A transgenic cell line with inducible transcription for studying (CGG)n repeat expansion mechanisms

There are more than 30 inherited human disorders connected with repeat expansion (myotonic dystrophy type I, Huntington’s disease, Fragile X syndrome). Fragile X syndrome is the most common reason for inherited intellectual disability in the human population. The ways of the expansion development re...

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Detalles Bibliográficos
Autores principales: Grishchenko, I.V., Tulupov, A.A., Rymareva, Y.M., Petrovskiy, E.D., Savelov, A.A., Korostyshevskaya, A.M., Maksimova, Y.V., Shorina, A.R., Shitik, E.M., Yudkin, D.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629361/
https://www.ncbi.nlm.nih.gov/pubmed/34901709
http://dx.doi.org/10.18699/VJ21.014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629361/
https://www.ncbi.nlm.nih.gov/pubmed/34901709
http://dx.doi.org/10.18699/VJ21.014

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