Literature DB >> 8784779

Inborn errors of metabolism: Garrod's legacy.

A G Bearn1.   

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Year:  1996        PMID： 8784779      PMCID： PMC2230147     

Source DB:  PubMed          Journal:  Mol Med        ISSN： 1076-1551            Impact factor:   6.354


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  6 in total

1.  The nature of the defect in tyrosine metabolism in alcaptonuria.

Authors:  B N LA DU; V G ZANNONI; L LASTER; J E SEEGMILLER
Journal:  J Biol Chem       Date:  1958-01       Impact factor: 5.157

2.  Characterization of the pigment from homogentisic acid and urine and tissue from an alkaptonuria patient.

Authors:  I A Menon; S D Persad; H F Haberman; P K Basu; J F Norfray; C C Felix; B Kalyanaraman
Journal:  Biochem Cell Biol       Date:  1991-04       Impact factor: 3.626

3.  A Contribution to the Study of Alkaptonuria.

Authors:  A E Garrod
Journal:  Med Chir Trans       Date:  1899

4.  aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16.

Authors:  X Montagutelli; A Lalouette; M Coudé; P Kamoun; M Forest; J L Guénet
Journal:  Genomics       Date:  1994-01-01       Impact factor: 5.736

5.  Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.

Authors:  M R Pollak; Y H Chou; J J Cerda; B Steinmann; B N La Du; J G Seidman; C E Seidman
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

Review 6.  Alcaptonuria and ochronotic arthritis.

Authors:  B N La Du
Journal:  Mol Biol Med       Date:  1991-02
  6 in total
  1 in total

Review 1.  The aryl hydrocarbon receptor complex and the control of gene expression.

Authors:  Timothy V Beischlag; J Luis Morales; Brett D Hollingshead; Gary H Perdew
Journal:  Crit Rev Eukaryot Gene Expr       Date:  2008       Impact factor: 1.807
  1 in total

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