Iron overload and gene expression in HepG2 cells: analysis by differential display (Q40894379)

24 September 2017

Iron overload and gene expression in HepG2 cells: analysis by differential display (English)

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24 September 2017

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Barisani D

1

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24 September 2017

Meneveri R

2

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24 September 2017

Ginelli E

3

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24 September 2017

Cassani C

4

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24 September 2017

Conte D

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24 September 2017

language of work or name

English

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publication date

1 March 2000

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24 September 2017

5

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inferred from page(s)

published in

FEBS Letters

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24 September 2017

469

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24 September 2017

2-3

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24 September 2017

208-212

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Role of free radicals and catalytic metal ions in human disease: an overview

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Iron regulates nitric oxide synthase activity by controlling nuclear transcription

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Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction

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Gluconate metabolism of Pasteurellapestis

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Rapid selection and classification of positive clones generated by mRNA differential display

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Organization of the human transferrin gene: direct evidence that it originated by gene duplication

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4-hydroxy-2,3-trans-nonenal induces transcription and expression of aldose reductase.

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Regulation of ferritin and transferrin receptor expression by iron in human hepatocyte cultures

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Nitric oxide reduces nontransferrin-bound iron transport in HepG2 cells

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Dietary iron overload and induced lipid peroxidation are associated with impaired plasma lipid transport and hepatic sterol metabolism in rats

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Liver gene expression during chronic dietary iron overload in rats

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Oxidative stress and cytotoxicity induced by ferric-nitrilotriacetate in HepG2 cells that express cytochrome P450 2E1.

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Aldose reductase induction: a novel response to oxidative stress of smooth muscle cells

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inferred from DOI database lookup

7 January 2021

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Identifiers

DOI

10.1016/S0014-5793(00)01280-1

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24 September 2017

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