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Frontiers in Endocrinology
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April 25, 2020
WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders
Yentl Huybrechts, Geert Mortier, Eveline Boudin, et al.
Seminars in Arthritis and Rheumatism
|
February 26, 2013
The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases
Eveline Boudin, Igor Fijalkowski, Elke Piters, et al.
International Journal of Molecular Sciences
|
November 27, 2025
The Paraoxonase (<i>PON</i>) Gene Family in Health, Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) and Other Diseases
Tammy Huybrechts, Kristien Franck, Ellen Steenackers, et al.
Frontiers in Endocrinology
|
April 18, 2022
Editorial: Innovative Models in Bone Biology: What can be Learned From Rare Bone Diseases?
Teun J de Vries, Wim Van Hul, E Marelise Eekhoff
European Journal of Human Genetics : EJHG
|
May 30, 2003
Clinical and molecular analysis of nine families with Adams-Oliver syndrome
Pieter Verdyck, Muriel Holder-Espinasse, Wim Van Hul, et al.
Calcified Tissue International
|
February 6, 2019
Camurati-Engelmann Disease
Wim Van Hul, Eveline Boudin, Filip M Vanhoenacker, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 13, 2004
LRP5 and Wnt signaling: a union made for bone
Mark L Johnson, Kimberley Harnish, Roel Nusse, et al.
Current Osteoporosis Reports
|
April 16, 2018
Human Genetics of Sclerosing Bone Disorders
Raphaël De Ridder, Eveline Boudin, Geert Mortier, et al.
Endocrine Reviews
|
May 20, 2005
Transforming growth factor-beta1 to the bone
Katrien Janssens, Peter ten Dijke, Sophie Janssens, et al.
Clinical Dysmorphology
|
September 13, 2012
Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndrome
Jenneke J van den Ende, Vere Borra, Wim Van Hul
Page
of 17
Search research articles
Search
Showing results (21-30 of 170) with videos related to
Sort By:
Page
of 17
Frontiers in Endocrinology
|
April 25, 2020
WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders
Yentl Huybrechts, Geert Mortier, Eveline Boudin, et al.
Seminars in Arthritis and Rheumatism
|
February 26, 2013
The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases
Eveline Boudin, Igor Fijalkowski, Elke Piters, et al.
International Journal of Molecular Sciences
|
November 27, 2025
The Paraoxonase (<i>PON</i>) Gene Family in Health, Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) and Other Diseases
Tammy Huybrechts, Kristien Franck, Ellen Steenackers, et al.
Frontiers in Endocrinology
|
April 18, 2022
Editorial: Innovative Models in Bone Biology: What can be Learned From Rare Bone Diseases?
Teun J de Vries, Wim Van Hul, E Marelise Eekhoff
European Journal of Human Genetics : EJHG
|
May 30, 2003
Clinical and molecular analysis of nine families with Adams-Oliver syndrome
Pieter Verdyck, Muriel Holder-Espinasse, Wim Van Hul, et al.
Calcified Tissue International
|
February 6, 2019
Camurati-Engelmann Disease
Wim Van Hul, Eveline Boudin, Filip M Vanhoenacker, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 13, 2004
LRP5 and Wnt signaling: a union made for bone
Mark L Johnson, Kimberley Harnish, Roel Nusse, et al.
Current Osteoporosis Reports
|
April 16, 2018
Human Genetics of Sclerosing Bone Disorders
Raphaël De Ridder, Eveline Boudin, Geert Mortier, et al.
Endocrine Reviews
|
May 20, 2005
Transforming growth factor-beta1 to the bone
Katrien Janssens, Peter ten Dijke, Sophie Janssens, et al.
Clinical Dysmorphology
|
September 13, 2012
Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndrome
Jenneke J van den Ende, Vere Borra, Wim Van Hul
Page
of 17