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Showing 1-7 of 7 results for "mabn77" within Papers
Yoshinori Otani et al.
Communications biology, 3(1), 121-121 (2020-03-15)
Charcot-Marie-Tooth (CMT) disease is a hereditary neuropathy mainly caused by gene mutation of peripheral myelin proteins including myelin protein zero (P0, MPZ). Large myelin protein zero (L-MPZ) is an isoform of P0 that contains an extended polypeptide synthesized by translational
Wen Li et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 42(26), 5130-5143 (2022-05-20)
Cerebellar inhibitory interneurons are important regulators of neural circuit activity for diverse motor and nonmotor functions. The molecular layer interneurons (MLIs), consisting of basket cells (BCs) and stellate cells (SCs), provide dendritic and somatic inhibitory synapses onto Purkinje cells, respectively.
O W Howell et al.
Brain : a journal of neurology, 129(Pt 12), 3173-3185 (2006-10-17)
Saltatory conduction in the nervous system is enabled through the intimate association between the leading edge of the myelin sheath and the axonal membrane to demarcate the node of Ranvier. The 186 kDa neuron specific isoform of the adhesion molecule
Nikki A McLean et al.
PloS one, 9(10), e110174-e110174 (2014-10-14)
Rapid and efficient axon remyelination aids in restoring strong electrochemical communication with end organs and in preventing axonal degeneration often observed in demyelinating neuropathies. The signals from axons that can trigger more effective remyelination in vivo are still being elucidated.
María T Dours-Zimmermann et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 29(24), 7731-7742 (2009-06-19)
The CNS-restricted versican splice-variant V2 is a large chondroitin sulfate proteoglycan incorporated in the extracellular matrix surrounding myelinated fibers and particularly accumulating at nodes of Ranvier. In vitro, it is a potent inhibitor of axonal growth and therefore considered to
De-En Xu et al.
Cell adhesion & migration, 8(4), 396-403 (2014-12-09)
Amyloid precursor protein (APP), commonly associated with Alzheimer disease, is upregulated and distributes evenly along the injured axons, and therefore, also known as a marker of demyelinating axonal injury and axonal degeneration. However, the physiological distribution and function of APP
Du-Yu Nie et al.
The EMBO journal, 22(21), 5666-5678 (2003-11-01)
We report Nogo-A as an oligodendroglial component congregating and interacting with the Caspr-F3 complex at paranodes. However, its receptor Nogo-66 receptor (NgR) does not segregate to specific axonal domains. CHO cells cotransfected with Caspr and F3, but not with F3
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