Found: 12
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Endoplasmic reticulum and mitochondria in diseases of motor and sensory neurons: a broken relationship?
- Published in:
- Cell Death & Disease, 2018, v. 9, n. 3, p. 1, doi. 10.1038/s41419-017-0125-1
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- Publication type:
- Article
Reduced Calreticulin Levels Link Endoplasmic Reticulum Stress and Fas-Triggered Cell Death in Motoneurons Vulnerable to ALS.
- Published in:
- Journal of Neuroscience, 2012, v. 32, n. 14, p. 4901, doi. 10.1523/JNEUROSCI.5431-11.2012
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- Publication type:
- Article
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4224, doi. 10.1093/hmg/ddt274
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- Publication type:
- Article
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 5, p. 1844, doi. 10.1093/brain/awac402
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- Publication type:
- Article
Physiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cells.
- Published in:
- PLoS ONE, 2022, v. 17, n. 10, p. 1, doi. 10.1371/journal.pone.0272097
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- Publication type:
- Article
Astrocyte‐targeting RNA interference against mutated superoxide dismutase 1 induces motoneuron plasticity and protects fast‐fatigable motor units in a mouse model of amyotrophic lateral sclerosis.
- Published in:
- Glia, 2022, v. 70, n. 5, p. 842, doi. 10.1002/glia.24140
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- Publication type:
- Article
Reply: Is SIGMAR1 a confirmed FTD/MND gene?
- Published in:
- 2015
- By:
- Publication type:
- commentary
Is SIGMAR1 a confirmed FTD/MND gene?
- Published in:
- 2015
- By:
- Publication type:
- commentary
Dysfunction in endoplasmic reticulummitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degeneration.
- Published in:
- Brain: A Journal of Neurology, 2015, v. 138, n. 4, p. 875, doi. 10.1093/brain/awv008
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- Publication type:
- Article
A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 ( CRMP4) Gene is Associated with ALS.
- Published in:
- Human Mutation, 2013, v. 34, n. 7, p. 953, doi. 10.1002/humu.22329
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- Article
Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 14, p. 2378, doi. 10.1093/hmg/ddz060
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- Publication type:
- Article
Parkin functionally interacts with PGC-1α to preserve mitochondria and protect dopaminergic neurons.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 3, p. 582, doi. 10.1093/hmg/ddw418
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- Publication type:
- Article