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Marjolijn Renard

Showing results (31-40 of 37) with videos related to

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Matrix Biology : Journal of the International Society for Matrix Biology|September 8, 2023
Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse modelsViolette Deleeuw, Eric Carlson, Marjolijn Renard, et al.
Nature Medicine|January 10, 2017
Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndromeJorge Oller, Nerea Méndez-Barbero, E Josue Ruiz, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionMarjolijn Renard, Catherine Francis, Rajarshi Ghosh, et al.
The Journal of Pediatrics|June 27, 2020
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan SyndromeSara L Van Driest, Lynn A Sleeper, Bruce D Gelb, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2022
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohortJosephina A N Meester, Silke Peeters, Lotte Van Den Heuvel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 29, 2020
Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysmSandy Elbitar, Marjolijn Renard, Pauline Arnaud, et al.
American Journal of Human Genetics|October 30, 2012
In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndromeVirginie Carmignac, Julien Thevenon, Lesley Adès, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Matrix Biology : Journal of the International Society for Matrix Biology|September 8, 2023
Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse modelsViolette Deleeuw, Eric Carlson, Marjolijn Renard, et al.
Nature Medicine|January 10, 2017
Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndromeJorge Oller, Nerea Méndez-Barbero, E Josue Ruiz, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionMarjolijn Renard, Catherine Francis, Rajarshi Ghosh, et al.
The Journal of Pediatrics|June 27, 2020
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan SyndromeSara L Van Driest, Lynn A Sleeper, Bruce D Gelb, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2022
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohortJosephina A N Meester, Silke Peeters, Lotte Van Den Heuvel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 29, 2020
Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysmSandy Elbitar, Marjolijn Renard, Pauline Arnaud, et al.
American Journal of Human Genetics|October 30, 2012
In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndromeVirginie Carmignac, Julien Thevenon, Lesley Adès, et al.
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