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32199 publications found in the database

*2011 (1784)

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

2011 Publications

Effects of genome architecture and epigenetic factors on susceptibility of promoter CpG islands to aberrant DNA methylation induction
Takeshima, H. et al. Genomics 98(3), 182-8, 2011, Human Genome U133 Plus 2.0 Array  PubMed

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements
Luo, Y. et al. Human Molecular Genetics 20(19), 3769-78, 2011, Genome-Wide Human SNP Array 6.0  PubMed

The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans
Menard, L. et al. Journal of Clinical Investigation 121(9), 3635-44, 2011, Human Genome U133 Plus 2.0 Array  PubMed

Insulin-like growth factor binding protein 5 suppresses tumor growth and metastasis of human osteosarcoma
Su, Y. et al. Oncogene 30(37), 3907-17, 2011  PubMed

Caspase-8 regulates TNF-alpha-induced epithelial necroptosis and terminal ileitis
Guenther, C. et al. Nature 477(7364), NPG, 2011, Mouse Genome 430 2.0 Array  PubMed

Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice
Kraft, M. et al. Journal of Clinical Investigation 121(9), 3479-91, 2011  PubMed

Upregulation of Rac GTPase-Activating Protein 1 Is Significantly Associated with the Early Recurrence of Human Hepatocellular Carcinoma
Wang, S. M. et al. Clinical Cancer Research 17(18), 6040-51, 2011  PubMed

Acquired genomic copy number aberrations and survival in chronic lymphocytic leukemia
Ouillette, P. et al. Blood 118(11), 3051-61, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group
Zhang, J. H. et al. Blood 118(11), 3080-7, 2011, Genome-Wide Human SNP Array 6.0  PubMed

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