Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype
about
Peroxisomes in brain development and functionThe Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder.Peroxisomes are required for lipid metabolism and muscle function in Drosophila melanogasterIdentifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.Redox interplay between mitochondria and peroxisomesDefects in myelination, paranode organization and Purkinje cell innervation in the ether lipid-deficient mouse cerebellumOverexpression of peroxisomal testis-specific 1 protein induces germ cell apoptosis and leads to infertility in male micealpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disorders.Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse.Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomesA New Immunomodulatory Role for Peroxisomes in Macrophages Activated by the TLR4 Ligand Lipopolysaccharide.Transcriptional coactivator PGC-1alpha promotes peroxisomal remodeling and biogenesisPEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress.Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models.Peroxisomes in dental tissues of the mouse.Deletion of a single allele of the Pex11β gene is sufficient to cause oxidative stress, delayed differentiation and neuronal death in mouse brainPeroxisomes in Different Skeletal Cell Types during Intramembranous and Endochondral Ossification and Their Regulation during Osteoblast Differentiation by Distinct Peroxisome Proliferator-Activated Receptors.Peroxisome deficient invertebrate and vertebrate animal modelsPeroxisome biogenesis and human peroxisome-deficiency disorders.Peroxisomal protein PEX13 functions in selective autophagy.Genetic Coding Variant in GPR65 Alters Lysosomal pH and Links Lysosomal Dysfunction with Colitis Risk.The biogenesis protein PEX14 is an optimal marker for the identification and localization of peroxisomes in different cell types, tissues, and species in morphological studies.
P2860
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P2860
Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype
description
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2003
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im August 2003 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2003/08/01)
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vědecký článek publikovaný v roce 2003
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wetenschappelijk artikel (gepubliceerd op 2003/08/01)
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наукова стаття, опублікована в серпні 2003
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مقالة علمية (نشرت في أغسطس 2003)
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name
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
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Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
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Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@nl
type
label
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@ast
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@en
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@nl
prefLabel
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@ast
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@en
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@nl
P2093
P2860
P1476
Pex13 inactivation in the mous ...... a Zellweger syndrome phenotype
@en
P2093
Barbara C. Paton
Carol Paterson
Denis I. Crane
Graham F. Kay
John Finnie
Jonas Bjorkman
Megan Maxwell
Peter Sharp
Tam Nguyen
P2860
P304
P356
10.1128/MCB.23.16.5947-5957.2003
P407
P577
2003-08-01T00:00:00Z