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    • Induction and regulatory function of miR-9 in human monocytes and neutrophils exposed to proinflammatory signals
    • Nuclear HBx binds the HBV minichromosome and modifies the epigenetic regulation of cccDNA function.
    • Molecular and clinical features of chronic lymphocytic leukaemia with stereotyped B cell receptors: results from an Italian multicentre study.
    • Che-1 activates XIAP expression in response to DNA damage.
    • Che-1 enhances cyclin-dependent kinase 5 expression and interacts with the active kinase-complex.
    • Selective modulation of PKA I and II reveals distinct roles in thyroid cell gene expression and growth.
    • Identification of key regions and genes important in the pathogenesis of sezary syndrome by combining genomic and expression microarrays.
    • Tandem repeats modify the structure of human genes hosted in segmental duplications.
    • Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instability.
    • Novel activation domain derived from Che-1 cofactor coupled with the artificial protein Jazz drives utrophin upregulation.
    • The artificial gene Jazz, a transcriptional regulator of utrophin, corrects the dystrophic pathology in mdx mice.
    • Standardized sample preparation phases for a quantitative measurement of plasma peptidome profiling by MALDI-TOF.
    • Complex Loci in human and mouse genomes.
    • Gene expression in chorionic villous samples at 11 weeks of gestation in women who develop preeclampsia later in pregnancy: implications for screening.
    • Relevance of CD49d protein expression as overall survival and progressive disease prognosticator in chronic lymphocytic leukemia.
    • Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.
    • Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteoc
    • Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
    • AntiHunter 2.0: increased speed and sensitivity in searching BLAST output for EST antisense transcripts.
    • Altered expression of selected microRNAs in melanoma: antiproliferative and proapoptotic activity of miRNA-155.
    • Partial logistic artificial neural network for competing risks regularized with automatic relevance determination.
    • Split hybridisation probes for electrochemical typing of single-nucleotide polymorphisms.
    • Challenges in projecting clustering results across gene expression-profiling datasets.
    • Time-course analysis of genome-wide gene expression data from hormone-responsive human breast cancer cells.
    • Canine tumor cross-species genomics uncovers targets linked to osteosarcoma progression.
    • hSirT1-dependent regulation of the PCAF-E2F1-p73 apoptotic pathway in response to DNA damage.
    • FancyGene: dynamic visualization of gene structures and protein domain architectures on genomic loci.
    • Differential regulation of iron homeostasis during human macrophage polarized activation.
    • Noncoding RNA synthesis and loss of Polycomb group repression accompanies the colinear activation of the human HOXA cluster.
    • Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes.
    • A methodology to identify consensus classes from clustering algorithms applied to immunohistochemical data from breast cancer patients.
    • Conditional independence relations among biological markers may improve clinical decision as in the case of triple negative breast cancers.
    • The MYD88-independent pathway is not mobilized in human neutrophils stimulated via TLR4.
    • Macrophage polarization comes of age
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