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32199 publications found in the database

*2012 (1980)

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

2012 Publications

The Origin and Nature of Tightly Clustered BTG1 Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution
Waanders, E. et al. Plos Genetics 8(2), NPG, 2012, Genome-Wide Human SNP Array 6.0  PubMed

The Receptor Tyrosine Kinase EphA2 Is a Direct Target Gene of Hypermethylated in Cancer 1 (HIC1)
Foveau, B. et al. Journal of Biological Chemistry 287(8), 5366-78, 2012, Human Genome U133 Set  PubMed

Loss of Hypermethylated in Cancer 1 (HIC1) in Breast Cancer Cells Contributes to Stress-induced Migration and Invasion through beta-2 Adrenergic Receptor (ADRB2) Misregulation
Boulay, G. et al. Journal of Biological Chemistry 287(8), 5379-89, 2012, Human Genome U133 Set  PubMed

Trinucleotide Repeat Containing 6a (Tnrc6a)-mediated MicroRNA Function Is Required for Development of Yolk Sac Endoderm
Jiang, Z. H. et al. Journal of Biological Chemistry 287(8), 5979-87, 2012, Mouse Gene 1.0 ST array  PubMed

DNA hypermethylation in lung cancer is targeted at differentiation- associated genes
Helman, E. et al. Oncogene 31(9), 1181-8, 2012  PubMed

A refined molecular taxonomy of breast cancer
Guedj, M. et al. Oncogene 31(9), 1196-206, 2012  PubMed

Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation
Shamseldin, H. E. et al. Journal of Medical Genetics 49(3), 184-6, 2012  PubMed

Global transcriptional profiling reveals similarities and differences between human stem cell-derived cardiomyocyte clusters and heart tissue
Synnergren, J. et al. Physiological Genomics 44(4), 245-58, 2012, Human Gene 1.0 ST Array  PubMed

X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development
Webb, T. R. et al. American Journal of Human Genetics 90(2), 247-59, 2012, Human Exon Array  PubMed

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