about
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme functionThe complete nucleotide sequence of the gene coding for the human aldolase CCracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesThe multi-faceted aspects of the complex cardiac Nav1.5 protein in membrane function and pathophysiologyThe impact of nanoparticle protein corona on cytotoxicity, immunotoxicity and target drug deliveryDistribution of human beta-defensin polymorphisms in various control and cystic fibrosis populationsComplete sequencing of Novosphingobium sp. PP1Y reveals a biotechnologically meaningful metabolic patternFunctional and molecular modelling studies of two hereditary fructose intolerance-causing mutations at arginine 303 in human liver aldolaseGenetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants.Genetic modifiers of liver disease in cystic fibrosis.A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in miceBiomimetic carriers mimicking leukocyte plasma membrane to increase tumor vasculature permeability.Therapeutic angiogenesis in diabetic apolipoprotein E-deficient mice using bone marrow cells, functional hemangioblasts and metabolic intervention.Partial purification and MALDI-TOF MS analysis of UN1, a tumor antigen membrane glycoprotein.Gaining insights into the Bcr-Abl activity-independent mechanisms of resistance to imatinib mesylate in KCL22 cells: a comparative proteomic approach.The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA targetProtein network study of human AF4 reveals its central role in RNA Pol II-mediated transcription and in phosphorylation-dependent regulatory mechanisms.A novel anti-aldolase C antibody specifically interacts with residues 85-102 of the proteinA new human species of aldolase A mRNA from fibroblasts.Human aldolase A gene. Structural organization and tissue-specific expression by multiple promoters and alternate mRNA processing.ABCG2, a novel antigen to sort luminal progenitors of BRCA1- breast cancer cells.Diverse human aldolase C gene promoter regions are required to direct specific LacZ expression in the hippocampus and Purkinje cells of transgenic mice.Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavalpha1S-subunit.Quality of Life (QoL) assessment in a cohort of patients with phenylketonuria.Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.Altered brain protein expression profiles are associated with molecular neurological dysfunction in the PKU mouse model.Haemophilia B: from molecular diagnosis to gene therapy.The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches.Human anti-nucleolin recombinant immunoagent for cancer therapy.Functional assay of tRNA molecules transcribed from a purified gene.Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal disease.Metagenomics Reveals Dysbiosis and a Potentially Pathogenic N. flavescens Strain in Duodenum of Adult Celiac Patients.Design and activity of a cyclic mini-β-defensin analog: a novel antimicrobial tool.The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing.Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndromeThe complete sequence of a full length cDNA for human liver glyceraldehyde-3-phosphate dehydrogenase: evidence for multiple mRNA species.One-pot synthesis of pH-responsive hybrid nanogel particles for the intracellular delivery of small interfering RNA.Haemophilia A: molecular insights.Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis.Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Francesco Salvatore
@ast
Francesco Salvatore
@en
Francesco Salvatore
@es
Francesco Salvatore
@sl
type
label
Francesco Salvatore
@ast
Francesco Salvatore
@en
Francesco Salvatore
@es
Francesco Salvatore
@sl
prefLabel
Francesco Salvatore
@ast
Francesco Salvatore
@en
Francesco Salvatore
@es
Francesco Salvatore
@sl
P1053
A-1966-2011
P106
P1153
35397252800
P21
P31
P3829
P496
0000-0002-2346-3564