Adult stem cell deficits drive Slc29a3 disorders in mice

Mutations exclusively in equilibrative nucleoside transporter 3 (ENT3), the only intracellular nucleoside transporter within the solute carrier 29 (SLC29) gene family, cause an expanding spectrum of human genetic disorders (e.g., H syndrome, PHID syndrome, and SHML/RDD syndrome). Here, we identify a...

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Detalles Bibliográficos
Autores principales: Nair, Sreenath, Strohecker, Anne M., Persaud, Avinash K., Bissa, Bhawana, Muruganandan, Shanmugam, McElroy, Craig, Pathak, Rakesh, Williams, Michelle, Raj, Radhika, Kaddoumi, Amal, Sparreboom, Alex, Beedle, Aaron M., Govindarajan, Rajgopal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610100/
https://www.ncbi.nlm.nih.gov/pubmed/31270333
http://dx.doi.org/10.1038/s41467-019-10925-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610100/
https://www.ncbi.nlm.nih.gov/pubmed/31270333
http://dx.doi.org/10.1038/s41467-019-10925-3

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