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Laura Calabresi

Showing results (101-110 of 169) with videos related to

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Atherosclerosis|October 18, 2008
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemiaAngelo B Cefalù, Davide Noto, Lucia Magnolo, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 3, 2011
[LCAT deficiency: a nephrological diagnosis]Giuliano Boscutti, Laura Calabresi, Stefano Pizzolitto, et al.
Atherosclerosis|June 24, 2003
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiencyLivia Pisciotta, Roberto Miccoli, Alfredo Cantafora, et al.
Journal of Clinical Lipidology|December 22, 2015
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)Livia Pisciotta, Cecilia Vitali, Elda Favari, et al.
Biologicals : Journal of the International Association of Biological Standardization|October 22, 2013
Recombinant human LCAT normalizes plasma lipoprotein profile in LCAT deficiencySara Simonelli, Cristina Tinti, Laura Salvini, et al.
Journal of Lipid Research|August 24, 2017
Plasma cholesterol homeostasis, HDL remodeling and function during the acute phase reactionFrancesca Zimetti, Stefano De Vuono, Monica Gomaraschi, et al.
Atherosclerosis|February 10, 2009
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindredLaura Calabresi, Peter Nilsson, Elisa Pinotti, et al.
Atherosclerosis|September 19, 2023
Apolipoprotein E isoforms differentially affect LCAT-dependent cholesterol esterificationCecilia Vitali, Chiara Pavanello, Marta Turri, et al.
Journal of Cellular and Molecular Medicine|October 30, 2009
Native LDL-induced oxidative stress in human proximal tubular cells: multiple players involvedClaudia Piccoli, Giovanni Quarato, Annamaria D'Aprile, et al.
International Journal of Molecular Sciences|January 11, 2022
Reduced Levels of ABCA1 Transporter Are Responsible for the Cholesterol Efflux Impairment in β-Amyloid-Induced Reactive Astrocytes: Potential Rescue from Biomimetic HDLsGiulia Sierri, Roberta Dal Magro, Barbara Vergani, et al.
Pageof 17

Showing results (101-110 of 169) with videos related to

Sort By:
Pageof 17
Atherosclerosis|October 18, 2008
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemiaAngelo B Cefalù, Davide Noto, Lucia Magnolo, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 3, 2011
[LCAT deficiency: a nephrological diagnosis]Giuliano Boscutti, Laura Calabresi, Stefano Pizzolitto, et al.
Atherosclerosis|June 24, 2003
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiencyLivia Pisciotta, Roberto Miccoli, Alfredo Cantafora, et al.
Journal of Clinical Lipidology|December 22, 2015
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)Livia Pisciotta, Cecilia Vitali, Elda Favari, et al.
Biologicals : Journal of the International Association of Biological Standardization|October 22, 2013
Recombinant human LCAT normalizes plasma lipoprotein profile in LCAT deficiencySara Simonelli, Cristina Tinti, Laura Salvini, et al.
Journal of Lipid Research|August 24, 2017
Plasma cholesterol homeostasis, HDL remodeling and function during the acute phase reactionFrancesca Zimetti, Stefano De Vuono, Monica Gomaraschi, et al.
Atherosclerosis|February 10, 2009
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindredLaura Calabresi, Peter Nilsson, Elisa Pinotti, et al.
Atherosclerosis|September 19, 2023
Apolipoprotein E isoforms differentially affect LCAT-dependent cholesterol esterificationCecilia Vitali, Chiara Pavanello, Marta Turri, et al.
Journal of Cellular and Molecular Medicine|October 30, 2009
Native LDL-induced oxidative stress in human proximal tubular cells: multiple players involvedClaudia Piccoli, Giovanni Quarato, Annamaria D'Aprile, et al.
International Journal of Molecular Sciences|January 11, 2022
Reduced Levels of ABCA1 Transporter Are Responsible for the Cholesterol Efflux Impairment in β-Amyloid-Induced Reactive Astrocytes: Potential Rescue from Biomimetic HDLsGiulia Sierri, Roberta Dal Magro, Barbara Vergani, et al.
Pageof 17