Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Caetano Da Silva, Caroline"'
Autor:
Caetano da Silva, Caroline1, Macias Trevino, Claudio2, Mitchell, Jason3, Murali, Hemma4, Tsimbal, Casey1,5, Dalessandro, Eileen1, Carroll, Shannon H.1,5, Kochhar, Simren6, Curtis, Sarah W.6, Cheng, Ching Hsun Eric1, Wang, Feng7, Kutschera, Eric7, Carstens, Russ P.8, Xing, Yi4,7, Wang, Kai4, Leslie, Elizabeth J.6, Liao, Eric C.1,2,5,9 liaoce@chop.edu
Publikováno v:
Communications Biology. 8/23/2024, Vol. 7 Issue 1, p1-14. 14p.
Autor:
Raman, Ratish, Antony, Mishal, Nivelle, Renaud, Lavergne, Arnaud, Zappia, Jérémie, Guerrero-Limón, Gustavo, Caetano da Silva, Caroline, Kumari, Priyanka, Sojan, Jerry Maria, Degueldre, Christian, Bahri, Mohamed Ali, Ostertag, Agnes, Collet, Corinne, Cohen-Solal, Martine, Plenevaux, Alain, Henrotin, Yves, Renn, Jörg, Muller, Marc
Publikováno v:
Biomolecules (2218-273X); Feb2024, Vol. 14 Issue 2, p139, 26p
Autor:
Raman, Ratish, Bahri, Mohamed Ali, Degueldre, Christian, Caetano da Silva, Caroline, Sanchez, Christelle, Ostertag, Agnes, Collet, Corinne, Cohen-Solal, Martine, Plenevaux, Alain, Henrotin, Yves, Muller, Marc
Publikováno v:
Animals (2076-2615); Jan2024, Vol. 14 Issue 1, p74, 14p
Autor:
Caetano da Silva, Caroline1 (AUTHOR), Ricquebourg, Manon1,2 (AUTHOR), Orcel, Philippe1,2 (AUTHOR), Fabre, Stéphanie1,2 (AUTHOR), Funck‐Brentano, Thomas1,2 (AUTHOR), Cohen‐Solal, Martine1,2 (AUTHOR), Collet, Corinne1,3 (AUTHOR) corinne.collet@aphp.fr
Publikováno v:
Molecular Genetics & Genomic Medicine. Jun2021, Vol. 9 Issue 6, p1-9. 9p.
Akademický článek
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Autor:
Caetano da Silva, Caroline, Ostertag, Agnes, Raman, Ratish, Muller, Marc, Cohen-Solal, Martine, Collet, Corinne
Publikováno v:
Zebrafish; February 2023, Vol. 20 Issue: 1 p1-9, 9p
Autor:
Ventura Fernandes, Bianca H., Caetano da Silva, Caroline, Bissegato, Debora, Kent, Michael L., Carvalho, Luciani R.
Publikováno v:
Journal of Fish Diseases; Jan2022, Vol. 45 Issue 1, p35-39, 5p
Autor:
Caetano Da Silva, Caroline, Kollár, Tímea, Csenki-Bakos, Zsolt, Fernandes, Bianca H.V., Horváth, Ákos, Carvalho, Luciani R.
Publikováno v:
Zebrafish; Jun2019, Vol. 16 Issue 3, p321-323, 3p
Autor:
Raman R; Laboratory for Organogenesis and Regeneration (LOR), GIGA Institute, University of Liège, 4000 Liège, Belgium., Bahri MA; GIGA CRC In Vivo Imaging, University of Liege, Sart Tilman, 4000 Liège, Belgium., Degueldre C; GIGA CRC In Vivo Imaging, University of Liege, Sart Tilman, 4000 Liège, Belgium., Caetano da Silva C; Hospital Lariboisière, Reference Centre for Rare Bone Diseases, INSERM U1132, Université de Paris-Cité, F-75010 Paris, France., Sanchez C; MusculoSKeletal Innovative Research Lab, Center for Interdisciplinary Research on Medicines, University of Liège, 4000 Liège, Belgium., Ostertag A; Hospital Lariboisière, Reference Centre for Rare Bone Diseases, INSERM U1132, Université de Paris-Cité, F-75010 Paris, France., Collet C; Hospital Lariboisière, Reference Centre for Rare Bone Diseases, INSERM U1132, Université de Paris-Cité, F-75010 Paris, France.; UF de Génétique Moléculaire, Hôpital Robert Debré, APHP, F-75019 Paris, France., Cohen-Solal M; Hospital Lariboisière, Reference Centre for Rare Bone Diseases, INSERM U1132, Université de Paris-Cité, F-75010 Paris, France., Plenevaux A; GIGA CRC In Vivo Imaging, University of Liege, Sart Tilman, 4000 Liège, Belgium., Henrotin Y; MusculoSKeletal Innovative Research Lab, Center for Interdisciplinary Research on Medicines, University of Liège, 4000 Liège, Belgium., Muller M; Laboratory for Organogenesis and Regeneration (LOR), GIGA Institute, University of Liège, 4000 Liège, Belgium.
Publikováno v:
Animals : an open access journal from MDPI [Animals (Basel)] 2023 Dec 24; Vol. 14 (1). Date of Electronic Publication: 2023 Dec 24.
Autor:
Caetano da Silva C; INSERM U1132 and Université de Paris, Reference Centre for Rare Bone Diseases, Hospital Lariboisière, Paris F-75010, France., Edouard T; Endocrine Bone Diseases and Genetics Unit, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism, ERN BOND, OSCAR Network, Pediatric Clinical Research Unit, Children's Hospital, RESTORE INSERM U1301, Toulouse University Hospital, Toulouse 31300, France., Fradin M; Service de Génétique Clinique, Centre de Référence des Anomalies du Développement de l'Ouest, Hôpital Sud de Rennes, Rennes F-35033, France., Aubert-Mucca M; Endocrine Bone Diseases and Genetics Unit, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism, ERN BOND, OSCAR Network, Pediatric Clinical Research Unit, Children's Hospital, RESTORE INSERM U1301, Toulouse University Hospital, Toulouse 31300, France., Ricquebourg M; INSERM U1132 and Université de Paris, Reference Centre for Rare Bone Diseases, Hospital Lariboisière, Paris F-75010, France., Raman R; Laboratory for Organogenesis and Regeneration (LOR), GIGA-Research, Liège University, Liège 4000, Belgium., Salles JP; Endocrine Bone Diseases and Genetics Unit, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism, ERN BOND, OSCAR Network, Pediatric Clinical Research Unit, Children's Hospital, RESTORE INSERM U1301, Toulouse University Hospital, Toulouse 31300, France., Charon V; Department of Radiology, CHU de Rennes, Rennes F-35000, France., Guggenbuhl P; Department of Rheumatology, CHU de Rennes, Rennes F-35000, France., Muller M; Laboratory for Organogenesis and Regeneration (LOR), GIGA-Research, Liège University, Liège 4000, Belgium., Cohen-Solal M; INSERM U1132 and Université de Paris, Reference Centre for Rare Bone Diseases, Hospital Lariboisière, Paris F-75010, France., Collet C; INSERM U1132 and Université de Paris, Reference Centre for Rare Bone Diseases, Hospital Lariboisière, Paris F-75010, France.; Département de Génétique, UF de Génétique Moléculaire, Hôpital Robert Debré, APHP, Paris F-75019, France.
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2022 May 19; Vol. 31 (10), pp. 1622-1634.