Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26-Reference-Cited by-同舟云学术

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Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26

Published:2019-03 Issue:3 Volume:1866 Page:518-531
ISSN:0167-4889
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Cell Research

Author:

Guder Philipp,Lotz-Havla Amelie S.,Woidy Mathias,Reiß Dunja D.,Danecka Marta K.,Schatz Ulrich A.,Becker Marc,Ensenauer Regina,Pagel Philipp,Büttner Lars,Muntau Ania C.,Gersting Søren W.

Funder

Bavarian Genome Research Network

LMUexcellent

Federal Ministry of Education and Research

Fritz Thyssen Stiftung

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference75 articles.

1. Peroxisome biogenesis disorders in the Zellweger spectrum: an overview of current diagnosis, clinical manifestations, and treatment guidelines;Braverman;Mol. Genet. Metab.,2016

2. The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders;Ferdinandusse;J. Inherit. Metab. Dis.,2016

3. Human disorders of peroxisome metabolism and biogenesis;Waterham;Biochim. Biophys. Acta,2016

4. Metabolic functions of peroxisomes in health and disease;Wanders;Biochimie,2014

5. Peroxisomes take shape;Smith;Nat. Rev. Mol. Cell Biol.,2013

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Insights into the Structure and Function of the Pex1/Pex6 AAA-ATPase in Peroxisome Homeostasis;Cells;2022-06-29

2. Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency;Frontiers in Genetics;2021-11-04

3. PEX26 gene genotype-phenotype correlation in neonates with Zellweger syndrome;Translational Pediatrics;2021-07

4. A novel mutation in the PEX26 gene in a family from Dagestan with members affected by Zellweger spectrum disorder;Molecular Genetics and Metabolism Reports;2021-06

5. Identification of a Homozygous PEX26 Mutation in a Heimler Syndrome Patient;Genes;2021-04-26

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