Coucke PJ - Search Results

1

G protein-coupled receptor kinase 6 (GRK6) regulates insulin processing and secretion via effects on proinsulin conversion to insulin.

Varney MJ, Steyaert W, Coucke PJ, Delanghe JR, Uehling DE, Joseph B, Marcellus R, Al-Awar R, Benovic JL. Varney MJ, et al. Among authors: coucke pj. J Biol Chem. 2022 Oct;298(10):102421. doi: 10.1016/j.jbc.2022.102421. Epub 2022 Aug 25. J Biol Chem. 2022. PMID: 36030052 Free PMC article.

2

[No title available]

[No authors listed] [No authors listed] PMID: 35554718

3

Hypergastrinemia, a clue leading to the identification of an atypical form of diabetes mellitus type 2.

Steyaert W, Varney MJ, Benovic JL, Creemers J, Speeckaert MM, Coucke PJ, Delanghe JR. Steyaert W, et al. Among authors: coucke pj. Clin Chim Acta. 2022 Jul 1;532:79-83. doi: 10.1016/j.cca.2022.05.016. Epub 2022 May 24. Clin Chim Acta. 2022. PMID: 35623402

4

Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family.

Syx D, Symoens S, Steyaert W, De Paepe A, Coucke PJ, Malfait F. Syx D, et al. Among authors: coucke pj. Dis Markers. 2015;2015:828970. doi: 10.1155/2015/828970. Epub 2015 Oct 4. Dis Markers. 2015. PMID: 26504261 Free PMC article.

5

Comprehensive validation of a diagnostic strategy for sequencing genes with one or multiple pseudogenes using pseudoxanthoma elasticum as a model.

Steyaert W, Verschuere S, Coucke PJ, Vanakker OM. Steyaert W, et al. Among authors: coucke pj. J Genet Genomics. 2021 Apr 20;48(4):289-299. doi: 10.1016/j.jgg.2021.02.009. Epub 2021 Mar 25. J Genet Genomics. 2021. PMID: 34049798

6

Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome.

Symoens S, Steyaert W, Demuynck L, De Paepe A, Diderich KE, Malfait F, Coucke PJ. Symoens S, et al. Among authors: coucke pj. Am J Med Genet A. 2017 Apr;173(4):1047-1050. doi: 10.1002/ajmg.a.38135. Epub 2017 Mar 6. Am J Med Genet A. 2017. PMID: 28261977

7

BATCH-GE: Analysis of NGS Data for Genome Editing Assessment.

Steyaert W, Boel A, Coucke P, Willaert A. Steyaert W, et al. Methods Mol Biol. 2018;1865:83-90. doi: 10.1007/978-1-4939-8784-9_6. Methods Mol Biol. 2018. PMID: 30151760

8

Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA.

Meerschaut I, Steyaert W, Bové T, François K, Martens T, De Groote K, De Wilde H, Muiño Mosquera L, Panzer J, Vandekerckhove K, Moons L, Vermassen P, Symoens S, Coucke PJ, De Wolf D, Callewaert B. Meerschaut I, et al. Among authors: coucke pj. Genes (Basel). 2022 Jul 7;13(7):1214. doi: 10.3390/genes13071214. Genes (Basel). 2022. PMID: 35885997 Free PMC article.

9

Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment.

Boel A, Steyaert W, De Rocker N, Menten B, Callewaert B, De Paepe A, Coucke P, Willaert A. Boel A, et al. Sci Rep. 2018 Oct 29;8(1):15845. doi: 10.1038/s41598-018-33869-y. Sci Rep. 2018. PMID: 30374100 Free PMC article.

10

Flexible, scalable, and efficient targeted resequencing on a benchtop sequencer for variant detection in clinical practice.

De Leeneer K, Hellemans J, Steyaert W, Lefever S, Vereecke I, Debals E, Crombez B, Baetens M, Van Heetvelde M, Coppieters F, Vandesompele J, De Jaegher A, De Baere E, Coucke P, Claes K. De Leeneer K, et al. Hum Mutat. 2015 Mar;36(3):379-87. doi: 10.1002/humu.22739. Hum Mutat. 2015. PMID: 25504618

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