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Mitochondrial Dysfunction in Aging and Diseases of Aging
Mitochondrial Dysfunction in Aging and Diseases of Aging
Autore Haas Richard H
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (270 p.)
Soggetto non controllato age-related diseases
sphingolipids
glaucoma
ALS
neurodegeneration
mitochondrial dysfunction
adaptive immunity
senescence
de-emergence
innate immunity
cell danger response
mitochondrial transfer
axonal transport
cytokines
mitochondrial
age-related macular degeneration
prevention
heart failure
purinergic signaling
autophagy
Alzheimer's disease
diabetic retinopathy
proteostasis
1
immunosenescence
Miro1
ROS
metabolism
optic nerve
polypharmacy
eIF2?
Parkin
coenzyme Q10
neurodegenerative disease
DNA damage
skin
exercise
nucleotide metabolism
pasteur effect
stress response
inflammation
retina
drug-induced mitochondrial toxicity
neuroinflammation
exosomes
reactive oxygen species
25(OH)D
cardiomyopathy
crabtree effect
insulin resistance
cardiovascular disease
ageing
genetic mutations
metabokines
mitochondria
multiple sclerosis
aerobic
healing cycle
SOD1
mitophagy
PINK1
type 2 diabetes
integrated cell stress response
morbidity and mortality
ultraviolet
photoageing
cancer
aging
25(OH)2D
lysosome
NAD+
Parkinson's disease
ISBN 3-03921-328-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367756303321
Haas Richard H  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Understanding Neuromuscular Health and Disease: Advances in Genetics, Omics, and Molecular Function
Understanding Neuromuscular Health and Disease: Advances in Genetics, Omics, and Molecular Function
Autore Duddy William
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (318 p.)
Soggetto topico Research & information: general
Soggetto non controllato LMNA
Emery-Dreifuss muscular dystrophy
Omics
ALS
MND
ALS variants
genotype-phenotype
ALS genes
FSHD
DUX4
transcription
muscle
regulation
spinal muscular atrophy
adult patients
disease heterogeneity
Nusinersen
disease modifiers
functional outcomes
biomarkers
epigenetic changes
-omics approaches
oxidative stress
mitochondria dysfunction
axonal transport
autophagy
endocytosis
secretion
excitotoxicity
RNA metabolism
Duchenne muscular dystrophy (DMD)
exon-skipping therapies
next-generation sequencing (NGS)
Sanger sequencing
multiplex ligation probe amplification (MLPA)
multiplex polymerase chain reaction (PCR)
comparative genomic hybridization array (CGH)
viltolarsen
eteplirsen
golodirsen
rheumatoid arthritis
SNP
DMARD
methotrexate
pharmacogenomics
Duchenne muscular dystrophy
pharmacodynamic biomarkers
prednisone
deflazacort
glucocorticoids
corticosteroids
safety
neuromuscular diseases
translational research
disease models
precision medicine
miRNA
proteomics
calprotectin
dystrophy
Becker muscular dystrophy
dystrophinopathy
genotype-phenotype correlations
Canadian Neuromuscular Disease Registry
reading frame rule
dystrophin
multiple logistic regression analysis
exon skipping therapy
Amyotrophic Lateral Sclerosis
machine learning
genome-wide association studies
GWAS
genomics
ALS pathology
gene prioritization
AAV
genetic neuromuscular disorders
gene therapy
clinical trials
toxicity
SMA
DMD
XLMTM
facioscapulohumeral dystrophy
TALEN
CRISPR-Cas9
gene editing
polyadenylation
D4Z4
duchenne muscular dystrophy (DMD)
becker muscular dystrophy (BMD)
exon skipping
skip-equivalent deletions
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Understanding Neuromuscular Health and Disease
Record Nr. UNINA-9910557669103321
Duddy William  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui