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Select item 21328911.

Peroxisome Synthesis in the Absence of Preexisting Peroxisomes

Sarah T. South, Stephen J. Gould

J Cell Biol. 1999 Jan 25; 144(2): 255–266. doi: 10.1083/jcb.144.2.255

PMCID:: PMC2132891

Abstract Article PDF–1.7M

Select item 12260462.

Disorders of Peroxisome Biogenesis Due to Mutations in PEX1: Phenotypes and PEX1 Protein Levels

Claudia Walter, Jeannette Gootjes, Petra A. Mooijer, Herma Portsteffen, Christina Klein, Hans R. Waterham, Peter G. Barth, Jörg T. Epplen, Wolf-H. Kunau, Ronald J. A. Wanders, Gabriele Dodt

Am J Hum Genet. 2001 Jul; 69(1): 35–48. Published online 2001 Jun 1. doi: 10.1086/321265

PMCID:: PMC1226046

Abstract Article PDF–857K

Select item 12878983.

Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

Ania C. Muntau, Peter U. Mayerhofer, Barbara C. Paton, Stefan Kammerer, Adelbert A. Roscher

Am J Hum Genet. 2000 Oct; 67(4): 967–975. Published online 2000 Aug 24. doi: 10.1086/303071

PMCID:: PMC1287898

Abstract Article PDF–1.0M

Select item 12878994.

PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G

Kamran Ghaedi, Masanori Honsho, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki

Am J Hum Genet. 2000 Oct; 67(4): 976–981. Published online 2000 Aug 31. doi: 10.1086/303086

PMCID:: PMC1287899

Abstract Article PDF–585K

Select item 13773045.

Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

D S Warren, J C Morrell, H W Moser, D Valle, S J Gould

Am J Hum Genet. 1998 Aug; 63(2): 347–359. doi: 10.1086/301963

PMCID:: PMC1377304

Summary PDF–1.5M

Select item 13776336.

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

M Honsho, S Tamura, N Shimozawa, Y Suzuki, N Kondo, Y Fujiki

Am J Hum Genet. 1998 Dec; 63(6): 1622–1630. doi: 10.1086/302161

PMCID:: PMC1377633

Summary PDF–1.2M

Select item 17151437.

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of Acyl-CoA oxidase (pseudo–Neonatal adrenoleukodystrophy)

Bwee Tien Poll-The, Frank Roels, Hélène Ogier, Jacques Scotto, Joseph Vamecq, Ruud B. H. Schutgens, Ronald J. A. Wanders, Carlo W. T. van Roermund, Michil J. A. van Wijland, Adre W. Schram, Joseph M. Tager, Jean-Marie Saudubray

Am J Hum Genet. 1988 Mar; 42(3): 422–434.

PMCID:: PMC1715143

Summary Page Browse PDF–3.2M

Select item 17342448.

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders

N. Shimozawa, A. Imamura, Z. Zhang, Y. Suzuki, T. Orii, T. Tsukamoto, T. Osumi, Y. Fujiki, R. Wanders, G. Besley, N. Kondo

J Med Genet. 1999 Oct; 36(10): 779–781. doi: 10.1136/jmg.36.10.779

PMCID:: PMC1734244

Summary PDF–109K

Select item 17361349.

Genetic and clinical aspects of Zellweger spectrum patients with PEX1 mutations

H Rosewich, A Ohlenbusch, J Gartner

J Med Genet. 2005 Sep; 42(9): e58. doi: 10.1136/jmg.2005.033324

PMCID:: PMC1736134

Summary PDF–79K

Select item 191486410.

Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

S. Fukuda, N. Shimozawa, Y. Suzuki, Z. Zhang, S. Tomatsu, T. Tsukamoto, N. Hashiguchi, T. Osumi, M. Masuno, K. Imaizumi, Y. Kuroki, Y. Fujiki, T. Orii, N. Kondo

Am J Hum Genet. 1996 Dec; 59(6): 1210–1220.