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Editorial for special issue “genetic basis and epidemiology of myopathies”

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Συγγραφέας
Peristeri E., Dardiotis E.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.3390/ijms22042152
Λέξη-κλειδί
glucocorticoid
glucocorticoid receptor
transcription factor NFAT
transcription factor NFAT5
tropomyosin
unclassified drug
NFAT5 protein, human
TPM2 protein, human
transcription factor
tropomyosin
antiproliferative activity
cognition
cognitive defect
Duchenne muscular dystrophy
Editorial
facioscapulohumeral muscular dystrophy
genotype
glycogen storage disease
heredity
human
microfluorometry
myopathy
nonhuman
pathogenesis
phenotype
skeletal muscle cell
spinal muscular atrophy
animal
disease model
genetic association study
genetics
metabolism
muscle disease
mutation
psychology
Animals
Disease Models, Animal
Genetic Association Studies
Humans
Muscular Diseases
Mutation
Transcription Factors
Tropomyosin
MDPI AG
Εμφάνιση Μεταδεδομένων
Επιτομή
We are pleased to announce a Special Issue on the Genetic Basis and Epidemiology of Myopathies. This Special Issue is collecting papers pertaining to various lines of research focusing on the genetic basis and the epidemiology of myopathies. The Guest Editors’ note combines the contributing authors’ reviews and findings of relevant research, and we hope that future studies on myopathies will attempt to confirm these findings and, additionally, evaluate supplementary phenotypic and histological expressions of myopathies, as well as genetic factors in their pathogenesis. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/78064
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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    SARS-CoV-2 pathophysiology and its clinical implications: An integrative overview of the pharmacotherapeutic management of COVID-19 

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    Common manifestations of COVID-19 are respiratory and can extend from mild symptoms to severe acute respiratory distress. The severity of the illness can also extend from mild disease to life-threatening acute respiratory ...
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