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32199 publications found in the database

*2011 (1784)

*Starting in 2010, coverage has been refocused on core journals.

2011 Publications

Pleiotropic platelet defects in mice with disrupted FOG1-NuRD interaction
Wang, Y. H. et al. Blood 118(23), 6183-91, 2011, Mouse Genome 430 2.0 Array  PubMed

AML1/RUNX1 functions as a cytoplasmic attenuator of NF-kappaB signaling in the repression of myeloid tumors
Nakagawa, M. et al. Blood 118(25), 6626-37, 2011, Mouse Genome 430 2.0 Array  PubMed

Transcriptomic analyses of murine resolution-phase macrophages
Stables, M. J. et al. Blood 118(26), E192-208, 2011, Mouse Genome 430 2.0 Array  PubMed

Etv2/ER71 induces vascular mesoderm from Flk1 (+) PDGFRalpha (+) primitive mesoderm
Kataoka, H. et al. Blood 118(26), 6975-86, 2011, Mouse Genome 430 2.0 Array  PubMed

Regulation of Autophagy by Neuropathological Protein TDP-43
Bose, J. K. et al. Journal of Biological Chemistry 286(52), 44441-8, 2011, Mouse Genome 430 2.0 Array  PubMed

Expression QTL mapping in regulatory and helper T cells from the BXD family of strains reveals novel cell-specific genes, gene-gene interactions and candidate genes for auto-immune disease
Alberts, R. et al. BMC Genomics 12(), NPG, 2011, Mouse Genome 430 2.0 Array  PubMed

Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis
de Laar, I. M. B. H. V. et al. Nature Genetics 43(2), NPG, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

The Populus Class III HD ZIP Transcription Factor POPCORONA Affects Cell Differentiation during Secondary Growth of Woody Stems
Du, J. et al. Plos One 6(2), NPG, 2011, Poplar Genome Array  PubMed

CEP152 is a genome maintenance protein disrupted in Seckel syndrome
Kalay, E. et al. Nature Genetics 43(1), 23-6, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

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