Understanding the Human RECQ5 Helicase—Connecting the Dots from DNA to Clinics

RECQ5, a member of the conserved RECQ helicase family, is the sole human RECQ homolog that has not been linked to a hereditary developmental syndrome. Nonetheless, dysregulation of RECQ5 has emerged as a significant clinical concern, being linked to cancer predisposition, cardiovascular disease, and...

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Detalles Bibliográficos
Autores principales: Mo, Chiefe, Shiozaki, Yukari, Omabe, Kenneth, Liu, Yilun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453775/
https://www.ncbi.nlm.nih.gov/pubmed/37626846
http://dx.doi.org/10.3390/cells12162037

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453775/
https://www.ncbi.nlm.nih.gov/pubmed/37626846
http://dx.doi.org/10.3390/cells12162037

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