(Q24677416)

2

0 references

M Souri

3

0 references

S Miyazawa

4

0 references

S Fukuda

5

0 references

Z Zhang

6

0 references

M Une

7

0 references

N Shimozawa

8

0 references

N Kondo

9

0 references

T Orii

10

0 references

T Hashimoto

American Journal of Human Genetics

11

0 references

language of work or name

English

0 references

publication date

November 1997

0 references

published in

0 references

volume

61

0 references

issue

5

0 references

page(s)

1153-62

0 references

cites work

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Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

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Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

28 September 2017

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Molecular structure of the human cytoplasmic beta-actin gene: interspecies homology of sequences in the introns

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The deficient degradation of synthetic 2- and 3-methyl-branched fatty acids in fibroblasts from patients with peroxisomal disorders

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30 May 2018

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The presence of a new 3-oxoacyl-CoA thiolase in rat liver peroxisomes

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12 December 2020

Properties of mitochondria and peroxisomal enoyl-CoA hydratases from rat liver

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12 December 2020

Individual peroxisomal beta-oxidation enzymes

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12 December 2020

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

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12 December 2020

A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities

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12 December 2020

Pristanic acid and phytanic acid in plasma from patients with a single peroxisomal enzyme deficiency

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12 December 2020

Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: Evidence for a Distinct peroxisomal pristanyl-CoA oxidase

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12 December 2020

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

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12 December 2020

A case of pseudo-Zellweger syndrome with a possible bifunctional enzyme deficiency but detectable enzyme protein. Comparison of two cases of Zellweger syndrome.

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12 December 2020

Two mitochondrial 3-hydroxyacyl-CoA dehydrogenases in bovine liver

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12 December 2020

Urinary bile acids and peroxisomal bifunctional enzyme deficiency

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12 December 2020