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| - artículu científicu espublizáu en 1999 (ast)
- vědecký článek publikovaný v roce 1999 (cs)
- 1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw)
- наукова стаття, опублікована в жовтні 1999 (uk)
- vedecký článok (publikovaný 1999/10/01) (sk)
- 1999 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy)
- مقالة علمية (نشرت في أكتوبر 1999) (ar)
- article scientifique publié en 1999 (fr)
- wetenschappelijk artikel (gepubliceerd op 1999/10/01) (nl)
- scientific journal article (en)
- im Oktober 1999 veröffentlichter wissenschaftlicher Artikel (de)
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author name string
| - J. F. Mercer
- M. J. Petris
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rdfs:label
| - The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (en)
- The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (nl)
- The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (ast)
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skos:prefLabel
| - The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (en)
- The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (nl)
- The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (ast)
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name
| - The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (en)
- The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (nl)
- The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (ast)
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title
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title
| - The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal (en)
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is cites work
of | - SLC11A1 (formerly NRAMP1) and disease resistance
- Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage
- Cellular copper distribution: a mechanistic systems biology approach
- Copper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B)
- Protein kinase-dependent phosphorylation of the Menkes copper P-type ATPase.
- Copper and genomic stability in mammals
- Copper promotes the trafficking of the amyloid precursor protein
- Autoantigen Golgin-97, an effector of Arl1 GTPase, participates in traffic from the endosome to the trans-golgi network
- The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein
- MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy
- Structure, Function, and Regulation of a Subfamily of Mouse Zinc Transporter Genes
- Signals regulating trafficking of Menkes (MNK; ATP7A) copper-translocating P-type ATPase in polarized MDCK cells
- Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A
- ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
- Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes ATPase
- Copper stimulates trafficking of a distinct pool of the Menkes copper ATPase (ATP7A) to the plasma membrane and diverts it into a rapid recycling pool
- Cell biology of membrane trafficking in human disease
- Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps
- Advances in the understanding of mammalian copper transporters
- Molecular mechanisms of copper uptake and distribution
- RAB-6.2 and the retromer regulate glutamate receptor recycling through a retrograde pathway
- Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes
- Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance
- Copper metalloregulation of gene expression
- Regulated transport of the glucose transporter GLUT4
- Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.
- Copper-stimulated endocytosis and degradation of the human copper transporter, hCtr1
- The mechanism of copper uptake mediated by human CTR1: a mutational analysis.
- Actin and microtubule regulation of trans-Golgi network architecture, and copper-dependent protein transport to the cell surface
- Iron Imports. V. Transport of iron through the intestinal epithelium
- Zn Transporter Levels and Localization Change Throughout Lactation in Rat Mammary Gland and Are Regulated by Zn in Mammary Cells
- Effects of copper supplementation on copper absorption, tissue distribution, and copper transporter expression in an infant rat model
- What can flies tell us about copper homeostasis?
- Functional understanding of the versatile protein copper metabolism MURR1 domain 1 (COMMD1) in copper homeostasis
- The transcytosis of divalent metal transporter 1 and apo-transferrin during iron uptake in intestinal epithelium
- A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation.
- COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux
- Mycobacteria, metals, and the macrophage
- Posttranslational regulation of copper transporters
- Trace elements in human physiology and pathology. Copper
- Understanding the mechanism and function of copper P-type ATPases
- A single PDZ domain protein interacts with the Menkes copper ATPase, ATP7A. A new protein implicated in copper homeostasis
- Copper-regulated trafficking of the Menkes disease copper ATPase is associated with formation of a phosphorylated catalytic intermediate
- Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking
- "Pulling the plug" on cellular copper: the role of mitochondria in copper export
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