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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 2
1991 1
1997 3
1999 3
2000 2
2002 2
2003 2
2004 3
2005 1
2006 4
2007 5
2008 3
2009 4
2010 6
2011 6
2012 8
2013 6
2014 10
2015 7
2016 6
2017 8
2018 6
2019 4
2020 7
2021 10
2022 9
2023 5
2024 4
2025 0

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124 results

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Page 1
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC. Loeys BL, et al. Among authors: coucke pj. N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695. N Engl J Med. 2006. PMID: 16928994 Free 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
DFNA 2, 5, 8, 12.
Van Camp G, Coucke PJ, Van Hauwe P, Van Laer L, Verhoeven K, Wuyts F, Smith RJ. Van Camp G, et al. Among authors: coucke pj. Adv Otorhinolaryngol. 2000;56:68-77. doi: 10.1159/000059084. Adv Otorhinolaryngol. 2000. PMID: 10868216 Review. No abstract available.
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. Among authors: coucke pj. 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.
Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders.
Tonelli F, Bek JW, Besio R, De Clercq A, Leoni L, Salmon P, Coucke PJ, Willaert A, Forlino A. Tonelli F, et al. Among authors: coucke pj. Front Endocrinol (Lausanne). 2020 Jul 31;11:489. doi: 10.3389/fendo.2020.00489. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32849280 Free PMC article. Review.
The corneoscleral shape in Marfan syndrome.
Vanhonsebrouck E, Consejo A, Coucke PJ, Leroy BP, Kreps EO. Vanhonsebrouck E, et al. Among authors: coucke pj. Acta Ophthalmol. 2021 Jun;99(4):405-410. doi: 10.1111/aos.14636. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996688 Free article.
Human germline nuclear transfer to overcome mitochondrial disease and failed fertilization after ICSI.
Tang M, Boel A, Castelluccio N, Cardona Barberán A, Christodoulaki A, Bekaert B, Popovic M, Vanden Meerschaut F, De Sutter P, Menten B, Symoens S, Vanlander AV, Stoop D, Coucke PJ, Heindryckx B. Tang M, et al. Among authors: coucke pj. J Assist Reprod Genet. 2022 Mar;39(3):609-618. doi: 10.1007/s10815-022-02401-7. Epub 2022 Jan 22. J Assist Reprod Genet. 2022. PMID: 35064435 Free PMC article.
124 results