Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata
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Peroxisomes in brain development and functionMolecular regulators of nerve conduction - Lessons from inherited neuropathies and rodent genetic modelsAlkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient miceDefects 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 miceHomeostasis of phospholipids - The level of phosphatidylethanolamine tightly adapts to changes in ethanolamine plasmalogens.Peripheral nervous system plasmalogens regulate Schwann cell differentiation and myelination.A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeletonDrosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomesA PEX7-centered perspective on the peroxisomal targeting signal type 2-mediated protein import pathway.Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome.The neurology of rhizomelic chondrodysplasia punctata.Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models.Tysnd1 deficiency in mice interferes with the peroxisomal localization of PTS2 enzymes, causing lipid metabolic abnormalities and male infertility.Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice.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 modelsPeroxisomes, myelination, and axonal integrity in the CNS.Peroxisome biogenesis disorders: Biological, clinical and pathophysiological perspectives.Plasmalogens and fatty alcohols in rhizomelic chondrodysplasia punctata and Sjögren-Larsson syndrome.Peroxisomal Disorders: A Review on Cerebellar Pathologies.Structural and functional roles of ether lipids.Plasmalogen homeostasis - regulation of plasmalogen biosynthesis and its physiological consequence in mammals.Fatty acid metabolism by the osteoblast.From peroxisomal disorders to common neurodegenerative diseases - the role of ether phospholipids in the nervous system.Association between peroxisomal biogenesis factor 7 and autism spectrum disorders in a Korean population.Differential contribution of two peroxisomal protein receptors to the maintenance of peroxisomal functions in Arabidopsis.Peroxisome biogenesis disorders.Role of Hydroxysteroid Dehydrogenase-Like 2 (HSDL2) in Human Ovarian Cancer.Rhizomelic chondrodysplasia punctata type 1 and fulminant neonatal respiratory failure, a case report and discussion of pathophysiology
P2860
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P2860
Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata
description
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2003
@ast
im September 2003 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
@en
vedecký článok (publikovaný 2003/09/15)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/09/15)
@nl
наукова стаття, опублікована у вересні 2003
@uk
مقالة علمية (نشرت في 15-9-2003)
@ar
name
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@ast
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@en
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@nl
type
label
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@ast
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@en
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@nl
prefLabel
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@ast
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@en
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@nl
P2093
P50
P921
P356
P1476
Impaired neuronal migration an ...... elic chondrodysplasia punctata
@en
P2093
Alison M. Motley
Hans R. Waterham
Ingrid Ploegaert
Luc Schoonjans
Marinus Duran
Myriam Baes
Petra A. W. Mooyer
Vincent Everts
P304
P356
10.1093/HMG/DDG236
P577
2003-09-15T00:00:00Z