Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structure

A loss-of-function mutation in tetratricopeptide repeat domain 7A (TTC7A) is a recently identified cause of human intestinal and immune disorders. However, clues to related underlying molecular dysfunctions remain elusive. It is now shown based on the study of TTC7A-deficient and wild-type cells tha...

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Publicado en:Cell Discov
Main Authors: El-Daher, Marie-Therese, Cagnard, Nicolas, Gil, Marine, Da Cruz, Marie Chansel, Leveau, Claire, Sepulveda, Fernando, Zarhrate, Mohammed, Tores, Frédéric, Legoix, Patricia, Baulande, Sylvain, de Villartay, Jean Pierre, Almouzni, Geneviève, Quivy, Jean-Pierre, Fischer, Alain, de Saint Basile, Geneviève
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group UK 2018
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6232119/
https://ncbi.nlm.nih.gov/pubmed/30455981
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41421-018-0061-y
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