Search Results - "Blondet, Brigitte"
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Pleiotrophin Cellular Localization in Nerve Regeneration after Peripheral Nerve Injury
Published in The journal of histochemistry and cytochemistry (01-08-2005)“…Pleiotrophin (PTN) is a member of the family of heparin-binding growth factors that displays mitogenic activities and promotes neurite outgrowth in vitro. In…”
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Localization of Butyrylcholinesterase at the Neuromuscular Junction of Normal and Acetylcholinesterase Knockout Mice
Published in The journal of histochemistry and cytochemistry (01-12-2010)“…At the mouse neuromuscular junction (NMJ), there are two distinct cholines-terases (ChE): acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Until…”
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3
Localization of butyrylcholinesteraseat the neuromuscular junction of normal and acetylcholinesterase knockout mice
Published in The journal of histochemistry and cytochemistry (2010)“…At the mouse neuromuscular junction (NMJ), there are two distinct cholinesterases (ChE): acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Until…”
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4
Exogenous pleiotrophin applied to lesioned nerve impairs muscle reinnervation
Published in Neurochemical research (01-07-2006)“…Pleiotrophin (PTN) is a heparin-binding growth factor involved in nerve regeneration after peripheral nerve injury. After crush injury, PTN is found in distal…”
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5
Motoneuron morphological alterations before and after the onset of the disease in the wobbler mouse
Published in Brain research (15-03-2002)“…The wobbler mutant mouse displays a recessively inherited neurological disease with degeneration of motoneurons and is considered to be an animal model for…”
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Transient massive DNA fragmentation in nervous system during the early course of a murine neurodegenerative disease
Published in Neuroscience letters (15-06-2001)“…In neurodegenerative diseases, such as Alzheimer's disease or HIV encephalitis, neuronal DNA fragmentation has been observed at unexpected high frequencies,…”
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Modulation of HSP25 expression during anterior horn motor neuron degeneration in the paralysé mouse mutant
Published in Journal of neuroscience research (01-08-2001)“…The paralysé spontaneous mutation in mice involves degeneration and death of anterior horn motor neurons. Mutant mice are not viable past postnatal day 16. At…”
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Brain-derived neurotrophic factor fails to arrest neuromuscular disorders in the paralysé mouse mutant, a model of motoneuron disease
Published in Journal of the neurological sciences (09-12-1997)“…Several new neurotrophic factors have been recently identified and shown to prevent motoneuron death in vitro and in vivo. One such agent is brain-derived…”
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The Paralysé Mouse Mutant: A New Animal Model of Anterior Horn Motor Neuron Degeneration
Published in Journal of neuropathology and experimental neurology (01-06-1996)“…The survival and morphometric characteristics of lumbar spinal motoneurons were examined in the paralysé mouse mutant. Affected (par/par) mice can be first…”
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10
Plasminogen activators in the neuromuscular system of the wobbler mutant mouse
Published in Brain research (15-05-1992)“…Wobbler, the neurological mutant mouse, carries an autosomal recessive gene (wr) and has been characterized as a model of lower motoneuron disorders with…”
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11
Activity-independent modulation of acetylcholine receptor levels in rat skeletal muscle following neonatal denervation
Published in Neuroscience letters (31-07-1989)“…Following denervation of adult muscle, levels of acetylcholine receptor (AChR) increase; normal, low levels are restored only after muscle reinnervation. After…”
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Difference in the ability of neonatal and adult denervated muscle to accumulate acetylcholinesterase at the old sites of innervation
Published in Developmental biology (01-09-1986)“…In adult rat sternocleidomastoid muscle, AChE is concentrated in the region rich in motor end-plates (MEP). All major AChE forms, “16 S,” “10 S,” and “4 S,”…”
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Distribution and quantification of ACh receptors and innervation in diaphragm muscle of normal and mdg mouse embryos
Published in Developmental biology (1984)“…Muscular dysgenesis ( mdg) in the mouse is an autosomal recessive mutation, expressed in the homozygous state ( in vivo and in vitro) as an absence of skeletal…”
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