(Q44671768)

English

Extensive changes in liver gene expression induced by hereditary tyrosinemia type I are not normalized by treatment with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC).

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Europe PubMed Central

PubMed publication ID

5 December 2017

Extensive changes in liver gene expression induced by hereditary tyrosinemia type I are not normalized by treatment with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC). (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

tyrosinemia type I

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inferred from title

author name string

Marjanka C Luijerink

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Saskia M M Jacobs

2

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Europe PubMed Central

PubMed publication ID

5 December 2017

Ellen A C M van Beurden

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Leander P Koornneef

4

1 reference

Europe PubMed Central

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5 December 2017

Leo W J Klomp

5

1 reference

Europe PubMed Central

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5 December 2017

Ruud Berger

6

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5 December 2017

Inge E T van den Berg

7

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5 December 2017

publication date

1 December 2003

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Europe PubMed Central

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5 December 2017

Journal of Hepatology

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Europe PubMed Central

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5 December 2017

39

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Europe PubMed Central

PubMed publication ID

5 December 2017

6

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Europe PubMed Central

PubMed publication ID

5 December 2017

901-909

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

The mutagenicity of the tyrosine metabolite, fumarylacetoacetate, is enhanced by glutathione depletion

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Cyclin B-dependent kinase and caspase-1 activation precedes mitochondrial dysfunction in fumarylacetoacetate-induced apoptosis.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Hepatocyte injury in tyrosinemia type 1 is induced by fumarylacetoacetate and is inhibited by caspase inhibitors

1 reference

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7 January 2021

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inferred from DOI database lookup

Fumarylacetoacetate, the metabolite accumulating in hereditary tyrosinemia, activates the ERK pathway and induces mitotic abnormalities and genomic instability

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase

1 reference

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7 January 2021

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Nontransplant treatment of tyrosinemia

1 reference

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Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice.

1 reference

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7 January 2021

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inferred from DOI database lookup

Deficiency of an enzyme of tyrosine metabolism underlies altered gene expression in newborn liver of lethal albino mice.

1 reference

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Rescue of mice homozygous for lethal albino deletions: implications for an animal model for the human liver disease tyrosinemia type 1

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term therapy with NTBC and tyrosine-restricted diet in a murine model of hereditary tyrosinemia type I.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Two genetically defined trans-acting loci coordinately regulate overlapping sets of liver-specific genes

1 reference

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based on heuristic

inferred from DOI database lookup

Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

1 reference

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based on heuristic

inferred from DOI database lookup

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

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based on heuristic

inferred from DOI database lookup

Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione).

1 reference

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based on heuristic

inferred from DOI database lookup

Role of the aromatic hydrocarbon receptor and [Ah] gene battery in the oxidative stress response, cell cycle control, and apoptosis

1 reference

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based on heuristic

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Complete rescue of lethal albino c14CoS mice by null mutation of 4-hydroxyphenylpyruvate dioxygenase and induction of apoptosis of hepatocytes in these mice by in vivo retrieval of the tyrosine catabolic pathway

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Biochemical studies of a patient with hereditary hepatorenal tyrosinemia: evidence of glutathione deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900433-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal glutathione conjugation in patients with tyrosinaemia type I

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900433-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparison of oxidative stress response parameters in newborn mouse liver versus simian virus 40 (SV40)-transformed hepatocyte cell lines

1 reference

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7 January 2021

based on heuristic

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The H2O2 stimulon in Saccharomyces cerevisiae

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Yap1 and Skn7 control two specialized oxidative stress response regulons in yeast.

1 reference

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7 January 2021

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Genomic expression programs in the response of yeast cells to environmental changes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0168-8278(03)00433-1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

release_k54rmjso5faefp57jne7h44wii

1 reference

https://api.fatcat.wiki/v0/release/k54rmjso5faefp57jne7h44wii

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

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