Found: 13
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Effects of early crush on aging wild type and Connexin 32 knockout mice: Evidence for a neuroprotective state in CMT1X mouse nerve.
- Published in:
- Journal of the Peripheral Nervous System, 2021, v. 26, n. 2, p. 167, doi. 10.1111/jns.12436
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- Article
Two Distinct Heterotypic Channels Mediate Gap Junction Coupling between Astrocyte and Oligodendrocyte Connexins.
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- Journal of Neuroscience, 2007, v. 27, n. 51, p. 13949, doi. 10.1523/JNEUROSCI.3395-07.2007
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- Article
Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).
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- Human Molecular Genetics, 2013, v. 22, n. 21, p. 4329, doi. 10.1093/hmg/ddt282
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- Article
Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32.
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- BMC Cell Biology, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12860-018-0173-0
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- Article
GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems.
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- Cell & Tissue Research, 2015, v. 360, n. 3, p. 659, doi. 10.1007/s00441-014-2014-6
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- Article
A new mutation in GJC2 associated with subclinical leukodystrophy.
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- Journal of Neurology, 2014, v. 261, n. 10, p. 1929, doi. 10.1007/s00415-014-7429-1
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- Article
Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild‐type forms of Cx47 do not contribute to or modulate gap junction function.
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- Glia, 2021, v. 69, n. 8, p. 1882, doi. 10.1002/glia.23999
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- Article
Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination.
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- Glia, 2018, v. 66, n. 12, p. 2589, doi. 10.1002/glia.23513
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- Article
Assessment of blood-brain barrier leakage and brain oxygenation in Connexin-32 knockout mice with systemic neuroinflammation using pulse electron paramagnetic resonance imaging techniques.
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- Magnetic Resonance in Medicine, 2024, v. 91, n. 6, p. 2519, doi. 10.1002/mrm.29994
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- Article
Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.
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- Scientific Reports, 2017, p. 40166, doi. 10.1038/srep40166
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- Article
Pathogenesis of X-Linked Charcot-Marie-Tooth Disease: Differential Effects of Two Mutations in Connexin 32.
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- Journal of Neuroscience, 2003, v. 23, n. 33, p. 10548, doi. 10.1523/JNEUROSCI.23-33-10548.2003
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- Article
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
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- Brain: A Journal of Neurology, 2009, v. 132, n. 2, p. 426, doi. 10.1093/brain/awn328
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- Article
Regulation of Substance P Expression in Sympathetic Neurons.
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- Annals of the New York Academy of Sciences, 1991, v. 632, n. 1, p. 10, doi. 10.1111/j.1749-6632.1991.tb33089.x
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- Article