Literature DB >> 14755332

Tandem mass spectrometry in discovery of disorders of the metabolome.

Arnold W Strauss1.   

Abstract

Genetic disorders of amino acid and fatty acid metabolism can be detected with tandem mass spectrometry (MS/MS). MS/MS screening of mice subjected to chemical mutagenesis (see the related article beginning on page 434) defined a new disorder of branched-chain amino acid metabolism resembling human maple syrup urine disease. This approach has general application to the discovery of gene function in developmental and metabolic disorders.

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Year:  2004        PMID: 14755332      PMCID: PMC324547          DOI: 10.1172/JCI20924

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  3 in total

Review 1.  Parsing the heart: genetic modules for organ assembly.

Authors:  M C Fishman; E N Olson
Journal:  Cell       Date:  1997-10-17       Impact factor: 41.582

2.  Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.

Authors:  T H Zytkovicz; E F Fitzgerald; D Marsden; C A Larson; V E Shih; D M Johnson; A W Strauss; A M Comeau; R B Eaton; G F Grady
Journal:  Clin Chem       Date:  2001-11       Impact factor: 8.327

3.  ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease.

Authors:  Jer-Yuarn Wu; Hsiao-Jung Kao; Sing-Chung Li; Robert Stevens; Steven Hillman; David Millington; Yuan-Tsong Chen
Journal:  J Clin Invest       Date:  2004-02       Impact factor: 14.808

  3 in total
  1 in total

1.  Analysis of the zebrafish proteome during embryonic development.

Authors:  Margaret B Lucitt; Thomas S Price; Angel Pizarro; Weichen Wu; Anastasia K Yocum; Christoph Seiler; Michael A Pack; Ian A Blair; Garret A Fitzgerald; Tilo Grosser
Journal:  Mol Cell Proteomics       Date:  2008-01-22       Impact factor: 5.911

  1 in total

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