Ribosomal Dysfunction Is a Common Pathomechanism in Different Forms of Trichothiodystrophy

Mutations in a broad variety of genes can provoke the severe childhood disorder trichothiodystrophy (TTD) that is classified as a DNA repair disease or a transcription syndrome of RNA polymerase II. In an attempt to identify the common underlying pathomechanism of TTD we performed a knockout/knockdo...

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Detalles Bibliográficos
Autores principales: Zhu, Gaojie, Khalid, Fatima, Zhang, Danhui, Cao, Zhouli, Maity, Pallab, Kestler, Hans A., Orioli, Donata, Scharffetter-Kochanek, Karin, Iben, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377840/
https://www.ncbi.nlm.nih.gov/pubmed/37508541
http://dx.doi.org/10.3390/cells12141877

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377840/
https://www.ncbi.nlm.nih.gov/pubmed/37508541
http://dx.doi.org/10.3390/cells12141877

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