(Q67581812)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434512%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

title

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets (English)

1 reference

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15 September 2019

3

1 reference

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15 September 2019

author name string

R W Taylor

1

1 reference

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15 September 2019

S Jackson

2

1 reference

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15 September 2019

K Bartlett

4

1 reference

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15 September 2019

D M Turnbull

5

1 reference

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15 September 2019

publication date

1 January 1992

1 reference

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Journal of Inherited Metabolic Disease

15 September 2019

published in

1 reference

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15 September 2019

volume

15

1 reference

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15 September 2019

issue

5

1 reference

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15 September 2019

page(s)

727-732

1 reference

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Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary carnitine deficiency

15 September 2019

cites work

1 reference

12 December 2020

Isolation of human platelets from plasma by centrifugation and washing.

1 reference

12 December 2020

Immunoreactive enzyme protein in medium-chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts

1 reference

12 December 2020

An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion

1 reference

12 December 2020

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards

1 reference

12 December 2020

Purification and properties of short chain acyl-CoA, medium chain acyl-CoA, and isovaleryl-CoA dehydrogenases from human liver

1 reference

12 December 2020

Medium chain acyl CoA dehydrogenase deficiency

1 reference

12 December 2020

Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation

1 reference

12 December 2020

The inborn errors of mitochondrial fatty acid oxidation

1 reference

12 December 2020

Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020