نتایج جستجو برای: motoneurons like cell

تعداد نتایج: 2217356  

Journal: :Journal of neurobiology 1998
B Grünewald R B Levine

The steroid hormone 20-hydroxyecdysone (20-HE) regulates several processes during insect metamorphosis. We studied the effects of 20-HE on the development of voltage-sensitive ionic currents of thoracic leg motoneurons of Manduca sexta. The larval leg motoneurons persist throughout metamorphosis but undergo substantial morphological reorganization, which is under the control of 20-HE and accomp...

Journal: :Folia neuropathologica 2006
Anna Fidziańska Roman Gadamski Janina Rafałowska Hanna Chrzanowska Paweł Grieb

The purpose of this study was to determine structural changes which trigger the onset and progression of amyotrophic lateral sclerosis in rats expressing a human SOD1 transgene with mutation G93A. Lumbar spinal cord of affected rats in early and late presymptomatic (PM, 60 and 93 days of age) and symptomatic (S, 120 days of age) stage of the disease were analyzed ultrastructurally. At 60 days t...

Journal: :The International journal of developmental biology 2002
Glen B Banks Peter G Noakes

Approximately half of the motoneurons generated during normal embryonic development undergo programmed cell death. Most of this death occurs during the time when synaptic connections are being formed between motoneurons and their target, skeletal muscle. Subsequent muscle activity stemming from this connection helps determine the final number of surviving motoneurons. These observations have gi...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2004
Daniel Perrelet Florence E Perrin Peter Liston Robert G Korneluk Alex MacKenzie Marcel Ferrer-Alcon Ann C Kato

Apoptotic cell death occurs in motoneurons in the neonate but not in the adult after a lesion of a peripheral nerve. To investigate the molecular basis for this difference, we have analyzed the expression and localization of inhibitors of apoptosis proteins (IAPs) and their inhibitors X-linked IAP (XIAP)-associated factor 1 (XAF1), Smac/DIABLO, and Omi/HtrA2 in motoneurons at both ages. Quantit...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Laure Duplan Nathalie Bernard Wilfrid Casseron Keith Dudley Eric Thouvenot Jérôme Honnorat Véronique Rogemond Béatrice De Bovis Patrick Aebischer Philippe Marin Cédric Raoul Christopher E Henderson Brigitte Pettmann

Embryonic motoneurons from mutant SOD1 (mSOD1) mouse models of amyotrophic lateral sclerosis (ALS), but not wild-type motoneurons, can be triggered to die by exposure to nitric oxide (NO), leading to activation of a motoneuron-specific signaling pathway downstream of the death receptor Fas/CD95. To identify effectors of mSOD1-dependent cell death, we performed a proteomic analysis. Treatment of...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1991
S D Meriney M J Ford D Oliva G Pilar

Most studies on the trophic regulation of the normal neuronal competition for survival have focused on interactions between neurons and their target environment. However, it is also likely that trophic modulators are released from premotor inputs onto motoneurons. We have examined the developmental distribution of endogenous enkephalin-like immunoreactivity and the role that these endogenous op...

2000
A. Garcès G. Haase M. S. Airaksinen

Glial cell-line derived neurotrophic factor (GDNF) and its relative neurturin (NTN) are potent trophic factors for motoneurons. They exert their biological effects by activating the RET tyrosine kinase in the presence of a glycosyl-phosphatidylinositol-linked co-receptor, either GFRa1 or GFRa2. By whole-mount in situ hybridization on embryonic mouse spinal cord, we demonstrate that whereas Ret ...

2009
Sandra Westmark Eugenio E. Oliveira

18 Stick insect middle leg (mesothoracic) motoneurons receive tonic excitatory input during front leg 19 stepping on a treadmill. We studied the pharmacology of this excitatory input to the motoneurons 20 during single-legged treadmill walking (in situ). During bath application of drugs restricted to the 21 mesothoracic ganglion activity in motoneurons contralateral to the stepping front leg wa...

Journal: :Human molecular genetics 2015
Le Thi Hao Phan Q Duy James D Jontes Christine E Beattie

Low levels of the survival motor neuron protein (SMN) cause the disease spinal muscular atrophy. A primary characteristic of this disease is motoneuron dysfunction and paralysis. Understanding why motoneurons are affected by low levels of SMN will lend insight into this disease and to motoneuron biology in general. Motoneurons in zebrafish smn mutants develop abnormally; however, it is unclear ...

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