sarcolemma

This means that the sarcolemma is not attached to the cytoskeleton.

Pressed against the inside of the sarcolemma are the unusual flattened nuclei.

The nuclei lie just adjacent to the sarcolemma, at the periphery of the fiber.

In the human fetus during muscle differentiation, utrophin is found at the sarcolemma.

Therefore during muscle contraction, the sarcolemma is not synchronized with the interior of the cell.

The looseness of the sarcolemma permits membrane calcium channels to open.

The sarcolemma, about 7.5 nm thick, is a unit-membrane like that investigating other cells.

The plasma membrane is called the sarcolemma with the cytoplasm known as the sarcoplasm.

Depolarization of the sarcolemma and transmission of an action potential through the T-tubules.

The muscle fibre has many cells with a plasma membrane and outer sheath or sarcolemma.

The same may be true for intercostal muscle, in which case, association with the sarcolemma, mitochondria or other organelles is possible.

Alterations in the sarcolemma membrane stability and repair system can lead to muscular dystrophy.

All muscular contraction happens inside the sarcolemma.

It overlies the muscle fiber's cell membrane: the Sarcolemma.

Satellite cells are described as quiescent myoblasts and neighbor muscle fiber sarcolemma.

Each muscle fibre is surrounded by a sarcolemma (the muscle fiber's plasma membrane).

The sarcolemma is invaginated and can make contact with the tracheole carrying oxygen to the muscle fibre.

Originates in the myofibrae, affecting the sarcolemma, or skeletal muscle cell membrane.

The end-plate potential propagates throughout the myocyte's sarcolemma and into the T-tubule system.

The sarcolemma contains the cytoplasm called sarcoplasm.

When enough receptors are stimulated, an action potential is generated and the permeability of the sarcolemma is altered.

Transverse tubules are invaginations of the sarcolemma.

Cardiac sarcolemma enzymes & liver microsomal cytochrome P450 in isoproterenol treated rats.

The sarcolemma possess microdomains specialized to cell-signaling events and ion channels called caveolae.

Dystrophin, a structural protein, connects the sarcomere, sarcolemma, and extracellular matrix components.