Related by context. All words. (Click for frequent words.) 64 DQB1 * 64 spontaneous mutation 64 familial ALS 63 inherited mutations 63 neuropsychiatric disorder 63 epigenetic changes 63 familial pancreatic cancer 63 monogenic 62 hippocampal function 62 Atopic eczema 62 Fragile X gene 62 mitochondrial mutations 62 TCF#L# gene 62 neuritic 62 methylation patterns 62 ADPKD 62 Irritable bowel syndrome IBS 62 circadian cycle 61 Peutz Jeghers syndrome 61 apoE4 61 GBA mutations 61 progressive neurodegenerative disorder 61 Kufs disease 61 de novo mutations 61 CYP#A# gene 61 klotho 61 Circadian rhythm 61 TP# mutation 61 inherit predisposition 61 FMR1 gene 61 pathogenic mutations 61 CYP#D# gene 61 Hypertrophic cardiomyopathy 61 APOE genotype 61 germline mutations 61 penetrance 61 Li Fraumeni syndrome 60 spontaneous mutations 60 Cryptococcus neoformans 60 phthalate syndrome 60 pea aphid 60 Generalized anxiety disorder 60 PTPN# 60 Hutchinson Gilford progeria 60 basal forebrain 60 KCNH2 60 differential gene expression 60 circadian genes 60 LRRK2 gene 60 EoE 60 adrenal function 60 TMEM#B 60 DNA methylation patterns 60 allostatic load 60 CYP#C# gene 60 genes predisposing 60 fatal neuromuscular disorder 60 circadian misalignment 60 Lafora disease 60 Bacterial vaginosis 60 LRP5 60 HLA DRB1 60 Neurofibromatosis type 60 Obsessive compulsive disorder 60 corticosterone levels 60 COMT gene 60 dyskeratosis congenita 60 G#S mutation 59 Genetic variants 59 LRRK2 mutation 59 circadian cycles 59 epigenetic markers 59 synaptic function 59 underlying pathophysiology 59 INF2 59 evolvability 59 salivary cortisol 59 dysbindin gene 59 serum BDNF 59 CDH1 59 MC4R gene 59 autonomic dysfunction 59 multi infarct dementia 59 achromatopsia 59 autosomal dominant disorder 59 brain neurochemistry 59 HbF 59 prefrontal cortical 59 intestinal microflora 59 euthymic patients 59 MLL2 59 DNA rearrangements 59 BMPR2 59 metabolic abnormality 59 epigenetically 59 Obstructive sleep apnea OSA 59 fatal myelination disorder 59 amyloid cascade 59 KIBRA 59 Genetic predisposition 59 developmental abnormalities 59 folate deficiency 59 predisposing factor 59 dopamine signaling 59 Brugada syndrome 59 myotonic dystrophy 59 thyroid hormone levels 59 WDR# 59 Leydig cell 59 Alternative splicing 59 chromosomal aberrations 59 APOE ε4 59 prefrontal regions 59 PER2 59 Chronic sinusitis 59 MECP2 gene 59 brain lesions 59 autosomal dominant inheritance 59 Aortic stenosis 59 dysbindin 59 Thyroid hormone 58 neuro developmental disorder 58 Chronic insomnia 58 sporadic ALS 58 causative genes 58 FXTAS 58 multifactorial disease 58 epigenetic modification 58 parkinsonism 58 phenotypic variation 58 dopamine D4 receptor 58 apolipoprotein E gene 58 Atopic dermatitis 58 pyloric stenosis 58 microcephalin 58 tic severity 58 airway hyperresponsiveness 58 mtDNA mutations 58 subclinical hyperthyroidism 58 phenotypic expression 58 CC genotype 58 mutant worms 58 mammary gland tumors 58 HMGA2 58 affective psychosis 58 dominantly inherited 58 CYP#C# [002] 58 histone methylation 58 Thyroid nodules 58 Magnesium deficiency 58 infantile hemangioma 58 LQTS 58 Irritable bowel syndrome 58 molecular underpinnings 58 Male pattern baldness 58 Hsp# [001] 58 biochemical imbalance 58 alexithymia 58 C. neoformans 58 inherited retinal degeneration 58 familial clustering 58 Angelman syndrome 58 insulin signaling pathways 58 missense mutations 58 galanin 58 REM sleep behavior 58 #q# deletion 58 FGFs 58 Alport syndrome 58 metabolic disturbances 58 neurodegenerative disorder 58 aldehyde dehydrogenase 58 Leber hereditary optic neuropathy 58 genomic imprinting 58 neuronal dysfunction 58 Essential tremor 58 Klinefelter syndrome 58 bronchopulmonary dysplasia 58 amyloid deposition 58 obstructive sleep 58 epigenetic modifications 58 APOE4 58 autoimmune thyroiditis 58 autoregulation 58 Zinc deficiency 58 endocannabinoid signaling 58 Seasonal affective disorder 58 Telomere length 58 epigenetic alterations 58 galactosemia 58 autosomal recessive 57 hamartomas 57 BCL#A 57 Genetic mutation 57 IGF2 57 cortical thinning 57 recessive genetic 57 comorbid disorders 57 EBV infection 57 lichen planus 57 #q#.# deletion syndrome 57 ataxias 57 Spinal muscular atrophy 57 spinal muscle atrophy 57 Picky eating 57 rhythmicity 57 locomotor activity 57 microdeletions 57 daytime alertness 57 metabolic dysfunction 57 p# mutations 57 Von Willebrand disease 57 NPHP 57 M. vaccae 57 allergic sensitization 57 PCOD 57 K ras mutations 57 ORMDL3 57 SGK1 57 GPC5 57 neurological abnormalities 57 ciliopathies 57 amyloid plaque formation 57 Chronic constipation 57 STAT4 57 genetic polymorphism 57 chromosome deletion 57 Helicobacter 57 protein conformation 57 gamma oscillations 57 neuroendocrine 57 toxoplasma 57 generalized epilepsy 57 circadian rhythm 57 single celled yeast 57 hyperactivation 57 SCN5A 57 Endometrial cancer 57 HFE gene 57 Premature Aging 57 HGPS 57 leptin deficiency 57 hemagglutinin gene 57 electrophysiologic 57 LIS1 57 fat malabsorption 57 serotonin transporter 57 epigenetic inheritance 57 synaptic proteins 57 Obstructive sleep apnea 57 hereditary deafness 57 GPx 57 neuroligins 57 GH deficiency 57 affective psychoses 57 Parkinson Disease PD 57 chromosomal anomalies 57 SIRT1 protein 57 olfactory dysfunction 57 transfusion syndrome 57 OSAHS 57 motor neuron degeneration 57 Hyperthyroidism 57 p# activation 57 recessive trait 57 phenothiazines 57 RUNX3 57 Major depressive disorder 57 multi factorial disease 57 EP3 receptor 57 Prostatitis 57 glial tumors 57 Chronic ITP 57 Rotavirus infection 57 PIK3CA 57 circadian 57 epigenetic silencing 57 nondemented 57 Six3 57 MC1R 57 primary biliary cirrhosis 57 subsyndromal 57 yeast roundworms 57 CP CPPS 57 ovarian hormones 57 amyloid beta plaque 57 lactase persistence 57 QT intervals 57 dopamine transporter 57 degenerative neurological diseases 57 chromosome #q#.# [001] 57 biochemical imbalances 57 biochemical abnormalities 57 NRF2 gene 57 CEACAM1 57 GBM tumors 57 Dilated cardiomyopathy 57 atypical neuroleptics 57 AAT deficiency 57 parasitic worm infection 57 huntingtin 57 NF1 57 postoperative delirium 57 Prostate enlargement 57 Myotonic dystrophy 57 Daytime sleepiness 57 residual confounding 57 schizotypal 57 familial aggregation 56 PTEN protein 56 serotonin receptor 56 polygenic 56 cellular prion protein 56 heterozygotes 56 KLF# gene 56 nematode Caenorhabditis elegans 56 atherosclerotic lesion 56 heritable variation 56 GSTM1 gene 56 spinocerebellar ataxia type 56 SHANK3 56 idiopathic PAH 56 glucocorticoid hormones 56 epistasis 56 narcolepsy cataplexy 56 inherited neurological disorder 56 B. subtilis 56 ichthyosis vulgaris 56 hypertrophic cardiomyopathy HCM 56 melatonin receptor 56 Sacktor 56 CHI#L# 56 carotid atherosclerosis 56 dopamine receptor gene 56 Fatty liver 56 apolipoprotein E4 56 tiny roundworm 56 chromosomal deletions 56 basal cell nevus syndrome 56 persistent pulmonary hypertension 56 E. faecalis 56 Genetic mutations 56 Bipolar disorder 56 leptin deficient mice 56 Subclinical 56 overt hypothyroidism 56 circadian clock 56 maternally inherited 56 Chronic pancreatitis 56 mutation 56 thyrotropin 56 nitrotyrosine 56 AAT Deficiency 56 shorten telomeres 56 Lactose intolerance 56 serotonin signaling 56 adiponectin levels 56 Haptoglobin 56 somatic mutations 56 hormones leptin 56 neurodevelopmental disorder 56 JAK mutations 56 gene MECP2 56 metapneumovirus 56 monozygotic twins 56 Enlarged prostate 56 heterotaxy 56 homeostatic mechanism 56 chromosomal alterations 56 clinically insignificant 56 cortisol secretion 56 autoinflammatory diseases 56 dizygotic twins 56 autosomal dominant polycystic kidney 56 lactase deficiency 56 Joubert syndrome 56 leptin receptor 56 A. fumigatus 56 adrenal cortex 56 left ventricular diastolic 56 autosomal recessive disease 56 ethosuximide 56 diabetic kidney 56 neuro endocrine 56 MCAD deficiency 56 MECP2 56 Binge eating 56 MeCP2 gene 56 hypothalamic pituitary 56 neurofibromatosis type 56 neurofibromas 56 genomewide 56 fruitfly Drosophila 56 Roenneberg 56 MGUS 56 FGFR2 gene 56 nerve degeneration 56 chromosomal rearrangements 56 white matter hyperintensities 56 tau protein tangles 56 triacylglycerol concentrations 56 overactivity 56 GABRA2 56 postnatally 56 polycystic ovary syndrome PCOS 56 cypin 56 hypoactive 56 G6PD 56 HER2 positivity 56 CALHM1 56 mutated K ras 56 phenotypic variability 56 alkalosis 56 ACh 56 Nicotine dependence 56 aortic stiffness 56 glucose homeostasis 56 nematode worm 56 hydrops 56 familial hypercholesterolemia 56 vascular cognitive impairment 56 exocrine 56 hippocampal cells 56 allele frequencies 56 hypocretin neurons 56 progranulin 56 Thyroid disorders 56 androgen depletion 56 hormone secretion 56 MSH2 56 MC4R 56 intestinal microbiota 56 VHL gene 56 miRNA expression 56 nonhereditary 56 medulloblastomas 56 CHD7 56 PrPC 56 ependymomas 56 Tay Sachs thalassemia 56 KRAS oncogene 56 C. difficile colitis 56 tumor suppressor protein 56 FTLD 56 sickle cell cystic fibrosis 56 neurofibrillary 56 gene rearrangements 56 alpha synuclein gene 56 assortative mating 56 Pathological gambling 56 rhinovirus infection 56 Apert syndrome 56 nephron 56 excitatory synapses 56 Coeliac disease 56 untreated celiac disease 56 GSTP1 56 chromosomal instability 56 Stress hormones 56 APOL1 56 Amyloid beta protein 56 Alopecia areata 56 palmitoleate 56 huntingtin protein 56 Meckel Gruber 56 SMN protein 56 MLH1 56 laforin 56 malarial anemia 56 colorectal adenoma 56 X chromosome inactivation 56 Disordered eating 56 vivax 56 hyperprolactinemia 56 parasite Trypanosoma cruzi 56 highly heritable 56 metabolic syndrome MetS 56 TGFBR1 56 calcium homeostasis 56 amyloid beta plaques 56 spermidine 56 undiagnosed celiac disease 56 hyperphagia 56 demodex 56 alpha synuclein protein 56 intermittent hypoxia 56 neuropsychiatric diseases 56 APOE gene 56 nucleus Chinnery 56 myotonia 56 antibody IgE 56 huntingtin gene 56 progranulin protein 55 secretory pathway 55 hyperemesis 55 TP# gene 55 trophoblast cells 55 Ovarian cysts 55 allergic inflammation 55 IGF1 55 hypocretin 55 airborne fungal spores 55 #ß HSD1 55 JAK2 enzyme 55 diurnal variation 55 hypothalamic pituitary adrenal axis 55 chromosomal rearrangement 55 psychobiological 55 Beta thalassemia 55 TRAF1 C5 55 neurodevelopmental disability 55 irregular menstrual cycles 55 Peritoneal mesothelioma 55 neuropeptide Y NPY 55 torsade de pointes 55 hypercapnia 55 Atlantic Multidecadal Oscillation AMO 55 neurobehavioral disorder 55 T. vaginalis 55 G6PD deficiency 55 circadian rhythms 55 locus coeruleus 55 Genetic Variation 55 fungal genomes 55 tau mutation 55 GAB2 55 previously uncharacterized 55 genetic variant 55 SAPAP3 55 SIDS infants 55 fronto temporal dementia 55 vitamin D receptors 55 lactose malabsorption 55 Pulmonary hypertension 55 inherited predisposition 55 albumin excretion 55 neuron degeneration 55 suprachiasmatic nuclei 55 yeast worms 55 thyroid hormone deficiency 55 obesity insulin resistance 55 microdeletion 55 CNVs 55 lymphangioleiomyomatosis LAM 55 chronic granulomatous disease 55 mutant proteins 55 LRAT 55 synaptogenesis 55 premenstrual syndrome PMS 55 sCJD 55 nongenetic 55 IKZF1 55 ADAMTS# 55 genetic determinants 55 Contagious yawning 55 Mitral regurgitation 55 orthologous genes 55 hereditary predisposition 55 paraneoplastic 55 Alzheimer pathology 55 hypersomnia 55 telomere lengths 55 occipital regions 55 diurnal rhythm 55 type 1diabetes 55 fatty acid metabolism 55 brassinosteroid 55 serotonin deficiency 55 cAMP signaling 55 PTEN gene 55 PKU genetic 55 ABCB1 55 Mitochondrial diseases 55 Functional neuroimaging 55 hypokalemia hypomagnesemia 55 androgen receptor gene 55 nicotinamide 55 transthyretin 55 SLC#A# [002] 55 infantile hemangiomas 55 Trypanosoma brucei 55 neurite outgrowth 55 male reproductive tract 55 epigenome 55 modifier genes 55 hypermethylated 55 neurotransmitter GABA 55 unprovoked seizures 55 mitochondrial dysfunction 55 TLR5 deficient mice 55 unmeasured confounders 55 Nonalcoholic fatty liver 55 SORL1 gene 55 neurosensory 55 Proteus syndrome 55 IRS1 55 sporadic Creutzfeldt Jakob 55 Hirschsprung disease 55 Vitamin D insufficiency 55 probiotic supplementation 55 microvascular disease 55 serum IGF 55 Purkinje cell 55 Orthostatic hypotension 55 debilitating neurodegenerative disorder 55 unmeasured factors 55 BRAF V#E 55 striatal neurons 55 roseola 55 microscopic lesions 55 Anopheles gambiae mosquitoes 55 holoprosencephaly 55 homozygosity 55 mutated gene 55 progressive degenerative neurological 55 molecular abnormalities 55 beta adrenergic receptor 55 Single Nucleotide Polymorphisms SNPs 55 comorbid anxiety 55 Systemic lupus 55 Clusterin 55 gut microbes 55 Oxidative stress 55 telogen 55 MTHFR gene 55 5 HTTLPR 55 Vitamin B# deficiency 55 childhood disintegrative disorder 55 sleep deprivation impairs 55 lateral habenula 55 ANCA associated 55 liver metastasis 55 autosomal dominant 55 serum calcium 55 sexually dimorphic 55 5 HTT gene 55 WAGR syndrome 55 Wnt1 55 HSV1 55 Ulcerative colitis 55 Dr. Zoe Arvanitakis 55 DISC1 gene 55 palladin 55 inflammatory demyelinating 55 arterial stiffening 55 SSc 55 K ras gene 55 inflammatory bowel 55 chromosome #q#.# deletion 55 SLITRK1 55 enteroviral 55 Leptospira 55 myopathies 55 T1DM 55 HIV HCV coinfected 55 atopy 55 autoimmune thyroid 55 gene variation 55 mutant genes 55 fungus infects 55 perilipin 55 P. falciparum parasites 55 Polycystic ovary syndrome 55 cause cardiac channelopathies 55 Basal cell carcinoma 55 familial hypercholesterolemia FH 55 SGPT 55 TPMT 55 NPC1 55 Lipodystrophy 55 neuropsychiatric disorders 55 protozoan parasites 55 antiphospholipid antibodies 55 gestational diabetes mellitus GDM 55 Chlamydia psittaci 55 neurobiological disorder 55 prenatal exposures 55 ERK signaling 55 genetic underpinnings 55 complement inhibitor eculizumab 55 Celiac sprue 55 vanA gene 55 beta1 integrin 55 progranulin mutations 55 genetic mutation 55 T. gondii 55 Apolipoprotein E 55 SOD1 gene 55 cultured neurons 55 hepatic steatosis 55 chronic inflammatory bowel 55 El Sohemy 55 Li Fraumeni 55 Bronchiolitis 55 arterial thickening 55 heritable genetic 55 GSTT1 55 inherited genetic mutations 55 Hashimoto thyroiditis 55 IGFBP2 55 retinal dysfunction 55 Diabetic neuropathy 55 impaired cognition 55 monoamine neurotransmitters 55 carbohydrate metabolism 55 metabolic abnormalities 55 fasting glucose levels 55 oesophageal adenocarcinoma 55 autistic regression 55 Naegleria 55 interferon induced 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 genetic loci 55 sortilin 55 Secondhand smoke exposure 55 Leber congenital amaurosis 55 genetic locus 55 Igf2 55 hypovitaminosis D 55 clefting 55 ApoE4 55 infantile amnesia 55 incurable genetic 55 dysglycemia 55 circadian clocks 55 TTR amyloidosis 55 CCR5 delta# 55 diabetes mellitus DM 55 spontaneous remission 55 DLX5 55 neuronal synapses 55 SLC#A# [001] 55 collagen VI 55 neurofibromin 55 genetic variation 55 palmitate 55 glucocorticoid receptors 55 Trichophyton rubrum 55 circadian rhythm sleep 55 MYH9 gene 55 TSC1 55 CYP#D# 55 overactivated 55 xeroderma pigmentosum 55 Hyperactivity 55 cardiolipin 54 Endothelial function 54 induce orthostatic hypotension 54 Leukemias 54 serotonin transporter gene 54 Heidi Rehm 54 thermophilum 54 Klotho gene 54 Mild cognitive impairment 54 congenital cataract 54 IFN beta 54 V#F mutation 54 indels 54 pleiotropic effects 54 #p#.# [001] 54 mutated genes 54 Epstein Barr Virus EBV 54 perimenopausal women 54 Beckwith Wiedemann syndrome 54 MMP# 54 Liver cirrhosis 54 FKBP# 54 Postnatal depression 54 stress hormone corticosterone 54 HLA B# 54 Dr. Bezprozvanny 54 Hypothalamic 54 stress cardiomyopathy 54 MYH9 54 cystic fibrosis chronic pancreatitis 54 SETDB1 54 inbred strains 54 osteosarcomas 54 multigenic 54 eosinophilic esophagitis 54 impair fertility 54 Caenorhabditis 54 Prevotella 54 psychiatric comorbidity 54 leucocytes 54 Treg cell 54 C EBP alpha 54 lysosomal storage disease 54 nongenetic factors 54 somatostatin 54 autosomal recessive genetic 54 trans palmitoleate 54 underactive thyroid gland 54 subcortical regions 54 histone modification 54 impaired glucose metabolism 54 microglial 54 hormone aldosterone 54 VIPR2 54 1 diabetes T1D 54 Uncontrolled diabetes 54 receptor gene 54 worm Caenorhabditis elegans 54 ENPP1 54 Electrophysiological 54 thiopurine 54 Peanut allergy 54 mammalian brains 54 fruitflies 54 IgA deficiency 54 leptin resistant 54 herpes viruses 54 deleterious mutations 54 Alpha synuclein 54 podocytes 54 hyperemesis gravidarum 54 electroencephalographic 54 mitochondrial defects 54 dopamine antagonists 54 puerperal psychosis 54 PLMs 54 behavioral disinhibition 54 Sir2 54 Polycystic ovary syndrome PCOS 54 Amino acid 54 Febrile seizures 54 gametophyte 54 circadian clock genes 54 symptom flare ups 54 B7 H3 54 myocardial fibrosis 54 MAP#K# 54 rCBF 54 gastric carcinoma 54 FGF2 54 hyperactivated 54 SNPs pronounced snips 54 histologic subtype 54 airflow limitation 54 inactive X chromosome 54 shorter telomere length 54 filaggrin 54 PCNSL 54 causative pathogens 54 Dicer enzyme 54 BARD1 54 giant danio 54 SRBD 54 haemochromatosis 54 inhibitory receptor 54 CFTR gene 54 SERT gene 54 VKORC1 54 neurological degeneration 54 Peptide YY 54 Personality traits 54 Epileptic seizures 54 attention-deficit/hyperactivity disorder ADHD 54 allergic eczema 54 syndrome gastroesophageal reflux 54 unrefreshing sleep 54 Dental caries 54 worm C. elegans 54 bacterial virulence 54 atherosclerotic lesions 54 S. cerevisiae 54 Tasigna prolongs 54 genetic polymorphisms 54 Sleep disturbances 54 Entamoeba histolytica 54 susceptibility gene 54 Acute pancreatitis 54 defensin 54 vitamin D inadequacy 54 Alleles 54 fetal hemoglobin 54 Wnt proteins 54 BRCA1 mutations 54 Schistosoma 54 ipRGCs 54 mutant allele 54 cognitively normal 54 neutrino mass 54 treating psychiatric disorders 54 Plasmodium parasites 54 cortical dysplasia 54 Neurogenesis 54 bronchoalveolar 54 authors hypothesize 54 hyperphenylalaninemia HPA due 54 endocrine tumors 54 Anxiety disorders 54 TP# mutations 54 endocasts 54 serum leptin 54 gene deletions 54 noncoding RNAs 54 KIF6 gene 54 granzyme B 54 myelin breakdown 54 Neuregulin 1 54 Skeletal muscle 54 Genetic variation 54 Bardet Biedl syndrome 54 MCADD 54 intracellular signal transduction 54 phylogenetically 54 serum homocysteine 54 TCF#L# 54 invasive secretory carcinoma 54 glutamate neurotransmission 54 connexin 54 nonmelanoma skin cancers 54 Farzaneh Far 54 NR#A# 54 enuresis 54 vermis 54 norepinephrine dopamine 54 Folic acid deficiency 54 beta amyloid peptides 54 mitochondrial DNA mutations 54 dermatologic reactions 54 parkinsonian 54 fibrous tangles 54 Severe Combined Immunodeficiency 54 elevated serum ALT 54 epigenetic regulation 54 hippocampal volumes 54 Mycoplasma pneumoniae 54 Inhibitory 54 SCN1A 54 breast cancer subtypes 54 serum estradiol 54 Depressive disorders 54 Chronic bronchitis 54 Antisocial personality 54 neurodevelopmental outcomes 54 dietary restriction 54 telomere length 54 dentate gyrus 54 Chronic fatigue 54 Sporadic CJD 54 ß amyloid 54 myofascial pain syndrome 54 XLHED 54 ventricular enlargement 54 MEF2A 54 vasopressin receptors 54 DRD2 gene 54 SCA5 54 hippocampal volume 54 granule cells 54 IRF6 54 toxic beta amyloid 54 CNTNAP2 54 microtubule dynamics 54 chromatin structure 54 neuronal plasticity 54 diathesis 54 Sjögren syndrome 54 histone modifications 54 Li Huei Tsai 54 Ribavirin causes 54 elevated triglyceride levels 54 Candida species 54 Hurler syndrome 54 Südhof 54 APOE e4 gene 54 Epstein Barr virus EBV 54 Cognitive dysfunction 54 Plasmodium vivax 54 polydactylism 54 dysthymic 54 prodynorphin 54 Chlamydia pneumoniae 54 OGG1 54 cortical excitability 54 anterior temporal 54 Dysregulation 54 C. elegans worm 54 Cockayne syndrome 54 neuroblastoma tumors 54 hyperexcitability 54 Calorie restriction 54 Wnt signaling 54 Telomere shortening 54 paralogs 54 parasomnias 54 parkin gene 54 pathophysiologic 54 inhibitory transmitter 54 EphB2 levels 54 Androgenetic alopecia 54 genetic makeups 54 hypothalamus pituitary 54 Hair follicles 54 low ptau levels 54 ALI ARDS 54 TGFBR1 * 6A