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Martine Verdière-Sahuqué

Researcher at French Institute of Health and Medical Research

Publications -  10
Citations -  432

Martine Verdière-Sahuqué is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Skeletal muscle & Acetylcholinesterase. The author has an hindex of 7, co-authored 10 publications receiving 424 citations.

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Expression of matrix metalloproteinases 2 and 9 in regenerating skeletal muscle: a study in experimentally injured and mdx muscles.

TL;DR: The data allow the correlation of the differential expression of pro and/or active forms of M MP-2 and MMP-9 with different stages of the degeneration-regeneration process: MMP -9 expression is related to the inflammatory response and probably to the activation of satellite cells, whereas Mmp-2 activation is concomitant with the regeneration of new myofibers.
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A 295-kDA intermediate filament-associated protein in radial glia and developing muscle cells in vivo and in vitro.

TL;DR: The RC2 antibody recognizes a developmentally regulated cytoskeletal protein that is expressed by cells of the glial and myogenic lineages and whose expression in vitro seems to be controlled by a signaling mechanism known to modulate astroglial morphology.
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Apolipoprotein E expression at neuromuscular junctions in mouse, rat and human skeletal muscle

TL;DR: It is demonstrated that Alzheimer β‐amyloid precursor protein and a serpin α1‐antichymotrypsin also found accumulated in senile plaques in AD brain, were also localized at neuromuscular junctions (NMJs).
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External and internal acetylcholinesterase in rat sympathetic neurones in vivo and in vitro.

TL;DR: Specific AChE externalization probably occurs in neuronal cells as a developmentally regulated process in SCG neurones.
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A dimeric form of acetylcholinesterase anchored through a glycolipid in mouse skeletal muscle.

TL;DR: It is reported that a phosphatidylinositol-specific phospholipase C (PIPLC) solubilizes AChE from microsomal membranes of mouse intercostal muscle and one molecular form which migrates on linear sucrose gradients as a single peak of sedimentation coefficient 6.3 s.