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Alejandro Giorgetti

Showing results (91-100 of 100) with videos related to

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Scientific Reports|July 13, 2017
All muscarinic acetylcholine receptors (M<sub>1</sub>-M<sub>5</sub>) are expressed in murine brain microvascular endotheliumBeatrice Mihaela Radu, Antonio Marco Maria Osculati, Eda Suku, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 20, 2025
Prasugrel Intermediate Metabolite Modulates Platelet Inhibition by Negatively Interfering With an Active Metabolite: An Ex Vivo, In Vitro, and In Silico StudyPietro Minuz, Alejandro Giorgetti, Alessandra Meneguzzi, et al.
Genes|February 25, 2022
A Gain-of-Function Mutation on <i>BCKDK</i> Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid MetabolismAlice Maguolo, Giulia Rodella, Alejandro Giorgetti, et al.
BMC Genomics|August 29, 2014
Mesencephalic dopaminergic neurons express a repertoire of olfactory receptors and respond to odorant-like moleculesAlice Grison, Silvia Zucchelli, Alice Urzì, et al.
Viruses|May 25, 2024
Wide Real-Life Data Support Reduced Sensitivity of Antigen Tests for Omicron SARS-CoV-2 InfectionsChiara Piubelli, Davide Treggiari, Denise Lavezzari, et al.
Annals of Clinical and Translational Neurology|March 19, 2021
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorderTanja Schmitz-Hübsch, Silke Lux, Peter Bauer, et al.
International Journal of Molecular Sciences|April 3, 2020
Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early DiagnosisMarc Vila Cuenca, Giacomo Marchi, Anna Barqué, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2007
The implications of alternative splicing in the ENCODE protein complementMichael L Tress, Pier Luigi Martelli, Adam Frankish, et al.
Brain : a Journal of Neurology|May 2, 2017
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxiaMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
American Journal of Human Genetics|June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxiasPaulina Cunha, Emilien Petit, Marie Coutelier, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Scientific Reports|July 13, 2017
All muscarinic acetylcholine receptors (M<sub>1</sub>-M<sub>5</sub>) are expressed in murine brain microvascular endotheliumBeatrice Mihaela Radu, Antonio Marco Maria Osculati, Eda Suku, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 20, 2025
Prasugrel Intermediate Metabolite Modulates Platelet Inhibition by Negatively Interfering With an Active Metabolite: An Ex Vivo, In Vitro, and In Silico StudyPietro Minuz, Alejandro Giorgetti, Alessandra Meneguzzi, et al.
Genes|February 25, 2022
A Gain-of-Function Mutation on <i>BCKDK</i> Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid MetabolismAlice Maguolo, Giulia Rodella, Alejandro Giorgetti, et al.
BMC Genomics|August 29, 2014
Mesencephalic dopaminergic neurons express a repertoire of olfactory receptors and respond to odorant-like moleculesAlice Grison, Silvia Zucchelli, Alice Urzì, et al.
Viruses|May 25, 2024
Wide Real-Life Data Support Reduced Sensitivity of Antigen Tests for Omicron SARS-CoV-2 InfectionsChiara Piubelli, Davide Treggiari, Denise Lavezzari, et al.
Annals of Clinical and Translational Neurology|March 19, 2021
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorderTanja Schmitz-Hübsch, Silke Lux, Peter Bauer, et al.
International Journal of Molecular Sciences|April 3, 2020
Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early DiagnosisMarc Vila Cuenca, Giacomo Marchi, Anna Barqué, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2007
The implications of alternative splicing in the ENCODE protein complementMichael L Tress, Pier Luigi Martelli, Adam Frankish, et al.
Brain : a Journal of Neurology|May 2, 2017
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxiaMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
American Journal of Human Genetics|June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxiasPaulina Cunha, Emilien Petit, Marie Coutelier, et al.
Pageof 10