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Items: 3

1.
The Pex1-G844D Mouse: A Model for Mild Human Zellweger Spectrum Disorder
Shandi Hiebler, Tomohiro Masuda, Joseph G. Hacia, Ann B. Moser, Phyllis L. Faust, Anita Liu, Nivedita Chowdhury, Ning Huang, Amanda Lauer, Jean Bennett, Paul A. Watkins, Donald J. Zack, Nancy E. Braverman, Gerald V. Raymond, Steven J. Steinberg
Mol Genet Metab. Author manuscript; available in PMC 2016 Jun 10.
Published in final edited form as: Mol Genet Metab. 2014 Apr; 111(4): 522–532. Published online 2014 Jan 23. doi: 10.1016/j.ymgme.2014.01.008
PMCID:
PMC4901203
AbstractArticlePDF–1.2M
2.
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
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

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