Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
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Late onset neuropathy with spontaneous clinical remission in mice lacking the POZ domain of the transcription factor Myc-interacting zinc finger protein 1 (Miz1) in Schwann cellsDominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology.Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.Glutamate signals through mGluR2 to control Schwann cell differentiation and proliferationGenetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success.Therapeutic options in Charcot-Marie-Tooth diseases.Muscle spindle alterations precede onset of sensorimotor deficits in Charcot-Marie-Tooth type 2E.Schwann cell Miz without POZ: degeneration meets regeneration.PMP22 messenger RNA levels in skin biopsies: testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker.Decreased ceramide underlies mitochondrial dysfunction in Charcot-Marie-Tooth 2F.Structure, function, and regulation of mitofusin-2 in health and disease.Locomotor and skeletal muscle abnormalities in trembler J neuropathic mice.CSF-1-activated macrophages are target-directed and essential mediators of Schwann cell dedifferentiation and dysfunction in Cx32-deficient mice.
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Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
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article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
@pt-br
artikel ilmiah
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artikull shkencor
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artículo científico
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name
Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
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type
label
Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
@en
prefLabel
Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
@en
P2860
P356
P1433
P1476
Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
@en
P2093
Delphine Bouhy
Vincent Timmerman
P2860
P304
P356
10.1002/ANA.23987
P577
2013-09-01T00:00:00Z