Literature DB >> 2246865

Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: a murine model for hereditary tyrosinaemia type III.

F Endo1, H Katoh, I Matsuda.   

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Year:  1990        PMID: 2246865     DOI: 10.1007/bf01799587

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


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  5 in total

1.  Biochemical studies in a patient with "tyrosinosis".

Authors:  W J Louis; D D Pitt; H Davies
Journal:  Aust N Z J Med       Date:  1974-06

2.  Chronic tyrosinemia associated with 4-hydroxyphenylpyruvate dioxygenase deficiency with acute intermittent ataxia and without visceral and bone involvement.

Authors:  O Giardini; A Cantani; N G Kennaway; P D'Eufemia
Journal:  Pediatr Res       Date:  1983-01       Impact factor: 3.756

3.  Assay, properties and tissue distribution of p-hydroxyphenylpyruvate hydroxylase.

Authors:  J H Fellman; T S Fujita; E S Roth
Journal:  Biochim Biophys Acta       Date:  1972-09-19

4.  Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia.

Authors:  R Berger; G P Smit; S A Stoker-de Vries; M Duran; D Ketting; S K Wadman
Journal:  Clin Chim Acta       Date:  1981-07-18       Impact factor: 3.786

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

Authors:  F Endo; A Kitano; I Uehara; N Nagata; I Matsuda; T Shinka; T Kuhara; I Matsumoto
Journal:  Pediatr Res       Date:  1983-02       Impact factor: 3.756

  5 in total
  2 in total

1.  Tyrosinaemia type III: immunochemical studies on 4-hydroxyphenylpyruvic acid dioxygenase and molecular cloning of cDNA for the enzyme.

Authors:  F Endo; H Awata; A Tanoue; Y Eda; I Matsuda
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

Review 2.  Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations.

Authors:  Jeffrey M Chinsky; Rani Singh; Can Ficicioglu; Clara D M van Karnebeek; Markus Grompe; Grant Mitchell; Susan E Waisbren; Muge Gucsavas-Calikoglu; Melissa P Wasserstein; Katie Coakley; C Ronald Scott
Journal:  Genet Med       Date:  2017-08-03       Impact factor: 8.822

  2 in total

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