Literature DB >> 14623232

Radiographic analysis of zebrafish skeletal defects.

Shannon Fisher1, Pudur Jagadeeswaran, Marnie E Halpern.   

Abstract

Systematic identification of skeletal dysplasias in model vertebrates provides insight into the pathogenesis of human skeletal disorders and can aid in the identification of orthologous human genes. We are undertaking a mutagenesis screen for skeletal dysplasias in adult zebrafish, using radiography to detect abnormalities in skeletal anatomy and bone morphology. We have isolated chihuahua, a dominant mutation causing a general defect in bone growth. Heterozygous chihuahua fish have phenotypic similarities to human osteogenesis imperfecta, a skeletal dysplasia caused by mutations in the type I collagen genes. Mapping and molecular characterization of the chihuahua mutation indicates that the defect resides in the gene encoding the collagen I(alpha1) chain. Thus, chihuahua accurately models osteogenesis imperfecta at the biologic and molecular levels, and will prove an important resource for studies on the disease pathophysiology. Radiography is a practical screening tool to detect subtle skeletal abnormalities in the adult zebrafish. The identification of chihuahua demonstrates that mutant phenotypes analogous to human skeletal dysplasias will be discovered.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14623232     DOI: 10.1016/s0012-1606(03)00399-3

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


  70 in total

1.  Proliferative and mineralogenic effects of insulin, IGF-1, and vanadate in fish osteoblast-like cells.

Authors:  Daniel M Tiago; M Leonor Cancela; Vincent Laizé
Journal:  J Bone Miner Metab       Date:  2010-12-23       Impact factor: 2.626

2.  Adult Zebrafish Injury Models to Study the Effects of Prednisolone in Regenerating Bone Tissue.

Authors:  Karina Geurtzen; Franziska Knopf
Journal:  J Vis Exp       Date:  2018-10-18       Impact factor: 1.355

3.  A new model system swims into focus: using the zebrafish to visualize intestinal metabolism in vivo.

Authors:  Juliana D Carten; Steven A Farber
Journal:  Clin Lipidol       Date:  2009-08-01

4.  Establishment of primary cell cultures from fish calcified tissues.

Authors:  Cátia L Marques; Marta S Rafael; M Leonor Cancela; Vincent Laizé
Journal:  Cytotechnology       Date:  2007-10-11       Impact factor: 2.058

5.  Development of an in vitro cell system from zebrafish suitable to study bone cell differentiation and extracellular matrix mineralization.

Authors:  Parameswaran Vijayakumar; Vincent Laizé; João Cardeira; Marlene Trindade; M Leonor Cancela
Journal:  Zebrafish       Date:  2013-08-02       Impact factor: 1.985

6.  Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.

Authors:  Kathrin Laue; Hans-Martin Pogoda; Philip B Daniel; Arie van Haeringen; Yasemin Alanay; Simon von Ameln; Martin Rachwalski; Tim Morgan; Mary J Gray; Martijn H Breuning; Gregory M Sawyer; Andrew J Sutherland-Smith; Peter G Nikkels; Christian Kubisch; Wilhelm Bloch; Bernd Wollnik; Matthias Hammerschmidt; Stephen P Robertson
Journal:  Am J Hum Genet       Date:  2011-10-20       Impact factor: 11.025

7.  A gain of function mutation causing skeletal overgrowth in the rapunzel mutant.

Authors:  Julie Green; Jennifer J Taylor; Anna Hindes; Stephen L Johnson; Matthew I Goldsmith
Journal:  Dev Biol       Date:  2009-07-24       Impact factor: 3.582

8.  Zebrafish grainyhead-like1 is a common marker of different non-keratinocyte epidermal cell lineages, which segregate from each other in a Foxi3-dependent manner.

Authors:  Martina Janicke; Bjorn Renisch; Matthias Hammerschmidt
Journal:  Int J Dev Biol       Date:  2010       Impact factor: 2.203

9.  Regulation of neural crest cell fate by the retinoic acid and Pparg signalling pathways.

Authors:  Nan Li; Robert N Kelsh; Peter Croucher; Henry H Roehl
Journal:  Development       Date:  2010-02       Impact factor: 6.868

10.  RANKL inhibition improves bone properties in a mouse model of osteogenesis imperfecta.

Authors:  Renee Bargman; Alice Huang; Adele L Boskey; Cathleen Raggio; Nancy Pleshko
Journal:  Connect Tissue Res       Date:  2010-04       Impact factor: 3.417

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.