SAMHD1‐deficient fibroblasts from Aicardi‐Goutières Syndrome patients can escape senescence and accumulate mutations-Reference-Cited by-同舟云学术

SAMHD1‐deficient fibroblasts from Aicardi‐Goutières Syndrome patients can escape senescence and accumulate mutations

Published:2019-11-26 Issue:1 Volume:34 Page:631-647
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Franzolin Elisa¹,Coletta Sara¹,Ferraro Paola¹,Pontarin Giovanna¹,D'Aronco Giulia¹,Stevanoni Martina¹,Palumbo Elisa²,Cagnin Stefano¹³⁴,Bertoldi Loris¹,Feltrin Erika¹,Valle Giorgio¹,Russo Antonella²,Bianchi Vera¹,Rampazzo Chiara¹

Affiliation:

1. Department of Biology University of Padova Padova Italy

2. Department of Molecular Medicine University of Padova Padova Italy

3. CRIBI Biotechnology Center University of Padova Padova Italy

4. CIR‐Myo Myology Center University of Padova Padova Italy

Funder

Associazione Italiana per la Ricerca sul Cancro

Fondazione Telethon

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201902508R

Reference63 articles.

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5. p53R2-dependent Ribonucleotide Reduction Provides Deoxyribonucleotides in Quiescent Human Fibroblasts in the Absence of Induced DNA Damage

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