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Calling on a million minds for community annotation in WikiProteinsHundreds of variants clustered in genomic loci and biological pathways affect human heightEnhanced exon-skipping induced by U7 snRNA carrying a splicing silencer sequence: Promising tool for DMD therapyAntisense-mediated exon skipping: a versatile tool with therapeutic and research applicationsGeneHopper: a web-based search engine to link gene-expression platforms through GenBank accession numbersGene expression variation between mouse inbred strainsThe Implicitome: A Resource for Rationalizing Gene-Disease AssociationsGenome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levelsThe Complete Genome Sequence of the Murine Pathobiont Helicobacter typhlonius.Novel protein-protein interactions inferred from literature contextMutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeBBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert CentresGenome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsThe Genome of the Netherlands: design, and project goalsToward a roadmap in global biobanking for healthTargeting several CAG expansion diseases by a single antisense oligonucleotideIn silico discovery and experimental validation of new protein-protein interactionsHypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophyIntegrated analysis of DNA copy number and gene expression microarray data using gene setsLow dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double-knockout miceLiterature-aided meta-analysis of microarray data: a compendium study on muscle development and disease.Antisense-induced exon skipping for duplications in Duchenne muscular dystrophySerum protein profiling in mice: identification of Factor XIIIa as a potential biomarker for muscular dystrophy.CORE_TF: a user-friendly interface to identify evolutionary conserved transcription factor binding sites in sets of co-regulated genes.Assessment of the feasibility of exon 45-55 multiexon skipping for Duchenne muscular dystrophyCost-effective HRMA pre-sequence typing of clone libraries; application to phage display selectionTargeting TGF-β Signaling by Antisense Oligonucleotide-mediated Knockdown of TGF-β Type I Receptor.Effect of post-mortem delay on N-terminal huntingtin protein fragments in human control and Huntington disease brain lysates.Human papillomavirus deregulates the response of a cellular network comprising of chemotactic and proinflammatory genes.Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause diseaseAn immune response network associated with blood lipid levels.Genome-wide assessment of differential roles for p300 and CBP in transcription regulation.Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distributionFacioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.Systemic administration of PRO051 in Duchenne's muscular dystrophy.Advances in Duchenne muscular dystrophy gene therapy.Advances in therapeutic RNA-targeting.Therapeutic exon skipping for dysferlinopathies?Transcriptome and genome sequencing uncovers functional variation in humansEntries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.
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P50
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