeloma 63 plasma lipids 63 VHL gene 63 soluble CD# ligand 63 Polycythemia vera 63 innate immune responses 63 colonic polyps 63 cardiac hypertrophy 63 neoplastic 63 limbic encephalitis 63 ductal adenocarcinoma 62 IL#R 62 autocrine 62 transfusion syndrome 62 klotho gene 62 CaM kinase II 62 radiosensitivity 62 oncogenic transformation 62 Squamous cell 62 atypical neuroleptics 62 hormone angiotensin II 62 idiopathic PAH 62 glaucomatous 62 fetal chromosomal 62 Marc Weisskopf 62 multiple sclerosis psoriasis 62 receptor subtypes 62 arterial thickening 62 gestational diabetes mellitus 62 von Hippel Lindau 62 thiopurine 62 galanin 62 prion infection 62 inflammatory cytokine 62 HLA DQ2 62 SRBD 62 Notch signaling 62 abnormal lipid 62 Kufs disease 62 neurotrophic 62 hedgehog signaling 62 thyroid abnormalities 62 precancerous cervical 62 mitochondrial function 62 asthmas 62 TCF4 62 intact parathyroid hormone 62 Helicobacter pylori infection 62 cystic fibrosis muscular dystrophy 62 Squamous 62 dopamine synthesis 62 CDK8 62 SIADH 62 oligodendrogliomas 62 pathophysiologic mechanism 62 cardio metabolic 62 recessive genetic 62 esophageal squamous cell carcinoma 62 familial adenomatous polyposis 62 hamartomas 62 inducible nitric oxide synthase 62 IL6 62 virulence genes 62 B7 H3 62 Cathepsin B 62 phenotypic variation 62 Testosterone deficiency 62 protein tyrosine phosphatase 62 PI3K AKT 62 STAT3 signaling 62 neurite outgrowth 62 Li Fraumeni syndrome 62 FMRP protein 62 polyp recurrence 62 skeletal metastases 62 PHD2 62 Hyperparathyroidism 62 hypocretin neurons 62 Iron deficiency anemia 62 dopamine D4 receptor 62 serum selenium 62 neuritic 62 NFkB 62 hypertension diabetes mellitus 62 SNP rs# [001] 62 abnormal proteins 62 TYMS 62 myelofibrosis polycythemia vera 62 gene MECP2 62 microglial activation 62 sporadic ALS 62 immuno compromised individuals 62 cardiac conduction 62 GABRA2 gene 62 VKORC1 62 multiple sclerosis lupus 62 hepatic steatosis 62 gene variants 62 neuro developmental disorders 62 WDR# 62 abnormal vaginal bleeding 62 atopic diseases 62 cognitive dysfunctions 62 progranulin gene 62 lactate dehydrogenase LDH 62 thromboxane A2 62 vascular reactivity 62 genetic aberrations 62 nonhuman primate model 62 leukaemias 62 underlying vasculopathy 62 autopsied brains 62 intermittent hypoxia 62 NOMID 62 beta amyloid peptides 62 adrenal hormones 62 lipid synthesis 62 beta adrenergic receptors 62 transthyretin 62 lymph node enlargement 62 gonococcal 62 Parkinson Disease PD 62 chitinase 62 NOD2 62 Mild hypothermia 62 familial predisposition 62 mammary stem cells 62 S#A# [002] 62 idiopathic pulmonary arterial hypertension 62 hyperinsulinemia 62 Neurodegenerative diseases 62 genetic locus 62 TGF b 62 choroidal neovascularization 62 enterocolitis 62 signaling cascades 62 FTIs 62 renal tubular 62 vascular endothelial dysfunction 62 dopamine D2 receptors 62 eicosanoids 62 epigenetic regulation 62 serous ovarian cancer 62 Chlamydia pneumoniae 62 node metastases 62 sporadic Creutzfeldt Jakob 62 ERBB2 62 bacterial virulence 62 SFRP1 62 epithelial tissues 62 CRF antagonists 62 transgene expression 62 PPARγ 62 Premature Aging 62 synaptogenesis 62 benign uterine 62 Pelvic inflammatory 62 gene BRCA2 62 respiratory viral infections 62 Metastases 62 PPAR γ 62 chronic hepatitis cirrhosis 62 chemoresistance 62 protein kinase C 62 oncogenic mutations 62 cholesterol metabolism 62 receptor gamma 62 BRCA2 gene mutation 62 affective psychosis 62 mitochondrial proteins 62 ANCA associated 62 trophoblast cells 62 SORL1 gene 62 aneuploid cells 62 Lowering cholesterol 62 Sjogren Syndrome 62 dermatologic reactions 62 TMEM#B 62 HSF1 62 facioscapulohumeral muscular dystrophy 62 NR#A# 62 angiotensin receptor blockers ARBs 62 colorectal cancer CRC 62 Ets2 62 BRCA carriers 62 pancreatic endocrine 62 growth hormone secretion 62 IDH1 mutations 62 synovial fibroblasts 62 neoplastic diseases 62 periodontal tissues 62 nitrotyrosine 62 remnant lipoproteins 62 facial clefts 62 progressive neurodegenerative 62 leiomyomas 62 Rho GTPases 62 Prostatitis 62 atherosclerotic cardiovascular 62 parietal cortices 62 intracranial stenosis 62 CCR5 delta# 62 precancerous tumors 62 underactive thyroid gland 62 breast cancer subtypes 62 immunological mechanisms 62 behavioral disturbances 62 neuronal stem cells 62 lymphatic cancers 62 vascular cognitive impairment 62 bacterial prostatitis 62 serum GGT 62 EphB2 levels 62 CYP#E# gene 62 blood coagulation disorders 62 caveolin 1 62 endothelial activation 62 serologic tests 62 endophenotypes 62 gene polymorphism 62 metabolic parameters 62 micro RNAs 62 granzyme B 62 upregulating 62 renal scarring 62 cryptogenic 62 HER2 positive cancers 62 IGFBP 62 chromosome #q# [001] 62 IgG4 62 Lipoic acid