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Showing 1 to 4 of 4 for “"myelin protein zero"”.

  1. Charcot-Marie-Tooth-Neuropathie Typ 2 : neue Myelinprotein-P0-Punktmutationen und Haplotypenanalyse in europäischen Familien

    … and nerve pathology, CMT is subdivided in demyelinating CMT1 and axonal CMT2. Causative gene mutations can be identified in about 80-90% of CMT1 patients while no major CMT2 gene has been identified so far. In the present study, 49 CMT2 patients were tested for mutations in the myelin protein

    aachen Repository record for Charcot-Marie-Tooth-Neuropathie Typ 2 : neue Myelinprotein-P0-Punktmutationen und Haplotypenanalyse in europäischen Familien (opens in a new tab)

  2. Entwicklung von Merkelzellen in der Haut von P0-defizienten Mäusen

    … als Mechanorezeptor der Haut wird von einer myelinisierten langsam adaptierenden Afferenz (Aß) innerviert. Deshalb wurde in der vorliegenden Arbeit als sekundärer Indikator für die distale Innervation in P0-defizienten Mäusen, ein Tiermodell der hereditären motorisch-sensorischen …

    wurz-thes Repository record for Entwicklung von Merkelzellen in der Haut von P0-defizienten Mäusen (opens in a new tab)

  3. Elevated Cochlear Adenosine Causes Hearing Loss Via Adora2B Signaling

    … observed nerve fiber density loss and aberrant myelin compaction. More importantly, we found that treatment of FDA-approved drug, polyethylene glycol-ADA (PEG-ADA), lowered cochlear adenosine levels and improved functional and structural phenotypes of <em>Ada<sup>-/-</sup></em> mice. In addition …

    uthsc Repository record for Elevated Cochlear Adenosine Causes Hearing Loss Via Adora2B Signaling (opens in a new tab)