Peroxisomal Fatty Acid Alpha-and Beta-Oxidation in Health and Disease: New insights-Reference-Cited by-同舟云学术

Peroxisomal Fatty Acid Alpha-and Beta-Oxidation in Health and Disease: New insights

Published:2003 Issue: Volume: Page:293-302
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
Short-container-title:

Author:

Wanders Ronald J.A.,Van Roermund Carlo W.T.,Visser Wouter F.,Ferdinandusse Sacha,Jansen Gerbert A.,Van den Brink Daan M.,Gloerich Jolein,Waterham Hans R.

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4419-9072-3_37

Reference24 articles.

1. Casteels M., Foulon V., Mannaerts G.P., and Van Veldhoven P.P., 2003, Alpha-oxidation of 3-methyl-substituted fatty acids and its thiamine dependence. EurJ.Biochem. 270: 1619–1627.

2. Ferdinandusse S., Denis S., Clayton P.T., Graham A., Rees J.E., Allen J.T., Mclean B.N., Brown A.Y., Vreken P., Waterham H.R. and Wanders R.J.A., 2000, Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy. Nat.Genet. 24: 188–191.

3. Ferdinandusse S., van Grunsven E.G., Oostheim W., Denis S., Hogenhout E.M., Ulst L., van Roermund C.W., Waterham H.R., Goldfischer S., Wanders R.J.A., 2002, Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of D-Bifunctional Protein. A mJ. Hum. Genet. 70: 1589–1593.

4. Goldfîscher S., Collins J., Rapin I., Neumann P., Neglia W., Spiro A.J., Ishii T., Roels F., Vamecq J. and Van Hoof F., 1986, Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities. J.Pediatr. 108: 25–32.

5. Jansen G.A., Hogenhout E.M., Ferdinandusse S., Waterham H.R., Ofman R., Jakobs C, Skjeldal O.H. and Wanders R.J.A., 2000, Human phytanoyl-CoA hydroxylase: resolution of the gene structure and the molecular basis of Refsum’s disease. Hum.Mol.Genet. 9: 1195–1200.

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Disturbed brain energy metabolism in a rodent model of DYT-TOR1A dystonia;Neurobiology of Disease;2024-05

2. A founder mutation in PEX12 among Egyptian patients in peroxisomal biogenesis disorder;Neurological Sciences;2020-10-29

3. Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy;International Journal of Molecular Sciences;2020-07-26

4. Visualized Networking of Co-Regulated Lipids in Human Blood Based on High-Throughput Screening Data: Implications for Exposure Assessment;Environmental Science & Technology;2019-02-11

5. Characterization of Peroxisomal Regulation Networks;Proteomics of Peroxisomes;2018