Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Rossella Spina"'
Autor:
Letizia Scola, Maria Rita Bongiorno, Giusi Irma Forte, Anna Aiello, Giulia Accardi, Chiara Scrimali, Rossella Spina, Domenico Lio, Giuseppina Candore
Publikováno v:
Genes, Vol 13, Iss 7, p 1235 (2022)
Differential genetically determined expression of transforming growth factor-β (TGF-β pathway and of vascular endothelial growth factor-A (VEGF-A) might modulate the molecular “milieu” involved in the etio-pathogenesis of non-melanoma skin canc
Externí odkaz:
https://doaj.org/article/757a2b5abfc9496ea69c53330066f4f9
Autor:
Davide Noto, Antonina Giammanco, Rossella Spina, Francesca Fayer, Angelo B Cefalù, Maurizio R Averna
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0247402 (2021)
SREBP1 and 2, are cholesterol sensors able to modulate cholesterol-related gene expression responses. SREBPs binding sites are characterized by the presence of multiple target sequences as SRE, NFY and SP1, that can be arranged differently in differe
Externí odkaz:
https://doaj.org/article/0a96cec23d9d44018fde3423c9fe4cd5
Autor:
Davide Noto, Rossella Spina, Antonina Giammanco, Carlo M. Barbagallo, Antonina Ganci, Chiara Scrimali, Federica Brucato, Gabriella Misiano, Marcello Ciaccio, Rosalia Caldarella, Angelo B. Cefalù, Maurizio Averna
Publikováno v:
Atherosclerosis. 347:63-67
Background and aims: Familial hypercholesterolemia (FH) is the most relevant genetic cause of early cardiovascular disease (CVD). FH is suspected when low density lipoprotein cholesterol (LDL-C) levels exceed the 95th percentile of the population dis
Purpose of Review Apolipoprotein C-III (ApoC-III) is a widely known player in triglyceride metabolism, and it has been recently recognized as a polyhedric factor which may regulate several pathways beyond lipid metabolism by influencing cardiovascula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffece0bbd9a7f516ff16acccf84f1a14
https://hdl.handle.net/10447/580173
https://hdl.handle.net/10447/580173
Autor:
G.I. Altieri, Marco Caruso, Oliviero Olivieri, Filippo M. Sarullo, V. Ingrassia, F. Brucato, Nicola Martinelli, Vincenzo Pernice, Rossella Spina, Carlo M. Barbagallo, C. Scrimali, Domenico Girelli, Francesca Fayer, Gabriella Misiano, Angelo B. Cefalù, Maurizio Averna, Antonina Giammanco, Davide Noto, Salvatore Novo
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 31:1542-1547
Background and aims Novel genetic determinants associated with coronary artery disease (CAD) have been discovered by genome wide association studies. Variants encompassing the CELSR2- PSRC1-SORT1 gene cluster have been associated with CAD. This study
Autor:
Angelo B. Cefalù, Rossella Spina, Davide Noto, Claudio Rabacchi, Antonina Giammanco, Maria Luisa Simone, Federica Brucato, Chiara Scrimali, Maria Grazia Gueli-Alletti, Carlo M. Barbagallo, Patrizia Tarugi, Maurizio R. Averna
Publikováno v:
Journal of clinical lipidology. 16(4)
Primary Hypobetalipoproteinemias (HBL) are a group of dominant and recessive monogenic genetic disorders caused by mutations in APOB, PCSK9, ANGPTL3, MTTP, Sar1b genes and characterized by plasma levels of total cholesterol (TC), low density lipoprot
Autor:
Davide Noto, Salvatore Petta, Antonina Giammanco, Rossella Spina, Daniela Cabibbi, Rossana Porcasi, Rosalia Caldarella, Marcello Ciaccio, Roberto Muratore, Angelo B. Cefalù, Antonio Craxi, Maurizio Averna
Publikováno v:
Nutrition, metabolism, and cardiovascular diseases : NMCD. 32(5)
Background and aims: The LISTEN trial (ClinicalTrial.gov accession: NCT01950884) is a phase IV 52 weeks double blind parallel randomized controlled trial that evaluated the effect of ezetimibe plus lifestyle and dietary intervention (eze) vs. lifesty
Autor:
Rossella Spina, Maurizio Averna, Francesca Fayer, Angelo B. Cefalù, Davide Noto, Antonina Giammanco
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0247402 (2021)
PLoS ONE
PLoS ONE
SREBP1 and 2, are cholesterol sensors able to modulate cholesterol-related gene expression responses. SREBPs binding sites are characterized by the presence of multiple target sequences as SRE, NFY and SP1, that can be arranged differently in differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a32cce41a26426c63d98e49379844adb
http://hdl.handle.net/10447/541039
http://hdl.handle.net/10447/541039
Autor:
Angelo B. Cefalù, Maurizio Averna, Davide Noto, Carlo M. Barbagallo, Francesca Fayer, Rossella Spina, Antonina Giammanco
Publikováno v:
Internal medicine journalReferences. 51(4)
Familial defective apolipoprotein (apo) B (FDB) and familial hypercholesterolaemia (FH) are the two common genetic conditions that cause hypercholesterolaemia. R3531C mutation of the APOB gene is a rare cause of FDB. Individuals with both FDB and FH
Autor:
A. Moregola, Fabio Pellegatta, Maurizio Averna, Alberico L. Catapano, V. Zampoleri, Rossella Spina, Angelo Baldassarre Cefalù, Fabrizia Bonacina, Lorenzo Da Dalt, Liliana Grigore, Andrea Baragetti, Giuseppe Danilo Norata, Angela Pirillo
Aims Leucocyte telomere length (LTL) shortening is a marker of cellular senescence and associates with increased risk of cardiovascular disease (CVD). A number of cardiovascular risk factors affect LTL, but the correlation between elevated LDL choles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffd95914c031ab6af52fd587aa87a884
http://hdl.handle.net/10447/522500
http://hdl.handle.net/10447/522500