ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model
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Mottled Mice and Non-Mammalian Models of Menkes DiseaseCopper signaling in the mammalian nervous system: synaptic effectsTranslational research investigations on ATP7A: an important human copper ATPaseConditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesisRegulation of copper transport crossing brain barrier systems by Cu-ATPases: effect of manganese exposureMaternofetal and neonatal copper requirements revealed by enterocyte-specific deletion of the Menkes disease protein.Inborn errors of copper metabolism.Neurodevelopment and brain growth in classic Menkes disease is influenced by age and symptomatology at initiation of copper treatment.Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse modelInvestigation of iron metabolism in mice expressing a mutant Menke's copper transporting ATPase (Atp7a) protein with diminished activity (Brindled; Mo (Br) (/y) ).Wilson's disease and other neurological copper disorders.Increased frequency of congenital heart defects in Menkes diseaseIn utero copper treatment for Menkes disease associated with a severe ATP7A mutationAutonomous requirements of the Menkes disease protein in the nervous system.L-threo-dihydroxyphenylserine corrects neurochemical abnormalities in a Menkes disease mouse modelFetal Brain-directed AAV Gene Therapy Results in Rapid, Robust, and Persistent Transduction of Mouse Choroid Plexus EpitheliaCopper: an essential metal in biologyRole of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis.Diagnostic copper imaging of Menkes disease by synchrotron radiation-generated X-ray fluorescence analysisProgress in gene therapy for neurological disorders.Copper trafficking to the secretory pathway.Bioavailable Trace Metals in Neurological Diseases.Drosophila melanogaster Models of Metal-Related Human Diseases and Metal Toxicity.Varicella-zoster virus ORF7 interacts with ORF53 and plays a role in its trans-Golgi network localization.Localization of copper and copper transporters in the human brain.New insights into CNS requirements for the copper-ATPase, ATP7A. Focus on "Autonomous requirements of the Menkes disease protein in the nervous system".Menkes disease with discordant phenotype in female monozygotic twins.
P2860
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P2860
ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model
description
2011 nî lūn-bûn
@nan
2011年の論文
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2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
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2011年论文
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2011年论文
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name
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@ast
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@en
type
label
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@ast
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@en
prefLabel
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@ast
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@en
P2093
P2860
P356
P1433
P1476
ATP7A gene addition to the cho ...... n a Menkes disease mouse model
@en
P2093
David S Goldstein
Elisabeth Rushing
Jose A Centeno
Joseph Prohaska
Lauren R Brinster
Patricia M Zerfas
Patricia Sullivan
Stephen G Kaler
P2860
P304
P356
10.1038/MT.2011.143
P577
2011-08-30T00:00:00Z