about
Insights into GATA-1-mediated gene activation versus repression via genome-wide chromatin occupancy analysisBridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity.A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer dataDOTS-Finder: a comprehensive tool for assessing driver genes in cancer genomes.LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancerIn Vivo Genetic Screens of Patient-Derived Tumors Revealed Unexpected Frailty of the Transformed Phenotype.RNAi screens identify CHD4 as an essential gene in breast cancer growth.Poly-glutamine expanded huntingtin dramatically alters the genome wide binding of HSF1.Genomics of acute myeloid leukemia: the next generation.The hidden genomic landscape of acute myeloid leukemia: subclonal structure revealed by undetected mutations.PML-RARA-associated cooperating mutations belong to a transcriptional network that is deregulated in myeloid leukemias.Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups.Peak shape clustering reveals biological insightsThe genomic and epigenomic landscapes of AML.In Vivo Functional Platform Targeting Patient-Derived Xenografts Identifies WDR5-Myc Association as a Critical Determinant of Pancreatic Cancer.Silencer elements as possible inhibitors of pseudoexon splicingComparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common feature.INSPEcT: a computational tool to infer mRNA synthesis, processing and degradation dynamics from RNA- and 4sU-seq time course experiments.Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups.A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.Effects of reboxetine on sleep and nocturnal cardiac autonomic activity in patients with dysthymia.Skeletal muscle gene expression profiling in mitochondrial disorders.Over-representation of exonic splicing enhancers in human intronless genes suggests multiple functions in mRNA processingWhole exome sequencing identifies driver mutations in asymptomatic computed tomography-detected lung cancers with normal karyotypeA wavelet based method to predict the alpha helix content in the secondary structure of globular proteinsNo unexpected CRISPR-Cas9 off-target activity revealed by trio sequencing of gene-edited miceMutational signatures in tumours induced by high and low energy radiation in Trp53 deficient miceDevelopment of Personalized Therapeutic Strategies by Targeting Actionable Vulnerabilities in Metastatic and Chemotherapy-Resistant Breast Cancer PDXs
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Laura Riva
@ast
Laura Riva
@en
Laura Riva
@es
Laura Riva
@nl
type
label
Laura Riva
@ast
Laura Riva
@en
Laura Riva
@es
Laura Riva
@nl
prefLabel
Laura Riva
@ast
Laura Riva
@en
Laura Riva
@es
Laura Riva
@nl
P1053
R-2562-2016
P106
P1153
7003865379
P21
P31
P3829
P496
0000-0001-5688-4915