Francesco Salvatore


Ontology type: schema:Person     


Person Info

NAME

Francesco

SURNAME

Salvatore

Publications in SciGraph latest 50 shown

  • 2018-12 Oropharyngeal microbiome evaluation highlights Neisseria abundance in active celiac patients in SCIENTIFIC REPORTS
  • 2017-12 Proteotoxicity in cardiac amyloidosis: amyloidogenic light chains affect the levels of intracellular proteins in human heart cells in SCIENTIFIC REPORTS
  • 2017-12 Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants in BMC MEDICAL GENETICS
  • 2017-08 “Classical organic acidurias”: diagnosis and pathogenesis in CLINICAL AND EXPERIMENTAL MEDICINE
  • 2017-04 Effect of lifelong football training on the expression of muscle molecular markers involved in healthy longevity in EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY
  • 2017-01 Corrigendum: No Change in the Mucosal Gut Microbiome is Associated with Celiac Disease-Specific Microbiome Alteration in Adult Patients in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2016-12 Biomimetic carriers mimicking leukocyte plasma membrane to increase tumor vasculature permeability in SCIENTIFIC REPORTS
  • 2016-12 Epigenetic features of FoxP3 in children with cow’s milk allergy in CLINICAL EPIGENETICS
  • 2016-12 The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase in SCIENTIFIC REPORTS
  • 2016-11 An ancestral host defence peptide within human β-defensin 3 recapitulates the antibacterial and antiviral activity of the full-length molecule in SCIENTIFIC REPORTS
  • 2016-11 No Change in the Mucosal Gut Microbiome is Associated With Celiac Disease-Specific Microbiome Alteration in Adult Patients in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2016-06 Metagenomics Reveals Dysbiosis and a Potentially Pathogenic N. flavescens Strain in Duodenum of Adult Celiac Patients in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2015-12 Differences in DNA methylation profile of Th1 and Th2 cytokine genes are associated with tolerance acquisition in children with IgE-mediated cow’s milk allergy in CLINICAL EPIGENETICS
  • 2015-12 Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal disease in BMC RESEARCH NOTES
  • 2015-02 A role for D-aspartate oxidase in schizophrenia and in schizophrenia-related symptoms induced by phencyclidine in mice in TRANSLATIONAL PSYCHIATRY
  • 2015 Carcinoembryonic Antigen Family Cell Adhesion Molecules (CEACAM) as Colorectal Cancer Biomarkers in BIOMARKERS IN CANCER
  • 2015 Oncoproteomic Approaches to Cancer Marker Discovery: The Case of Colorectal Cancer in BIOMARKERS IN CANCER
  • 2014-12 Complete sequencing of Novosphingobium sp. PP1Y reveals a biotechnologically meaningful metabolic pattern in BMC GENOMICS
  • 2014-12 ABCG2, a novel antigen to sort luminal progenitors of BRCA1- breast cancer cells in MOLECULAR CANCER
  • 2014-12 Quality of Life (QoL) assessment in a cohort of patients with Phenylketonuria in BMC PUBLIC HEALTH
  • 2014 Carcinoembryonic Antigen-Family Cell Adhesion Molecules (CEACAM) as Colorectal Cancer Biomarkers in BIOMARKERS IN CANCER
  • 2014 Oncoproteomic Approaches to Cancer Marker Discovery: The Case of Colorectal Cancer in BIOMARKERS IN CANCER
  • 2013-12 PEGylated helper-dependent adenoviral vector expressing human Apo A-I for gene therapy in LDLR-deficient mice in GENE THERAPY
  • 2013-12 PEGylated helper-dependent adenoviral vector expressing human Apo A-I for gene therapy in LDLR-deficient mice in GENE THERAPY
  • 2013-05 An Altered Gut Microbiome Profile in a Child Affected by Crohn's Disease Normalized After Nutritional Therapy in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2010-12 The first case of mitochondrial acetoacetyl-CoA thiolase deficiency identified by expanded newborn metabolic screening in Italy: the importance of an integrated diagnostic approach in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2006-12 CMRL-T, a novel T-cell line showing asynchronous phenotype (CD34+/CD1a−/TCRαβ+) and dual T-cell receptor β chain in LEUKEMIA
  • 2006 Epistasis in Cystic Fibrosis in ENCYCLOPEDIC REFERENCE OF GENOMICS AND PROTEOMICS IN MOLECULAR MEDICINE
  • 2005-04 Significant reduction of the hybrid BCR/ABL transcripts after induction and consolidation therapy is a powerful predictor of treatment response in adult Philadelphia-positive acute lymphoblastic leukemia in LEUKEMIA
  • 2004-12 Genetic Typing of Corallium rubrum in JOURNAL OF MARINE BIOTECHNOLOGY
  • 2002-12 BCR/ABL genes and leukemic phenotype: from molecular mechanisms to clinical correlations in ONCOGENE
  • 2002-02 Evaluation of circulating levels and renal clearance of natural amino acids in patients with Cushing’s disease in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2001-12 Differential distribution of aldolase A and C in the human central nervous system in BRAIN CELL BIOLOGY
  • 2001-10 Characterization of two novel cell lines, DERL-2 (CD56+/CD3+/TCRγδ+) and DERL-7 (CD56+/CD3−/TCRγδ−), derived from a single patient with CD56+ non-Hodgkin's lymphoma in LEUKEMIA
  • 2001-05 Transglutaminase 1 Gene Mutations in Italian Patients with Autosomal Recessive Lamellar Ichthyosis in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2000-02 Identification of a novel mutation in the ryanodine receptor gene (RYR1) in a malignant hyperthermia Italian family in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-05 Novel six-nucleotide deletion in the hepatic fructose-1,6-bisphosphate aldolase gene in a patient with hereditary fructose intolerance and enzyme structure-function implications in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-05 A case of discordance between genotype and phenotype in a malignant hyperthermia family in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1997-09 JURL-MK1 (c-kithigh/CD30−/CD40−) and JURL-MK2 (c-kitlow/CD30+/CD40+) cell lines: ‘two-sided’ model for investigating leukemic megakaryocytopoiesis in LEUKEMIA
  • 1994-06 A unique origin for Sicilian (δβ)∘-thalassemia in 33 unrelated families and its rapid diagnostic characterization by PCR analysis in HUMAN GENETICS
  • 1989-08 Human glyceraldehyde-3-phosphate dehydrogenase pseudogenes: Molecular evolution and a possible mechanism for amplification in BIOCHEMICAL GENETICS
  • 1989-08 Human glyceraldehyde-3-phosphate dehydrogenase pseudogenes: Molecular evolution and a possible mechanism for amplification in BIOCHEMICAL GENETICS
  • 1989-06 Assignment of human aldolase C gene to chromosome 17, region cen→q21.1 in HUMAN GENETICS
  • 1989 The Serum Gamma-glutamyltransferase Isoenzyme System and its Diagnostic Role in Hepatobiliary Diseases in CLINICAL BIOCHEMISTRY IN HEPATOBILIARY DISEASES
  • 1989 Molecular Biology of the Human Aldolase Isoenzyme Gene Family in CLINICAL CHEMISTRY
  • 1987-10 Mapping of a restriction fragment length polymorphism within the human aldolase B gene in HUMAN GENETICS
  • 1984 Pseudouridine: A Biochemical Marker for Cancer in GENETIC AND PHENOTYPIC MARKERS OF TUMORS
  • 1983-09 Isolation and characterization of a tRNA(guanine-7-)-methyltransferase from Salmonella typhimurium in MOLECULAR AND CELLULAR BIOCHEMISTRY
  • 1983 Modified Nucleosides in Body Fluids of Tumor-Bearing Patients in MODIFIED NUCLEOSIDES AND CANCER
  • 1982 Modified nucleosides from transfer ribonucleic acid as tumor markers in BIOCHEMISTRY OF S-ADENOSYLMETHIONINE AND RELATED COMPOUNDS
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