Zobrazeno 1 - 10
of 197
pro vyhledávání: '"Eric M. SHOOTER"'
Publikováno v:
Neurobiology of Disease, Vol 17, Iss 2, Pp 300-309 (2004)
A characteristic feature of mouse models of the peripheral neuropathies caused by dominant mutations in peripheral myelin protein 22 (pmp22) is the appearance, in Schwann cells, of pmp22 aggregates. Using a set of dominant and recessive pmp22 mutatio
Externí odkaz:
https://doaj.org/article/8bdd1bfe5c004330bc1eaf2fd5464a75
Publikováno v:
Neurobiology of Disease, Vol 10, Iss 2, Pp 109-118 (2002)
Alterations in peripheral myelin protein 22 (PMP22) gene expression are associated with demyelinating peripheral neuropathies. Overexpression of wild type (wt) PMP22 or inhibition of proteasomal degradation lead to the formation of aggresomes, intrac
Externí odkaz:
https://doaj.org/article/ee47366d9cd9464a8967c0de60d60003
Publikováno v:
Neurobiology of Disease, Vol 7, Iss 4, Pp 416-428 (2000)
Under some circumstances neurons can be primed to rapidly regenerate injured neuritic processes independent of new gene expression. Such transcription-independent neurite extension occurs in adult rat sensory neurons cultured after sciatic nerve crus
Externí odkaz:
https://doaj.org/article/fef61fd4f209431c879c36e6db4f59ec
Publikováno v:
Neurobiology of Disease, Vol 6, Iss 5, Pp 450-460 (1999)
Peripheral myelin protein 22 (PMP22) is a 22-kDa glycoprotein mainly expressed by Schwann cells (SCs). Duplication or deletion of the PMP22 gene locus is associated with heritable peripheral neuropathies suggesting that the correct level of PMP22 pro
Externí odkaz:
https://doaj.org/article/d95f369203bf4da884dcb13d1d47699d
Autor:
Jose Miguel Cosgaya, Eric M. Shooter
Publikováno v:
Journal of Neurochemistry. 79:391-399
Nerve growth factor (NGF) regulates the activity of the transcription factor NF-κB (nuclear factor-κB) through its low affinity receptor, p75. In the present study we found that NGF binding to p75 induces nuclear translocation of p65 and increases
Publikováno v:
Journal of Neuroscience Research. 85:2863-2869
The heterozygous Trembler-J (TrJ/+) mouse, containing a point mutation in the peripheral myelin protein 22 (Pmp22) gene, is characterized by severe hypomyelination and is a representative model of Charcot-Marie-Tooth 1A (CMT1A) disease/Dejerine-Sotta
Publikováno v:
Proceedings of the National Academy of Sciences. 102:5198-5203
During the development of the peripheral nervous system, Schwann cells, the myelin-forming glia, migrate along axons before initiating myelination. We previously demonstrated that endogenous neurotrophin-3 (NT3) acting through the TrkC tyrosine kinas
Publikováno v:
Neurobiology of Disease, Vol 17, Iss 2, Pp 300-309 (2004)
A characteristic feature of mouse models of the peripheral neuropathies caused by dominant mutations in peripheral myelin protein 22 (pmp22) is the appearance, in Schwann cells, of pmp22 aggregates. Using a set of dominant and recessive pmp22 mutatio
Publikováno v:
Proceedings of the National Academy of Sciences. 101:8774-8779
Neurotrophins are recognized widely as essential factors in the developing nervous system. Previously, we demonstrated that neurotrophin 3 activation of TrkC inhibits Schwann cell myelination and enhances the migration of primary Schwann cells throug
Autor:
Jonah R. Chan, Y.J. Wu, Alex Krüttgen, Jens Carsten Möller, Jose Miguel Cosgaya, D. Shine, Eric M. Shooter
Publikováno v:
Journal of Neuroscience Research. 75:825-834
Neurotrophins (NTs) play an important role in the modulation of synaptic transmission and in morphological changes in synaptic structures. Although there is agreement that brain-derived neurotrophic factor (BDNF) is sorted to large dense-core vesicle