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PEX10 gene

Known as: PEROXIN 10, RNF69, peroxisomal biogenesis factor 10 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
PEX10-related autosomal recessive cerebellar ataxia with hearing loss
Peroxisomes are present in all cells with a nucleus and contain many different enzymes. Peroxisomes have an important role in the… 
2017
2017
Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case report
BackgroundThe peroxisome biogenesis disorders, which are caused by mutations in any of 13 different PEX genes, include the… 
2017
2017
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype
2017
2017
Agrobacterium tumefaciens-mediated transformation of oleaginous yeast Lipomyces species
Interest in using renewable sources of carbon, especially lignocellulosic biomass, for the production of hydrocarbon fuels and… 
2016
2016
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia
Peroxisomal biogenesis disorders (PBDs) consist of a heterogeneous group of autosomal recessive diseases, in which peroxisome… 
2013
2013
A caffeine fix for human nuclear transfer?
Efficient human nuclear-transfer embryo cloning is here at last, prompting renewed efforts to explore hidden variables in the… 
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