Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 6 of 6 for “"MPZ"”.
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Comparing Schools: From Value Added to Sound Policy
… Student Value Added (SVA), and Mean Prior Z (MPZ). The models are compared based on four properties: fairness, stability, validity, and transparency. I find that the Similar Schools Comparisons (SSC) model is more stable than SGP and SVA, but similar to MPZ. On fairness, defined as the …
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Untersuchungen zur neurogenen Differenzierung von humanen mesenchymalen Stammzellen gewonnen aus dem Knochenmark und aus trabekulären Knochenfragmenten
… und zeigten eine Expression der für Myelinmarker MPZ und PMP 22 sowie des Schwann-Zell-Markers S 100. Abschließend wurden mhMSCs und bhMSCs für 6 Tage in einem Schwann-Zell-Differenzierungsmedium mit Forskolin kultiviert. Die differenzierten spindelförmigen Zellen zeigten eine für Schwann-Zellen …
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Charcot-Marie-Tooth-Neuropathie Typ 2 : neue Myelinprotein-P0-Punktmutationen und Haplotypenanalyse in europäischen Familien
… for mutations in the myelin protein zero (P0, MPZ) gene that had initially been thought to be exclusively involved in the advent of demyelinating hereditary neuropathies. Three heterozygous single nucleotide changes were detected: two novel missense mutations, Asp61Gly and Tyr119Cys, and the …
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Genetics of hearing impairment and peripheral neuropathy in Mali
… GJB1 (OMIM: 304040), MFN2 (OMIM: 608507), MPZ (OMIM: 159440) genes. HI is the common audiological symptom associated with CMT and is caused by several genes including PMP22 and GJB1. HI and IPN are inherited in autosomal (dominant and recessive), X-linked, and mitochondrial transmission. …
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P0 specific T-cell repertoire in wild-type and P0 deficient mice
Zusammenfassung Das Myelinprotein P0 stellt eine zentrale Komponente für die Stabilität und Funktionalität der Myelinscheiden des peripheren Nervensystems dar. Mutationen des P0-Proteins führen zu verschiedenen, schwer behindernden peripheren Neuropathien wie der Charcot-Marie-Tooth- oder der …
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Zur Differenzierung hereditärer sensomotorischer Neuropathien mittels Mutationsanalyse des P0-Gens an Paraffin-eingebetteten Suralnervenbiopsien
HMSN is a heterogenous entity of genetically determined disorders of the peripheral nervous system. Clinical and morphological data sometimes do not allow to come to a definite diagnosis regarding the subtype of the disease. Therefore, genetic investigations are essential. The present dissertation …