Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded byPEX11
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(98)00815-1/fullpdf
Reference52 articles.
1. Biogenesis of Peroxisomes
2. A unified nomenclature for peroxisome biogenesis factors.
3. Molecular defects in genetic diseases of peroxisomes
4. Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
5. Peroxisomal assembly defects: Clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group
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3. Compound heterozygous p. Arg949Trp and p. Gly970Ala mutations deteriorated the function of PEX1p: A study on PEX1 in a patient with Zellweger syndrome;Journal of Cellular Biochemistry;2021-05-06
4. A Mouse Model System to Study Peroxisomal Roles in Neurodegeneration of Peroxisome Biogenesis Disorders;Advances in Experimental Medicine and Biology;2020
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