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Characterization and Clinical Management of Dilated Cardiomyopathy
Characterization and Clinical Management of Dilated Cardiomyopathy
Autore Merlo Marco
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (232 p.)
Soggetto topico Medicine
Soggetto non controllato SCN5A
cardiac sodium channel
cardiac channelopathy
dilated cardiomyopathy
precision medicine
arrhythmias
atrial fibrillation
cardiomyopathy
heart failure
supraventricular arrhythmia
systolic dysfunction
tachycardiomyopathy
ventricular arrhythmia
left atrial strain
cardiac resynchronization therapy
muscular dystrophy
calcium
heart
gene therapy
phospholamban
Serca2a
mdx
oxidative stress
membrane stabilization
left ventricular noncompaction
congenital heart disease
congestive heart failure
non-ischemic cardiomyopathy
genetics
desmin
mitochondrial dysfunction
myopathy
whole exome sequencing
laminopathy
LMNA
biomarkers
troponin T
NT-proBNP
malignant ventricular arrhythmia
arrhythmic risk stratification
DNA methylation
alternative splicing
epigenetics
nonischemic dilated cardiomyopathy
cardiac magnetic resonance imaging
late gadolinium enhancement
long axis strain
left ventricle sphericity index
major adverse cardiovascular events
sex differences
left ventricular reverse remodelling
long-term outcomes
left ventricle non-compaction cardiomyopathy
cardiac magnetic resonance
titin
RNA binding motif protein 20 (RBM20)
sarcomere
diastolic dysfunction
phosphorylation
non-sense mRNA decay
mammalian target of rapamycin (mTOR) complex-1
duchenne muscular distrophy
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557595503321
Merlo Marco  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Creatine Supplementation for Health and Clinical Diseases
Creatine Supplementation for Health and Clinical Diseases
Autore Kreider Richard B
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (562 p.)
Soggetto topico Research & information: general
Biology, life sciences
Food & society
Soggetto non controllato ergogenic aids
cellular metabolism
phosphagens
sarcopenia
cognition
diabetes
creatine synthesis deficiencies
concussion
traumatic brain injury
spinal cord injury
muscle atrophy
rehabilitation
pregnancy
immunity
anti-inflammatory
antioxidant
anticancer
creatine
nutritional supplements
fertility
newborn
development
brain injury
post-viral fatigue syndrome
chronic fatigue syndrome
GAA
creatine kinase
dietary supplements
exercise
skeletal muscle
glycemic control
type 2 diabetes mellitus
phosphorylcreatine
dietary supplement
ergogenic aid
youth
athletes
osteoporosis
osteosarcopenia
frailty
cachexia
innate immunity
adaptive immunity
inflammation
macrophage polarization
cytotoxic T cells
toll-like receptors
vascular pathology
cardiovascular disease
oxidative stress
vascular health
female
menstrual cycle
hormones
exercise performance
menopause
mood
children
height
BMI-for-age
stature-for-age
growth
phosphocreatine
creatine transporter
supplementation
treatment
heart
heart failure
ischemia
myocardial infarction
anthracycline
cardiac toxicity
energy metabolism
cell survival
bioinformatics
systems biology
cellular allostasis
dynamic biosensor
pleiotropic effects of creatine (Cr) supplementation
inflammatory bowel diseases (IBD)
ulcerative colitis
Crohn’s disease
creatine kinase (CK)
phosphocreatine (PCr)
creatine transporter (CrT)
intestinal epithelial cell protection
intestinal tissue protection
creatine perfusion
organ transplantation
Adenosine mono-phosphate (AMP)
activated protein kinase (AMPK)
liver kinase B1 (LKB1)
mitochondrial permeability transition pore (mPTP)
reactive oxygen species (ROS)
glucose transporter (GLUT)
T cell antitumor immunity
metabolic regulator
cancer immunotherapy
supplements
muscle damage
recovery
immobilization
atrophy
muscular dystrophy
amyotrophic lateral sclerosis
Parkinson’s Disease
cardiopulmonary disease
mitochondrial cytopathy
hypertrophy
athletic performance
weightlifting
resistance exercise
training
muscular power
muscular adaptation
muscle fatigue
adipose tissue
muscle strength
physiological adaptation
mitochondria
thermogenesis
MAP kinase signaling system
sodium-chloride-dependent neurotransmitter symporters
signal transduction
intradialytic creatine supplementation
hemodialysis
muscle
protein energy wasting
clinical trial
muscle weakness
chronic fatigue
cognitive impairment
depression
anemia
resistance training
sports nutrition
strength
toxicity
methylation
hyperhomocysteinemia
neuromodulation
MCDA
mitochondriopathia
cardiac infarction
long COVID
hypoxia
stroke
neurodegenerative diseases
noncommunicable disease
adenosine 5′-monopnophosphate-activated protein kinase
anthracyclines
creatine supplementation
cardiac signaling
cardiotoxicity
doxorubicin
soy
vegetarian/vegan diet
amino acids
dietary ingredients
performance
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566476003321
Kreider Richard B  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Genome Editing in Neurosciences [[electronic resource] /] / edited by Rudolf Jaenisch, Feng Zhang, Fred Gage
Genome Editing in Neurosciences [[electronic resource] /] / edited by Rudolf Jaenisch, Feng Zhang, Fred Gage
Autore Feng Zhang
Edizione [1st ed. 2017.]
Pubbl/distr/stampa Springer Nature, 2017
Descrizione fisica 1 online resource (XI, 123 p. 16 illus. in color.)
Disciplina 611.01816
599.935
Collana Research and Perspectives in Neurosciences
Soggetto topico Human genetics
Neurosciences
Biomedical engineering
Human Genetics
Biomedical Engineering/Biotechnology
Soggetto non controllato CRISPR
muscular dystrophy
Parkinson's disease
DNA
Rett syndrome
double-strand breaks
Huntington's disease
genetic engineering
ISBN 3-319-60192-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction -- In vitro modeling of complex neurological diseases -- Aquatic model organisms in neurosciences : the genome editing revolution -- Genome-wide genetic screening in the mammalian CNS -- CRISPR/Cas9-mediated Knockin and Knockout in Zebrafish -- Dissecting the role of synaptic proteins with CRISPR -- Recurrently Breaking Genes in Neural Progenitors: Potential Roles of DNA Breaks in Neuronal Function, Degeneration and Cancer -- Neuroscience research using non-human primate models and genome editing -- Multiscale genome engineering: Genome-wide screens and targeted approaches -- Using Genome Engineering to Understand Huntington’s Disease -- Therapeutic gene editing in muscles and muscle stem cells.
Record Nr. UNINA-9910231247003321
Feng Zhang  
Springer Nature, 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Muscle Homeostasis and Regeneration : From Molecular Mechanisms to Therapeutic Opportunities
Muscle Homeostasis and Regeneration : From Molecular Mechanisms to Therapeutic Opportunities
Autore Musarò Antonio
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 electronic resource (500 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato lysine
mTORC1
satellite cells
proliferation
skeletal muscle growth
muscle satellite cell
transthyretin
thyroid hormone
myogenesis
exosomes
skeletal muscle
genotype
genetic variation
muscle phenotypes
sarcopenia
aging
calcium homeostasis
hibernation
mitochondria
sarcoplasmic reticulum
Acvr1b
Tgfbr1
myostatin
Col1a1
fibrosis
atrophy
IGF2R
muscle homeostasis
inflammation
muscular dystrophy
pericytes
macrophages
Nfix
phagocytosis
RhoA-ROCK1
splicing isoforms
CRISPR-Cas9
exon deletion
NF-Y
muscle differentiation
C2C12 cells
denervation
neuromuscular junction
heavy resistance exercise
acetylcholine receptor
cell culture
neonatal myosin
neural cell adhesion molecule
biomarkers
mitophagy
mitochondrial dynamics
mitochondrial quality control
mitochondrial-derived vesicles (MDVs)
mitochondrial-lysosomal axis
Hibernation
electron microscopy
immunocytochemistry
α-smooth muscle actin
confocal microscopy
connexin 43
connexin 26
gap junctions
myofibroblasts
Platelet-Rich Plasma
transforming growth factor (TGF)-β1
muscle regeneration
inflammatory response
cell precursors
experimental methods
stem cell markers
muscles
heterotopic ossification
skeletal muscle stem and progenitor cells
HO precursors
muscle atrophy
septicemia
mitochondrial fusion
mitochondrial fission
iPSC
extracellular vesicles
Drosophila
muscle
genetic control
muscle diversification
fascicle
myofiber
myofibril
sarcomere
hypertrophy
hyperplasia
splitting
radial growth
longitudinal growth
exercise
muscle stem cells
stem cells niche
neuromuscular disorders
Duchenne muscular dystrophy
pharmacological approach
single-cell
mass cytometry
skeletal muscle regeneration
skeletal muscle homeostasis
fibro/adipogenic progenitors
myogenic progenitors
muscle populations
evolution
metazoans
differentiation
transdifferentiation
muscle precursors
regenerative medicine
stem cells
FAPs
tissue niche
growth factors
muscle pathology
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Muscle Homeostasis and Regeneration
Record Nr. UNINA-9910557587003321
Musarò Antonio  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Pathophysiological Mechanisms of Sarcopenia in Aging and in Muscular Dystrophy: A Translational Approach
Pathophysiological Mechanisms of Sarcopenia in Aging and in Muscular Dystrophy: A Translational Approach
Autore Paolo Bonaldo
Pubbl/distr/stampa Frontiers Media SA, 2015
Descrizione fisica 1 electronic resource (248 p.)
Collana Frontiers Research Topics
Soggetto non controllato Aging sarcopenia
muscular dystrophy
Mitochondrial dysfunction
therapy
skeletal muscle
Autophagy
Animal Models
Apoptosis
satellite cells
muscle imaging
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Pathophysiological Mechanisms of Sarcopenia in Aging and in Muscular Dystrophy
Record Nr. UNINA-9910136802403321
Paolo Bonaldo  
Frontiers Media SA, 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Recent Developments in Annexin Biology
Recent Developments in Annexin Biology
Autore Jaiswal Jyoti K
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (266 p.)
Soggetto topico Research & information: general
Soggetto non controllato inflammation
nigericin
pyroptosis
mass spectrometry
lipidomics
anxA2
Birbeck granules
Langerhans cell
A2t
annexin
plasma membrane repair
membrane curvature
membrane curvature sensing
membrane shaping
interdisciplinary research
cell rupture
membrane damage
bias analysis
G protein-coupled receptor (GPCR)
formyl peptide receptor 1
danger-associated molecular pattern (DAMP)
pathogen-associated molecular pattern (PAMP)
annexin A1 peptide Ac2-26
cholesterol
AnxA6
chaperone-mediated autophagy
endolysosomes
NPC1
Lamp2A
annexin A2
microdomain
cross-linker
quartz crystal microbalance with dissipation monitoring (QCM-D)
mucin-1
claudin-1
zona occludens
ERK1/2 pathway
angiogenesis
F-actin polymerization
BeWo spheroids
Ishikawa cells
influenza
RNA-sequencing
transcriptomics
autophagy
Annexin-A1
infection
adherens junction
macroautophagy
breast cancer
estrogen receptor negative
Annexin A2
metastasis
annexin-A6
membrane repair
human skeletal muscle
cap subdomain
fluorescence
electron microscopy
CLEM
annexin A6
RasGRF2
EGFR
cell growth
cell motility
acquired resistance
tyrosine kinase inhibitors
muscle injury
plasma membrane
vesicle
muscular dystrophy
annexinA2 egress
exocytosis
chromaffin cells
thrombosis
Annexin A1
formyl peptide receptors
sickle cell disease
sepsis
Annexin
membrane
injury
virus
lipid
cancer
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557351303321
Jaiswal Jyoti K  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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