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Items: 4

1.
Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability
Kristin D. Kernohan, Martine Tétreault, Urszula Liwak-Muir, Michael T. Geraghty, Wen Qin, Sunita Venkateswaran, Jorge Davila, Care4Rare Canada Consortium, Martin Holcik, Jacek Majewski, Julie Richer, Kym M. Boycott
Hum Mol Genet. 2015 Nov 15; 24(22): 6293–6300. Published online 2015 Aug 24. doi: 10.1093/hmg/ddv337
PMCID:
PMC4614701
AbstractArticlePDF–357K
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.
Inhibition of a constitutive translation initiation factor 2α phosphatase, CReP, promotes survival of stressed cells
Céline Jousse, Seiichi Oyadomari, Isabel Novoa, Phoebe Lu, Yuhong Zhang, Heather P. Harding, David Ron
J Cell Biol. 2003 Nov 24; 163(4): 767–775. doi: 10.1083/jcb.200308075
PMCID:
PMC2173671
AbstractArticlePDF–449K
4.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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