References and Further Reading
Baker, A. , Paudyal, R. (2014)The life of the peroxisome: From birth to death. Current Opinion in Plant Biology 22: 39-47
Brites, P. Waterham, H.R., Wanders, R.J.A. (2004) Functions and biosynthesis of plasmalogens in health and disease. Biochimica et Biophysica Acta 1636: 219-231
Cooper, G.M. (2000). The Cell: A Molecular Approach. Sunderland M.A.:Sinauer Associates, 2nd Ed.
Danpure, C.J. and Rumsby, G. (2004). Molecular aetiology of primary hyperoxaluria and its implications for clinical management. Expert Reviews in Molecular Medicine. 6:1-16.
Davidson, M. 2015. Molecular Expressions Cell Biology: Animal Cell Structure - Peroxisomes [Online]. Available at: http://micro.magnet.fsu.edu/cells/peroxisomes/peroxisomes.html [Accessed: 7 March 2015].
Erdmann, R. and Schliebs, W. 2005. Peroxisomal matrix protein import: the transient pore model. Nature Reviews Molecular Cell Biology 6(9), pp. 738-742.
Guo, C. and McMartin, K. E. (2005). The cytotoxicity of oxalate, metabolite of ethylene glycol, is due to calcium oxalate monohydrate formation. Toxicology 208:347-355.
Hu, J., Baker A., Bartel B., Linka N., Mullen R.T., Reumann S., Zolman B.K. (2012). Plant peroxisomes: biogenesis and function. Plant Cell 24:2279-2303
Kunau, W.H., (2005). Peroxisome Biogenesis: End of the Debate. Current Biology, 15: 774-776
Lodhi, I.J., Semenkovich, C.F. (2014) Peroxisomes: A Nexus for Lipid Metabolisms and Cellular Signalling. Cell Metabolism 19: 380-392
Lodish H., Berk A., Zipursky S.L. (2000). Molecular Cell Biology. New York:WH Freeman, 4th Ed.
Mannaerts, G. P., Van Veldhoven, P. P. and Casteels, M. (2000) Peroxisomal lipid degradation via beta- and alpha-oxidation in mammals. Cell Biochemistry Biophysiology 32:73-87
Reddy, J. K. (2000) Peroxisomal β-oxidation, PPARα, and steatohepatitis. American Journal of Physiology 281:1333-1339
Rucktaschel R., Halbach A., Girzalsky W., Rottensteiner H., Erdmann R. (2010). De novo synthesis of peroxisomes upon mitochondrial targeting of Pex3p. European Journal of Cell Biology 89:947-954.
Salido, E., Pey, A. L., Rodriguez, R. and Lorenzo, V. (2012). Primary hyperoxalurias: Disorders of glyoxylate detoxification. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1822:1453-1464.
Schrader, M. and Fahimi, H. 2008. The peroxisome: still a mysterious organelle. Histochemistry and Cell Biology 129(4), pp. 421-440.
Smith J.J., Aitchison J.D. (2013). Peroxisomes take shape. Nature Reviews Molecular Cell Biology 14:803-817.
Subramani, S. (1996). Protein translocation into peroxisomes. Journal of Biological Chemistry 271:32483-32486
Thai, T-P., Rodemer, C., Jauch, A., Hunziker, A., Moser, A., Gorgas, K., Just, W.W. (2001) Impaired membrane traffic in defective ether lipid biosynthesis. Human Molecular Genetics 10: 127-136
Wanders, R. J. A. (2014). Metabolic functions of peroxisomes in health and disease. Biochimie 98:36-44.
Wanders, R.J.A., Waterham, H.R. (2006) Biochemistry of Mammalian Peroxisomes Revisited. Annual Reviews of Biochemistry 75: 295-332
Wills, A. J., Manning, N. J. and Reilly, M. M. (2001). Refsum's disease. QJM 94:403-406.
Brites, P. Waterham, H.R., Wanders, R.J.A. (2004) Functions and biosynthesis of plasmalogens in health and disease. Biochimica et Biophysica Acta 1636: 219-231
Cooper, G.M. (2000). The Cell: A Molecular Approach. Sunderland M.A.:Sinauer Associates, 2nd Ed.
Danpure, C.J. and Rumsby, G. (2004). Molecular aetiology of primary hyperoxaluria and its implications for clinical management. Expert Reviews in Molecular Medicine. 6:1-16.
Davidson, M. 2015. Molecular Expressions Cell Biology: Animal Cell Structure - Peroxisomes [Online]. Available at: http://micro.magnet.fsu.edu/cells/peroxisomes/peroxisomes.html [Accessed: 7 March 2015].
Erdmann, R. and Schliebs, W. 2005. Peroxisomal matrix protein import: the transient pore model. Nature Reviews Molecular Cell Biology 6(9), pp. 738-742.
Guo, C. and McMartin, K. E. (2005). The cytotoxicity of oxalate, metabolite of ethylene glycol, is due to calcium oxalate monohydrate formation. Toxicology 208:347-355.
Hu, J., Baker A., Bartel B., Linka N., Mullen R.T., Reumann S., Zolman B.K. (2012). Plant peroxisomes: biogenesis and function. Plant Cell 24:2279-2303
Kunau, W.H., (2005). Peroxisome Biogenesis: End of the Debate. Current Biology, 15: 774-776
Lodhi, I.J., Semenkovich, C.F. (2014) Peroxisomes: A Nexus for Lipid Metabolisms and Cellular Signalling. Cell Metabolism 19: 380-392
Lodish H., Berk A., Zipursky S.L. (2000). Molecular Cell Biology. New York:WH Freeman, 4th Ed.
Mannaerts, G. P., Van Veldhoven, P. P. and Casteels, M. (2000) Peroxisomal lipid degradation via beta- and alpha-oxidation in mammals. Cell Biochemistry Biophysiology 32:73-87
Reddy, J. K. (2000) Peroxisomal β-oxidation, PPARα, and steatohepatitis. American Journal of Physiology 281:1333-1339
Rucktaschel R., Halbach A., Girzalsky W., Rottensteiner H., Erdmann R. (2010). De novo synthesis of peroxisomes upon mitochondrial targeting of Pex3p. European Journal of Cell Biology 89:947-954.
Salido, E., Pey, A. L., Rodriguez, R. and Lorenzo, V. (2012). Primary hyperoxalurias: Disorders of glyoxylate detoxification. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1822:1453-1464.
Schrader, M. and Fahimi, H. 2008. The peroxisome: still a mysterious organelle. Histochemistry and Cell Biology 129(4), pp. 421-440.
Smith J.J., Aitchison J.D. (2013). Peroxisomes take shape. Nature Reviews Molecular Cell Biology 14:803-817.
Subramani, S. (1996). Protein translocation into peroxisomes. Journal of Biological Chemistry 271:32483-32486
Thai, T-P., Rodemer, C., Jauch, A., Hunziker, A., Moser, A., Gorgas, K., Just, W.W. (2001) Impaired membrane traffic in defective ether lipid biosynthesis. Human Molecular Genetics 10: 127-136
Wanders, R. J. A. (2014). Metabolic functions of peroxisomes in health and disease. Biochimie 98:36-44.
Wanders, R.J.A., Waterham, H.R. (2006) Biochemistry of Mammalian Peroxisomes Revisited. Annual Reviews of Biochemistry 75: 295-332
Wills, A. J., Manning, N. J. and Reilly, M. M. (2001). Refsum's disease. QJM 94:403-406.