Mutation of foxl1 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 FOXL1 has been identified as the causative gene in a family wi...

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Detalles Bibliográficos
Autores principales: Hawkey-Noble, Alexia, Pater, Justin A., Kollipara, Roshni, Fitzgerald, Meriel, Maekawa, Alexandre S., Kovacs, Christopher S., Young, Terry-Lynn, French, Curtis R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319681/
https://www.ncbi.nlm.nih.gov/pubmed/35885890
http://dx.doi.org/10.3390/genes13071107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319681/
https://www.ncbi.nlm.nih.gov/pubmed/35885890
http://dx.doi.org/10.3390/genes13071107

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