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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 online resource (5793 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato adenosine A1 receptor
adjunctive therapy
age-related hearing loss
aging
astrocytes
auditory brainstem
brain-derived neurotrophic factor
CCG-4986
chronic oral treatment
circadian dysregulation
clock genes
cochlear nucleus
cochlear rescue
d-galactose
deafness
development
gap junctions
hearing loss
hearing protection
high-fat diet
hyperbaric oxygenation
hypoxic
inferior colliculus
inner ear
intratympanic drug delivery
KCNQ4 activator
lateral superior olive
microRNAs
mitochondria dysfunction
mouse model
n/a
neuroplasticity
noise-induced cochlear injury
noise-induced hearing loss
nonsyndromic hearing loss
otoferlin
otoprotection
potassium
potassium voltage-gated channel subfamily q member 4
reactive oxygen species
regulator of G protein signalling 4
selegiline
sensorineural hearing loss
sensory hair cells
spontaneous activity
synaptic ribbons
TrkB
voltage-activated calcium channel 1.3
zebrafish
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 online resource (318 p.)
Soggetto topico Research & information: general
Research and information: general
Soggetto non controllato -omics approaches
adult patients
autophagy
axonal transport
becker muscular dystrophy (BMD)
biomarkers
calprotectin
clinical trials
comparative genomic hybridization array (CGH)
corticosteroids
deflazacort
disease heterogeneity
disease models
disease modifiers
duchenne muscular dystrophy (DMD)
dystrophin
dystrophinopathy
dystrophy
endocytosis
epigenetic changes
eteplirsen
excitotoxicity
exon skipping
exon skipping therapy
exon-skipping therapies
facioscapulohumeral dystrophy
functional outcomes
gene editing
gene prioritization
gene therapy
genetic neuromuscular disorders
genome-wide association studies
genomics
genotype-phenotype
genotype-phenotype correlations
glucocorticoids
golodirsen
machine learning
methotrexate
miRNA
mitochondria dysfunction
multiple logistic regression analysis
multiplex ligation probe amplification (MLPA)
multiplex polymerase chain reaction (PCR)
muscle
neuromuscular diseases
next-generation sequencing (NGS)
oxidative stress
pharmacodynamic biomarkers
pharmacogenomics
polyadenylation
precision medicine
prednisone
proteomics
reading frame rule
regulation
rheumatoid arthritis
safety
secretion
skip-equivalent deletions
spinal muscular atrophy
toxicity
transcription
translational research
viltolarsen
AAV
ALS genes
ALS pathology
ALS variants
Amyotrophic Lateral Sclerosis
Becker muscular dystrophy
Canadian Neuromuscular Disease Registry
CRISPR-Cas9
D4Z4
DMARD
DMD
Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD)
DUX4
Emery-Dreifuss muscular dystrophy
FSHD
GWAS
LMNA
MND
Nusinersen
Omics
RNA metabolism
Sanger sequencing
SMA
SNP
TALEN
XLMTM
ISBN 9783036516226
9783036516219
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