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29 results for Caputo,+Viviana

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Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode
Author / Creator:Hauser, Jonas ; Pisa, Edoardo ; Arias Vásquez, Alejandro ; Tomasi, Flavio ; Traversa, Alice ; Chiodi, Valentina ; Martin, Francois-Pierre ; Sprenger, Norbert ; Lukjancenko, Oksana ; Zollinger, Alix ; Metairon, Sylviane ; Schneider, Nora ; Steiner, Pascal ; Martire, Alberto ; Caputo, Viviana ; Macrì, Simone
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2021-07, Vol.26 (7), p.2854-2871
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Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
Author / Creator:Kortüm, Fanny ; Caputo, Viviana ; Bauer, Christiane K ; Stella, Lorenzo ; Ciolfi, Andrea ; Alawi, Malik ; Bocchinfuso, Gianfranco ; Flex, Elisabetta ; Paolacci, Stefano ; Dentici, Maria Lisa ; Grammatico, Paola ; Korenke, Georg Christoph ; Leuzzi, Vincenzo ; Mowat, David ; Nair, Lal D V ; Nguyen, Thi Tuyet Mai ; Thierry, Patrick ; White, Susan M ; Dallapiccola, Bruno ; Pizzuti, Antonio ; Campeau, Philippe M ; Tartaglia, Marco ; Kutsche, Kerstin
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2015-06, Vol.47 (6), p.661-667
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APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants
Author / Creator:Bianco, Salvatore Daniele ; Parca, Luca ; Petrizzelli, Francesco ; Biagini, Tommaso ; Giovannetti, Agnese ; Liorni, Niccolò ; Napoli, Alessandro ; Carella, Massimo ; Procaccio, Vincent ; Lott, Marie T. ; Zhang, Shiping ; Vescovi, Angelo Luigi ; Wallace, Douglas C. ; Caputo, Viviana ; Mazza, Tommaso
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2023-08, Vol.14 (1), p.5058-13, Article 5058
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Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities
Author / Creator:Pisa, Edoardo ; Traversa, Alice ; Caputo, Viviana ; Ottomana, Angela Maria ; Hauser, Jonas ; Macrì, Simone
Publisher:Switzerland: Frontiers Research Foundation
Journal title:Frontiers in cellular neuroscience, 2023-01, Vol.17, p.1091890-1091890
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Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding
Author / Creator:Caputo, Viviana ; Sinibaldi, Lorenzo ; Fiorentino, Alessia ; Parisi, Chiara ; Catalanotto, Caterina ; Pasini, Augusto ; Cogoni, Carlo ; Pizzuti, Antonio
Publisher:United States: Public Library of Science
Journal title:PloS one, 2011-12, Vol.6 (12), p.e28656-e28656
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Prenatal expression of d-aspartate oxidase causes early cerebral d-aspartate depletion and influences brain morphology and cognitive functions at adulthood
Author / Creator:De Rosa, Arianna ; Mastrostefano, Francesca ; Di Maio, Anna ; Nuzzo, Tommaso ; Saitoh, Yasuaki ; Katane, Masumi ; Isidori, Andrea M. ; Caputo, Viviana ; Marotta, Pina ; Falco, Geppino ; De Stefano, Maria Egle ; Homma, Hiroshi ; Usiello, Alessandro ; Errico, Francesco
Publisher:Vienna: Springer Vienna
Journal title:Amino acids, 2020-04, Vol.52 (4), p.597-617
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Genomic and physiological resilience in extreme environments are associated with a secure attachment style
Author / Creator:Caputo, Viviana ; Pacilli, Maria Giuseppina ; Arisi, Ivan ; Mazza, Tommaso ; Brandi, Rossella ; Traversa, Alice ; Casasanta, Giampietro ; Pisa, Edoardo ; Sonnessa, Michele ; Healey, Beth ; Moggio, Lorenzo ; D’Onofrio, Mara ; Alleva, Enrico ; Macrì, Simone
Publisher:London: Nature Publishing Group UK
Journal title:Translational psychiatry, 2020-06, Vol.10 (1), p.185, Article 185
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Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome
Author / Creator:Flex, Elisabetta ; Ciolfi, Andrea ; Caputo, Viviana ; Fodale, Valentina ; Leoni, Chiara ; Melis, Daniela ; Bedeschi, Maria Francesca ; Mazzanti, Laura ; Pizzuti, Antonio ; Tartaglia, Marco ; Zampino, Giuseppe
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2013-08, Vol.50 (8), p.493-499
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Investigating Mitochondrial Gene Expression Patterns in Drosophila melanogaster Using Network Analysis to Understand Aging Mechanisms
Author / Creator:Mangoni, Manuel ; Petrizzelli, Francesco ; Liorni, Niccolò ; Bianco, Salvatore Daniele ; Biagini, Tommaso ; Napoli, Alessandro ; Adinolfi, Marta ; Guzzi, Pietro Hiram ; Novelli, Antonio ; Caputo, Viviana ; Mazza, Tommaso
Publisher:Basel: MDPI AG
Journal title:Applied sciences, 2023-06, Vol.13 (12), p.7342
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Potential Role of eNOS Genetic Variants in Ischemic Heart Disease Susceptibility and Clinical Presentation
Author / Creator:Severino, Paolo ; D’Amato, Andrea ; Prosperi, Silvia ; Magnocavallo, Michele ; Mariani, Marco Valerio ; Netti, Lucrezia ; Birtolo, Lucia Ilaria ; De Orchi, Paolo ; Chimenti, Cristina ; Maestrini, Viviana ; Miraldi, Fabio ; Lavalle, Carlo ; Caputo, Viviana ; Palmirotta, Raffaele ; Mancone, Massimo ; Fedele, Francesco
Publisher:Basel: MDPI AG
Journal title:Journal of cardiovascular development and disease, 2021-09, Vol.8 (9), p.116
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Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy–Walker malformation
Author / Creator:Traversa, Alice ; Bernardo, Silvia ; Paiardini, Alessandro ; Giovannetti, Agnese ; Marchionni, Enrica ; Genovesi, Maria Luce ; Guadagnolo, Daniele ; Torres, Barbara ; Paolacci, Stefano ; Bernardini, Laura ; Mazza, Tommaso ; Carella, Massimo ; Caputo, Viviana ; Pizzuti, Antonio
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1054-n/a
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Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co‐inheritance
Author / Creator:Traversa, Alice ; Marchionni, Enrica ; Giovannetti, Agnese ; Genovesi, Maria L. ; Panzironi, Noemi ; Margiotti, Katia ; Napoli, Giulia ; Piceci Sparascio, Francesca ; De Luca, Alessandro ; Petrizzelli, Francesco ; Carella, Massimo ; Cardona, Francesco ; Bernardo, Silvia ; Manganaro, Lucia ; Mazza, Tommaso ; Pizzuti, Antonio ; Caputo, Viviana
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1336-n/a
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Exposure to 3′Sialyllactose-Poor Milk during Lactation Impairs Cognitive Capabilities in Adulthood
Author / Creator:Pisa, Edoardo ; Martire, Alberto ; Chiodi, Valentina ; Traversa, Alice ; Caputo, Viviana ; Hauser, Jonas ; Macrì, Simone
Publisher:Basel: MDPI AG
Journal title:Nutrients, 2021-12, Vol.13 (12), p.4191
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Intussusception After Roux-en-Y Gastric Bypass: Laparoscopic Management
Author / Creator:Facchiano, Enrico ; Soricelli, Emanuele ; Leuratti, Luca ; Caputo, Viviana ; Quartararo, Giovanni ; Lucchese, Marcello
Publisher:New York: Springer US
Journal title:Obesity surgery, 2018-07, Vol.28 (7), p.2145-2147
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Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis
Author / Creator:Napoli, Giulia ; Panzironi, Noemi ; Traversa, Alice ; Catalanotto, Caterina ; Pace, Valentina ; Petrizzelli, Francesco ; Giovannetti, Agnese ; Lazzari, Sara ; Cogoni, Carlo ; Tartaglia, Marco ; Carella, Massimo ; Mazza, Tommaso ; Pizzuti, Antonio ; Parisi, Chiara ; Caputo, Viviana
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2022-08, Vol.59 (8), p.4825-4838
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Protection against Ischemic Heart Disease: A Joint Role for eNOS and the K[sub.ATP] Channel
Author / Creator:Severino, Paolo ; D’Amato, Andrea ; Mancone, Massimo ; Palazzuoli, Alberto ; Mariani, Marco Valerio ; Prosperi, Silvia ; Myftari, Vincenzo ; Lavalle, Carlo ; Forleo, Giovanni Battista ; Birtolo, Lucia Ilaria ; Caputo, Viviana ; Miraldi, Fabio ; Chimenti, Cristina ; Badagliacca, Roberto ; Maestrini, Viviana ; Palmirotta, Raffaele ; Vizza, Carmine Dario ; Fedele, Francesco
Publisher:MDPI AG
Journal title:International journal of molecular sciences, 2023-04, Vol.24 (9)
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Protection against Ischemic Heart Disease: A Joint Role for eNOS and the KATP Channel
Author / Creator:Severino, Paolo ; D’Amato, Andrea ; Mancone, Massimo ; Palazzuoli, Alberto ; Mariani, Marco Valerio ; Prosperi, Silvia ; Myftari, Vincenzo ; Lavalle, Carlo ; Forleo, Giovanni Battista ; Birtolo, Lucia Ilaria ; Caputo, Viviana ; Miraldi, Fabio ; Chimenti, Cristina ; Badagliacca, Roberto ; Maestrini, Viviana ; Palmirotta, Raffaele ; Vizza, Carmine Dario ; Fedele, Francesco
Publisher:Basel: MDPI AG
Journal title:International journal of molecular sciences, 2023-04, Vol.24 (9), p.7927
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Craniofacial and Dental Anomalies of a Patient Carrying Two MicroRNA Variants: A Proof-Of-Concept Case Report
Author / Creator:Grenga, Camilla ; Guarnieri, Rosanna ; Mezio, Martina ; De Stefano, Adriana Assunta ; Galluccio, Gabriella ; Di Giorgio, Roberto ; Giovannetti, Agnese ; Pizzuti, Antonio ; Caputo, Viviana ; Barbato, Ersilia
Publisher:England: John Wiley and Sons Inc
Journal title:Clinical case reports, 2025-04, Vol.13 (4), p.e70137
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Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study
Author / Creator:Putotto, Carolina ; Pulvirenti, Federica ; Pugnaloni, Flaminia ; Isufi, Ina ; Unolt, Marta ; Anaclerio, Silvia ; Caputo, Viviana ; Bernardini, Laura ; Messina, Elisa ; Moretti, Corrado ; Tarani, Luigi ; Marino, Bruno ; Versacci, Paolo
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2022-12, Vol.13 (12), p.2334
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Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Author / Creator:Valente, Enza Maria ; Abou-Sleiman, Patrick M. ; Caputo, Viviana ; Miratul M. K. Muqit ; Harvey, Kirsten ; Gispert, Suzana ; Ali, Zeeshan ; Del Turco, Domenico ; Bentivoglio, Anna Rita ; Healy, Daniel G. ; Albanese, Alberto ; Nussbaum, Robert ; González-Maldonado, Rafael ; Deller, Thomas ; Salvi, Sergio ; Cortelli, Pietro ; Gilks, William P. ; Latchman, David S. ; Harvey, Robert J. ; Dallapiccola, Bruno ; Auburger, Georg ; Wood, Nicholas W.
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2004-05, Vol.304 (5674), p.1158-1160
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Showing 1 to 20 of 29 results

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Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode

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Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome

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APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

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Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities

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Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding

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Prenatal expression of d-aspartate oxidase causes early cerebral d-aspartate depletion and influences brain morphology and cognitive functions at adulthood

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Genomic and physiological resilience in extreme environments are associated with a secure attachment style

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Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome

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Investigating Mitochondrial Gene Expression Patterns in Drosophila melanogaster Using Network Analysis to Understand Aging Mechanisms

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Potential Role of eNOS Genetic Variants in Ischemic Heart Disease Susceptibility and Clinical Presentation

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Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy–Walker malformation

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Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co‐inheritance

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Exposure to 3′Sialyllactose-Poor Milk during Lactation Impairs Cognitive Capabilities in Adulthood

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Intussusception After Roux-en-Y Gastric Bypass: Laparoscopic Management

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Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis

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Protection against Ischemic Heart Disease: A Joint Role for eNOS and the K[sub.ATP] Channel

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Protection against Ischemic Heart Disease: A Joint Role for eNOS and the KATP Channel

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Craniofacial and Dental Anomalies of a Patient Carrying Two MicroRNA Variants: A Proof-Of-Concept Case Report

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Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study

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Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

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