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Page 1
Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development.
Guillemyn B, De Saffel H, Bek JW, Tapaneeyaphan P, De Clercq A, Jarayseh T, Debaenst S, Willaert A, De Rycke R, Byers PH, Rosseel T, Coucke P, Blaumeiser B, Syx D, Malfait F, Symoens S. Guillemyn B, et al. Among authors: coucke p. J Bone Miner Res. 2023 Nov;38(11):1718-1730. doi: 10.1002/jbmr.4914. Epub 2023 Sep 30. J Bone Miner Res. 2023. PMID: 37718532
Zebrafish Tric-b is required for skeletal development and bone cells differentiation.
Tonelli F, Leoni L, Daponte V, Gioia R, Cotti S, Fiedler IAK, Larianova D, Willaert A, Coucke PJ, Villani S, Busse B, Besio R, Rossi A, Witten PE, Forlino A. Tonelli F, et al. Among authors: coucke pj. Front Endocrinol (Lausanne). 2023 Jan 23;14:1002914. doi: 10.3389/fendo.2023.1002914. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36755921 Free PMC article.
Cell differentiation and matrix organization are differentially affected during bone formation in osteogenesis imperfecta zebrafish models with different genetic defects impacting collagen type I structure.
Daponte V, Tonelli F, Masiero C, Syx D, Exbrayat-Héritier C, Biggiogera M, Willaert A, Rossi A, Coucke PJ, Ruggiero F, Forlino A. Daponte V, et al. Matrix Biol. 2023 Aug;121:105-126. doi: 10.1016/j.matbio.2023.06.003. Epub 2023 Jun 17. Matrix Biol. 2023. PMID: 37336269 Free article.
High rate of detected variants in male PLCZ1 and ACTL7A genes causing failed fertilization after ICSI.
Cardona Barberán A, Reddy Guggilla R, Colenbier C, Van der Velden E, Rybouchkin A, Stoop D, Leybaert L, Coucke P, Symoens S, Boel A, Vanden Meerschaut F, Heindryckx B. Cardona Barberán A, et al. Among authors: coucke p. Hum Reprod Open. 2024 Sep 28;2024(4):hoae057. doi: 10.1093/hropen/hoae057. eCollection 2024. Hum Reprod Open. 2024. PMID: 39411542 Free PMC article.
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.
Schuermans N, El Chehadeh S, Hemelsoet D, Gautheron J, Vantyghem MC, Nouioua S, Tazir M, Vigouroux C, Auclair M, Bogaert E, Dufour S, Okawa F, Hilbert P, Van Doninck N, Taquet MC, Rosseel T, De Clercq G, Debackere E, Van Haverbeke C, Cherif FR, Urtizberea JA, Chanson JB, Funalot B, Authier FJ, Kaya S, Terryn W, Callens S, Depypere B, Van Dorpe J; Program for Undiagnosed Diseases (UD-PrOZA); Poppe B, Impens F, Mizushima N, Depienne C, Jéru I, Dermaut B. Schuermans N, et al. Nat Genet. 2023 Nov;55(11):1929-1940. doi: 10.1038/s41588-023-01535-3. Epub 2023 Nov 2. Nat Genet. 2023. PMID: 37919452
Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing.
Aalders J, Léger L, Demolder A, Muiño Mosquera L, Coucke P, Menten B, De Backer J, van Hengel J. Aalders J, et al. Among authors: coucke p. Stem Cell Res. 2023 Mar;67:103036. doi: 10.1016/j.scr.2023.103036. Epub 2023 Jan 25. Stem Cell Res. 2023. PMID: 36724552 Free article.
Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos.
Bekaert B, Boel A, De Witte L, Vandenberghe W, Popovic M, Stamatiadis P, Cosemans G, Tordeurs L, De Loore AM, Chuva de Sousa Lopes SM, De Sutter P, Stoop D, Coucke P, Menten B, Heindryckx B. Bekaert B, et al. Among authors: coucke p. Mol Ther. 2023 Aug 2;31(8):2326-2341. doi: 10.1016/j.ymthe.2023.06.013. Epub 2023 Jun 27. Mol Ther. 2023. PMID: 37376733 Free PMC article.
538 results