arrow
返回
P

Paul Coucke

Ghent University

68H指数
473论文数
1.9W被引数
收录论文 140
发表时间
Evaluating variants of uncertain significance in adult zebrafish via prime editing: a proof of concept with a COL1A2 variant通过碱基编辑技术评估成年斑马鱼中意义未明的变异:一项关于COL1A2变异的可行性研究
err2025-12-02
err0
PREAI
errVanhooydonck, Michiel; Debaenst, Sophie; Vanbelleghem, Eva; De Saffel, Hanna; Syx, Delfien; Sips, Patrick; Coucke, Paul J.; Willaert, Andy; Callewaert, Bert
err分享
err收藏
Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney Disease结构-活性分析揭示MAPKBP1相关肾脏病中纤毛- Jun N末端激酶信号通路紊乱
err2025-06-04
err0
errOAAI
errChristin Findeisen; Maria Papazian; Linda Pöschla; Anastasia Ertel; Wenjun Jin; Nydia Panitz; Elena Hantmann; Paul Coucke; Firdous Abdulwahab; Lama AlAbdi; Fawzan S. Alkuraya; May Salem; Hamad Alzaidan; Kai-Uwe Eckardt; Søren T. Christensen; Alexandre Benmerah; Sophie Saunier; Jan Halbritter; Ria Schönauer
err分享
err收藏
Genetic screening in patients with oocyte/zygote/embryo maturation arrest and failed fertilization卵母细胞/合子/胚胎成熟阻滞及受精失败患者的遗传筛查
err2025-06-01
err0
errOAAI
errMu, H.; Cardona Barberan, A.; Decroos, E.; Vuylsteke, S.; Jalali, F.; Syryn, H.; De Baere, E.; Janssens, S.; Coucke, P.; Menten, B.; Stoop, D.; Heindryckx, B.
err分享
err收藏
Mito-TALENs reduce mitochondrial DNA mutation load following pronuclear transferMito-TALENs 通过原核转移降低线粒体DNA突变负荷
err2025-06-01
err0
errOAAI
errCastelluccio, N.; Rybouchkin, A.; Bacman, S. R.; Symoens, S.; Coucke, P.; Menten, B.; Moraes, C. T.; De Spiegelaere, W.; Stoop, D.; Heindryckx, B.
err分享
err收藏
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease (Jan, 10.1038/s41431-025-01788-y, 2025)RNA测序揭示了可变先天性心脏病中的FLT4剪接位点变异 (1月,10.1038/s41431-025-01788-y,2025)
err2025-04-01
err0
PREAI
errVerlee, Maxim; D'haenens, Erika; De Cock, Laurenz; Mosquera, Laura Muino; De Groote, Katya; Vandekerckhove, Kristof; Panzer, Joseph; Roets, Ellen; Menten, Bjoern; Symoens, Sofie; Coucke, Paul; Van Damme, Tim; Vergult, Sarah; Callewaert, Bert
err分享
err收藏
Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone
err2025-03-14
err0
PREAI
errHuybrechts, Yentl; De Ridder, Raphael; Bergen, Dylan; De Samber, Bjoern; Boudin, Eveline; Tonelli, Francesca; Knapen, Dries; Vergauwen, Lucia; Schepers, Dorien; Van Dijck, Evelien; Tong, Qiao; Verhulst, Anja; De Beenhouwer, Jan; Sijbers, Jan; Hammond, Chrissy; Forlino, Antonella; Mortier, Geert; Coucke, Paul; Witten, P. Eckhard; Kwon, Ronald Young; Willaert, Andy; Hendrickx, Gretl; Van Hul, Wim
err分享
err收藏
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease
err2025-01-27
err1
PREAI
errVerlee, Maxim; D'haenens, Erika; De Cock, Laurenz; Mosquera, Laura Muino; De Groote, Katya; Vandekerckhove, Kristof; Panzer, Joseph; Roets, Ellen; Menten, Bjorn; Symoens, Sofie; Coucke, Paul; Vandamme, Tim; Vergult, Sarah; Callewaert, Bert
err分享
err收藏
Bmpr1aa modulates the severity of the skeletal phenotype in an fkbp10-deficient Bruck syndrome zebrafish modelBmpr1aa调节fkbp10-deficient布鲁克综合征斑马鱼模型中骨骼表型的严重程度
err2024-11-20
err1
PREAI
errJarayseh, Tamara; Debaenst, Sophie; De Saffel, Hanna; Rosseel, Toon; Milazzo, Mauro; Bek, Jan Willem; Hudson, David M.; Van Nieuwerburgh, Filip; Gansemans, Yannick; Josipovic, Ivan; Boone, Matthieu N.; Witten, P. Eckhard; Willaert, Andy; Coucke, Paul J.
err分享
err收藏
High rate of detected variants in male PLCZ1 and ACTL7A genes causing failed fertilization after ICSI
err2024-09-28
err1
errOAAI
errCardona Barberan, Arantxa; Reddy Guggilla, Ramesh; Colenbier, Cora; van der Velden, Emma; Rybouchkin, Andrei; Stoop, Dominic; Leybaert, Luc; Coucke, Paul; Symoens, Sofie; Boel, Annekatrien; Meerschaut, Frauke Vanden; Heindryckx, Bjorn
err分享
err收藏
An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome
err2024-07-01
err1
PREAI
errVan Den Heuvel, Lotte J. F.; Peeters, Silke; Meester, Josephina A. N.; Coucke, Paul J.; Loeys, Bart L.
err分享
err收藏
Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos
err2024-04-01
err0
PREAI
errBekaert, B.; Boel, A.; Rybouchkin, A.; Cosemans, G.; Declercq, S.; Lopes, S. M. Chuva de Sousa; Parrington, J.; Stoop, D.; Coucke, P.; Menten, B.; Heindryckx, B.
err分享
err收藏
Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development
err2023-11-01
err1
errOAAI
errGuillemyn, Brecht; De Saffel, Hanna; Bek, Jan Willem; Tapaneeyaphan, Piyanoot; De Clercq, Adelbert; Jarayseh, Tamara; Debaenst, Sophie; Willaert, Andy; De Rycke, Riet; Byers, Peter H.; Rosseel, Toon; Coucke, Paul; Blaumeiser, Bettina; Syx, Delfien; Malfait, Fransiska; Symoens, Sofie
err分享
err收藏
Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos
err2023-08-01
err1
PREAI
errBekaert, Bieke; Boel, Annekatrien; De Witte, Lisa; Vandenberghe, Winter; Popovic, Mina; Stamatiadis, Panagiotis; Cosemans, Gwenny; Tordeurs, Lise; De Loore, Athina-Maria; Lopes, Susana Marina Chuva de Sousa; De Sutter, Petra; Stoop, Dominic; Coucke, Paul; Menten, Bjoern; Heindryckx, Bjoern
err分享
err收藏
Assisted oocyte activation does not overcome recurrent embryo developmental problems
err2023-03-17
err6
PREAI
errCardona Barberan, 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.
err分享
err收藏
A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract
err2023-01-25
err4
PREAI
errJarayseh, Tamara; Guillemyn, Brecht; De Saffel, Hanna; Bek, Jan Willem; Syx, Delfien; Symoens, Sofie; Gansemans, Yannick; Nieuwerburgh, Filip; Jagadeesh, Sujatha; Raja, Jayarekha; Malfait, Fransiska; Coucke, Paul J.; De Clercq, Adelbert; Willaert, Andy
err分享
err收藏
Zebrafish Tric-b is required for skeletal development and bone cells differentiation
err2023-01-23
err8
errOAAI
errTonelli, Francesca; Leoni, Laura; Daponte, Valentina; Gioia, Roberta; Cotti, Silvia; Fiedler, Imke A. K.; Larianova, Daria; Willaert, Andy; Coucke, Paul J.; Villani, Simona; Busse, Bjoern; Besio, Roberta; Rossi, Antonio; Witten, P. Eckhard; Forlino, Antonella
err分享
err收藏
G protein-coupled receptor kinase 6 (GRK6) regulates insulin processing and secretion via effects on proinsulin conversion to insulin
err2022-10-01
err2
errOAAI
errVarney, Matthew J.; Steyaert, Wouter; Coucke, Paul J.; Delanghe, Joris R.; Uehling, David E.; Joseph, Babu; Marcellus, Richard; Al-awar, Rima; Benovic, Jeffrey L.
err分享
err收藏
Hypergastrinemia, a clue leading to the identification of an atypical form of diabetes mellitus type 2
err2022-07-01
err6
errOAAI
errSteyaert, Wouter; Varney, Matthew J.; Benovic, Jeffrey L.; Creemers, John; Speeckaert, Marijn M.; Coucke, Paul J.; Delanghe, Joris R.
err分享
err收藏