Search Results - "Allodi, I"
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Motor neurons with differential vulnerability to degeneration show distinct protein signatures in health and ALS
Published in Neuroscience (16-04-2015)“…Highlights • The motor protein dynein is down-regulated in resistant and vulnerable motor neurons (MNs) in ALS. • The high level of Gabra1 in oculomotor MNs in…”
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Synaptotagmin 13 is neuroprotective across motor neuron diseases
Published in Acta neuropathologica (01-05-2020)“…In amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA), spinal and lower brainstem motor neurons degenerate, but some motor neuron subtypes…”
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Locomotor deficits in a mouse model of ALS are paralleled by loss of V1-interneuron connections onto fast motor neurons
Published in Nature communications (31-05-2021)“…ALS is characterized by progressive inability to execute movements. Motor neurons innervating fast-twitch muscle-fibers preferentially degenerate. The reason…”
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LCM-seq reveals unique transcriptional adaptation mechanisms of resistant neurons and identifies protective pathways in spinal muscular atrophy
Published in Genome research (01-08-2020)“…Somatic motor neurons are selectively vulnerable in spinal muscular atrophy (SMA), which is caused by a deficiency of the ubiquitously expressed survival of…”
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Differential neuronal vulnerability identifies IGF-2 as a protective factor in ALS
Published in Scientific reports (16-05-2016)“…The fatal disease amyotrophic lateral sclerosis (ALS) is characterized by the loss of somatic motor neurons leading to muscle wasting and paralysis. However,…”
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Intact single muscle fibres from SOD1G93A amyotrophic lateral sclerosis mice display preserved specific force, fatigue resistance and training‐like adaptations
Published in The Journal of physiology (01-06-2019)“…Key points How defects in muscle contractile function contribute to weakness in amyotrophic lateral sclerosis (ALS) were systematically investigated. Weakness…”
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Modeling Motor Neuron Resilience in ALS Using Stem Cells
Published in Stem cell reports (11-06-2019)“…Oculomotor neurons, which regulate eye movement, are resilient to degeneration in the lethal motor neuron disease amyotrophic lateral sclerosis (ALS). It would…”
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Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish
Published in Frontiers in neuroscience (20-05-2014)“…Induction of specific neuronal fates is restricted in time and space in the developing CNS through integration of extrinsic morphogen signals and intrinsic…”
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Intact single muscle fibres from SOD1 G93A amyotrophic lateral sclerosis mice display preserved specific force, fatigue resistance and training-like adaptations
Published in The Journal of physiology (01-06-2019)“…How defects in muscle contractile function contribute to weakness in amyotrophic lateral sclerosis (ALS) were systematically investigated. Weakness in whole…”
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Journal Article -
10
Increased fatigue resistance and preserved specific force in intact single muscle fibres from the SOD1G93A mouse model of ALS
Published in ACTA PHYSIOLOGICA (2017)“…Introduction : Amyotrophic lateral sclerosis (ALS) is a motor neurone disease characterized by degeneration and loss of motor neurones, leading to severe…”
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Journal Article Conference Proceeding -
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The oculomotor restricted protein synaptotagmin 13 protects motor neurons from degeneration in ALS and SMA (P3.131)
Published in NEUROLOGY (18-04-2017)“…Abstract only…”
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Journal Article Conference Proceeding -
12
Neurturin is a PGC-1α1-controlled myokine that promotes motor neuron recruitment and neuromuscular junction formation
Published in Molecular metabolism (Germany) (01-01-2018)“…We examined whether skeletal muscle overexpression of PGC-1α1 or PGC-1α4 affected myokine secretion and neuromuscular junction (NMJ) formation. A microfluidic…”
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