Detalhe da pesquisa
1.
Macrophages influence Schwann cell myelin autophagy after nerve injury and in a model of Charcot-Marie-Tooth disease.
J Peripher Nerv Syst
; 28(3): 341-350, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37209383
2.
Early targeting of endoneurial macrophages alleviates the neuropathy and affects abnormal Schwann cell differentiation in a mouse model of Charcot-Marie-Tooth 1A.
Glia
; 70(6): 1100-1116, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35188681
3.
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
Am J Hum Genet
; 99(3): 607-623, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588448
4.
Cell-Surface and Secreted Isoforms of CSF-1 Exert Opposing Roles in Macrophage-Mediated Neural Damage in Cx32-Deficient Mice.
J Neurosci
; 36(6): 1890-901, 2016 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26865613
5.
Progression of motor axon dysfunction and ectopic Nav1.8 expression in a mouse model of Charcot-Marie-Tooth disease 1B.
Neurobiol Dis
; 93: 201-14, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27215377
6.
Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice.
Brain
; 138(Pt 11): 3193-205, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26297559
7.
CSF-1-activated macrophages are target-directed and essential mediators of Schwann cell dedifferentiation and dysfunction in Cx32-deficient mice.
Glia
; 63(6): 977-86, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25628221
8.
Endogenous antibodies contribute to macrophage-mediated demyelination in a mouse model for CMT1B.
J Neuroinflammation
; 12: 49, 2015 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25879857
9.
Nonuniform molecular features of myelinating Schwann cells in models for CMT1: distinct disease patterns are associated with NCAM and c-Jun upregulation.
Glia
; 62(5): 736-50, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24526449
10.
Long-lasting significant functional improvement in chronic severe spinal cord injury following scar resection and polyethylene glycol implantation.
Neurobiol Dis
; 67: 165-79, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24713436
11.
Similarities between inherited demyelinating neuropathies and Wallerian degeneration: an old repair program may cause myelin and axon perturbation under nonlesion conditions.
Am J Pathol
; 183(3): 655-60, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23831295
12.
Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot-Marie-Tooth disease type 1X.
Brain
; 135(Pt 1): 88-104, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22094537
13.
Attenuation of MCP-1/CCL2 expression ameliorates neuropathy in a mouse model for Charcot-Marie-Tooth 1X.
Hum Mol Genet
; 19(18): 3530-43, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20591826
14.
Na(v)1.8 channelopathy in mutant mice deficient for myelin protein zero is detrimental to motor axons.
Brain
; 134(Pt 2): 585-601, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21169333
15.
Presymptomatic macrophage targeting has a long-lasting therapeutic effect on treatment termination in a mouse model of Charcot-Marie-Tooth 1.
Exp Neurol
; 357: 114195, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35931123
16.
MCP-1/CCL2 modifies axon properties in a PMP22-overexpressing mouse model for Charcot-Marie-tooth 1A neuropathy.
Am J Pathol
; 176(3): 1390-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20093502
17.
Physical exercise mitigates neuropathic changes in an animal model for Charcot-Marie-Tooth disease 1X.
Exp Neurol
; 343: 113786, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34153322
18.
Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A.
Neurobiol Dis
; 38(1): 78-84, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20064611
19.
The alpha-chemokine CXCL14 is up-regulated in the sciatic nerve of a mouse model of Charcot-Marie-Tooth disease type 1A and alters myelin gene expression in cultured Schwann cells.
Neurobiol Dis
; 33(3): 448-58, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19111616
20.
Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder.
J Cell Biol
; 165(4): 565-73, 2004 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-15148307