U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

Links from Nucleotide

Items: 2

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.
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

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center