Literature DB >> 31325453

Zebrafish and medaka as models for biomedical research of bone diseases.

L Lleras-Forero1, C Winkler2, S Schulte-Merker3.   

Abstract

The identification of disease-causing mutations has in recent years progressed immensely due to whole genome sequencing approaches using patient material. The task accordingly is shifting from gene identification to functional analysis of putative disease-causing genes, preferably in an in vivo setting which also allows testing of drug candidates or biotherapeutics in whole animal disease models. In this review, we highlight the advances made in the field of bone diseases using small laboratory fish, focusing on zebrafish and medaka. We particularly highlight those human conditions where teleost models are available.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Year:  2019        PMID: 31325453     DOI: 10.1016/j.ydbio.2019.07.009

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  14 in total

1.  Cxcl9l and Cxcr3.2 regulate recruitment of osteoclast progenitors to bone matrix in a medaka osteoporosis model.

Authors:  Quang Tien Phan; Wen Hui Tan; Ranran Liu; Sudha Sundaram; Anita Buettner; Susanne Kneitz; Benedict Cheong; Himanshu Vyas; Sinnakaruppan Mathavan; Manfred Schartl; Christoph Winkler
Journal:  Proc Natl Acad Sci U S A       Date:  2020-07-27       Impact factor: 11.205

Review 2.  Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy of the Royal Osteoporosis Society on October 5th 2020.

Authors:  Jonathan H Tobias; Emma L Duncan; Erika Kague; Chrissy L Hammond; Celia L Gregson; Duncan Bassett; Graham R Williams; Josine L Min; Tom R Gaunt; David Karasik; Claes Ohlsson; Fernando Rivadeneira; James R Edwards; Fadil M Hannan; John P Kemp; Sophie J Gilbert; Nerea Alonso; Neelam Hassan; Juliet E Compston; Stuart H Ralston
Journal:  Front Endocrinol (Lausanne)       Date:  2021-02-15       Impact factor: 5.555

3.  Pharmacological Manipulation of Early Zebrafish Skeletal Development Shows an Important Role for Smad9 in Control of Skeletal Progenitor Populations.

Authors:  Georgina L K McDonald; Mengdi Wang; Chrissy L Hammond; Dylan J M Bergen
Journal:  Biomolecules       Date:  2021-02-13

Review 4.  Tissue-Nonspecific Alkaline Phosphatase-A Gatekeeper of Physiological Conditions in Health and a Modulator of Biological Environments in Disease.

Authors:  Daniel Liedtke; Christine Hofmann; Franz Jakob; Eva Klopocki; Stephanie Graser
Journal:  Biomolecules       Date:  2020-12-08

Review 5.  Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders.

Authors:  Francesca Tonelli; Jan Willem Bek; Roberta Besio; Adelbert De Clercq; Laura Leoni; Phil Salmon; Paul J Coucke; Andy Willaert; Antonella Forlino
Journal:  Front Endocrinol (Lausanne)       Date:  2020-07-31       Impact factor: 5.555

Review 6.  High Fidelity of Mouse Models Mimicking Human Genetic Skeletal Disorders.

Authors:  Robert Brommage; Claes Ohlsson
Journal:  Front Endocrinol (Lausanne)       Date:  2020-02-04       Impact factor: 5.555

7.  Investigation of alpl expression and Tnap-activity in zebrafish implies conserved functions during skeletal and neuronal development.

Authors:  Barbara Ohlebusch; Angela Borst; Daniel Liedtke; Stephanie Graser; Tina Frankenbach; Eva Klopocki; Franz Jakob
Journal:  Sci Rep       Date:  2020-08-07       Impact factor: 4.379

8.  Zebrafish mafbb Mutants Display Osteoclast Over-Activation and Bone Deformity Resembling Osteolysis in MCTO Patients.

Authors:  Yujie Han; Weihao Shao; Dan Zhong; Cui Ma; Xiaona Wei; Abrar Ahmed; Tingting Yu; Wei Jing; Lili Jing
Journal:  Biomolecules       Date:  2021-03-23

9.  Endospanin Is a Candidate for Regulating Leptin Sensitivity.

Authors:  Richard L Londraville; Matthew Tuttle; Qin Liu; Janna M Andronowski
Journal:  Front Physiol       Date:  2022-01-07       Impact factor: 4.566

10.  Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease.

Authors:  John P Kemp; Chrissy L Hammond; Juriaan R Metz; Dylan J M Bergen; Qiao Tong; Ankit Shukla; Elis Newham; Jan Zethof; Mischa Lundberg; Rebecca Ryan; Scott E Youlten; Monika Frysz; Peter I Croucher; Gert Flik; Rebecca J Richardson
Journal:  BMC Biol       Date:  2022-01-21       Impact factor: 7.431

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