Hnf1b renal expression directed by a distal enhancer responsive to Pax8

Xenopus provides a simple and efficient model system to study nephrogenesis and explore the mechanisms causing renal developmental defects in human. Hnf1b (hepatocyte nuclear factor 1 homeobox b), a gene whose mutations are the most commonly identified genetic cause of developmental kidney disease,...

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Detalles Bibliográficos
Autores principales: Goea, L., Buisson, I., Bello, V., Eschstruth, A., Paces-Fessy, M., Le Bouffant, R., Chesneau, A., Cereghini, S., Riou, J. F., Umbhauer, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675860/
https://www.ncbi.nlm.nih.gov/pubmed/36402859
http://dx.doi.org/10.1038/s41598-022-21171-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675860/
https://www.ncbi.nlm.nih.gov/pubmed/36402859
http://dx.doi.org/10.1038/s41598-022-21171-x

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