Skeletal biology and disease modeling in zebrafish

K Dietrich, IAK Fiedler, A Kurzyukova… - Journal of Bone and …, 2020 - academic.oup.com
Zebrafish are teleosts (bony fish) that share with mammals a common ancestor belonging to
the phylum Osteichthyes, from which their endoskeletal systems have been inherited …

Zebrafish as an emerging model for osteoporosis: a primary testing platform for screening new osteo-active compounds

DJM Bergen, E Kague, CL Hammond - Frontiers in Endocrinology, 2019 - frontiersin.org
Osteoporosis is metabolic bone disease caused by an altered balance between bone
anabolism and catabolism. This dysregulated balance is responsible for fragile bones that …

Zebrafish models of human skeletal disorders: embryo and adult swimming together

M Carnovali, G Banfi, M Mariotti - BioMed Research …, 2019 - Wiley Online Library
Danio rerio (zebrafish) is an elective model organism for the study of vertebrate
development because of its high degree of homology with human genes and organs …

Zebrafish models for human skeletal disorders

M Marí-Beffa, AB Mesa-Román, I Duran - Frontiers in Genetics, 2021 - frontiersin.org
In 2019, the Nosology Committee of the International Skeletal Dysplasia Society provided an
updated version of the Nosology and Classification of Genetic Skeletal Disorders. This is a …

Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies

G Unlu, X Qi, ER Gamazon, DB Melville, N Patel… - Nature medicine, 2020 - nature.com
Discovery of genotype–phenotype relationships remains a major challenge in clinical
medicine. Here, we combined three sources of phenotypic data to uncover a new …

Zebrafish endochondral growth zones as they relate to human bone size, shape and disease

P Le Pabic, DB Dranow, DJ Hoyle… - Frontiers in …, 2022 - frontiersin.org
Research on the genetic mechanisms underlying human skeletal development and disease
have largely relied on studies in mice. However, recently the zebrafish has emerged as a …

[HTML][HTML] Fgfr3 mutation disrupts chondrogenesis and bone ossification in zebrafish model mimicking CATSHL syndrome partially via enhanced Wnt/β-catenin …

X Sun, R Zhang, H Chen, X Du, S Chen, J Huang… - Theranostics, 2020 - ncbi.nlm.nih.gov
CATSHL syndrome, characterized by camptodactyly, tall stature and hearing loss, is caused
by loss-of-function mutations of fibroblast growth factor receptors 3 (FGFR3) gene. Most …

Fishing for collagen function: About development, regeneration and disease

S Bretaud, P Nauroy, M Malbouyres… - Seminars in Cell & …, 2019 - Elsevier
Collagens are the most abundant vertebrate extracellular matrix proteins. They form a
superfamily of 28 members that show a remarkable diversity in molecular and …

Screening of mineralogenic and osteogenic compounds in zebrafish—Tools to improve assay throughput and data accuracy

JT Rosa, M Tarasco, PJ Gavaia, ML Cancela, V Laizé - Pharmaceuticals, 2022 - mdpi.com
Bone disorders affect millions of people worldwide and treatments currently available often
produce undesirable secondary effects or have limited efficacy. It is therefore of the utmost …

The role of starter diets in the development of skeletal abnormalities in zebrafish Danio rerio (Hamilton, 1822)

A Antinero, A Printzi, C Kourkouta… - Journal of Fish …, 2023 - Wiley Online Library
Fish skeletal development has long been correlated with nutritional factors. Lack of zebrafish
nutritional standardization, especially during the early stages, decreases the reproducibility …