(Q34757260)

4 August 2017

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title

Tyrosinaemia type I and apoptosis of hepatocytes and renal tubular cells (English)

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4 August 2017

Endo F

1

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4 August 2017

Sun MS

series ordinal

2

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4 August 2017

language of work or name

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1 May 2002

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Journal of Inherited Metabolic Disease

4 August 2017

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4 August 2017

25

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4 August 2017

3

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4 August 2017

227-234

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https://scigraph.springernature.com/pub.10.1023/a:1015646400182

4 August 2017

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cites work

Genetic control of morphogenetic and biochemical differentiation: Lethal albino deletions in the mouse

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12 December 2020

Neurologic crises in hereditary tyrosinemia

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12 December 2020

A mouse model of renal tubular injury of tyrosinemia type 1: development of de Toni Fanconi syndrome and apoptosis of renal tubular cells in Fah/Hpd double mutant mice.

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12 December 2020

On the enzymic defects in hereditary tyrosinemia

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12 December 2020

A murine model for type III tyrosinemia: lack of immunologically detectable 4-hydroxyphenylpyruvic acid dioxygenase enzyme protein in a novel mouse strain with hypertyrosinemia

1 reference

12 December 2020

Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Assay of fumarylacetoacetate fumarylhydrolase in human liver-deficient activity in a case of hereditary tyrosinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A nonsense mutation in the 4-hydroxyphenylpyruvic acid dioxygenase gene (Hpd) causes skipping of the constitutive exon and hypertyrosinemia in mouse strain III.

1 reference

12 December 2020

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

12 December 2020

Ultrastructural basis of biochemical effects in a series of lethal alleles in the mouse. Neonatal and developmental studies

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient

1 reference

12 December 2020

Structural organization and analysis of the human fumarylacetoacetate hydrolase gene in tyrosinemia type I.

1 reference

12 December 2020

In vivo correction with recombinant adenovirus of 4-hydroxyphenylpyruvic acid dioxygenase deficiencies in strain III mice.

1 reference

12 December 2020

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

1 reference

12 December 2020

Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1015646400182

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Dimensions Publication ID

4 August 2017

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