Skeletal malformations of Meox1-deficient zebrafish resemble human Klippel-Feil syndrome

Author:

Dauer Mervyn V. P.12,Currie Peter D.12,Berger Joachim12ORCID

Affiliation:

1. Australian Regenerative Medicine Institute; Monash University; Clayton VIC Australia

2. Victoria Node; EMBL Australia; Clayton VIC Australia

Funder

National Health and Medical Research Council

State Government of Victoria and the Australian Government

Publisher

Wiley

Subject

Cell Biology,Developmental Biology,Molecular Biology,Ecology, Evolution, Behavior and Systematics,Histology,Anatomy

Reference30 articles.

1. Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype;Bayrakli;BMC Genet,2013

2. Developmental morphology of the axial skeleton of the zebrafish, Danio rerio (Ostariophysi: Cyprinidae);Bird;Dev Dyn,2003

3. Understanding idiopathic scoliosis: a new zebrafish school of thought;Boswell;Trends Genet,2017

4. Differential localization of Mox-1 and Mox-2 proteins indicates distinct roles during development;Candia;Int J Dev Biol,1996

5. Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos;Candia;Development,1992

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