about
Matrin 3 binds and stabilizes mRNAA high-resolution anatomical atlas of the transcriptome in the mouse embryoCell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteinsComparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strainsThe nerve growth factor receptor CD271 is crucial to maintain tumorigenicity and stem-like properties of melanoma cellsAtaxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granulesThe BTB and CNC homology 1 (BACH1) target genes are involved in the oxidative stress response and in control of the cell cycleDissecting the genomic complexity underlying medulloblastomaRegulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicingAn endoribonuclease-prepared siRNA screen in human cells identifies genes essential for cell divisionARH-seq: identification of differential splicing in RNA-seq dataInfluence of RNA extraction methods and library selection schemes on RNA-seq data.A gene expression map of human chromosome 21 orthologues in the mouse.Construction and analysis of a human-chimpanzee comparative clone map.Functional analysis and identification of cis-regulatory elements of human chromosome 21 gene promotersA simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods.Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma.Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndromeChIP-Seq and RNA-Seq analyses identify components of the Wnt and Fgf signaling pathways as Prep1 target genes in mouse embryonic stem cells.The direction of cross affects [corrected] obesity after puberty in male but not female offspringGene expression variation in Down's syndrome mice allows prioritization of candidate genesGenomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options.Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age GroupsMedulloblastoma-associated DDX3 variant selectively alters the translational response to stress.Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.Hypermutation of the inactive X chromosome is a frequent event in cancer.Active medulloblastoma enhancers reveal subgroup-specific cellular origins.Network and systems biology: essential steps in virtualising drug discovery and development.Cancer Precision Medicine: Why More Is More and DNA Is Not Enough.Human Lineage-Specific Transcriptional Regulation through GA-Binding Protein Transcription Factor Alpha (GABPa).BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence.Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing.Parallel profiling of the transcriptome, cistrome, and epigenome in the cellular response to ionizing radiation.Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments.Screening of human gene promoter activities using transfected-cell arrays.Primary differentiation in the human blastocyst: comparative molecular portraits of inner cell mass and trophectoderm cells.Erratum to: 'The direction of cross affects obesity after puberty in male but not female offspring'.Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer.
P50
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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Marie-Laure Yaspo
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