WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders von Huybrechts, Yentl, Mortier, Geert, Boudin, Eveline, Van Hul, Wim

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A Panel-Based Sequencing Analysis of Patients with Paget’s Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importanc... von De Ridder, Raphaël, Vandeweyer, Geert, Boudin, Eveline, Hendrickx, Gretl, Huybrechts, Yentl, Cremers, Tycho Canter, Devogelaer, Jean-Pierre, Mortier, Geert, Fransen, Erik, Van Hul, Wim

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Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking von Huybrechts, Yentl, Van Hul, Wim

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Compound heterozygosity of mutations located in the first and third β-propeller domain of LRP4 causes sclerosteosis in a Spanish patient von Huybrechts, Yentl, Steenackers, Ellen, Hamdy, Neveen, Mortier, Geert, Martinez, Guillermo, Bracamonte, Milagros Sierra, Appelman-Dijkstra, Natasha, Van Hul, Wim, Boudin, Eveline

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A Mosaic Variant in CTNNB1/β-catenin as a Novel Cause for Osteopathia Striata With Cranial Sclerosis von Huybrechts, Yentl, Appelman-Dijkstra, Natasha M, Steenackers, Ellen, Van Beylen, Wouter, Mortier, Geert, Hendrickx, Gretl, Van Hul, Wim

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A mosaic variant in CTNNB1/β-catenin as a novel cause for osteopathia striata with cranial sclerosis von Huybrechts, Yentl, Appelman-Dijkstra, Natasha M, Steenackers, Ellen, Van Beylen, Wouter, Mortier, Geert, Hendrickx, Gretl, Van Hul, Wim

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Genetic Screening of ZNF687 and PFN1 in a Paget's Disease of Bone Cohort Indicates an Important Role for the Nuclear Localization Signal of ZNF687 von Huybrechts, Yentl, De Ridder, Raphael, Steenackers, Ellen, Devogelaer, Jean-Pierre, Mortier, Geert, Hendrickx, Gretl, Van Hul, Wim

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Genetic Screening of ZNF687 and PFN1 in a Paget’s Disease of Bone Cohort Indicates an Important Role for the Nuclear Localization Signal of ZNF687 von Huybrechts, Yentl, De Ridder, Raphaël, Steenackers, Ellen, Devogelaer, Jean-Pierre, Mortier, Geert, Hendrickx, Gretl, Van Hul, Wim

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Osteocytic Sclerostin Expression as an Indicator of Altered Bone Turnover von Huybrechts, Yentl, Evenepoel, Pieter, Haarhaus, Mathias, Cavalier, Etienne, Dams, Geert, Van Hul, Wim, D'Haese, Patrick C.C, Verhulst, Anja

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WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders von Huybrechts, Yentl, Mortier, Geert, Boudin, Eveline, Van Hul, Wim

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A Panel-Based Sequencing Analysis of Patients with Paget's Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importanc... von De Ridder, Raphael, Vandeweyer, Geert, Boudin, Eveline, Hendrickx, Gretl, Huybrechts, Yentl, Cremers, Tycho Canter, Devogelaer, Jean-Pierre, Mortier, Geert, Fransen, Erik, Van Hul, Wim

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Osteocytic Sclerostin Expression as an Indicator of Altered Bone Turnover von Huybrechts, Yentl, Evenepoel, Pieter, Haarhaus, Mathias, Cavalier, Etienne, Dams, Geert, Van Hul, Wim, D'Haese, Patrick C, Verhulst, Anja

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Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis von Huybrechts, Yentl, Boudin, Eveline, Hendrickx, Gretl, Steenackers, Ellen, Hamdy, Neveen, Mortier, Geert, Martinez Diaz-Guerra, Guillermo, Bracamonte, Milagros Sierra, Appelman-Dijkstra, Natasha M, Van Hul, Wim

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Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis von Huybrechts, Yentl, Boudin, Eveline, Hendrickx, Gretl, Steenackers, Ellen, Hamdy, Neveen, Mortier, Geert, Martínez Díaz-Guerra, Guillermo, Bracamonte, Milagros Sierra, Appelman-Dijkstra, Natasha M, Van Hul, Wim

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The sqstm1tmΔUBA zebrafish model, a proof-of-concept in vivo model for Paget’s disease of bone? von Huybrechts, Yentl, De Ridder, Raphaël, De Samber, Björn, Boudin, Eveline, Tonelli, Francesca, Knapen, Dries, Schepers, Dorien, De Beenhouwer, Jan, Sijbers, Jan, Forlino, Antonella, Mortier, Geert, Coucke, Paul, Witten, P. Eckhard, Kwon, Ronald, Willaert, Andy, Hendrickx, Gretl, Van Hul, Wim

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A Novel in Vivo Model for Paget's Disease of Bone: The sqstm1tmΔUBA Zebrafish Line von Huybrechts, Yentl, De Ridder, Raphael, De Samber, Bjorn, Boudin, Eveline, Tonelli, Francesca, Knapen, Dries, Schepers, Dorien, De Beenhouwer, Jan, Sijbers, Jan, Bergen, Dylan, Hammond, Chrissy, Forlino, Antonella, Mortier, Geert, Coucke, Paul, Witten, P. Eckhard, Kwon, Ronald, Willaert, Andy, Hendrickx, Gretl, Van Hul, Wim

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