RNAi-mediated silencing of ABCD3 gene expression in rat C6 glial cells: A model system to study PMP70 function-Reference-Cited by-同舟云学术

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RNAi-mediated silencing of ABCD3 gene expression in rat C6 glial cells: A model system to study PMP70 function

Published:2008-05 Issue:6 Volume:52 Page:1106-1113
ISSN:0197-0186
Container-title:Neurochemistry International
language:en
Short-container-title:Neurochemistry International

Author:

Di Benedetto Rita,Denti Michela Alessandra,Salvati Serafina,Sanchez Massimo,Attorri Lucilla,David Giulia,Di Biase Antonella

Publisher

Elsevier BV

Subject

Cell Biology,Cellular and Molecular Neuroscience

Reference39 articles.

1. Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy;Asheuer;Hum. Mol. Gen.,2005

2. Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (Pex5 knockout mouse);Baumgart;Am. J. Pathol.,2001

3. X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects;Berger;Biochim. Biophys. Acta,2006

4. The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression;Berger;Eur. J. Biochem.,1999

5. Suppression of peroxisomal membrane protein defects by ATP-binding cassette (ABC) proteins;Braiterman;Hum. Mol. Genet.,1998

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2. 1q42.12q42.2 Deletion in a Child with Midline Defects and Hypoplasia of the Corpus Callosum;Molecular Syndromology;2019

3. Functional Characterization of IPSC-Derived Brain Cells as a Model for X-Linked Adrenoleukodystrophy;PLOS ONE;2015-11-18

4. Peroxisomal ABC transporters: functions and mechanism;Biochemical Society Transactions;2015-10-01

5. A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3;Human Molecular Genetics;2014-08-28

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