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Endothelial Dysfunction: From Pathophysiology to Novel Therapeutic Approaches
Endothelial Dysfunction: From Pathophysiology to Novel Therapeutic Approaches
Autore Jeon Byeong Hwa
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (368 p.)
Soggetto topico Technology: general issues
Biotechnology
Soggetto non controllato endothelial cells
oxidative stress
inflammageing
endothelial dysfunction
aldehyde dehydrogenase-2
cardiovascular disease
neurovascular disease
vascular inflammation
APE1/Ref-1
cardiovascular diseases
subcellular localization
serological biomarkers
atherosclerosis
aerobic exercise
PCSK9
LOX-1
insulin resistance
macrophage polarity
serum γ-glutamyltransferase
essential hypertension
cardiovascular risk factors
angiogenesis
nargenicin A1
compound 9
VEGF
VEGFR2
HIF-1α
electronegative low-density lipoprotein
LDL(-)
L5 LDL
oxidized LDL
oxLDL
ADMA
arginine
arginine paradox
BH4
blood pressure
COVID-19
dietary supplements
endothelium
eNOS uncoupling
heart failure
hypertension
L-arginine
myocardial infarction
NADPH
nitric oxide
peripheral artery disease
ApoE knockout mouse
atorvastatin
VCAM-1
galectin-3
neutrophil/lymphocyte ratio
electronegative LDL
LDL(−)
lectin-like oxLDL receptor-1
dyslipidemia
chronic venous insufficiency
prolyl oligopeptidase (POP)
inflammation
endothelial disfunction
lung disease
endothelial to mesenchymal transition
pulmonary hypertension
pulmonary fibrosis
metformin
diabetes
CV risk
hyperglycemia
glycated lipoproteins
glycated LDL
glycated HDL
endothelial cell dysfunction
molecular mechanisms
epigenetic factors
therapeutic approaches
vasoactive factors
EndoMT
TGF-β
epigenetics
endothelial cell
glycolysis
metabolism
pathological angiogenesis
tumor microenvironment
MRI (magnetic resonance imaging)
high-fat diets
plaque burden
low-level laser therapy
phototherapy
vascular disease
healing
ischemia
vascular calcification
chronic kidney disease
CKD
uremic toxins
hyperphosphatemia
vascular smooth muscle cells
VSMCs
macrophages
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Endothelial Dysfunction
Record Nr. UNINA-9910566471803321
Jeon Byeong Hwa  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Epigenetics Traits in Mammalian Tissues. From New Technology to New Hypotheses
Epigenetics Traits in Mammalian Tissues. From New Technology to New Hypotheses
Autore Symonds Michael E
Pubbl/distr/stampa Frontiers Media SA, 2019
Descrizione fisica 1 electronic resource (70 p.)
Soggetto topico Science: general issues
Medical genetics
Soggetto non controllato histone deacetylation
CpG methylation
cytocrin
epigenetic factors
Epigenetic traits
Pregnancy
Sugar metabolism
eye epigenetics
in vitro fertilization
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910688484703321
Symonds Michael E  
Frontiers Media SA, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020
Autore Butler Merlin G
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (204 p.)
Soggetto topico Research & information: general
Biology, life sciences
Genetics (non-medical)
Soggetto non controllato autism
ASD
genetics
heterogeneity
syndromes
assessment
medications
treatment
causes
autism spectrum disorders (ASDs)
proteomics
metabolomics
interactomics
disease biomarkers
clinical decision support systems (CDSSs)
phenotypic subgroups stratified by ASD severity
simplex families
DNA methylation
subgroup-associated genes and biological functions
Broader Autism Phenotype
genetic
autism spectrum disorder
multiplex family
genetic factors
epigenetic factors
environmental factors
pervasive developmental disorder
post-synaptic density
CNV
SNP
gene fusion
CACNA1C
CaV1.2
short QT syndrome
dental enamel defect
bioinformatics
human genetics
pharmacogenomics
15q11.2 BP1-BP2 deletion
Burnside-Butler syndrome
clinical findings
cognition
neuropsychiatric behavior development
genomic characterization
exome sequencing
protein–protein interaction
22q13.3 duplication
auditory steady-state response
ASSR
SHANK3
biomarker
auditory event-related potential
ERP
autism spectrum disorders
intellectual disabilities
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566463603321
Butler Merlin G  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui