Pages that link to "Q35623439"

The following pages link to ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model (Q35623439):

Displaying 31 items.

• Mottled Mice and Non-Mammalian Models of Menkes Disease (Q26770905) (← links)
• Copper signaling in the mammalian nervous system: synaptic effects (Q26849773) (← links)
• Translational research investigations on ATP7A: an important human copper ATPase (Q26996596) (← links)
• Conditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesis (Q28482175) (← links)
• Regulation of copper transport crossing brain barrier systems by Cu-ATPases: effect of manganese exposure (Q29347141) (← links)
• Maternofetal and neonatal copper requirements revealed by enterocyte-specific deletion of the Menkes disease protein (Q30530787) (← links)
• Inborn errors of copper metabolism (Q34429101) (← links)
• Neurodevelopment and brain growth in classic Menkes disease is influenced by age and symptomatology at initiation of copper treatment (Q34617579) (← links)
• Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse model (Q34657353) (← links)
• Investigation of iron metabolism in mice expressing a mutant Menke's copper transporting ATPase (Atp7a) protein with diminished activity (Brindled; Mo (Br) (/y) ). (Q34776142) (← links)
• Wilson's disease and other neurological copper disorders (Q35106874) (← links)
• Increased frequency of congenital heart defects in Menkes disease (Q36064679) (← links)
• In utero copper treatment for Menkes disease associated with a severe ATP7A mutation (Q36240640) (← links)
• Autonomous requirements of the Menkes disease protein in the nervous system (Q36297557) (← links)
• L-threo-dihydroxyphenylserine corrects neurochemical abnormalities in a Menkes disease mouse model (Q36684997) (← links)
• Fetal Brain-directed AAV Gene Therapy Results in Rapid, Robust, and Persistent Transduction of Mouse Choroid Plexus Epithelia (Q36968202) (← links)
• Copper: an essential metal in biology (Q37031388) (← links)
• Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis (Q37112824) (← links)
• Diagnostic copper imaging of Menkes disease by synchrotron radiation-generated X-ray fluorescence analysis (Q37257560) (← links)
• Progress in gene therapy for neurological disorders. (Q38100997) (← links)
• Catecholamine metabolites affected by the copper-dependent enzyme dopamine-beta-hydroxylase provide sensitive biomarkers for early diagnosis of menkes disease and viral-mediated ATP7A gene therapy. (Q38140162) (← links)
• Copper trafficking to the secretory pathway (Q38559272) (← links)
• Bioavailable Trace Metals in Neurological Diseases (Q38967236) (← links)
• Drosophila melanogaster Models of Metal-Related Human Diseases and Metal Toxicity (Q39419474) (← links)
• Varicella-zoster virus ORF7 interacts with ORF53 and plays a role in its trans-Golgi network localization. (Q45325126) (← links)
• Localization of copper and copper transporters in the human brain. (Q48331794) (← links)
• New insights into CNS requirements for the copper-ATPase, ATP7A. Focus on "Autonomous requirements of the Menkes disease protein in the nervous system". (Q50559602) (← links)
• Menkes disease with discordant phenotype in female monozygotic twins. (Q53396365) (← links)
• Cerebrospinal Fluid-Directed rAAV9-rsATP7A Plus Subcutaneous Copper Histidinate Advance Survival and Outcomes in a Menkes Disease Mouse Model (Q59354904) (← links)
• Estimated birth prevalence of Menkes disease and ATP7A-related disorders based on the Genome Aggregation Database (gnomAD) (Q96304586) (← links)
• Targeted next generation sequencing for newborn screening of Menkes disease (Q97885766) (← links)