AbstractBiological sensors and their ability to detect and respond to change in the cellular environment can be modulated by protein scaffolds acting within their interaction network. The skeletal muscle α-actinins have been considered as primarily structural scaffold proteins. However, deficiency of α-actinin-3 due to a common null polymorphism results in predominantly metabolic changes in skeletal muscle function. In this review, we explore the range of phenotypes associated with α-actinin-3 deficiency, and draw supporting evidence from known interaction partners for its role as a scaffold which acts to modulate biological sensors that result in changes in muscle metabolism and structure
A common null polymorphism (R577X) in ACTN3 causes α-actinin-3 deficiency in ~18% of the global popu...
A common nonsense polymorphism in the ACTN3 gene results in the absence of a-actinin-3 in XX individ...
α-Actinin-3 deficiency occurs in approximately 16% of the global population due to homozygosity for ...
AbstractBiological sensors and their ability to detect and respond to change in the cellular environ...
An estimated 1.5 billion people worldwide are deficient in the skeletal muscle protein α-actinin-3 d...
The spectrin superfamily of proteins plays key roles in assembling the actin cytoskeleton in various...
SummaryThe spectrin superfamily of proteins plays key roles in assembling the actin cytoskeleton in ...
Muscle contracts when thick and thin filaments within the sarcomere slide past one another, shorteni...
Sarcomeric α-actinins (α-actinin-2 and -3) are a major component of the Z-disk in skeletal muscle, w...
Approximately one billion people worldwide are homozygous for a stop codon polymorphism in the ACTN3...
Homozygosity for a common null polymorphism (R577X) in the ACTN3 gene results in the absence of the ...
A common nonsense polymorphism in the ACTN3 gene results in the absence of α-actinin-3 in XX individ...
The association between the ACTN3 genotype and human performance has been intensively studied in a n...
A common nonsense polymorphism (R577X) in the ACTN3 gene results in complete deficiency of the fast ...
Background: A common polymorphism (R577X) in the ACTN3 gene results in the complete absence of the Z...
A common null polymorphism (R577X) in ACTN3 causes α-actinin-3 deficiency in ~18% of the global popu...
A common nonsense polymorphism in the ACTN3 gene results in the absence of a-actinin-3 in XX individ...
α-Actinin-3 deficiency occurs in approximately 16% of the global population due to homozygosity for ...
AbstractBiological sensors and their ability to detect and respond to change in the cellular environ...
An estimated 1.5 billion people worldwide are deficient in the skeletal muscle protein α-actinin-3 d...
The spectrin superfamily of proteins plays key roles in assembling the actin cytoskeleton in various...
SummaryThe spectrin superfamily of proteins plays key roles in assembling the actin cytoskeleton in ...
Muscle contracts when thick and thin filaments within the sarcomere slide past one another, shorteni...
Sarcomeric α-actinins (α-actinin-2 and -3) are a major component of the Z-disk in skeletal muscle, w...
Approximately one billion people worldwide are homozygous for a stop codon polymorphism in the ACTN3...
Homozygosity for a common null polymorphism (R577X) in the ACTN3 gene results in the absence of the ...
A common nonsense polymorphism in the ACTN3 gene results in the absence of α-actinin-3 in XX individ...
The association between the ACTN3 genotype and human performance has been intensively studied in a n...
A common nonsense polymorphism (R577X) in the ACTN3 gene results in complete deficiency of the fast ...
Background: A common polymorphism (R577X) in the ACTN3 gene results in the complete absence of the Z...
A common null polymorphism (R577X) in ACTN3 causes α-actinin-3 deficiency in ~18% of the global popu...
A common nonsense polymorphism in the ACTN3 gene results in the absence of a-actinin-3 in XX individ...
α-Actinin-3 deficiency occurs in approximately 16% of the global population due to homozygosity for ...