Yentl Huybrechts

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 8 publications

Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone.

Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone.

Journal: Calcified tissue international

Published: November 14, 2024

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.

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.

Journal: Calcified tissue international

Published: July 19, 2023

A Mosaic Variant in CTNNB1/β-catenin as a Novel Cause for Osteopathia Striata With Cranial Sclerosis.

A Mosaic Variant in CTNNB1/β-catenin as a Novel Cause for Osteopathia Striata With Cranial Sclerosis.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 12, 2023

Osteocytic Sclerostin Expression as an Indicator of Altered Bone Turnover.

Osteocytic Sclerostin Expression as an Indicator of Altered Bone Turnover.

Journal: Nutrients

Published: December 21, 2022

Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking.

Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking.

Journal: Bone

Published: June 14, 2022

Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis.

Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis.

Journal: Genes

Published: December 03, 2021

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 Importance of the 7q33 Locus.

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 Importance of the 7q33 Locus.

Journal: Calcified tissue international

Published: April 07, 2021

WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders.

WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders.

Journal: Frontiers in endocrinology

Published: December 20, 2019

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Last Updated: 09/26/2026