Results 171 to 180 of about 1,135,071 (192)

Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis Defect

Frontiers in Cell and Developmental Biology, 2021
Hans Waterham, Ronald Wanders, Kim Falkenberg   +2 more
exaly  

Hypomorphic mutation of PEX3 with peroxisomal mosaicism reveals the oscillating nature of peroxisome biogenesis coupled with differential metabolic activities

Molecular Genetics and Metabolism, 2022
Shigeo Takashima, Kentaro Oh-Hashi, Yoko Hirata   +2 more
exaly  

Peroxisome Biogenesis and Human Peroxisomal Disorders

Biochemical Society Transactions, 2000
openaire   +2 more sources

An overview of peroxisomal biogenesis disorders

Molecular Genetics and Metabolism, 2005
openaire   +2 more sources

Sequential lipidomic, metabolomic, and proteomic analyses of serum, liver, and heart tissue specimens from peroxisomal biogenesis factor 11α knockout mice

Analytical and Bioanalytical Chemistry, 2022
Claudia Colasante, Baumgart-Vogt E And Baumgart E, Bernhard Spengler   +2 more
exaly  

Novel retinal findings in peroxisomal biogenesis disorders

Ophthalmic Genetics, 2018
Gregg Lueder
exaly  

A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 °C

Journal of Human Genetics, 2007
Hans Waterham, Ronald Wanders, Andréea Nissenkorn   +2 more
exaly  

A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder

American Journal of Medical Genetics, Part A, 2010
Ronald Wanders
exaly  

A novel mutation in the PEX12 gene causing a peroxisomal biogenesis disorder

Molecular Biology Reports, 2015
Jana Konkolova, Robert Petrović, Jan Chandoga   +2 more
exaly  

The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders

Autophagy, 2017
Peter K Kim, John Brumell, Ann Moser
exaly