Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Corinne Collet

Showing results (51-60 of 93) with videos related to

Pageof 10
Sort By:
Bone|December 12, 2018
Sclerosing bone dysplasias with hallmarks of dysosteosclerosis in four patients carrying mutations in SLC29A3 and TCIRG1Antonia Howaldt, Sheela Nampoothiri, Lisa-Marie Quell, et al.
Ophthalmic Genetics|March 27, 2014
MSX2 Gene Duplication in a Patient with Eye Development DefectsJulie Plaisancié, Corinne Collet, Valerie Pelletier, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2021
Compromised Volumetric Bone Density and Microarchitecture in Men With Congenital Hypogonadotropic HypogonadismAgnès Ostertag, Georgios E Papadakis, Corinne Collet, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 30, 2006
Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlationsCorinne Collet, Laëtitia Michou, Maurice Audran, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|April 17, 2025
Respiratory and craniofacial management in children with Apert syndromeSonia Khirani, Giovanna Paternoster, Romain Luscan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2011
Ineffective erythropoiesis with reduced red blood cell survival in serotonin-deficient micePascal Amireault, Sarah Hatia, Elisa Bayard, et al.
Animals : an Open Access Journal From MDPI|January 11, 2024
A Zebrafish Mutant in the Extracellular Matrix Protein Gene <i>efemp1</i> as a Model for Spinal OsteoarthritisRatish Raman, Mohamed Ali Bahri, Christian Degueldre, et al.
European Journal of Medical Genetics|December 22, 2022
Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathyAdrien Bloch, Guillaume Couture, Bertrand Isidor, et al.
Blood|December 22, 2011
Serotonin 5-HT2B receptors are required for bone-marrow contribution to pulmonary arterial hypertensionJean-Marie Launay, Philippe Hervé, Jacques Callebert, et al.
The Journal of Craniofacial Surgery|June 9, 2025
Impact of SMAD6 Variants on Neurodevelopment in CraniosynostosisIsabelle Verlut, Sofia Guernouche, Massimiliano Rossi, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
Bone|December 12, 2018
Sclerosing bone dysplasias with hallmarks of dysosteosclerosis in four patients carrying mutations in SLC29A3 and TCIRG1Antonia Howaldt, Sheela Nampoothiri, Lisa-Marie Quell, et al.
Ophthalmic Genetics|March 27, 2014
MSX2 Gene Duplication in a Patient with Eye Development DefectsJulie Plaisancié, Corinne Collet, Valerie Pelletier, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2021
Compromised Volumetric Bone Density and Microarchitecture in Men With Congenital Hypogonadotropic HypogonadismAgnès Ostertag, Georgios E Papadakis, Corinne Collet, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 30, 2006
Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlationsCorinne Collet, Laëtitia Michou, Maurice Audran, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|April 17, 2025
Respiratory and craniofacial management in children with Apert syndromeSonia Khirani, Giovanna Paternoster, Romain Luscan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2011
Ineffective erythropoiesis with reduced red blood cell survival in serotonin-deficient micePascal Amireault, Sarah Hatia, Elisa Bayard, et al.
Animals : an Open Access Journal From MDPI|January 11, 2024
A Zebrafish Mutant in the Extracellular Matrix Protein Gene <i>efemp1</i> as a Model for Spinal OsteoarthritisRatish Raman, Mohamed Ali Bahri, Christian Degueldre, et al.
European Journal of Medical Genetics|December 22, 2022
Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathyAdrien Bloch, Guillaume Couture, Bertrand Isidor, et al.
Blood|December 22, 2011
Serotonin 5-HT2B receptors are required for bone-marrow contribution to pulmonary arterial hypertensionJean-Marie Launay, Philippe Hervé, Jacques Callebert, et al.
The Journal of Craniofacial Surgery|June 9, 2025
Impact of SMAD6 Variants on Neurodevelopment in CraniosynostosisIsabelle Verlut, Sofia Guernouche, Massimiliano Rossi, et al.
Pageof 10