(Q28335340)

English

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

scientific article (publication date: April 1991)

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scholarly article

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

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1 reference

based on heuristic

inferred from title

author name string

F Endo

1

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H Katoh

2

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S Yamamoto

3

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I Matsuda

4

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language of work or name

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publication date

April 1991

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American Journal of Human Genetics

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48

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4

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704-9

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

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4-Hydroxyphenylpyruvate dioxygenase from pig liver

1 reference

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4-Hydroxyphenylpyruvate dioxygenase from human liver

1 reference

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Purification and properties of avian liver p-hydroxyphenylpyruvate hydroxylase

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Purification and some properties of human 4-hydroxyphenylpyruvate dioxygenase (I)

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

1 reference

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X chromosome-linked muscular dystrophy (mdx) in the mouse

1 reference

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Purification and properties of hog liver 4-hydroxyphenylpyruvate dioxygenase

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Radiochemical assays for p-hydroxyphenylpyruvate hydroxylase activity in human liver

1 reference

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The enzymatic deficiency in tyrosinemia.

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inferred from PubMed ID database lookup

Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2014797

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based on heuristic

inferred from PubMed ID database lookup

Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia

1 reference

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based on heuristic

inferred from PubMed ID database lookup

Chronic Tyrosinemia Associated with 4-Hydroxyphenylpyruvate Dioxygenase Deficiency with Acute Intermittent Ataxia and without Visceral and Bone Involvement

1 reference

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based on heuristic

inferred from PubMed ID database lookup

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