Mouse Tbx3 Mutants Suggest Novel Molecular Mechanisms for Ulnar-Mammary Syndrome

The transcription factor TBX3 plays critical roles in development and TBX3 mutations in humans cause Ulnar-mammary syndrome. Efforts to understand how altered TBX3 dosage and function disrupt the development of numerous structures have been hampered by embryonic lethality of mice bearing presumed nu...

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Detalles Bibliográficos
Autores principales: Frank, Deborah U., Emechebe, Uchenna, Thomas, Kirk R., Moon, Anne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699485/
https://www.ncbi.nlm.nih.gov/pubmed/23844108
http://dx.doi.org/10.1371/journal.pone.0067841

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699485/
https://www.ncbi.nlm.nih.gov/pubmed/23844108
http://dx.doi.org/10.1371/journal.pone.0067841

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