(Q22011184)

bile acid metabolic process

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Peter Theodore Clayton

1 reference

ORCID Public Data File 2021

S Ferdinandusse

1

Sacha

Ferdinandusse

1 reference

28 September 2022

S Denis

2

Simone

Denis

1 reference

28 September 2022

P T Clayton

3

0 references

A Graham

4

Andrew

Graham

1 reference

28 September 2022

J E Rees

5

John E.

Rees

1 reference

28 September 2022

J T Allen

6

John T.

Allen

1 reference

28 September 2022

B N McLean

7

Brendan N.

McLean

1 reference

28 September 2022

A Y Brown

8

Ann Y.

Brown

1 reference

28 September 2022

P Vreken

9

Peter

Vreken

1 reference

28 September 2022

H R Waterham

10

Hans R.

Waterham

1 reference

28 September 2022

R J Wanders

11

Ronald J.A.

Wanders

1 reference

Charcot-Marie-Tooth disease and related inherited neuropathies

28 September 2022

language of work or name

English

0 references

publication date

February 2000

0 references

published in

Nature Genetics

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volume

24

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issue

2

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page(s)

188-91

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cites work

1 reference

Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms

21 January 2018

1 reference

The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder

21 January 2018

1 reference

Purification and properties of an alpha-methylacyl-CoA racemase from rat liver

21 January 2018

1 reference

Purification and Characterization of an alpha-Methylacyl-CoA Racemase from Human Liver

21 January 2018

1 reference

Substrate stereospecificity in oxidation of (25S)-3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoyl-CoA by peroxisomal trihydroxy-5 beta-cholestanoyl-CoA oxidase

21 January 2018

1 reference

Peroxisomal beta-oxidation of 2-methyl-branched acyl-CoA esters: stereospecific recognition of the 2S-methyl compounds by trihydroxycoprostanoyl-CoA oxidase and pristanoyl-CoA oxidase

21 January 2018

1 reference

Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene

21 January 2018

1 reference

Identification of PAHX, a Refsum disease gene

21 January 2018

1 reference

2-Methylacyl racemase: a coupled assay based on the use of pristanoyl-CoA oxidase/peroxidase and reinvestigation of its subcellular distribution in rat and human liver

21 January 2018

1 reference

Molecular cloning of cDNA species for rat and mouse liver alpha-methylacyl-CoA racemases

21 January 2018

1 reference

Plasma and red blood cell fatty acids in peroxisomal disorders

21 January 2018

1 reference

Refsum's disease: management by diet and plasmapheresis

21 January 2018

1 reference

Comparison of the binding affinities of acyl-CoA-binding protein and fatty-acid-binding protein for long-chain acyl-CoA esters

21 January 2018

1 reference

Substrate specificity of THCA-CoA oxidases from rat liver light mitochondrial fractions on dehydrogenation of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acid CoA thioester

21 January 2018

1 reference

The occurrence of diastereomers of phytanic and pristanic acids and their determination by gas-liquid chromatography

21 January 2018

1 reference

7 January 2021

Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates

1 reference

7 January 2021

Rapid stable isotope dilution analysis of very-long-chain fatty acids, pristanic acid and phytanic acid using gas chromatography-electron impact mass spectrometry

1 reference

7 January 2021

Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts

1 reference

7 January 2021

Bile acids in peroxisomal disorders

1 reference

7 January 2021

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein

1 reference

7 January 2021

Identifiers

DOI

10.1038/72861

0 references