Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I. (Q52507854)

2 May 2018

title

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

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2 May 2018

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author name string

Lindstedt S

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al-Dhalimy M

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Kennaway NG

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Papaconstantinou J

5

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2 May 2018

Torres-Ramos CA

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Ou CN

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Finegold M

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language of work or name

English

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publication date

1 August 1995

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2 May 2018

published in

Nature Genetics

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2 May 2018

volume

10

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2 May 2018

page(s)

453-460

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issue

4

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2 May 2018

https://scigraph.springernature.com/pub.10.1038/ng0895-453

exact match

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cites work

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Ionic calcium levels during pregnancy, at delivery and in the first hours of life

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

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

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Identifiers

DOI

10.1038/NG0895-453

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2 May 2018

Dimensions Publication ID

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1 reference

2 May 2018