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Items: 4

1.
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
2.
A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori’s disease
Alan Cheng, Mei Zhang, Matthew S. Gentry, Carolyn A. Worby, Jack E. Dixon, Alan R. Saltiel
Genes Dev. 2007 Oct 1; 21(19): 2399–2409. doi: 10.1101/gad.1553207
PMCID:
PMC1993871
AbstractArticlePDF–745K
3.
Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.
Y T Chen, J K He, J H Ding, B I Brown
Am J Hum Genet. 1987 Dec; 41(6): 1002–1015.
PMCID:
PMC1684360
SummaryPage BrowsePDF–1.9M
4.
Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle.
J Shen, Y Bao, H M Liu, P Lee, J V Leonard, Y T Chen
J Clin Invest. 1996 Jul 15; 98(2): 352–357. doi: 10.1172/JCI118799
PMCID:
PMC507437
SummaryPDF–195K

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