Literature DB >> 1700192

Metabolism of branched chain fatty acids in peroxisomal disorders.

H Singh1, S Usher, D Johnson, A Poulos.   

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Year:  1990        PMID： 1700192     DOI： 10.1007/bf01799402

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


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  5 in total

1.  Distinct long chain and very long chain fatty acyl CoA synthetases in rat liver peroxisomes and microsomes.

Authors:  H Singh; A Poulos
Journal:  Arch Biochem Biophys       Date:  1988-11-01       Impact factor: 4.013

2.  A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders.

Authors:  H Singh; S Usher; D Johnson; A Poulos
Journal:  J Lipid Res       Date:  1990-02       Impact factor: 5.922

3.  A comparative study of stearic and lignoceric acid oxidation by human skin fibroblasts.

Authors:  H Singh; A Poulos
Journal:  Arch Biochem Biophys       Date:  1986-10       Impact factor: 4.013

4.  Prenatal diagnosis of Zellweger syndrome and related disorders: impaired degradation of phytanic acid.

Authors:  A Poulos; C van Crugten; P Sharp; W F Carey; E Robertson; D M Becroft; J M Saudubray; B T Poll-The; E Christensen; N Brandt
Journal:  Eur J Pediatr       Date:  1986-12       Impact factor: 3.183

5.  Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction.

Authors:  A Poulos; P Sharp; A J Fellenberg; D W Johnson
Journal:  Eur J Pediatr       Date:  1988-02       Impact factor: 3.183
  5 in total

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