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Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone Huybrechts, 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 分享 收藏
A Case-Control Study Supports Genetic Contribution of the PON Gene Family in Obesity and Metabolic Dysfunction Associated Steatotic Liver Disease 一项病例对照研究支持PON基因家族在肥胖和代谢功能障碍相关的脂肪性肝病中的遗传贡献 Van Dijck, Evelien; Diels, Sara; Fransen, Erik; Cremers, Tycho Canter; Verrijken, An; Dirinck, Eveline; Hoischen, Alexander; Vandeweyer, Geert; Vanden Berghe, Wim; Van Gaal, Luc; Francque, Sven; Van Hul, Wim 分享 收藏
Evolutionary and functional analyses of LRP5 in archaic and extant modern humans Roca-Ayats, Neus; Maceda, Iago; Bruque, Carlos David; Martinez-Gil, Nuria; Garcia-Giralt, Natalia; Cozar, Monica; Mellibovsky, Leonardo; Van Hul, Wim; Lao, Oscar; Grinberg, Daniel; Balcells, Susanna 分享 收藏
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An Additional Lrp4 High Bone Mass Mutation Mitigates the Sost-Knockout Phenotype in Mice by Increasing Bone Remodeling Hendrickx, Gretl; Boudin, Eveline; Mateiu, Ligia; Yorgan, Timur A.; Steenackers, Ellen; Kneissel, Michaela; Kramer, Ina; Mortier, Geert; Schinke, Thorsten; Van Hul, Wim 分享 收藏
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Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia Beyltjens, Tessi; Boudin, Eveline; Revencu, Nicole; Boeckx, Nele; Bertrand, Miriam; Schuetz, Leon; Haack, Tobias B.; Weber, Axel; Biliouri, Eleni; Vinksel, Mateja; Zagozen, Anja; Peterlin, Borut; Pai, Shashidhar; Telegrafi, Aida; Henderson, Lindsay B.; Ells, Courtney; Turner, Lesley; Wuyts, Wim; Van Hul, Wim; Hendrickx, Gretl; Mortier, Geert R. 分享 收藏
High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench 高骨量障碍: 连接诊所和工作台的新见解 Bergen, Dylan J. M.; Maurizi, Antonio; Formosa, Melissa M.; McDonald, Georgina L. K.; El-Gazzar, Ahmed; Hassan, Neelam; Brandi, Maria-Luisa; Riancho, Jose A.; Rivadeneira, Fernando; Ntzani, Evangelia; Duncan, Emma L.; Gregson, Celia L.; Kiel, Douglas P.; Zillikens, M. Carola; Sangiorgi, Luca; Hogler, Wolfgang; Duran, Ivan; Makitie, Outi; Van Hul, Wim; Hendrickx, Gretl 分享 收藏
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Broadening the Spectrum of Loss-of-Function Variants in NPR-C-Related Extreme Tall Stature 扩大与npr-c相关的极端身材的功能丧失变体的范围 Lauffer, Peter; Boudin, Eveline; van der Kaay, Danielle C. M.; Koene, Saskia; van Haeringen, Arie; van Tellingen, Vera; Van Hul, Wim; Prickett, Timothy C. R.; Mortier, Geert; Espiner, Eric A.; van Duyvenvoorde, Hermine A. 分享 收藏
Perspective of the GEMSTONE Consortium on Current and Future Approaches to Functional Validation for Skeletal Genetic Disease Using Cellular, Molecular and Animal-Modeling Techniques Rauner, Martina; Foessl, Ines; Formosa, Melissa M.; Kague, Erika; Prijatelj, Vid; Lopez, Nerea Alonso; Banerjee, Bodhisattwa; Bergen, Dylan; Busse, Bjoern; Calado, Angelo; Douni, Eleni; Gabet, Yankel; Giralt, Natalia Garcia; Grinberg, Daniel; Lovsin, Nika M.; Solan, Xavier Nogues; Ostanek, Barbara; Pavlos, Nathan J.; Rivadeneira, Fernando; Soldatovic, Ivan; van de Peppel, Jeroen; van der Eerden, Bram; van Hul, Wim; Balcells, Susanna; Marc, Janja; Reppe, Sjur; Soe, Kent; Karasik, David 分享 收藏
A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders Formosa, Melissa M.; Bergen, Dylan J. M.; Gregson, Celia L.; Maurizi, Antonio; Kampe, Anders; Garcia-Giralt, Natalia; Zhou, Wei; Grinberg, Daniel; Ovejero Crespo, Diana; Zillikens, M. Carola; Williams, Graham R.; Bassett, J. H. Duncan; Brandi, Maria Luisa; Sangiorgi, Luca; Balcells, Susanna; Hoegler, Wolfgang; Van Hul, Wim; Makitie, Outi 分享 收藏
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