Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse

Peroxisome biogenesis disorders (PBD) are a group of multi-system human diseases due to mutations in the PEX genes that are responsible for peroxisome assembly and function. These disorders lead to global defects in peroxisomal function and result in severe brain, liver, bone and kidney disease. In...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS Genet
Päätekijät: Wangler, Michael F., Chao, Yu-Hsin, Bayat, Vafa, Giagtzoglou, Nikolaos, Shinde, Abhijit Babaji, Putluri, Nagireddy, Coarfa, Cristian, Donti, Taraka, Graham, Brett H., Faust, Joseph E., McNew, James A., Moser, Ann, Sardiello, Marco, Baes, Myriam, Bellen, Hugo J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2017
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5480855/
https://ncbi.nlm.nih.gov/pubmed/28640802
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006825
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