Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes

The peroxisome biogenesis disorders (PBDs) are currently difficult-to-treat multiple-organ dysfunction disorders that result from the defective biogenesis of peroxisomes. Genes encoding Peroxins, which are required for peroxisome biogenesis or functions, are known causative genes of PBDs. The human...

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Hlavní autoři: Nakayama, Minoru, Sato, Hiroyasu, Okuda, Takayuki, Fujisawa, Nao, Kono, Nozomu, Arai, Hiroyuki, Suzuki, Emiko, Umeda, Masato, Ishikawa, Hiroyuki O., Matsuno, Kenji
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2011
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3149631/
https://ncbi.nlm.nih.gov/pubmed/21826223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0022984
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