Drupal-Biblio17<style face="normal" font="default" size="100%">Metatranscriptomic analysis reveals gut microbiome bacterial genes in pyruvate and amino acid metabolism associated with hyperuricemia and gout in humans.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Aripiprazole as protector against COVID-19 mortality.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Characterization of the Common Genetic Variation in the Spanish Population of Navarre.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genotypic characterization and antimicrobial susceptibility of human isolates in Southern Spain.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel Variant and Possible Modifier Gene.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Shared germline genomic variants in two patients with double primary gastrointestinal stromal tumours (GISTs).</style>Drupal-Biblio17<style face="normal" font="default" size="100%">De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Real world evidence of calcifediol or vitamin D prescription and mortality rate of COVID-19 in a retrospective cohort of hospitalized Andalusian patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Community Assessment of the Predictability of Cancer Protein and Phosphoprotein Levels from Genomics and Transcriptomics.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mechanistic Models of Signaling Pathways Reveal the Drug Action Mechanisms behind Gender-Specific Gene Expression for Cancer Treatments.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nivolumab and sunitinib combination in advanced soft tissue sarcomas: a multicenter, single-arm, phase Ib/II trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pazopanib for treatment of typical solitary fibrous tumours: a multicentre, single-arm, phase 2 trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pazopanib for treatment of advanced malignant and dedifferentiated solitary fibrous tumour: a multicentre, single-arm, phase 2 trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">LRH-1 agonism favours an immune-islet dialogue which protects against diabetes mellitus.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The modular network structure of the mutational landscape of Acute Myeloid Leukemia.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations in TRAPPC11 are associated with a congenital disorder of glycosylation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Human DNA methylomes of neurodegenerative diseases show common epigenomic patterns.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Serum metabolomic profiling facilitates the non-invasive identification of metabolic biomarkers associated with the onset and progression of non-small cell lung cancer.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The EGR2 gene is involved in axonal Charcot-Marie-Tooth disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Two novel mutations in the BCKDK (branched-chain keto-acid dehydrogenase kinase) gene are responsible for a neurobehavioral deficit in two pediatric unrelated patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Differential gene-expression analysis defines a molecular pattern related to olive pollen allergy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Grape antioxidant dietary fiber inhibits intestinal polyposis in ApcMin/+ mice: relation to cell cycle and immune response.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel genes detected by transcriptional profiling from whole-blood cells in patients with early onset of acute coronary syndrome.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pathways systematically associated to Hirschsprung's disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Role of CPI-17 in restoring skin homoeostasis in cutaneous field of cancerization: effects of topical application of a film-forming medical device containing photolyase and UV filters.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hypoxia promotes efficient differentiation of human embryonic stem cells to functional endothelium.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecular profiling related to poor prognosis in thyroid carcinoma. Combining gene expression data and biological information.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Evidence for systems-level molecular mechanisms of tumorigenesis.</style>