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Corinne Collet

Showing results (81-90 of 93) with videos related to

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The Journal of Experimental Medicine|March 7, 2022
FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse modelMaxence Cornille, Stéphanie Moriceau, Roman H Khonsari, et al.
Biomolecules|February 24, 2024
The Osteoblast Transcriptome in Developing Zebrafish Reveals Key Roles for Extracellular Matrix Proteins Col10a1a and Fbln1 in Skeletal Development and HomeostasisRatish Raman, Mishal Antony, Renaud Nivelle, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|May 30, 2017
Imbalanced Angiogenesis in Peripartum Cardiomyopathy - Diagnostic Value of Placenta Growth FactorAlexandre Mebazaa, Marie-France Seronde, Etienne Gayat, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|August 26, 2024
AI-based diagnosis and phenotype - Genotype correlations in syndromic craniosynostosesQuentin Hennocq, Giovanna Paternoster, Corinne Collet, et al.
International Journal of Cardiology|March 30, 2013
Incremental value of biomarkers to clinical variables for mortality prediction in acutely decompensated heart failure: the Multinational Observational Cohort on Acute Heart Failure (MOCA) studyJohan Lassus, Etienne Gayat, Christian Mueller, et al.
Calcified Tissue International|September 24, 2024
Early-Onset Osteoporosis: Molecular Analysis in Large Cohort and Focus on the PLS3 GeneMaxence Mancini, Roland Chapurlat, Bertrand Isidor, et al.
Journal of the American College of Cardiology|January 22, 2013
Association between elevated blood glucose and outcome in acute heart failure: results from an international observational cohortAlexandre Mebazaa, Etienne Gayat, Johan Lassus, et al.
European Heart Journal|June 27, 2012
Unbiased plasma proteomics for novel diagnostic biomarkers in cardiovascular disease: identification of quiescin Q6 as a candidate biomarker of acutely decompensated heart failureAlexandre Mebazaa, Griet Vanpoucke, Gregoire Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2023
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetranceRebecca S Tooze, Kerry A Miller, Sigrid M A Swagemakers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2019
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4Elodie Sanchez, Béryl Laplace-Builhé, Frédéric Tran Mau-Them, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
The Journal of Experimental Medicine|March 7, 2022
FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse modelMaxence Cornille, Stéphanie Moriceau, Roman H Khonsari, et al.
Biomolecules|February 24, 2024
The Osteoblast Transcriptome in Developing Zebrafish Reveals Key Roles for Extracellular Matrix Proteins Col10a1a and Fbln1 in Skeletal Development and HomeostasisRatish Raman, Mishal Antony, Renaud Nivelle, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|May 30, 2017
Imbalanced Angiogenesis in Peripartum Cardiomyopathy - Diagnostic Value of Placenta Growth FactorAlexandre Mebazaa, Marie-France Seronde, Etienne Gayat, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|August 26, 2024
AI-based diagnosis and phenotype - Genotype correlations in syndromic craniosynostosesQuentin Hennocq, Giovanna Paternoster, Corinne Collet, et al.
International Journal of Cardiology|March 30, 2013
Incremental value of biomarkers to clinical variables for mortality prediction in acutely decompensated heart failure: the Multinational Observational Cohort on Acute Heart Failure (MOCA) studyJohan Lassus, Etienne Gayat, Christian Mueller, et al.
Calcified Tissue International|September 24, 2024
Early-Onset Osteoporosis: Molecular Analysis in Large Cohort and Focus on the PLS3 GeneMaxence Mancini, Roland Chapurlat, Bertrand Isidor, et al.
Journal of the American College of Cardiology|January 22, 2013
Association between elevated blood glucose and outcome in acute heart failure: results from an international observational cohortAlexandre Mebazaa, Etienne Gayat, Johan Lassus, et al.
European Heart Journal|June 27, 2012
Unbiased plasma proteomics for novel diagnostic biomarkers in cardiovascular disease: identification of quiescin Q6 as a candidate biomarker of acutely decompensated heart failureAlexandre Mebazaa, Griet Vanpoucke, Gregoire Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2023
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetranceRebecca S Tooze, Kerry A Miller, Sigrid M A Swagemakers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2019
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4Elodie Sanchez, Béryl Laplace-Builhé, Frédéric Tran Mau-Them, et al.
Pageof 10