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Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function.
- Published in:
- eLife, 2019, p. 1, doi. 10.7554/eLife.42404
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- Publication type:
- Article
RIUSO DI COMPONENTI EDILIZI: Sistema di valutazione a supporto delle decisioni negli interventi di ridistribuzione interna.
- Published in:
- Agathon: International Journal of Architecture, Art & Design, 2024, v. 15, p. 266, doi. 10.19229/2464-9309/15212024
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- Publication type:
- Article
Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice.
- Published in:
- Journal of Neuroscience, 2006, v. 26, n. 8, p. 2358, doi. 10.1523/JNEUROSCI.3819-05.2006
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- Publication type:
- Article
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot–Marie–Tooth disease type 1B.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 7, p. 2032, doi. 10.1093/brain/aws140
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- Publication type:
- Article
Dynamin 2 mutations in Charcot–Marie–Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 5, p. 1395, doi. 10.1093/brain/aws061
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- Publication type:
- Article
Author Correction: Global network analysis in Schizosaccharomycespombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-85471-4
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- Publication type:
- Article
Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 8, p. 1253, doi. 10.1093/hmg/ddaa034
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- Publication type:
- Article
Muscle-specific function of the centronuclear myopathy and Charcot–Marie–Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 21, p. 4417, doi. 10.1093/hmg/ddt292
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- Publication type:
- Article
P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 11, p. 2081, doi. 10.1093/hmg/ddr081
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- Publication type:
- Article