Mutation of <i>foxl1</i> Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis

Mutation of <i>foxl1</i> Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis

Bone diseases such as otosclerosis (conductive hearing loss) and osteoporosis (low bone mineral density) can result from the abnormal expression of genes that regulate cartilage and bone development. The forkhead box transcription factor <i>FOXL1</i> has been identified as the causative...

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Bibliographic Details
Main Authors: Alexia Hawkey-Noble, Justin A. Pater, Roshni Kollipara, Meriel Fitzgerald, Alexandre S. Maekawa, Christopher S. Kovacs, Terry-Lynn Young, Curtis R. French
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Genes
Subjects:
<i>foxl1</i>
<i>foxc1</i>
zebrafish
otosclerosis
collagen
osteoporosis
Online Access:https://www.mdpi.com/2073-4425/13/7/1107

Internet

https://www.mdpi.com/2073-4425/13/7/1107

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