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Items: 4

1.
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.
PMCID:
PMC1914864
SummaryPage BrowsePDF–2.5M
2.
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.
T Yahraus, N Braverman, G Dodt, J E Kalish, J C Morrell, H W Moser, D Valle, S J Gould
EMBO J. 1996 Jun 17; 15(12): 2914–2923.
PMCID:
PMC450231
SummaryPage BrowsePDF–2.7M
3.
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
S Tamura, N Matsumoto, A Imamura, N Shimozawa, Y Suzuki, N Kondo, Y Fujiki
Biochem J. 2001 Jul 15; 357(Pt 2): 417–426. doi: 10.1042/0264-6021:3570417
PMCID:
PMC1221968
SummaryPDF–430K
4.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M

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