Study of Peroxisomal Proteins in Patients with Zellweger Syndrome
Overview
Overview
Authors
Affiliations
Affiliations
Soon will be listed here.
References
1.
Chen W, Watkins P, Osumi T, Hashimoto T, Moser H
. Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy. Proc Natl Acad Sci U S A. 1987; 84(5):1425-8.
PMC: 304443.
DOI: 10.1073/pnas.84.5.1425.
View
2.
Watkins P, Chen W, Harris C, Hoefler G, Hoefler S, Blake Jr D
. Peroxisomal bifunctional enzyme deficiency. J Clin Invest. 1989; 83(3):771-7.
PMC: 303746.
DOI: 10.1172/JCI113956.
View
3.
Fujiki Y, Hubbard A, Fowler S, Lazarow P
. Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum. J Cell Biol. 1982; 93(1):97-102.
PMC: 2112113.
DOI: 10.1083/jcb.93.1.97.
View
4.
Fujiki Y, Rachubinski R, Lazarow P
. Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes. Proc Natl Acad Sci U S A. 1984; 81(22):7127-31.
PMC: 392090.
DOI: 10.1073/pnas.81.22.7127.
View
5.
Lazarow P, Fujiki Y, SMALL G, Watkins P, Moser H
. Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome). Proc Natl Acad Sci U S A. 1986; 83(23):9193-6.
PMC: 387101.
DOI: 10.1073/pnas.83.23.9193.
View