Search Results - "Varret, Mathilde"

A tentative tracking of the SARS-Cov2 pandemic in France, based on a corrected SIR model including vaccination effects.

Authors: Varret, Mathilde Martin, François Xavier Varret, François

Source: EPJ Web of Conferences. 4/28/2022, Vol. 263, p1-12. 12p.

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Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects.

Authors: Saint-Jore, Bruno Varret, Mathilde Dachet, Christiane et al.

Source: European Journal of Human Genetics. Aug2000, Vol. 8 Issue 8, p621. 10p.

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DnaJA4 is a SREBP-regulated chaperone involved in the cholesterol biosynthesis pathway

Authors: Robichon, Céline Varret, Mathilde Le Liepvre, Xavier et al.

Source: BBA - Molecular & Cell Biology of Lipids. Sep2006, Vol. 1761 Issue 9, p1107-1113. 7p.

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Effect of the p.Arg357His mutation of PCSK9 on basal and postprandial lipoprotein metabolism.

Authors: Varret, Mathilde Abifadel, Marianne Despina Kalopissis, Athina et al.

Source: Atherosclerosis (00219150). Aug2017, Vol. 263, pe2-e2. 1p.

APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia.

Authors: Abou Khalil, Yara Marmontel, Oriane Ferrières, Jean et al.

Source: International Journal of Molecular Sciences. May2022, Vol. 23 Issue 10, p5792-5792. 19p.

PCSK9 expression in human atherosclerotic lesions and vascular smooth muscle cells.

Authors: Azar, Yara Abou Khalil, Yara Lebel, Marie-Nathalie et al.

Source: Atherosclerosis (00219150). May2026, Vol. 416, pN.PAG-N.PAG. 1p.

Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease).

Authors: Georges, Amandine Bonneau, Jessica Bonnefont-Rousselot, Dominique et al.

Source: Orphanet Journal of Rare Diseases. 2011, Vol. 6 Issue 1, p1-16. 16p. 2 Color Photographs, 1 Black and White Photograph, 2 Charts, 2 Graphs.

A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1.

Authors: Marques-Pinheiro, Alice Marduel, Marie Rabès, Jean-Pierre et al.

Source: European Journal of Human Genetics. Nov2010, Vol. 18 Issue 11, p1236-1242. 7p. 1 Diagram, 3 Charts, 1 Graph.

Rare variants in U2-spliceosome genes and autosomal dominant hypercholesterolemia.

Authors: Jan, Maëlle Lebel, Marie-Nathalie Diallo, Abdoul Karim et al.

Source: Atherosclerosis (00219150). 2025 Supplement, Vol. 407, pN.PAG-N.PAG. 1p.

Genetic screening and functional analysis of LIPA variants in autosomal dominant hypercholesterolemia.

Authors: Jan, Maëlle Diallo, Abdoul Karim Gallo, Antonio et al.

Source: Atherosclerosis (00219150). 2025 Supplement, Vol. 407, pN.PAG-N.PAG. 1p.

Familial hypercholesterolemia in Morocco: first report of mutations in the LDL receptor gene.

Authors: El Messal, Mariame Aït Chihab, Karima Chater, Rachid et al.

Source: Journal of Human Genetics. 2003, Vol. 48 Issue 4, p199. 5p.

APOE gene variants in primary dyslipidemia.

Authors: Khalil, Yara Abou Rabès, Jean-Pierre Boileau, Catherine et al.

Source: Atherosclerosis (00219150). Jul2021, Vol. 328, p11-22. 12p.

High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry.

Authors: Béliard, Sophie Boccara, Franck Cariou, Bertrand et al.

Source: Atherosclerosis (00219150). Oct2018, Vol. 277, p334-340. 7p.

Rare variants in U2-spliceosome genes are involved in autosomal dominant hypercholesterolemia.

Authors: Jan, Maëlle Khalil, Yara Abou Diallo, Abdoul Karim et al.

Source: Atherosclerosis (00219150). 2024 Supplement 1, Vol. 395, pN.PAG-N.PAG. 1p.

Plasma proprotein‐convertase‐subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes.

Authors: El Khoury, Petra Abou‐Khalil, Yara Abifadel, Marianne et al.

Source: Diabetes, Obesity & Metabolism. Apr2018, Vol. 20 Issue 4, p943-953. 11p.