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Activating RNAs associate with Mediator to enhance chromatin architecture and transcription. Nature 102.
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Foam cell specific LXRalpha ligand. PLoS One 103.
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Optimal precursor ion selection for LC-MALDI MS/MS. BMC Bioinformatics 104.
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DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer. PLoS Genetics 105.
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5 (2), p. 5:11 - 5:11 (2013)
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine 106.
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Evolutionary entropy predicts the outcome of selection: Competition for resources that vary in abundance and diversity. Theoretical Population Biology 107.
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Development and application of a DNA microarray-based yeast two-hybrid system. Nucleic Acids Research (London) 108.
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Evaluation of methods for modeling transcription factor sequence specificity. Nature biotechnology 109.
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The tissue-specific IncRNA Fendrr is an essential regulator of heart and body wall development in the mouse. Developmental Cell 110.
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Warburg effect and translocation-induced genomic instability: two yeast models for cancer cells. Frontiers in Oncology 111.
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Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Journal of Medical Genetics (London) 112.
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Human stromal (mesenchymal) stem cells from bone marrow, adipose tissue and skin exhibit differences in molecular phenotype and differentiation potential. Stem Cell Reviews 113.
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Janus-a comprehensive tool investigating the two faces of transcription. Bioinformatics 114.
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TREM2 and Neurodegenerative Disease. The New England Journal of Medicine: NEJM / Publ. by the Massachusetts Medical Society 115.
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Distinguishing true from false positives in genomic studies: p values. European Journal of Epidemiology 116.
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Transcriptomic responses generated by hepatocarcinogens in a battery of liver-based in vitro models. Carcinogenesis 117.
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LGALS3BP regulates centriole biogenesis and centrosome hypertrophy in cancer cells. Nature Communications 118.
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Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical Genetics: an international journal of genetics in medicine 119.
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Hypermutation of the inactive X chromosome is a frequent event in cancer. Cell 120.
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The enzymatic activity of the VEGFR2 receptor for the biosynthesis of dinucleoside polyphosphates. Journal of Molecular Medicine-JMM