Literature DB >> 6067402

Hypervalinemia. A defect in valine transamination.

J Dancis, J Hutzler, K Tada, Y Wada, T Morikawa, T Arakawa.   

Abstract

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Year:  1967        PMID： 6067402

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  5 in total

Review 1.  Food intolerance in humans.

Authors:  R H Herman; L Hagler
Journal:  West J Med       Date:  1979-02

2.  A sibship with hypervalinemia.

Authors:  O S Reddi; S V Reddy; K R Reddy
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

3.  Isovaleric acidemia.

Authors: 
Journal:  Can Med Assoc J       Date:  1967-11-11       Impact factor: 8.262

4.  Normal 2-aminobutyrate oxidation and increased valine oxidation in fibroblasts deficient in pyruvate dehydrogenase.

Authors:  O Borud; J E Pettersen
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

5.  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
  5 in total

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