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Corinne Collet

Showing results (61-70 of 93) with videos related to

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Frontiers in Immunology|October 26, 2018
Inflammatory Potential of Four Different Phases of Calcium Pyrophosphate Relies on NF-κB Activation and MAPK PathwaysLaure Campillo-Gimenez, Félix Renaudin, Maud Jalabert, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Clinical interest of molecular study in cases of isolated midline craniosynostosisFederico Di Rocco, Massimiliano Rossi, Isabelle Verlut, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disabilityMarie Vincent, Corinne Collet, Alain Verloes, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
CEP57 mutation in a girl with mosaic variegated aneuploidy syndromeLucile Pinson, Linda Mannini, Marjolaine Willems, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 16, 2023
Dysregulation of MicroRNAs in Adult Osteogenesis Imperfecta: The miROI StudyAlexandre Mercier-Guery, Marjorie Millet, Blandine Merle, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 1, 2014
Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromesYann Heuzé, Neus Martínez-Abadías, Jennifer M Stella, et al.
Human Molecular Genetics|December 7, 2021
WNT11, a new gene associated with early onset osteoporosis, is required for osteoblastogenesisCaroline Caetano da Silva, Thomas Edouard, Melanie Fradin, et al.
JBMR Plus|October 5, 2018
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal GenesCorinne Collet, Agnès Ostertag, Manon Ricquebourg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 8, 2014
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndromeElise Schaefer, Corinne Collet, David Genevieve, et al.
Human Molecular Genetics|January 16, 2016
Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosisCarole Le Henaff, Mélanie Faria Da Cunha, Aurélie Hatton, et al.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
Frontiers in Immunology|October 26, 2018
Inflammatory Potential of Four Different Phases of Calcium Pyrophosphate Relies on NF-κB Activation and MAPK PathwaysLaure Campillo-Gimenez, Félix Renaudin, Maud Jalabert, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Clinical interest of molecular study in cases of isolated midline craniosynostosisFederico Di Rocco, Massimiliano Rossi, Isabelle Verlut, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disabilityMarie Vincent, Corinne Collet, Alain Verloes, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
CEP57 mutation in a girl with mosaic variegated aneuploidy syndromeLucile Pinson, Linda Mannini, Marjolaine Willems, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 16, 2023
Dysregulation of MicroRNAs in Adult Osteogenesis Imperfecta: The miROI StudyAlexandre Mercier-Guery, Marjorie Millet, Blandine Merle, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 1, 2014
Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromesYann Heuzé, Neus Martínez-Abadías, Jennifer M Stella, et al.
Human Molecular Genetics|December 7, 2021
WNT11, a new gene associated with early onset osteoporosis, is required for osteoblastogenesisCaroline Caetano da Silva, Thomas Edouard, Melanie Fradin, et al.
JBMR Plus|October 5, 2018
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal GenesCorinne Collet, Agnès Ostertag, Manon Ricquebourg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 8, 2014
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndromeElise Schaefer, Corinne Collet, David Genevieve, et al.
Human Molecular Genetics|January 16, 2016
Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosisCarole Le Henaff, Mélanie Faria Da Cunha, Aurélie Hatton, et al.
Pageof 10