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Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The main proteins encoded by LMNA are Lamin A and C, which together with Lamin B1 and B2, form the nuclear lamina: a mesh-like structure located underneath the ...
Sara M. Maffioletti (5869217) +6 more
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Induced pluripotent stem cell platforms for disease modelling of skeletal muscle laminopathies [PDF]
Laminopathies are a clinically and genetically heterogeneous group of 16 disorders caused by mutations in LMNA. This gene codes for lamin A and lamin C, which together with lamin B1 and B2 form the nuclear lamina, a mesh-like structure located underneath
Steele-Stallard, Heather
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Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The main proteins encoded by LMNA are Lamin A and C, which together with Lamin B1 and B2, form the nuclear lamina: a mesh-like structure located underneath the ...
Sara M. Maffioletti (5869217) +6 more
core +1 more source
Fluorescent probes of the orientation of myosin regulatory light chains in relaxed, rigor, and contracting muscle. [PDF]
The orientation of the light-chain region of myosin heads in relaxed, rigor, and isometrically contracting fibers from rabbit psoas muscle was studied by fluorescence polarization. Cysteine 108 of chicken gizzard myosin regulatory light chain (cgRLC) was
Shrimpton, C. +10 more
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Nitric oxide synthase in skeletal muscle fibres of patients with type 2 diabetes [PDF]
Muscle-derived nitric oxide (NO) mediates fundamental physiological actions on skeletal muscle including glucose uptake into muscle cells. Recently, we have shown that the altered glucose metabolism in skeletal muscle of patients with type 2 diabetes ...
Karla Punkt +5 more
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Properties of Sphincteric Striated Muscle
External anal and urethral sphincters have several common features. Each has striated muscle fibers encircling those of smooth muscle that reflexly contract to guard an orifice or relax to allow evacuation.
T Adams, J Krier
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International audienceIntroductionEmery-Dreifuss muscular dystrophy is characterized by skeletal muscle atrophy and weakness, associated with dilated cardiomyopathy and cardiac conduction disorders.
Vignier, Nicolas
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Muscular laminopathies: Role of prelamin A in early steps of muscle differentiation.
Mutations in A-type lamins or lamin-binding proteins are involved in the pathogenesis of diseases referred to as laminopathies (Worman et al., 2009). They include both tissue-specific disorders affecting striated muscle (muscular laminopathies), adipose ...
MARALDI, NADIR +15 more
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International audienceMuscle forces are produced by repeated stereotypical actomyosin units called sarcomeres. Sarcomeres are chained into linear myofibrils spanning the entire muscle fiber.
Manuela Weitkunat +7 more
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The structure and function of striated muscle
THE STRUCTURE AND FUNCTION OF STRIATED MUSCLE The structure and function of striated muscle (2) (-
Macdonald, J. S.
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