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Maria Savino

Showing results (41-50 of 60) with videos related to

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Clinical Laboratory|January 14, 2012
Effectiveness of a high-throughput genetic analysis in the identification of responders/non-responders to CYP2D6-metabolized drugsMaria Savino, Davide Seripa, Antonietta P Gallo, et al.
Biomedicines|December 23, 2022
Circadian Genes Expression Patterns in Disorders Due to Enzyme Deficiencies in the Heme Biosynthetic PathwayMaria Savino, Claudio Carmine Guida, Maria Nardella, et al.
Cell Metabolism|December 28, 2020
High Fructose Drives the Serine Synthesis Pathway in Acute Myeloid Leukemic CellsSangmoo Jeong, Angela Maria Savino, Rachel Chirayil, et al.
Human Mutation|October 2, 2004
Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel allelesMaria Savino, Maria d'Apolito, Vincenza Formica, et al.
Heliyon|July 29, 2024
Synergistic drug interactions of the histone deacetylase inhibitor givinostat (ITF2357) in CRLF2-rearranged pediatric B-cell precursor acute lymphoblastic leukemia identified by high-throughput drug screeningAthanasios Oikonomou, Titus Watrin, Luigia Valsecchi, et al.
Human Mutation|September 5, 2003
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variantMaria Savino, Adriana Borriello, Maria D'Apolito, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|December 19, 2015
Cerebral Hypoperfusion in Hereditary Coproporphyria (HCP): A Single Photon Emission Computed Tomography (SPECT) StudyGuido Valle, Claudio Carmine Guida, Michelangelo Nasuto, et al.
Pain Medicine (Malden, Mass.)|May 20, 2015
Role of CYP2D6 Polymorphisms in the Outcome of Postoperative Pain TreatmentDavide Seripa, Paola Latina, Andrea Fontana, et al.
Human Genetics|April 6, 2002
Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 geneMarco Seri, Maria Savino, Domenico Bordo, et al.
Clinical Hemorheology and Microcirculation|October 16, 2018
Timing of clopidogrel loading dose on peripheral blood endothelial progenitor cells, SDF-1α and neointimal hyperplasia in carotid stentingGiuseppe Di Stolfo, Sandra Mastroianno, Maurizio Ruggieri, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Clinical Laboratory|January 14, 2012
Effectiveness of a high-throughput genetic analysis in the identification of responders/non-responders to CYP2D6-metabolized drugsMaria Savino, Davide Seripa, Antonietta P Gallo, et al.
Biomedicines|December 23, 2022
Circadian Genes Expression Patterns in Disorders Due to Enzyme Deficiencies in the Heme Biosynthetic PathwayMaria Savino, Claudio Carmine Guida, Maria Nardella, et al.
Cell Metabolism|December 28, 2020
High Fructose Drives the Serine Synthesis Pathway in Acute Myeloid Leukemic CellsSangmoo Jeong, Angela Maria Savino, Rachel Chirayil, et al.
Human Mutation|October 2, 2004
Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel allelesMaria Savino, Maria d'Apolito, Vincenza Formica, et al.
Heliyon|July 29, 2024
Synergistic drug interactions of the histone deacetylase inhibitor givinostat (ITF2357) in CRLF2-rearranged pediatric B-cell precursor acute lymphoblastic leukemia identified by high-throughput drug screeningAthanasios Oikonomou, Titus Watrin, Luigia Valsecchi, et al.
Human Mutation|September 5, 2003
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variantMaria Savino, Adriana Borriello, Maria D'Apolito, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|December 19, 2015
Cerebral Hypoperfusion in Hereditary Coproporphyria (HCP): A Single Photon Emission Computed Tomography (SPECT) StudyGuido Valle, Claudio Carmine Guida, Michelangelo Nasuto, et al.
Pain Medicine (Malden, Mass.)|May 20, 2015
Role of CYP2D6 Polymorphisms in the Outcome of Postoperative Pain TreatmentDavide Seripa, Paola Latina, Andrea Fontana, et al.
Human Genetics|April 6, 2002
Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 geneMarco Seri, Maria Savino, Domenico Bordo, et al.
Clinical Hemorheology and Microcirculation|October 16, 2018
Timing of clopidogrel loading dose on peripheral blood endothelial progenitor cells, SDF-1α and neointimal hyperplasia in carotid stentingGiuseppe Di Stolfo, Sandra Mastroianno, Maurizio Ruggieri, et al.
Pageof 6