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Investigation of peroxisomal disease entities

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dc.contributor.author Mizuno, Y.
dc.contributor.author Kurochkin, I.
dc.contributor.author Schönbach, C.
dc.contributor.author Okzaki, Y.
dc.date.accessioned 2015-10-30T04:05:18Z
dc.date.available 2015-10-30T04:05:18Z
dc.date.issued 2013
dc.identifier.uri http://nur.nu.edu.kz/handle/123456789/597
dc.description.abstract We applied a sequence- and motif-based, multi-step knowledge discovery strategy to identify novel peroxisome-targeted protein candidates in mouse and human in addition to in vitro and in vivo analyses of mouse regulatory circuits associated with lipid metabolism conditions.The results are likely to be of relevance for some patients with Zellweger Syndrome Spectrum disorders. Detailed structure-function relationships of Tysnd1 with regard to substrate interactions and processing and activation await the determination of its 3D structure. ru_RU
dc.language.iso en ru_RU
dc.publisher Nazarbayev University ru_RU
dc.subject first research week ru_RU
dc.subject peroxisomal disease ru_RU
dc.subject medicine ru_RU
dc.subject scientific research ru_RU
dc.title Investigation of peroxisomal disease entities ru_RU
dc.type Abstract ru_RU


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