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Molecular Mechanisms of Sensorineural Hearing Loss and Development of Inner Ear Therapeutics
Molecular Mechanisms of Sensorineural Hearing Loss and Development of Inner Ear Therapeutics
Autore Vlajkovic Srdjan M
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (5793 p.)
Soggetto topico Medicine
Soggetto non controllato brain-derived neurotrophic factor
TrkB
inner ear
development
zebrafish
mitochondria dysfunction
reactive oxygen species
hypoxic
d-galactose
high-fat diet
aging
hearing loss
astrocytes
auditory brainstem
lateral superior olive
gap junctions
voltage-activated calcium channel 1.3
otoferlin
spontaneous activity
deafness
circadian dysregulation
clock genes
noise-induced hearing loss
sensory hair cells
synaptic ribbons
sensorineural hearing loss
hyperbaric oxygenation
adjunctive therapy
microRNAs
cochlear nucleus
inferior colliculus
neuroplasticity
noise-induced cochlear injury
cochlear rescue
otoprotection
adenosine A1 receptor
regulator of G protein signalling 4
CCG-4986
intratympanic drug delivery
potassium voltage-gated channel subfamily q member 4
potassium
nonsyndromic hearing loss
KCNQ4 activator
age-related hearing loss
selegiline
chronic oral treatment
hearing protection
mouse model
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557463003321
Vlajkovic Srdjan M  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
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