Copper transport and its alterations in Menkes and Wilson diseases. (Q41374951)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061035%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

review article

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title

Copper transport and its alterations in Menkes and Wilson diseases (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061035%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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1

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1 November 2019

author name string

B Sarkar

series ordinal

2

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1 November 2019

publication date

1 February 1997

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Biochimica et Biophysica Acta

1 November 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061035%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

1360

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1 November 2019

page(s)

3-16

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1 November 2019

issue

1

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

1 November 2019

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

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

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7 January 2021

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

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7 January 2021

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

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7 January 2021

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

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7 January 2021

Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease

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7 January 2021

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OBSERVATIONS ON THE MECHANISM OF ABSORPTION OF COPPER BY THE SMALL INTESTINE

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Copper absorption and retention in young men at three levels of dietary copper by use of the stable isotope 65Cu

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Dietary ascorbic acid lowers the concentration of soluble copper in the small intestinal lumen of rats

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Studies on copper metabolism. XIII. Hepatolenticular degeneration

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The effect of dietary zinc on intestinal copper absorption

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The effect of cadmium on intestinal copper absorption and binding in the rat

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THE INCORPORATION OF COPPER INTO CERULOPLASMIN IN VIVO: STUDIES WITH COPPER AND COPPER

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7 January 2021

Metabolism of copper in Wilson's disease and in normal subjects; studies with Cu-64

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7 January 2021

The state of copper in human serum: evidence for an amino acid-bound fraction

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7 January 2021

Evidence for albumin--cu(II)--amino acid ternary complex

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7 January 2021

Copper-histidine therapy for Menkes disease

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7 January 2021

Early copper-histidine treatment for Menkes disease

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7 January 2021

The influence of amino acids on copper uptake by rat liver slices

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7 January 2021

Uptake of 67Cu by isolated human trophoblast cells

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7 January 2021

Synthesis of the native copper(II)-transport site of human serum albumin and its copper(II)-binding properties

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7 January 2021

Characterization of the copper(II)- and nickel(II)-transport site of human serum albumin. Studies of copper(II) and nickel(II) binding to peptide 1-24 of human serum albumin by 13C and 1H NMR spectroscopy

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7 January 2021

Circulating ceruloplasmin is an important source of copper for normal and malignant animal cells

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7 January 2021

Evidence for ceruloplasmin as a copper transport protein

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7 January 2021

Regulation of aortic CuZn-superoxide dismutase with copper. Caeruloplasmin and albumin re-activate and transfer copper to the enzyme in culture

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7 January 2021

Copper transport from ceruloplasmin: characterization of the cellular uptake mechanism

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7 January 2021

Ascorbate enhances copper transport from ceruloplasmin into human K562 cells

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7 January 2021

Ceruloplasmin receptors of erythrocytes

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7 January 2021

Ceruloplasmin receptors in liver cell suspensions are limited to the endothelium

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7 January 2021

Binding and uptake of copper from ceruloplasmin.

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7 January 2021

Specific receptor for ceruloplasmin in membrane fragments from aortic and heart tissues

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7 January 2021

Copper deficiency in the mitochondria of cultured skin fibroblasts from patients with Menkes syndrome

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7 January 2021

Secretion of lysyl oxidase by cultured human skin fibroblasts and effects of monensin, nigericin, tunicamycin and colchicine

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7 January 2021

Immunohistochemical demonstration of the cytoplasmic copper-associated protein in the liver in primary biliary cirrhosis: its identification as metallothionein

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7 January 2021

The lysosomal copper concentration in the liver in primary biliary cirrhosis

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7 January 2021

Copper(I) transfer into metallothionein mediated by glutathione

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7 January 2021

Reconstitution of ceruloplasmin by the Cu(I)-glutathione complex. Evidence for a role of Mg2+ and ATP

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7 January 2021

Binding of copper by human alimentary secretions

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7 January 2021

DISTRIBUTION OF COPPER IN THE RAT.

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7 January 2021

PROGRESSIVE LENTICULAR DEGENERATION: A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER

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7 January 2021

Copper metallothionein in patients with hepatic copper overload

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7 January 2021

Copper distribution among serum proteins in paediatric liver disorders and malignancies

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7 January 2021

The intracellular distribution of the radiocopper derived from ceruloplasmin and from albumin

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7 January 2021

Characterisation of the copper uptake mechanism and isolation of the ceruloplasmin receptor/copper transporter in human placental vesicles

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7 January 2021

The role of ceruloplasmin in iron metabolism

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7 January 2021

The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease).

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7 January 2021

Penicillamine, a new oral therapy for Wilson's disease

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7 January 2021

Wilson's disease. Development of neurological disease after beginning penicillamine therapy

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7 January 2021

Development of neurologic symptoms in a patient with asymptomatic Wilson's disease treated with penicillamine

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7 January 2021

Treatment of Wilson's disease with trientine (triethylene tetramine) dihydrochloride

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7 January 2021

The use of trientine in preventing the effects of interrupting penicillamine therapy in Wilson's disease

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7 January 2021

Copper: its role in the pathogenesis of liver disease

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7 January 2021

Treatment of Wilson's disease with ammonium tetrathiomolybdate. I. Initial therapy in 17 neurologically affected patients.

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7 January 2021

Oral zinc sulphate for Wilson's disease

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7 January 2021

Oral zinc in Wilson's disease

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7 January 2021

Oral zinc sulphate as long-term treatment in Wilson's disease (hepatolenticular degeneration)

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7 January 2021

Wilson's disease treated with trientine during pregnancy

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7 January 2021

Treatment of Wilson's disease: in D-penicillamine we trust--what about zinc?

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7 January 2021

Oral zinc therapy for Wilson's disease

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7 January 2021

Vitamin D and osteocalcin levels in liver transplant recipients. Is osteocalcin a reliable marker of bone turnover in such cases?

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7 January 2021

Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions

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7 January 2021

Induction of the putative copper ATPases, CopA and CopB, of Enterococcus hirae by Ag+ and Cu2+, and Ag+ extrusion by CopB.

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7 January 2021

The Wilson disease gene: spectrum of mutations and their consequences.

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7 January 2021

Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat.

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7 January 2021

The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene

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7 January 2021

The gene responsible for LEC hepatitis, located on rat chromosome 16, is the homolog to the human Wilson disease gene

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7 January 2021

Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis. A model of Wilson's disease

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7 January 2021

Failure of copper incorporation into ceruloplasmin in the Golgi apparatus of LEC rat hepatocytes

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7 January 2021

Toxic milk, a new mutation affecting cooper metabolism in the mouse

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7 January 2021

Menkes' kinky-hair syndrome.

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7 January 2021

Menkes' kinky hair disease: further definition of the defect in copper transport.

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7 January 2021

Uptake and efflux of copper-64 in Menkes'-disease and normal continuous lymphoid cell lines

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7 January 2021

Cell culture studies of Menkes kinky hair disease

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7 January 2021

64Cu metabolism in Menkes and normal cultured skin fibroblasts

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7 January 2021

Abnormal copper metabolism in menkes cultured fibroblasts

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7 January 2021

Metallothionein in Menkes' disease: induction in cultured muscle cells

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7 January 2021

Kinky hair disease: twenty five years later.

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7 January 2021

Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder.

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7 January 2021

Alterations in copper and collagen metabolism in Menkes' syndrome and a new subtype of Ehlers-Danlos syndrome

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7 January 2021

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7 January 2021

Comparisons of copper deficiency states in the murine mutants blotchy and brindled. Changes in copper-dependent enzyme activity in 13-day-old mice

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7 January 2021

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease

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7 January 2021

Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2

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7 January 2021

An ATPase operon involved in copper resistance by Enterococcus hirae.

1 reference

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7 January 2021

Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0925-4439%2896%2900064-6

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7 January 2021

The failure of parenteral copper therapy in Menkes Kinky Hair syndrome.

1 reference

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7 January 2021

Uptake of 67copper complexed to 3H-histidine by brain hypothalamic slices: evidence that dissociation of the complex is not the only factor determining 67copper uptake.

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7 January 2021

Further characterization of the process of in vitro uptake of radiolabeled copper by the rat brain

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7 January 2021

Clinical and biochemical consequences of copper-histidine therapy in Menkes disease.

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7 January 2021

Copper metabolism in mottled mouse mutants. The effect of copper therapy on lysyl oxidase activity in brindled (Mobr) mice

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7 January 2021

Primary defect in copper transport underlies mottled mutants in the mouse

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7 January 2021

Of mice and men, metals and mutations.

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7 January 2021

The mottled gene is the mouse homologue of the Menkes disease gene

1 reference

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7 January 2021

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

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7 January 2021

Expression of the Menkes gene homologue in mouse tissues lack of effect of copper on the mRNA levels

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7 January 2021

10.1016/S0925-4439(96)00064-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061035%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference