Coucke P - Search Results

1

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

2

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.

3

Assisted oocyte activation does not overcome recurrent embryo developmental problems.

Cardona Barberán A, Bonte D, Boel A, Thys V, Paredis R, Machtelinckx F, De Sutter P, De Croo I, Leybaert L, Stoop D, Coucke P, Vanden Meerschaut F, Heindryckx B. Cardona Barberán A, et al. Among authors: coucke p. Hum Reprod. 2023 May 2;38(5):872-885. doi: 10.1093/humrep/dead051. Hum Reprod. 2023. PMID: 36931261

4

Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos.

Bekaert B, Boel A, Rybouchkin A, Cosemans G, Declercq S, Chuva de Sousa Lopes SM, Parrington J, Stoop D, Coucke P, Menten B, Heindryckx B. Bekaert B, et al. Among authors: coucke p. J Assist Reprod Genet. 2024 Apr 1. doi: 10.1007/s10815-024-03095-9. Online ahead of print. J Assist Reprod Genet. 2024. PMID: 38557805

5

A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract.

Jarayseh T, Guillemyn B, De Saffel H, Bek JW, Syx D, Symoens S, Gansemans Y, Van Nieuwerburgh F, Jagadeesh S, Raja J, Malfait F, Coucke PJ, De Clercq A, Willaert A. Jarayseh T, et al. Hum Genet. 2023 Mar;142(3):457-476. doi: 10.1007/s00439-022-02518-w. Epub 2023 Jan 25. Hum Genet. 2023. PMID: 36697720

6

Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?

Clabout T, Maes L, Acke F, Wuyts W, Van Schil K, Coucke P, Janssens S, De Leenheer E. Clabout T, et al. Among authors: coucke p. Genes (Basel). 2022 Dec 29;14(1):105. doi: 10.3390/genes14010105. Genes (Basel). 2022. PMID: 36672845 Free PMC article.

7

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 Free article.

8

Inorganic Pyrophosphate Plasma Levels Are Decreased in Pseudoxanthoma Elasticum Patients and Heterozygous Carriers but Do Not Correlate with the Genotype or Phenotype.

Van Gils M, Depauw J, Coucke PJ, Aerts S, Verschuere S, Nollet L, Vanakker OM. Van Gils M, et al. J Clin Med. 2023 Feb 27;12(5):1893. doi: 10.3390/jcm12051893. J Clin Med. 2023. PMID: 36902680 Free PMC article.

9

A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation.

Van Den Heuvel LJF, Peeters S, Meester JAN, Perik M, Coucke P, Loeys BL. Van Den Heuvel LJF, et al. Among authors: coucke p. Stem Cell Res. 2023 Mar;67:103032. doi: 10.1016/j.scr.2023.103032. Epub 2023 Jan 23. Stem Cell Res. 2023. PMID: 36708686 Free article.

10

Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couples.

Van Tongerloo AJAG, Verdin H, Steyaert W, Coucke PJ, Janssens S. Van Tongerloo AJAG, et al. J Genet Couns. 2024 Apr 12. doi: 10.1002/jgc4.1899. Online ahead of print. J Genet Couns. 2024. PMID: 38610077

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