Search Results - "Altieri, Grazia I."

rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography by Noto, Davide, Cefalù, Angelo B., Martinelli, Nicola, Giammanco, Antonina, Spina, Rossella, Barbagallo, Carlo M., Caruso, Marco, Novo, Salvatore, Sarullo, Filippo, Pernice, Vincenzo, Brucato, Federica, Ingrassia, Valeria, Fayer, Francesca, Altieri, Grazia I., Scrimali, Chiara, Misiano, Gabriella, Olivieri, Oliviero, Girelli, Domenico, Averna, Maurizio R.

“…Novel genetic determinants associated with coronary artery disease (CAD) have been discovered by genome wide association studies. Variants encompassing the…”
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PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study by Valenti, Vincenza, Noto, Davide, Giammanco, Antonina, Fayer, Francesca, Spina, Rossella, Altieri, Grazia I., Ingrassia, Valeria, Scrimali, Chiara, Barbagallo, Carlo M., Brucato, Federica, Misiano, Gabriella, Cefalù, Angelo B., Averna, Maurizio R.

“…Proprotein convertase subtilisin/kexin type 9 (PCSK9) binds to low density lipoprotein receptor (LDLR) through the LDLR epidermal growth factor-like repeat A…”
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Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing by Spina, Rossella, Cefalu', Angelo B., Noto, Davide, Ingrassia, Valeria, Giammanco, Antonina, Fayer, Francesca, Misiano, Gabriella, Scrimali, Chiara, Altieri, Grazia I., Ganci, Antonina, Barbagallo, Carlo M., Averna, Maurizio

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Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily by Giammanco, Antonina, Spina, Rossella, Ingrassia, Valeria, Valenti, Vincenza, Scrimali, Chiara, Misiano, Gabriella, Altieri, Grazia I., Fayer, Francesca, Barbagallo, Carlo M., Ganci, Antonina, Noto, Davide, Cefalu', Angelo B., Averna, Maurizio

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Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing by Cefalù, Angelo B, Spina, Rossella, Noto, Davide, Ingrassia, Valeria, Valenti, Vincenza, Giammanco, Antonina, Fayer, Francesca, Misiano, Gabriella, Cocorullo, Gianfranco, Scrimali, Chiara, Palesano, Ornella, Altieri, Grazia I, Ganci, Antonina, Barbagallo, Carlo M, Averna, Maurizio R

“…Abstract Background Severe hypertriglyceridemia may result from mutations in genes affecting the intravascular lipolysis of triglyceride rich lipoproteins…”
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