Pages that link to "Q33280093"
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The following pages link to The pathogenesis of ACTA1-related congenital fiber type disproportion (Q33280093):
Displaying 17 items.
- Pathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focus (Q28087567) (← links)
- Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy (Q28252989) (← links)
- Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy (Q28293427) (← links)
- Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients (Q28295272) (← links)
- A genome scan for positive selection in thoroughbred horses (Q33463312) (← links)
- Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1). (Q34989619) (← links)
- Thin filament proteins mutations associated with skeletal myopathies: defective regulation of muscle contraction. (Q37198630) (← links)
- Actin isoform expression patterns during mammalian development and in pathology: insights from mouse models (Q37417675) (← links)
- Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms. (Q38028847) (← links)
- Profiling of the yak skeletal muscle tissue gene expression and comparison with the domestic cattle by genome array (Q38483450) (← links)
- alpha-Skeletal muscle actin mutants causing different congenital myopathies induce similar cytoskeletal defects in cell line cultures (Q39885443) (← links)
- A Case Report of Congenital Fiber Type Disproportion with an Increased Level of Anti-ACh Receptor Antibodies (Q41429301) (← links)
- Investigation of a transgenic mouse model of familial dilated cardiomyopathy. (Q42473760) (← links)
- Tropomyosin Must Interact Weakly with Actin to Effectively Regulate Thin Filament Function. (Q47323482) (← links)
- Bi-allelic mutations in MYL1 cause a severe congenital myopathy (Q63681671) (← links)
- The Molecular Mechanisms of Mutations in Actin and Myosin that Cause Inherited Myopathy. (Q64883689) (← links)
- Comprehensive Transcriptional Profiling of the Gastrointestinal Tract of Ruminants from Birth to Adulthood Reveals Strong Developmental Stage Specific Gene Expression (Q90364865) (← links)