Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage. - Wikidata - wikimedia - TriplyDB

Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage.

Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage.

http://www.wikidata.org/entity/Q36292959

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Charting the travels of copper in eukaryotes from yeast to mammals Mammalian copper-transporting P-type ATPases, ATP7A and ATP7B: emerging roles.Interactions between metal-binding domains modulate intracellular targeting of Cu(I)-ATPase ATP7B, as revealed by nanobody binding.Clusterin (apolipoprotein J), a molecular chaperone that facilitates degradation of the copper-ATPases ATP7A and ATP7B.Upregulated copper transporters in hypoxia-induced pulmonary hypertension.ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7B Host-Imposed Copper Poisoning Impacts Fungal Micronutrient Acquisition during Systemic Candida albicans Infections Molecular events initiating exit of a copper-transporting ATPase ATP7B from the trans-Golgi network The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders.Cellular transport and homeostasis of essential and nonessential metals.Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis.Copper transport in mammalian cells: special care for a metal with special needs.Human copper transporters: mechanism, role in human diseases and therapeutic potential.Orchestration of dynamic copper navigation - new and missing pieces.Anticancer activity of a chelating nitrogen mustard bearing tetrachloridoplatinum(iv) complex: better stability yet equipotent to the Pt(ii) analogue.Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin.Comparative features of copper ATPases ATP7A and ATP7B heterologously expressed in COS-1 cells.The six metal binding domains in human copper transporter, ATP7B: molecular biophysics and disease-causing mutations.HUMAN COPPER TRANSPORTER ATP7B (WILSON DISEASE PROTEIN) FORMS STABLE DIMERS IN VITRO AND IN CELLS.Dynamic changes in copper homeostasis and post-transcriptional regulation of Atp7a during myogenic differentiation.Full-length cellular β-secretase has a trimeric subunit stoichiometry, and its sulfur-rich transmembrane interaction site modulates cytosolic copper compartmentalization.Anticancer activity of a cis-dichloridoplatinum(ii) complex of a chelating nitrogen mustard: insight into unusual guanine binding mode and low deactivation by glutathione.

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P2860

Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage.

http://www.wikidata.org/entity/Q36292959

description

2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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2009年學術文章

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Cell-specific trafficking sugg ...... intracellular copper storage.

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Ann L Hubbard

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Arnab Gupta

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Jack H Kaplan

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Lita Braiterman

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Mee Y Bartee

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Natalie Barnes

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Svetlana Lutsenko

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Vesna Zuzel

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Vladimir Ustiyan

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P2860

The Menkes copper transporter is required for the activation of tyrosinase

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: a novel mechanism of regulated trafficking

WIF-B cells: an in vitro model for studies of hepatocyte polarity

Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

Isolation of a partial candidate gene for Menkes disease by positional cloning

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

Stable plasma membrane levels of hCTR1 mediate cellular copper uptake

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

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