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Marta Futema

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Biorxiv : the Preprint Server for Biology|June 12, 2026

The COPI coatomer influences LDL receptor activity, hepatic lipid storage, and apoB secretionGrigorios Panteloglou, Jérôme Robert, Marieke Smit, et al.

Nature Communications|September 17, 2014

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in EuropeansNicholas J Timpson, Klaudia Walter, Josine L Min, et al.

Circulation Research|November 23, 2021

Posttranscriptional Regulation of the Human LDL Receptor by the U2-SpliceosomePaolo Zanoni, Grigorios Panteloglou, Alaa Othman, et al.

European Heart Journal|July 15, 2021

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathyLuis R Lopes, Soledad Garcia-Hernández, Massimiliano Lorenzini, et al.

Nature|February 26, 2025

Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.

Medrxiv : the Preprint Server for Health Sciences|January 10, 2024

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.

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Search research articles

Showing results (41-50 of 46) with videos related to

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You have reached the last page of results.This site can display upto 46 results.

Biorxiv : the Preprint Server for Biology|June 12, 2026

The COPI coatomer influences LDL receptor activity, hepatic lipid storage, and apoB secretionGrigorios Panteloglou, Jérôme Robert, Marieke Smit, et al.

Nature Communications|September 17, 2014

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in EuropeansNicholas J Timpson, Klaudia Walter, Josine L Min, et al.

Circulation Research|November 23, 2021

Posttranscriptional Regulation of the Human LDL Receptor by the U2-SpliceosomePaolo Zanoni, Grigorios Panteloglou, Alaa Othman, et al.

European Heart Journal|July 15, 2021

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathyLuis R Lopes, Soledad Garcia-Hernández, Massimiliano Lorenzini, et al.

Nature|February 26, 2025

Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.

Medrxiv : the Preprint Server for Health Sciences|January 10, 2024

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.

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