Literature DB >> 3399966

Gene for lipoamide dehydrogenase maps to human chromosome 7.

G Otulakowski1, B H Robinson, H F Willard.   

Abstract

The gene for lipoamide dehydrogenase (LD) has been assigned to human chromosome 7 based on filter hybridization analysis of genomic DNA from rodent-human somatic cell hybrids using a cDNA probe for human LD. No indication of multiple copies of the gene was found, in accordance with previous evidence that LD in the pyruvate, alpha-ketoglutarate, and branched chain alpha-ketoacid dehydrogenase complexes is genetically as well as biochemically identical.

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Year:  1988        PMID： 3399966     DOI： 10.1007/bf01534650

Source DB:  PubMed          Journal:  Somat Cell Mol Genet        ISSN： 0740-7750


  6 in total

1.  Identification of two missense mutations in a dihydrolipoamide dehydrogenase-deficient patient.

Authors:  T C Liu; H Kim; C Arizmendi; A Kitano; M S Patel
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-01       Impact factor: 11.205

Review 2.  Maple syrup urine disease 1954 to 1993.

Authors:  F Peinemann; D J Danner
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

3.  Characterization of the transcriptional regulatory region of the human dihydrolipoamide dehydrogenase gene.

Authors:  G L Johanning; J I Morris; K T Madhusudhan; D Samols; M S Patel
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

4.  Formation of reactive oxygen species by human and bacterial pyruvate and 2-oxoglutarate dehydrogenase multienzyme complexes reconstituted from recombinant components.

Authors:  Attila Ambrus; Natalia S Nemeria; Beata Torocsik; Laszlo Tretter; Mattias Nilsson; Frank Jordan; Vera Adam-Vizi
Journal:  Free Radic Biol Med       Date:  2015-10-09       Impact factor: 7.376

5.  Three genes for enzymes of the pyruvate dehydrogenase complex map to human chromosomes 3, 7, and X.

Authors:  S Olson; B J Song; T L Huh; Y T Chi; R L Veech; O W McBride
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

6.  Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome 1.

Authors:  W J Herring; S Litwer; J L Weber; D J Danner
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025
  6 in total

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