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Capponi

Showing results (471-480 of 561) with videos related to

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JAMA Pediatrics|January 13, 2025
Pediatrician Perspectives on Incorporating Discussion of Police Encounters Into Anticipatory Guidance for Black Youth and Their CaregiversJeffrey M Eugene, Maria Nelson, Rebecca Neergaard, et al.
Nature Communications|May 5, 2026
Correction of the molecular phenotype of X-linked Dystonia-Parkinsonism reveals a non-canonical function of BRD4Simona Capponi, Sandra Ehret, Zeynep Camgöz, et al.
Frontiers in Cardiovascular Medicine|September 27, 2021
Case Report: Perioperative Kounis Syndrome in an Adolescent With Congenital GlaucomaGuglielmo Capponi, Mattia Giovannini, Ioanna Koniari, et al.
Contrast Media & Molecular Imaging|November 4, 2017
Labelling of <sup>90</sup>Y- and <sup>177</sup>Lu-DOTA-Bioconjugates for Targeted Radionuclide Therapy: A Comparison among Manual, Semiautomated, and Fully Automated SynthesisMichele Iori, Pier C Capponi, Sara Rubagotti, et al.
Frontiers in Immunology|June 12, 2023
Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosityAndrea Balduit, Anna Monica Bianco, Alessandro Mangogna, et al.
The American Journal of Cardiology|July 7, 2009
Safety and tolerability of dalcetrapibEvan A Stein, Erik S G Stroes, George Steiner, et al.
AIDS (London, England)|April 5, 2019
Distinct gut microbiota profile in antiretroviral therapy-treated perinatally HIV-infected patients associated with cardiac and inflammatory biomarkersLibera Sessa, Sofia Reddel, Emma Manno, et al.
Frontiers in Endocrinology|October 24, 2022
cAMP-specific phosphodiesterase 8A and 8B isoforms are differentially expressed in human testis and Leydig cell tumorFederica Campolo, Chiara Capponi, Maria Grazia Tarsitano, et al.
Annals of Neurology|March 28, 2012
Gain of glycosylation: a new pathomechanism of myelin protein zero mutationsValeria Prada, Mario Passalacqua, Maria Bono, et al.
Frontiers in Immunology|May 19, 2023
Case Report: Interindividual variability and possible role of heterozygous variants in a family with deficiency of adenosine deaminase 2: are all heterozygous born equals?Federica Pulvirenti, Bianca Laura Cinicola, Simona Ferrari, et al.
Pageof 57

Showing results (471-480 of 561) with videos related to

Sort By:
Pageof 57
JAMA Pediatrics|January 13, 2025
Pediatrician Perspectives on Incorporating Discussion of Police Encounters Into Anticipatory Guidance for Black Youth and Their CaregiversJeffrey M Eugene, Maria Nelson, Rebecca Neergaard, et al.
Nature Communications|May 5, 2026
Correction of the molecular phenotype of X-linked Dystonia-Parkinsonism reveals a non-canonical function of BRD4Simona Capponi, Sandra Ehret, Zeynep Camgöz, et al.
Frontiers in Cardiovascular Medicine|September 27, 2021
Case Report: Perioperative Kounis Syndrome in an Adolescent With Congenital GlaucomaGuglielmo Capponi, Mattia Giovannini, Ioanna Koniari, et al.
Contrast Media & Molecular Imaging|November 4, 2017
Labelling of <sup>90</sup>Y- and <sup>177</sup>Lu-DOTA-Bioconjugates for Targeted Radionuclide Therapy: A Comparison among Manual, Semiautomated, and Fully Automated SynthesisMichele Iori, Pier C Capponi, Sara Rubagotti, et al.
Frontiers in Immunology|June 12, 2023
Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosityAndrea Balduit, Anna Monica Bianco, Alessandro Mangogna, et al.
The American Journal of Cardiology|July 7, 2009
Safety and tolerability of dalcetrapibEvan A Stein, Erik S G Stroes, George Steiner, et al.
AIDS (London, England)|April 5, 2019
Distinct gut microbiota profile in antiretroviral therapy-treated perinatally HIV-infected patients associated with cardiac and inflammatory biomarkersLibera Sessa, Sofia Reddel, Emma Manno, et al.
Frontiers in Endocrinology|October 24, 2022
cAMP-specific phosphodiesterase 8A and 8B isoforms are differentially expressed in human testis and Leydig cell tumorFederica Campolo, Chiara Capponi, Maria Grazia Tarsitano, et al.
Annals of Neurology|March 28, 2012
Gain of glycosylation: a new pathomechanism of myelin protein zero mutationsValeria Prada, Mario Passalacqua, Maria Bono, et al.
Frontiers in Immunology|May 19, 2023
Case Report: Interindividual variability and possible role of heterozygous variants in a family with deficiency of adenosine deaminase 2: are all heterozygous born equals?Federica Pulvirenti, Bianca Laura Cinicola, Simona Ferrari, et al.
Pageof 57