Severe changes in colon epithelium in the Mecp2-null mouse model of Rett syndrome

BACKGROUND: Rett syndrome is best known due to its severe and devastating symptoms in the central nervous system. It is produced by mutations affecting the Mecp2 gene that codes for a transcription factor. Nevertheless, evidence for MECP2 activity has been reported for tissues other than those of th...

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Detalles Bibliográficos
Autores principales: Millar-Büchner, Pamela, Philp, Amber R., Gutierrez, Noemí, Villanueva, Sandra, Kerr, Bredford, Flores, Carlos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116442/
https://www.ncbi.nlm.nih.gov/pubmed/27868160
http://dx.doi.org/10.1186/s40348-016-0065-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116442/
https://www.ncbi.nlm.nih.gov/pubmed/27868160
http://dx.doi.org/10.1186/s40348-016-0065-3

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