Vincenza Valenti

Via Del Vespro 129
Palermo, 90127, Italy

Last Updated: 09/26/2026

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Found 8 publications

PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study.

PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study.

Journal: Atherosclerosis
Published: January 22, 2019

Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred.

Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred.

Journal: Journal of clinical lipidology
Published: August 10, 2017

Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.

Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.

Journal: Journal of clinical lipidology
Published: June 02, 2016

Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model.

Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model.

Journal: Atherosclerosis
Published: August 27, 2015

Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia.

Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia.

Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: July 06, 2015

Homozygous familial hypobetalipoproteinemia: two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature.

Homozygous familial hypobetalipoproteinemia: two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature.

Journal: Atherosclerosis
Published: September 28, 2014

A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia.

A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia.

Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: June 01, 2013

Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.

Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.

Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: January 17, 2012
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Last Updated: 09/26/2026