نتایج جستجو برای: motoneuron

تعداد نتایج: 2335  

Journal: :Journal of cell science 2002
Jonathan Corcoran Po Lin So Malcolm Maden

We generated retinoid-deficient adult rats by the removal of retinoids from their diet. We show that their motoneurons undergo neurodegeneration and that there is an accumulation of neurofilaments and an increase in astrocytosis, which is associated with motoneuron disease. These effects are mediated through the retinoic acid receptor alpha. The same receptor deficit is found in motoneurons fro...

Journal: :Neuroscience Letters 2009
Yu Wang Shreejith Pillai Jonathan R. Wolpaw Xiang Yang Chen

H-reflex down-conditioning increases GABAergic terminals on spinal cord motoneurons. To explore the origins of these terminals, we studied the numbers and distributions of spinal cord GABAergic interneurons. The number of identifiable GABAergic interneurons in the ventral horn was 78% greater in rats in which down-conditioning was successful than in naive rats or rats in which down-conditioning...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1986
Y M Yao J N Weakly

Recent studies suggest that the number of nerve terminals maintained per motoneuron and perhaps other motoneuron properties (Grinnell and Herrera, 1980a; Grinnell and Trussell, 1983) influence transmitter release. We have examined, in detail, the structure and function of motoneurons innervating two different twitch muscles, the sartorius and the ext. long. dig. IV (e.l.d.) in the adult frog us...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1986
H Tanaka L T Landmesser

During normal development chick motoneurons have been shown to project selectively to appropriate muscles by responding to a series of cues, both specific and nonspecific, within the limb. We tested the ability of motoneurons from another avian species, the Japanese quail, to respond to these cues by transplanting chick limb buds onto quail embryos and quail limb buds onto chick embryos between...

Journal: :Molecular pharmacology 2009
Manoj Kumar Jaiswal Bernhard U Keller

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the selective loss of defined motoneuron populations in the brainstem and spinal cord. Although low cytosolic calcium ([Ca(2+)](i)) buffering and a strong interaction between metabolic mechanisms and [Ca(2+)](i) have been associated with selective motoneuron vulnerability, the underlying cellular mechanis...

Journal: :Journal of neurophysiology 2016
Peter A Kirkwood

TO THE EDITOR: In recent years, De Luca and colleagues (De Luca et al. 1993; De Luca and Kline 2014) have expressed considerable scepticism for the conventionally accepted view that motoneuron synchronization results from activity in common inputs to the motoneurons concerned. Now Kline and De Luca (doi:10.1152/jn.00452.2015) have gone further. Exploiting the EMG decomposition technique develop...

Journal: :The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1989
G R Chalmers V R Edgerton

We have developed a quantitative histochemical assay for measurement of succinate dehydrogenase (SDH) activity in single motoneurons. A computer image processing system was used to quantify the histochemical enzyme reaction product and to follow the time course of the reaction. The optimal concentration for each of the ingredients of the incubation medium for the SDH reaction was determined and...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1998
J Cheng R B Stein K Jovanović K Yoshida D J Bennett Y Han

We tested the hypothesis that the neural networks for walking in the mudpuppy can be divided into a flexor and an extensor center, each of which contains collections of interneurons localized in the vicinity of their motoneuron pools. Combining a battery of techniques, we identified and localized the elbow flexor center and its motoneuron pool in the C2 segment and the elbow extensor center and...

Journal: :Neurobiology of disease 2014
Hans-Georg König Karen S Coughlan Sinéad Kinsella Bridget A Breen Jochen H M Prehn

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the loss of motoneurons in the spinal cord, brainstem and motor cortex. Mutations in the superoxide dismutase 1 (SOD1) gene represent a frequent genetic determinant and recapitulate a disease phenotype similar to ALS when expressed in mice. Previous studies using SOD1(G93A) transgenic mice have suggested a...

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