(Q34662081)

3 August 2017

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title

Metal transporters and disease (English)

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3 August 2017

1

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3 August 2017

publication date

1 April 2002

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Current Opinion in Chemical Biology

3 August 2017

published in

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3 August 2017

volume

6

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3 August 2017

issue

2

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3 August 2017

page(s)

181-186

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

3 August 2017

1 reference

7 January 2021

Cloning and characterization of a mammalian proton-coupled metal-ion transporter

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

The iron transport protein NRAMP2 is an integral membrane glycoprotein that colocalizes with transferrin in recycling endosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Nramp 2 (DCT1/DMT1) expressed at the plasma membrane transports iron and other divalent cations into a calcein-accessible cytoplasmic pool

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

An iron-regulated ferric reductase associated with the absorption of dietary iron

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

A novel mammalian iron-regulated protein involved in intracellular iron metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Chemistry and biology of eukaryotic iron metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Characterization of the hCTR1 gene: genomic organization, functional expression, and identification of a highly homologous processed gene

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Essential role for mammalian copper transporter Ctr1 in copper homeostasis and embryonic development

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

The molecular basis of copper-transport diseases

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Structure and chemistry of the copper chaperone proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Binding to the transferrin receptor is required for endocytosis of HFE and regulation of iron homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Interactions of the ectodomain of HFE with the transferrin receptor are critical for iron homeostasis in cells

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Congenital Atransferrinemia A Case Report and Review of the Literature

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

The cell biology of the Menkes disease protein.

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900307-1

7 January 2021

10.1016/S1367-5931(02)00307-1

Identifiers

DOI

1 reference

3 August 2017

1 reference