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Patrizia Tarugi

Showing results (41-50 of 78) with videos related to

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Human Gene Therapy|June 24, 2004
Low-density lipoprotein (LDL) receptor/transferrin fusion protein: in vivo production and functional evaluation as a potential therapeutic tool for lowering plasma LDL cholesterolGiorgia Razzini, Flavia Parise, Davide Calebiro, et al.
Atherosclerosis|May 25, 2005
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemiaEnza Di Leo, Sandra Lancellotti, Junia Y Penacchioni, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 1, 2013
A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemiaAngelo B Cefalù, James P Pirruccello, Davide Noto, et al.
Journal of Clinical Lipidology|June 5, 2012
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemiaPaola Conca, Silvana Pileggi, Sara Simonelli, et al.
Journal of Clinical Lipidology|October 21, 2019
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemiaClaudio Rabacchi, Maria Luisa Simone, Livia Pisciotta, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 14, 2004
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemiaClaudio Priore Oliva, Livia Pisciotta, Giovanni Li Volti, et al.
Gene|October 10, 2012
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemiaLucia Magnolo, Mohamed Najah, Tatiana Fancello, et al.
Atherosclerosis|October 18, 2008
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemiaAngelo B Cefalù, Davide Noto, Lucia Magnolo, et al.
Atherosclerosis|August 24, 2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genesLivia Pisciotta, Laura Calabresi, Graziana Lupattelli, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
Human Gene Therapy|June 24, 2004
Low-density lipoprotein (LDL) receptor/transferrin fusion protein: in vivo production and functional evaluation as a potential therapeutic tool for lowering plasma LDL cholesterolGiorgia Razzini, Flavia Parise, Davide Calebiro, et al.
Atherosclerosis|May 25, 2005
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemiaEnza Di Leo, Sandra Lancellotti, Junia Y Penacchioni, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 1, 2013
A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemiaAngelo B Cefalù, James P Pirruccello, Davide Noto, et al.
Journal of Clinical Lipidology|June 5, 2012
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemiaPaola Conca, Silvana Pileggi, Sara Simonelli, et al.
Journal of Clinical Lipidology|October 21, 2019
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemiaClaudio Rabacchi, Maria Luisa Simone, Livia Pisciotta, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 14, 2004
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemiaClaudio Priore Oliva, Livia Pisciotta, Giovanni Li Volti, et al.
Gene|October 10, 2012
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemiaLucia Magnolo, Mohamed Najah, Tatiana Fancello, et al.
Atherosclerosis|October 18, 2008
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemiaAngelo B Cefalù, Davide Noto, Lucia Magnolo, et al.
Atherosclerosis|August 24, 2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genesLivia Pisciotta, Laura Calabresi, Graziana Lupattelli, et al.
Pageof 8