A novel method for determining peroxisomal fatty acid β-oxidation-Reference-Cited by-同舟云学术

A novel method for determining peroxisomal fatty acid β-oxidation

Published:2016-06-20 Issue:5 Volume:39 Page:725-731
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Morita Masashi^ORCID,Matsumoto Shun,Okazaki Airi,Tomita Kaito,Watanabe Shiro,Kawaguchi Kosuke,Minato Daishiro,Matsuya Yuji,Shimozawa Nobuyuki,Imanaka Tsuneo

Funder

Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-016-9952-y.pdf

Reference19 articles.

1. Corzo D, Gibson W, Johnson K et al (2002) Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. Am J Hum Genet 70:1520–1531

2. Dubois-Dalcq M, Feigenbaum V, Aubourg P (1999) The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder. Trends Neurosci 22:4–12

3. Galla HJ, Hartmann W (1981) Pyrenedecanoic acid and pyrene lecithin. Methods Enzymol 72:471–479

4. Gatt S, Bremer J, Osmundsen H (1988) Pyrene dodecanoic acid coenzyme A ester: peroxisomal oxidation and chain shortening. Biochim Biophys Acta 958:130–133

5. Hoefler G, Paschke E, Hoefler S, Moser AB, Moser HW (1991) Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage. J Clin Invest 88:1873–1879

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