Related by context. All words. (Click for frequent words.) 69 mitochondrial dysfunction 69 dyskeratosis congenita 69 neurodegenerative disorder 68 degenerative disorder 67 brain malformation 67 holoprosencephaly 66 motor neuron diseases 66 muscular dystrophies 66 Angelman syndrome 65 Friedreich ataxia 65 progressive neurodegenerative disorder 65 Hutchinson Gilford progeria 65 Fanconi anemia 65 myelodysplasia 65 Joubert syndrome 65 NF2 64 fronto temporal dementia 64 Cockayne syndrome 64 Niemann Pick disease 64 Sanfilippo Syndrome 64 chromosome abnormality 64 FMR1 gene 64 ectodermal dysplasia 64 spinocerebellar ataxia 64 Myotonic dystrophy 64 Dravet syndrome 64 familial ALS 64 lysosomal storage disease 64 degenerative neurological disorder 64 Six3 63 chronic granulomatous disease 63 sporadic ALS 63 Hurler syndrome 63 blastoma 63 synaptic function 63 spastic diplegia 63 nonsense mutation 63 Brugada Syndrome 63 inherited neurological disorder 63 motor neurones 63 pseudotumor cerebri 63 genetic defect 63 ADPKD 63 mitochondrial myopathy 63 Becker muscular dystrophy 63 spastic paraplegia 63 nerve degeneration 63 genetic disorder 63 malignant transformation 63 neuronal degeneration 63 inherited retinal degeneration 63 Wnt signaling 63 autosomal dominant 63 HGPS 62 LKB1 62 Lafora disease 62 NF1 62 SOCS1 62 motor neuron degeneration 62 eosinophilic esophagitis 62 hereditary spastic paraplegia 62 fatal neuromuscular disorder 62 degenerative neurological disease 62 neurofibromin 62 Neurofibromatosis type 62 FTLD 62 Leber congenital amaurosis 62 myopathies 62 Cyclin D1 62 retinal degeneration 62 RPE# 62 Myasthenia gravis 62 galactosemia 62 type 1diabetes 62 Duchenne muscular dystrophy DMD 62 chromosomal translocation 62 lysosomal storage diseases 62 blood clotting disorder 62 Leber congenital amaurosis LCA 62 gastrointestinal stromal tumor 62 metabolic disorder 62 microdeletion 62 Fanconi Anemia 61 PTEN gene 61 LIS1 61 neurofibromatosis type 61 glutamate signaling 61 leukoencephalopathy 61 Von Willebrand disease 61 enzyme deficiency 61 MECP2 gene 61 Krabbe Leukodystrophy 61 Rett syndrome 61 incurable neurodegenerative disease 61 tau proteins 61 IRS1 61 neurodegenerative disease 61 hyperactivation 61 granule cells 61 FMRP protein 61 incurable neurological disorder 61 synaptogenesis 61 gene p# 61 Neurofibromatosis Type 61 allergic inflammation 61 neuronal dysfunction 61 genetic abnormality 61 cardiac hypertrophy 61 mitochondrial disease 61 systemic amyloidosis 61 medium chain acyl 61 mutated gene 61 hereditary disorder 61 CHD7 61 clotting disorder 61 motor neuron disease 61 dominantly inherited 61 hypertrophic cardiomyopathy HCM 61 alpha synuclein gene 61 myotonia 61 autosomal dominant disorder 61 ependymoma 61 dilated cardiomyopathy 61 von Willebrand 61 de novo mutations 61 myotonic muscular dystrophy 61 idiopathic PAH 61 excitotoxicity 60 inherited neurodegenerative disorder 60 galanin 60 leptin resistance 60 LQTS 60 vWD 60 autoimmune encephalitis 60 MELAS 60 long QT syndrome 60 chromosomal defect 60 C1q 60 lung fibrosis 60 mGluR5 antagonist 60 infantile spasms 60 dystrophin 60 Htt 60 embryonal rhabdomyosarcoma 60 calcineurin 60 protein misfolding 60 neuro degenerative disease 60 SOD1 60 filaggrin 60 hereditary blindness 60 inherited mutations 60 mitochondrial diseases 60 spinal muscular atrophy SMA 60 Peutz Jeghers syndrome 60 beta globin gene 60 G#S mutation 60 motor neurone 60 polymorphic ventricular tachycardia 60 podocytes 60 myoclonic epilepsy 60 dystrophin gene 60 neurofibromas 60 polycystic kidneys 60 parathyroid gland 60 Kufs disease 60 Hutchinson Gilford Progeria Syndrome 60 von Willebrand disease 60 microtubule dynamics 60 situs inversus 60 gene MECP2 60 fatal neurodegenerative disorder 60 ataxias 60 underlying pathophysiology 60 paraganglioma 60 Parkinson degenerative 60 Hirschsprung disease 60 protein misfolding diseases 60 homozygous FH 60 renal fibrosis 60 Hutchinson Gilford Progeria 60 neuronal plasticity 60 essential thrombocythemia 60 Hashimoto thyroiditis 60 facioscapulohumeral muscular dystrophy 60 NKX2 60 progressive degeneration 60 Spinal muscular atrophy 60 Pulmonary hypertension 60 huntingtin gene 60 mutant protein 60 CHARGE syndrome 60 tumor suppressor protein 60 chromosomal disorder 60 Hurler Syndrome 60 congenital blindness 60 polyomavirus nephropathy 60 monozygotic twin 60 neural cells 60 Aplastic anemia 60 Eisenmenger syndrome 60 interferon pathway 60 neurodegeneration 60 Myocarditis 60 dystrophy 60 torsade de pointes 60 neuropsychiatric disorder 60 Meckel Gruber 59 mutant proteins 59 fatal neurodegenerative 59 juvenile myelomonocytic leukemia 59 Acute Myelogenous Leukemia 59 achondroplasia 59 Leber Congenital Amaurosis LCA 59 euthymic patients 59 diabetic kidney 59 CFTR gene 59 epigenetically 59 Usher Syndrome 59 optica 59 amyloid formation 59 Parkinson disease neurodegenerative disorder 59 beta thalassemia 59 Long QT syndrome 59 epilepsy 59 myelination 59 Fragile X Syndrome 59 JMML 59 transgenic mouse models 59 progressive neurological disorder 59 cerebellar hypoplasia 59 Essential tremor 59 leukemia ALL 59 Przedborski 59 degenerative neurological condition 59 incurable genetic 59 multisystem disease 59 Alport syndrome 59 TTR amyloidosis 59 SCN5A 59 cellular pathways 59 Wnt signaling pathway 59 alpha synuclein protein 59 podocyte 59 SMN protein 59 neurodevelopmental disorder 59 ataxia telangiectasia 59 genetic syndromes 59 BRAF gene 59 dysgenesis 59 dystrophin protein 59 hypothalamic pituitary adrenal axis 59 Cushing syndrome 59 transfusion syndrome 59 DiGeorge syndrome 59 demyelinating disease 59 myelogenous leukemia 59 mastocytosis 59 Neuregulin 1 59 Epstein Barr 59 epilepsies 59 autosomal recessive 59 primary ciliary dyskinesia 59 chromosomal translocations 59 Myelodysplastic syndrome 59 serotonin receptor 59 leukaemic stem cells 59 epigenetic changes 59 folate metabolism 59 missense mutation 59 mitochondrial disorders 59 FXTAS 59 p# gene 59 basal cell nevus syndrome 59 Acute myeloid leukemia 59 autosomal dominant polycystic kidney 59 hematologic disorders 59 ANCA associated 59 mice lacking 59 Cowden syndrome 59 heart arrhythmias 59 monogenic 59 #beta HSD1 59 Long QT Syndrome 59 apoE4 59 FASPS 59 electrical conduction 59 untreated celiac disease 59 Chronic pancreatitis 59 cerebellar ataxia 59 fibrotic disease 59 Pdx1 59 fibrous dysplasia 59 protein dystrophin 59 huntingtin protein 59 transgenic mouse model 59 neuroligin 59 Glioblastoma Multiforme GBM 59 mutant huntingtin 59 Dystrophin 59 generalized seizures 59 Severe Combined Immunodeficiency 59 retinal dystrophy 59 acute myocarditis 59 Ets2 59 skeletal muscle cells 59 VHL gene 59 neurotrophic 59 progressive neurodegenerative 59 oncomodulin 59 lissencephaly 58 von Hippel Lindau 58 amyloid deposition 58 Dpp 58 NOTCH1 58 immunodeficiency 58 cerebri 58 Notch signaling 58 alzheimer disease 58 familial adenomatous polyposis 58 LRRK2 gene 58 achalasia 58 Parkinsons disease 58 lymphocyte activation 58 renal kidney 58 juvenile dermatomyositis 58 intractable epilepsy 58 HLA B# 58 cortical dysplasia 58 autoinflammatory diseases 58 Sandhoff disease 58 Leber Hereditary Optic Neuropathy 58 diaphragmatic hernia 58 inflammatory demyelinating 58 Chronic lymphocytic leukemia 58 lymphoblastic lymphoma 58 ectopic expression 58 epigenetic mechanisms 58 leptin deficiency 58 Brugada syndrome 58 demyelination 58 MYCN amplification 58 Notch1 58 nitric oxide synthase 58 MGUS 58 SLC#A# [002] 58 p# activation 58 activin 58 Muscular dystrophy 58 lymphoblastic leukemia 58 osteogenic sarcoma 58 Fibrosis 58 systemic scleroderma 58 interstitial fibrosis 58 cypin 58 discoid lupus 58 FSGS 58 Philadelphia Chromosome Positive 58 autoimmune thyroiditis 58 epidermolysis bullosa EB 58 epigenetic modification 58 Pompe Disease 58 osteogenesis imperfecta 58 Wiskott Aldrich syndrome 58 hemolytic anemia 58 mutant huntingtin protein 58 DUX4 58 Hyperthyroidism 58 artery stenosis 58 Stargardt Macular Dystrophy 58 hippocampal function 58 Joubert Syndrome 58 Alzheimers disease 58 arrhythmogenic right 58 LRAT 58 BCL#A 58 synaptic transmission 58 Akt1 58 Sanfilippo syndrome 58 neurologic disorder 58 optic atrophy 58 PTPN# 58 Von Willebrand 58 synapse formation 58 mosaicism 58 Raynaud disease 58 breast cancer metastasis 58 BH4 58 neuromuscular junction 58 Anencephaly 58 muscle degeneration 58 pulmonary hypertension PH 58 paraneoplastic 58 homozygous familial hypercholesterolemia 58 PCNSL 58 ADAM# 58 p# mutations 58 Leber hereditary optic neuropathy 58 neuro degenerative disorder 58 PECAM 1 58 Maroteaux Lamy syndrome 58 iPS derived 58 DiGeorge Syndrome 58 Pten 58 alpha synuclein 58 heterotaxy 58 DLX5 58 immunopathology 58 epigenetic alterations 58 ARVD 58 XBP1 58 behavioral abnormalities 58 DISC1 gene 58 Diamond Blackfan anemia 58 osteopetrosis 58 rhabdomyosarcoma 58 Maroteaux Lamy Syndrome 58 Prox1 58 beta arrestin 58 Epstein Barr Virus 58 neuroblastomas 58 epigenetic silencing 58 leukemia AML 58 neuro degenerative 58 protein tau 58 hyperinsulinism 58 meningeal 58 hemophagocytic lymphohistiocytosis 58 achromatopsia 58 antiphospholipid syndrome 58 PTLD 58 Aortic stenosis 58 INGAP 58 primary pulmonary hypertension 58 CD#L 58 cystic fibrosis transmembrane conductance 58 Duchenne muscular dystrophy 58 Li Fraumeni syndrome 58 diffuse intrinsic pontine glioma 58 telomere maintenance 58 WDR# 58 progranulin mutations 58 neuroblastoma tumor 58 polycystin 58 Fragile X syndrome 58 teratoma 58 desmin 57 MCAD deficiency 57 parkin gene 57 IgA deficiency 57 Peripheral neuropathy 57 lymphangioleiomyomatosis LAM 57 hyperammonemia 57 sortilin 57 recessive mutation 57 genetic alteration 57 WAGR syndrome 57 immunodeficiencies 57 lymphocytic leukemia 57 primary biliary cirrhosis 57 EBV infection 57 schizoaffective disorder bipolar 57 tuberous sclerosis complex 57 ADAMTS# 57 coagulation cascade 57 apoptotic pathway 57 muscarinic receptors 57 MEF2A 57 myelin insulation 57 Sonic hedgehog 57 unprovoked seizures 57 Noonan Syndrome 57 beta adrenergic receptors 57 Krabbe Disease 57 Rett Syndrome 57 motor neuropathy 57 neuronal synapses 57 myelopathy 57 DISC1 57 fibril formation 57 adult neurogenesis 57 pRb 57 Klinefelter syndrome 57 hereditary degenerative 57 TGF β 57 Wiskott Aldrich Syndrome 57 Diabetic neuropathy 57 medulloblastomas 57 GBA mutations 57 neurofibroma 57 subarachnoid haemorrhage 57 neurological dysfunction 57 liver scarring 57 tau protein 57 Sjögren syndrome 57 thymosin 57 spontaneous remission 57 AAT deficiency 57 intestinal inflammation 57 SOD1 gene 57 idiopathic pulmonary 57 hypothalamic pituitary 57 HMGA2 57 cAMP signaling 57 Ehlers Danlos syndrome 57 protein encoded 57 pyloric stenosis 57 autoimmune hemolytic anemia 57 chronic autoimmune disorder 57 Alzheimer Disease AD 57 SMN1 57 hedgehog pathway 57 autosomal recessive genetic 57 Lou Gehrigs disease 57 synovial sarcoma 57 neurite outgrowth 57 myeloproliferative neoplasms 57 intestinal epithelium 57 antibody mediated 57 microcephalin 57 Glioblastoma multiforme GBM 57 alveolar rhabdomyosarcoma 57 frontotemporal dementia 57 membrane fusion 57 multisystem disorder 57 CMV infections 57 MLL gene 57 Pervasive Developmental Disorder 57 Gorlin syndrome 57 Proteus syndrome 57 proNGF 57 excess glutamate 57 QT intervals 57 defective gene 57 eotaxin 57 cyclophilin D 57 diabetes mellitus T2DM 57 disc degeneration 57 nasopharyngeal carcinoma NPC 57 autosomal recessive disease 57 Krabbe disease 57 haematopoietic 57 Niemann Pick 57 biochemical imbalance 57 SSc 57 glomerulonephritis 57 transgenic rats 57 ethosuximide 57 PPARγ 57 Parkinsons Disease 57 alpha1 antitrypsin deficiency 57 progressive degenerative 57 MECP2 57 variable immunodeficiency 57 cholesterol metabolism 57 transcriptional repressor 57 GIST tumors 57 insulin secreting cells 57 MELAS syndrome 57 familial hypercholesterolemia 57 glutamate receptors 57 pulmonary thromboembolism 57 SOD1 protein 57 RNA splicing 57 Morquio 57 neuro developmental disorder 57 neuron degeneration 57 Hh 57 Skp2 57 glutamic acid decarboxylase 57 atypical hemolytic uremic syndrome 57 misregulation 57 recessive trait 57 Huntingtons disease 57 genotoxic stress 57 kalirin 57 Myelodysplastic Syndrome 57 congenital deafness 57 Pulmonary arterial hypertension 57 optic nerve hypoplasia 57 auditory neuropathy 57 IKZF1 57 peroxisomal 57 hamartomas 57 myasthenia gravis 57 aortic rupture 57 Retinoblastoma 57 myeloproliferative 57 autosomal recessive disorder 57 myelomeningocele 57 amyloids 57 NRG1 57 chromosome #q#.# [001] 57 dysautonomia 57 amyloid cascade 57 postoperative delirium 57 chorea 57 Obsessive compulsive disorder 57 gene rearrangements 57 Helicobacter 57 Hsp# [001] 57 pernicious anemia 57 amyloidosis 57 PTEN mutations 57 recurrent miscarriages 57 secreting insulin 57 spasmodic dysphonia 57 neuro degeneration 57 myalgic encephalomyelitis ME 57 Crouzon Syndrome 57 selective inhibition 57 medulloblastoma 57 L dopa 57 phenylketonuria 57 NR#A# 57 axon guidance 57 TP# mutation 57 IDH1 mutation 57 SHANK3 57 locus coeruleus 57 kidney insufficiency 57 BMP4 57 neuropilin 57 mtDNA mutations 57 Fanconi Anaemia 57 mutant genes 57 bronchopulmonary dysplasia 57 malignant hyperthermia 57 NPHP 57 Hypoplastic Left Heart 57 fibrogenesis 57 neuronal stem cells 57 NFkB 57 chromosomal imbalance 57 axon regeneration 57 prion disease 57 PGC 1α 57 multiforme 57 nonhereditary 57 Chronic fatigue 57 RDEB 57 dystonia 57 atherosclerotic lesions 57 involuntary tics 57 chronic myeloid 57 alkalosis 57 NF1 gene 57 neuropsychiatric disorders 57 Insulin resistance 57 immunodeficiency disorder 57 BMP signaling 57 mutant SOD1 57 spinocerebellar ataxia type 57 anemias 57 Purkinje cells 57 autonomic neuropathy 57 Hemophilia B 57 ATTR PN 57 sensory neuron 57 Duchenne Muscular Dystrophy DMD 57 Wilms tumor 57 Lennox Gastaut Syndrome 57 1 diabetes T1D 57 cardiac insufficiency 57 ADDLs 57 cardiac myocytes 57 ankyrin B 57 dysregulation 57 JAK2 gene 57 GRK2 57 neuro endocrine 57 Hh signaling 57 Hypophosphatasia 57 regulates gene expression 57 skeletal dysplasia 57 neuronal function 56 infantile hemangioma 56 MIF gene 56 Mitochondrial diseases 56 physiological abnormalities 56 Epstein Barr virus EBV 56 Acetylcholine 56 DICER1 56 intraventricular 56 amyloid deposits 56 autophagic 56 aP2 56 mutated protein 56 shortened telomeres 56 IGFBP2 56 dyskinetic 56 Gata4 56 acute myelogenous leukemia AML 56 misfolded protein 56 autoimmunity 56 airway remodeling 56 neuropsychiatric diseases 56 Sonic Hedgehog 56 HbF 56 Cystic fibrosis CF 56 micro RNAs 56 Mitochondrial 56 LRP5 56 brain lesions 56 allograft rejection 56 TACI 56 beta adrenergic receptor 56 rare autosomal recessive 56 neurological degeneration 56 polyglutamine diseases 56 retinal degenerative disease 56 Acute Myelogenous Leukemia AML 56 neuroendocrine 56 petit mal seizures 56 Spinal Muscular Atrophy SMA 56 ischemia induced 56 acute myeloid 56 amyloid proteins 56 Parkinson Disease PD 56 Vitamin B# deficiency 56 apoE 56 acyl CoA 56 Autoimmune disorders 56 POMC neurons 56 Retinitis pigmentosa 56 Genetic variants 56 beta1 integrin 56 HFE gene 56 regulator CFTR gene 56 hypoperfusion 56 degenerative nerve disorder 56 osteosarcomas 56 inosine 56 cholestasis 56 N Myc 56 casein kinase 56 serotonin signaling 56 susceptibility gene 56 Wnt pathway 56 Gleevec resistant 56 systemic mastocytosis 56 airway hyperresponsiveness 56 prostaglandin E2 56 Chiari malformation 56 septo optic dysplasia 56 TET2 56 fat malabsorption 56 motoneurons 56 acetylcholine receptor 56 axonal damage 56 VIPR2 56 Wolf Hirschhorn 56 metabolic abnormality 56 FSHD 56 EoE 56 reflex sympathetic dystrophy 56 obliterative bronchiolitis 56 gene mutation 56 FUS1 56 Proteus Syndrome 56 neurofibromatosis 56 chromosomal anomaly 56 retinitis pigmentosa RP 56 TEL AML1 56 degenerative neurological diseases 56 fatal myelination disorder 56 hemochromatosis 56 arterial calcification 56 persistent pulmonary hypertension 56 imatinib resistance 56 arrhythmogenic 56 pDCs 56 inherited neurodegenerative 56 degenerative disorders 56 endogenous cannabinoids 56 Symadex 56 thymoma 56 malarial infection 56 neuroinflammation 56 genomic instability 56 klotho 56 neurological manifestations 56 Medulloblastoma 56 cellular senescence 56 REM sleep behavior 56 CFTR protein 56 huntingtin 56 ischemic colitis 56 STAT4 56 Parkinsonian 56 glycogen synthase kinase 56 chronic myeloid leukemia CML 56 PAOD 56 hypokalemia hypomagnesemia 56 acute psychosis 56 Spasticity 56 infection progressive multifocal 56 Apert syndrome 56 mammary cells 56 truncus arteriosus 56 SMN2 gene 56 congenital deficiency 56 missense mutations 56 adrenal insufficiency 56 aortic valve stenosis 56 hyperparathyroidism 56 neurotransmission 56 COX2 56 bullous 56 chromosomal aberrations 56 recessive genetic 56 β thalassemia 56 chronic eosinophilic leukemia 56 normal karyotype 56 granzyme B 56 rare chromosomal disorder 56 PDGFR 56 genetic abnormalities 56 LHON 56 endostatin 56 metachromatic leukodystrophy 56 limb girdle muscular dystrophy 56 arthrogryposis multiplex congenita 56 demyelinating disorders 56 MC4R gene 56 IL 1ß 56 cultured neurons 56 immunocompetent 56 insoluble plaques 56 myelofibrosis polycythemia vera 56 CTEPH 56 endoplasmic reticulum stress 56 Purkinje cell 56 fibrous tangles 56 MPGN 56 KIBRA 56 beta globin 56 Prader Willi syndrome 56 JAK2 enzyme 56 neurogenic 56 biliary atresia 56 myeloproliferative disease 56 proliferative retinopathy 56 enzyme phosphodiesterase 56 T1DM 56 myelodysplastic syndrome MDS 56 electrophysiologic 56 inherited genetic mutation 56 Vpu 56 thyrotoxicosis 56 6 OHDA 56 genetic mutation 56 congenital disorders 56 Tourette syndrome neurological disorder 56 idiopathic thrombocytopenic purpura 56 Cryptococcus neoformans 56 chromosome condensation 56 epigenetic regulation 56 aneuploidies 56 GBM tumors 56 neurocysticercosis 56 somatic mutation 56 Treg cell 56 amylin 56 PTHrP 56 hydrops 56 p# MAPK 56 SCN9A gene 56 Morquio syndrome 56 chromosomal anomalies 56 alpha thalassemia 56 severe aplastic anemia 56 TCF4 56 overactivation 56 Progeria 56 β catenin 56 acute promyelocytic leukemia 56 catenin 56 clefting 56 Pelizaeus Merzbacher disease 56 degenerative retinal diseases 56 myelination disorders 56 Foxp3 56 Pseudomonas aeruginosa infections 56 familial dysautonomia 56 tumor suppressor genes 56 sulfatase 56 cardiac dysfunction 56 cohesin 56 malperfusion 56 transdifferentiation 56 neurological disorder characterized 56 SOD2 gene 56 diabetes mellitus DM 56 epithelial barrier 56 Angelman Syndrome 56 progeria rare 56 glial cell 56 NADPH oxidase 56 collagen VII 56 choroid plexus 56 hyperalgesia 56 metabolic abnormalities 56 chromatin remodeling 56 MAP#K# 56 leukemia CML 56 medulloblastoma tumors 56 enterocolitis 56 Wnt1 56 LDLR 56 neuroepithelial cells 56 rheumatic disease 56 spontaneous mutation 56 KCNE2 56 melanocyte stimulating hormone 56 catecholamine 56 parkinsonism 56 lymphoproliferative disorder 56 Abeta protein 56 progranulin 56 congenital muscular dystrophy 56 biochemical pathway 56 developmental abnormalities 56 molecular abnormalities 56 dopaminergic cells 56 Dysplasia 56 Cholangiocarcinoma 56 neuromotor 56 Angiotensin II 56 Ribavirin causes 56 carcinoid 56 spontaneous mutations 56 microdeletions 56 neuroligins 56 intracellular proteins 56 chitinase 56 nonalcoholic steatohepatitis NASH 56 urea cycle 56 metabolic enzymes 56 FGFR1 56 sickle cell hemoglobin 56 ERK1 2 56 Smad7 56 Hurthle cell 56 LRRK2 mutations 56 diabetes insipidus 56 M.tb 56 Severe Primary IGFD 56 chimeric mice 56 ubiquitylation 56 erythropoiesis 56 SGS# 56 fungal meningitis 56 abnormal chromosome 56 generalized epilepsy 56 nephritis 56 NF kB signaling 56 cardiac abnormalities 56 FGFs 55 lymphoblasts 55 Gaucher disease 55 Smac mimetic 55 PrP 55 metastatic uveal melanoma 55 SCD1 55 TGF beta 55 IKK2 55 prostaglandin synthesis 55 DNA methylation patterns 55 inhibitory transmitter 55 hepatic toxicity 55 5 hydroxymethylcytosine 55 lymphocytic 55 Thyroid hormone 55 leukaemic cells 55 neurotransmitter glutamate 55 PTEN protein 55 CDH1 55 remyelination 55 metabolic disturbances 55 zebrafish embryo 55 lysosomal storage disorder 55 abnormal proteins 55 mutation 55 misfolding 55 GABAergic neurons 55 acute decompensation 55 hormone angiotensin II 55 Kabuki syndrome 55 cardiac channelopathies 55 histone deacetylases 55 transplanted bone marrow 55 tumoral 55 Myelofibrosis 55 ABCB1 55 stress cardiomyopathy 55 epidermolysis bullosa 55 Prion proteins 55 Hypertrophic 55 leiomyosarcoma