Coucke PJ - Search Results

1

Gonadal Mosaicism as a Rare Inheritance Pattern in Recessive Genodermatoses: Report of Two Cases with Pseudoxanthoma Elasticum and Literature Review.

Dangreau L, Hosen MJ, De Zaeytijd J, Leroy BP, Coucke PJ, Vanakker OM. Dangreau L, et al. Among authors: coucke pj. Curr Issues Mol Biol. 2024 Sep 11;46(9):9998-10007. doi: 10.3390/cimb46090597. Curr Issues Mol Biol. 2024. PMID: 39329949 Free PMC article.

2

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. Among authors: coucke pj. J Clin Med. 2023 Feb 27;12(5):1893. doi: 10.3390/jcm12051893. J Clin Med. 2023. PMID: 36902680 Free PMC article.

3

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. Among authors: coucke pj. J Genet Couns. 2025 Feb;34(1):e1899. doi: 10.1002/jgc4.1899. Epub 2024 Apr 12. J Genet Couns. 2025. PMID: 38610077

4

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. 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.

5

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. J Assist Reprod Genet. 2024 Jun;41(6):1605-1617. doi: 10.1007/s10815-024-03095-9. Epub 2024 Apr 1. J Assist Reprod Genet. 2024. PMID: 38557805

6

Bmpr1aa modulates the severity of the skeletal phenotype in an fkbp10-deficient Bruck syndrome zebrafish model.

Jarayseh T, Debaenst S, De Saffel H, Rosseel T, Milazzo M, Bek JW, Hudson DM, Van Nieuwerburgh F, Gansemans Y, Josipovic I, Boone MN, Witten PE, Willaert A, Coucke PJ. Jarayseh T, et al. Among authors: coucke pj. J Bone Miner Res. 2024 Dec 31;40(1):154-166. doi: 10.1093/jbmr/zjae185. J Bone Miner Res. 2024. PMID: 39566080

7

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. 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.

8

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. Hum Reprod. 2023 May 2;38(5):872-885. doi: 10.1093/humrep/dead051. Hum Reprod. 2023. PMID: 36931261

9

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.

10

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. Genes (Basel). 2022 Dec 29;14(1):105. doi: 10.3390/genes14010105. Genes (Basel). 2022. PMID: 36672845 Free PMC article.

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