Adelbert De Clercq

Gent, VLG 9000, Belgium

Last Updated: 09/26/2026

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Found 18 publications

Smad3 deficiency attenuates disease severity in a zebrafish model for Smad6-related aortic disease.

Smad3 deficiency attenuates disease severity in a zebrafish model for Smad6-related aortic disease.

Journal: Angiogenesis
Published: October 08, 2025

Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development.

Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: May 03, 2023

Elevated Water CO2 Can Prevent Dietary-Induced Osteomalacia in Post-Smolt Atlantic Salmon (Salmo salar, L.).

Elevated Water CO2 Can Prevent Dietary-Induced Osteomalacia in Post-Smolt Atlantic Salmon (Salmo salar, L.).

Journal: Biomolecules
Published: January 27, 2023

A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract.

A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract.

Journal: Human genetics
Published: October 28, 2022

Alterations in glycosaminoglycan biosynthesis associated with the Ehlers-Danlos syndromes.

Alterations in glycosaminoglycan biosynthesis associated with the Ehlers-Danlos syndromes.

Journal: American journal of physiology. Cell physiology
Published: August 22, 2022

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.

Journal: American journal of human genetics
Published: December 03, 2021

An Overview of Investigational and Experimental Drug Treatment Strategies for Marfan Syndrome.

An Overview of Investigational and Experimental Drug Treatment Strategies for Marfan Syndrome.

Journal: Journal of experimental pharmacology
Published: May 01, 2021

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.

Journal: American journal of human genetics
Published: January 23, 2021

The ZE-Tunnel: An Affordable, Easy-to-Assemble, and User-Friendly Benchtop Zebrafish Swim Tunnel.

The ZE-Tunnel: An Affordable, Easy-to-Assemble, and User-Friendly Benchtop Zebrafish Swim Tunnel.

Journal: Zebrafish
Published: January 11, 2021

Lrp5 Mutant and Crispant Zebrafish Faithfully Model Human Osteoporosis, Establishing the Zebrafish as a Platform for CRISPR-Based Functional Screening of Osteoporosis Candidate Genes.

Lrp5 Mutant and Crispant Zebrafish Faithfully Model Human Osteoporosis, Establishing the Zebrafish as a Platform for CRISPR-Based Functional Screening of Osteoporosis Candidate Genes.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: December 23, 2020

b3galt6 Knock-Out Zebrafish Recapitulate β3GalT6-Deficiency Disorders in Human and Reveal a Trisaccharide Proteoglycan Linkage Region.

b3galt6 Knock-Out Zebrafish Recapitulate β3GalT6-Deficiency Disorders in Human and Reveal a Trisaccharide Proteoglycan Linkage Region.

Journal: Frontiers in cell and developmental biology
Published: August 22, 2020

Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders.

Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders.

Journal: Frontiers in endocrinology
Published: April 25, 2020
Showing 1-12 of 18

Last Updated: 09/26/2026