Marie-sylvie Gross

Paris, France

Last Updated: 09/26/2026

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Found 11 publications

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 03, 2020

Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability.

Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability.

Journal: Genes

Published: April 22, 2020

Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome.

Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome.

Journal: Genes

Published: January 07, 2019

Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells.

Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells.

Journal: Molecular therapy. Nucleic acids

Published: November 19, 2018

Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression.

Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression.

Journal: Genes

Published: June 21, 2018

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.

Journal: European journal of human genetics : EJHG

Published: September 04, 2017

The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele.

The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele.

Journal: Human molecular genetics

Published: December 16, 2014

MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.

MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.

Journal: American journal of human genetics

Published: September 10, 2014

Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures.

Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures.

Journal: PloS one

Published: July 01, 2012

Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placenta.

Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placenta.

Journal: PloS one

Published: June 08, 2012

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.

Journal: Nature genetics

Published: February 28, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026