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32199 publications found in the database

*2010 (1822)

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

2010 Publications

DNMT1 maintains progenitor function in self-renewing somatic tissue
Sen, G. L. et al. Nature 463(7280), NPG, 2010, Human Genome U133 Plus 2.0 Array  PubMed

Meta-analysis and imputation refines the association of 15q25 with smoking quantity
Liu, J. Z. et al. Nature Genetics 42(5), NPG, 2010  PubMed

regulatory feedback loop involving p63 and IRF6 links the pathogenesis of 2 genetically different human ectodermal dysplasias
Moretti, F. et al. Journal of Clinical Investigation 120(5), 1570-7, 2010, Mouse Genome 430 2.0 Array  PubMed

Sex determines the expression level of one third of the actively expressed genes in bovine blastocysts
Bermejo-Alvarez, P. et al. Proceedings of the National Academy of Sciences of the United States of America 107(8), 3394-9, 2010, Bovine Genome Array  PubMed

Aberrant overexpression and function of the miR-17-92 cluster in MLL-rearranged acute leukemia
Mi, S. L. et al. Proceedings of the National Academy of Sciences of the United States of America 107(8), 3710-5, 2010, Mouse Gene 1.0 ST array  PubMed

Nuclear Pore Proteins Nup153 and Megator Define Transcriptionally Active Regions in the Drosophila Genome
Vaquerizas, J. M. et al. Plos Genetics 6(2), NPG, 2010  PubMed

MMBGX: a method for estimating expression at the isoform level and detecting differential splicing using whole-transcript Affymetrix arrays
Turro, E. et al. Nucleic Acids Research 38(4), 1413, 2010  PubMed

Growth Factor Regulation of Prostaglandin-Endoperoxide Synthase 2 (Ptgs2) Expression in Colonic Mesenchymal Stem Cells
Walker, M. R. et al. Journal of Biological Chemistry 285(7), 5026-39, 2010, Mouse Genome 430A 2.0 Array  PubMed

Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome - Like Phenotype
Collins, S. C. et al. Plos One 5(3), NPG, 2010  PubMed

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