Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease. - Wikidata - wikimedia - TriplyDB

Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease.

Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease.

http://www.wikidata.org/entity/Q36088166

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Mottled Mice and Non-Mammalian Models of Menkes Disease Exposure to sodium metam during zebrafish somitogenesis results in early transcriptional indicators of the ensuing neuronal and muscular dysfunction Adaptor Protein-1 Complex Affects the Endocytic Trafficking and Function of Peptidylglycine α-Amidating Monooxygenase, a Luminal Cuproenzyme Pam heterozygous mice reveal essential role for Cu in amygdalar behavioral and synaptic function Elevated adult neurogenesis in brain subventricular zone following in vivo manganese exposure: roles of copper and DMT1.Optimizing production of Fc-amidated peptides by Chinese hamster ovary cells Neuronal copper homeostasis susceptibility by genetic defects in dysbindin, a schizophrenia susceptibility factor.Increased apoptosis and hypomyelination in cerebral white matter of macular mutant mouse brain.The genetics of essential metal homeostasis during development Peptidylgycine α-amidating monooxygenase and copper: a gene-nutrient interaction critical to nervous system function.Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis.Therapeutics for Alzheimer's disease based on the metal hypothesis Aberrant Adult Neurogenesis in the Subventricular Zone-Rostral Migratory Stream-Olfactory Bulb System Following Subchronic Manganese Exposure Interactions of peptide amidation and copper: novel biomarkers and mechanisms of neural dysfunction.Peptidylglycine α-amidating monooxygenase heterozygosity alters brain copper handling with region specificity.Zebrafish in the sea of mineral (iron, zinc, and copper) metabolism.Genetic and biologic classification of infantile spasms.Copper metabolism of astrocytes.Understanding copper sensitivity in zebrafish (Danio rerio) through the intracellular localization of copper transporters in a hepatocyte cell-line ZFL and the tissue expression profiles of copper transporters.Atp7a and Atp7b regulate copper homeostasis in developing male germ cells in mice.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".Functional significance of the copper transporter ATP7 in peptidergic neurons and endocrine cells in Drosophila melanogaster.Metabolic etiologies in West syndrome.

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P2860

Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease.

http://www.wikidata.org/entity/Q36088166

description

2007 nî lūn-bûn

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J.NBD.2007.05.004

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Neurobiology of Disease

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Altered ATP7A expression and o ...... urine model of Menkes disease.

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Betty A Eipper

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Joel S Pachter

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Mark J Niciu

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Rajaâ El Meskini

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Richard E Mains

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Xin-Ming Ma

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P2860

betaIV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system

The Menkes copper transporter is required for the activation of tyrosinase

Cholecystokinin modulates migration of gonadotropin-releasing hormone-1 neurons

The copper-transporting ATPases, menkes and wilson disease proteins, have distinct roles in adult and developing cerebellum

The copper transporter CTR1 provides an essential function in mammalian embryonic development

Metabolic consequences of the cytochrome c oxidase deficiency in brain of copper-deficient Mo(vbr) mice

Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity

Copper, zinc-superoxide dismutase protein but not mRNA is lower in copper-deficient mice and mice lacking the copper chaperone for superoxide dismutase

Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development

Menkes protein contributes to the function of peptidylglycine alpha-amidating monooxygenase

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278-291

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10.1016/J.NBD.2007.05.004

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