(Q43882459)

1 July 2018

title

Hereditary low level of plasma ceruloplasmin in LEC rats associated with spontaneous development of hepatitis and liver cancer (English)

1 reference

1 July 2018

author name string

T Ono

series ordinal

1

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1 July 2018

S Abe

series ordinal

2

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1 July 2018

M C Yoshida

series ordinal

3

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1 July 2018

publication date

1 May 1991

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1 July 2018

number of pages

4

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Japanese Journal of Cancer Research

inferred from page(s)

published in

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1 July 2018

volume

82

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1 July 2018

issue

5

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1 July 2018

page(s)

486-489

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1 July 2018

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Investigations on the nature of ceruloplasmin deficiency in the newborn

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Absorption, transport, and hepatic metabolism of copper and zinc: special reference to metallothionein and ceruloplasmin

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

The ontogeny of liver copper metabolism in the guinea pig: clues to the etiology of Wilson's disease

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Molecular studies of ceruloplasmin deficiency in Wilson's disease

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

New mutation causing hereditary hepatitis in the laboratory rat.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Hepatic copper and metallothionein distribution in Wilson's disease (hepatolenticular degeneration).

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Copper transport from Cu(I)-thionein into apo-caeruloplasmin mediated by activated leucocytes

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Complete cDNA sequence of human preceruloplasmin

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

High susceptibility to hepatocellular carcinoma development in LEC rats with hereditary hepatitis.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5918485

Spontaneous hepatitis in Long-Evans rats. A potential animal model for fulminant hepatitis in man

15 August 2018

1 reference

12 December 2020

Expression of the caeruloplasmin gene in the adult and neonatal rat liver

1 reference

12 December 2020

Reinvestigation of some physicochemical and chemical properties of human ceruloplasmin (ferroxidase)

1 reference

12 December 2020

Hereditary hepatitis of LEC rats is controlled by a single autosomal recessive gene

1 reference

12 December 2020

A micromethod for the determination of ferroxidase (ceruloplasmin) in human serums

1 reference

12 December 2020

10.1111/J.1349-7006.1991.TB01875.X

Identifiers

DOI

1 reference

1 July 2018

PMC publication ID

5918485

1 reference

1 July 2018

PubMed publication ID

1905693

1 reference

1 July 2018