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Changes in subcellular distribution of protocadherin gamma proteins accompany maturation of spinal neuronsA semaphorin code defines subpopulations of spinal motor neurons during mouse developmentSemaphorin 3E and plexin-D1 control vascular pattern independently of neuropilinsETS gene Pea3 controls the central position and terminal arborization of specific motor neuron poolsRole of neurotrophic factors in neuronal development.Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy.Collapsin response mediator protein 4a (CRMP4a) is upregulated in motoneurons of mutant SOD1 mice and can trigger motoneuron axonal degeneration and cell death.Chronic activation in presymptomatic amyotrophic lateral sclerosis (ALS) mice of a feedback loop involving Fas, Daxx, and FasL.Identification and characterization of cholest-4-en-3-one, oxime (TRO19622), a novel drug candidate for amyotrophic lateral sclerosis.A functionally characterized test set of human induced pluripotent stem cellsMotor columns caged by crest.Antennapedia homeobox peptide enhances growth and branching of embryonic chicken motoneurons in vitro.Programmed cell death of embryonic motoneurons triggered through the Fas death receptorAccelerated high-yield generation of limb-innervating motor neurons from human stem cells.Gating of Sema3E/PlexinD1 signaling by neuropilin-1 switches axonal repulsion to attraction during brain development.Met signaling is required for recruitment of motor neurons to PEA3-positive motor pools.Efficient gene transfer and expression of biologically active glial cell line-derived neurotrophic factor in rat motoneurons transduced wit lentiviral vectors.Expression of vesicular glutamate transporters, VGLUT1 and VGLUT2, in cholinergic spinal motoneurons.Loss of leukemia inhibitory factor receptor beta or cardiotrophin-1 causes similar deficits in preganglionic sympathetic neurons and adrenal medulla.Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS.Neuronal defects in the hindbrain of Hoxa1, Hoxb1 and Hoxb2 mutants reflect regulatory interactions among these Hox genes.Neurotrophins promote motor neuron survival and are present in embryonic limb bud.euroSCIENCE moves into sixth gear!Roles for retrograde factors in synapse formation at the nerve-muscle junction.Motoneuron death triggered by a specific pathway downstream of Fas. potentiation by ALS-linked SOD1 mutations.Role of neurotrophic factors in motoneuron developmentPurification of embryonic rat motoneurons by panning on a monoclonal antibody to the low-affinity NGF receptorEmbryonic rat motoneurons express a functional P-type voltage-dependent calcium channelRapid purification of embryonic rat motoneurons: an in vitro model for studying MND/ALS pathogenesisLow-affinity nerve growth factor receptor is associated with motoneuron axonal pathwaysInfluence of factors secreted by wobbler astrocytes on neuronal and motoneuronal survivalSpecific expression of the urotensin II gene in sacral motoneurons of developing rat spinal cordCardiotrophin-1 requires LIFRbeta to promote survival of mouse motoneurons purified by a novel techniqueKiller wiles: growing interest in Fas
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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type
label
Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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Christopher E. Henderson
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P106
P1153
7202491087
P21
P31
P496
0000-0002-9936-3279