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Annamaria Fra

Showing results (1-10 of 20) with videos related to

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Frontiers in Molecular Neuroscience|June 22, 2017
Cysteines as Redox Molecular Switches and Targets of DiseaseAnnamaria Fra, Edgar D Yoboue, Roberto Sitia
Methods in Molecular Biology (Clifton, N.J.)|September 9, 2018
Cellular Models for the SerpinopathiesAnnamaria Fra, Emanuela D'Acunto, Mattia Laffranchi, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 18, 2023
Characterization of Novel Alpha-1-Antitrypsin Coding Variants in a Mammalian Cellular ModelAndrea Denardo, Emna Ben Khlifa, Mattia Bignotti, et al.
Human Molecular Genetics|March 15, 2018
Heteropolymerization of α-1-antitrypsin mutants in cell models mimicking heterozygosityMattia Laffranchi, Romina Berardelli, Riccardo Ronzoni, et al.
Cellular and Molecular Life Sciences : CMLS|August 18, 2021
Neuroserpin: structure, function, physiology and pathologyEmanuela D'Acunto, Annamaria Fra, Cristina Visentin, et al.
Human Mutation|June 9, 2018
Real-world clinical applicability of pathogenicity predictors assessed on SERPINA1 mutations in alpha-1-antitrypsin deficiencyEdoardo Giacopuzzi, Mattia Laffranchi, Romina Berardelli, et al.
Cellular and Molecular Life Sciences : CMLS|December 12, 2023
Probing of the reactive center loop region of alpha-1-antitrypsin by mutagenesis predicts new type-2 dysfunctional variantsAndrea Denardo, Emna Ben Khlifa, Mattia Bignotti, et al.
Plos One|January 12, 2019
Characterisation of a type II functionally-deficient variant of alpha-1-antitrypsin discovered in the general populationMattia Laffranchi, Emma L K Elliston, Fabrizio Gangemi, et al.
Scientific Reports|January 19, 2018
Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural InsightSonia Caccia, Chiara Suffritti, Thomas Carzaniga, et al.
The FEBS Journal|October 15, 2020
The molecular species responsible for α<sub>1</sub> -antitrypsin deficiency are suppressed by a small molecule chaperoneRiccardo Ronzoni, Nina Heyer-Chauhan, Annamaria Fra, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Frontiers in Molecular Neuroscience|June 22, 2017
Cysteines as Redox Molecular Switches and Targets of DiseaseAnnamaria Fra, Edgar D Yoboue, Roberto Sitia
Methods in Molecular Biology (Clifton, N.J.)|September 9, 2018
Cellular Models for the SerpinopathiesAnnamaria Fra, Emanuela D'Acunto, Mattia Laffranchi, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 18, 2023
Characterization of Novel Alpha-1-Antitrypsin Coding Variants in a Mammalian Cellular ModelAndrea Denardo, Emna Ben Khlifa, Mattia Bignotti, et al.
Human Molecular Genetics|March 15, 2018
Heteropolymerization of α-1-antitrypsin mutants in cell models mimicking heterozygosityMattia Laffranchi, Romina Berardelli, Riccardo Ronzoni, et al.
Cellular and Molecular Life Sciences : CMLS|August 18, 2021
Neuroserpin: structure, function, physiology and pathologyEmanuela D'Acunto, Annamaria Fra, Cristina Visentin, et al.
Human Mutation|June 9, 2018
Real-world clinical applicability of pathogenicity predictors assessed on SERPINA1 mutations in alpha-1-antitrypsin deficiencyEdoardo Giacopuzzi, Mattia Laffranchi, Romina Berardelli, et al.
Cellular and Molecular Life Sciences : CMLS|December 12, 2023
Probing of the reactive center loop region of alpha-1-antitrypsin by mutagenesis predicts new type-2 dysfunctional variantsAndrea Denardo, Emna Ben Khlifa, Mattia Bignotti, et al.
Plos One|January 12, 2019
Characterisation of a type II functionally-deficient variant of alpha-1-antitrypsin discovered in the general populationMattia Laffranchi, Emma L K Elliston, Fabrizio Gangemi, et al.
Scientific Reports|January 19, 2018
Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural InsightSonia Caccia, Chiara Suffritti, Thomas Carzaniga, et al.
The FEBS Journal|October 15, 2020
The molecular species responsible for α<sub>1</sub> -antitrypsin deficiency are suppressed by a small molecule chaperoneRiccardo Ronzoni, Nina Heyer-Chauhan, Annamaria Fra, et al.
Pageof 2