Next Article in Journal
Continuous Reusability using Immobilized HasApf in Chemoenzymatic Deracemization: A New Heterogeneous Enzyme Catalysis
Previous Article in Journal
Intra- and Extra-Cellular Events Related to Altered Glycosylation of MUC1 Promote Chronic Inflammation, Tumor Progression, Invasion, and Metastasis
Previous Article in Special Issue
Cooperativity of the SUMO and Ubiquitin Pathways in Genome Stability
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Correction

Correction: Pennisi, R., et al. Hsp90: A New Player in DNA Repair? Biomolecules 2015, 5, 2589–2618

1
Department of Sciences, Roma Tre University, Viale Guglielmo Marconi 446, Roma I-00146, Italy
2
Istituto Nazionale di Biostrutture e Biosistemi, Viale Medaglie d’Oro 305, Roma I-00136, Italy
*
Author to whom correspondence should be addressed.
Submission received: 14 September 2016 / Accepted: 14 September 2016 / Published: 18 October 2016
(This article belongs to the Special Issue DNA Damage Response)
The authors of the published paper [1] wish to add the following two references on pages 2590 and 2597–2598 that were not originally cited in the text, consequently the paper has been updated:
11.
Kaplan, K.B.; Li, R. A prescription for ‘stress’—The role of Hsp90 in genome stability and cellular adaptation. Trends Cell Biol. 2012, 22, 576–583.
105.
Gullotta, F.; De Marinis, E.; Ascenzi, P.; di Masi, A. Targeting the DNA double strand breaks repair for cancer therapy. Curr. Med. Chem. 2010, 17, 2017–2048.
Furthermore, the following references were not correctly cited in the original paper, and have thus been updated:
122.
Fang, Q.; Inanc, B.; Schamus, S.; Wang, X.H.; Wei, L.; Brown, A.R.; Svilar, D.; Sugrue, K.F.; Goellner, E.M.; Zeng, X.; et al. HSP90 regulates DNA repair via the interaction between XRCC1 and DNA polymerase beta. Nat. Commun. 2014, 5, doi:10.1038/ncomms6513.
198.
Tung, C.L.; Jian, Y.J.; Syu, J.J.; Wang, T.J.; Chang, P.Y.; Chen, C.Y.; Jian, Y.T.; Lin, Y.W. Down-regulation of ERK1/2 and AKT-mediated X-ray repair cross-complement group 1 protein (XRCC1) expression by Hsp90 inhibition enhances the gefitinib-induced cytotoxicity in human lung cancer cells. Exp. Cell Res. 2015, 334, 126–135.
The authors apologize to the readers and authors of the cited papers for any inconvenience caused by these changes.

Reference

  1. Pennisi, R.; Ascenzi, P.; di Masi, A. Hsp90: A New Player in DNA Repair? Biomolecules 2015, 5, 2589–2618. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Pennisi, R.; Ascenzi, P.; Di Masi, A. Correction: Pennisi, R., et al. Hsp90: A New Player in DNA Repair? Biomolecules 2015, 5, 2589–2618. Biomolecules 2016, 6, 40. https://0-doi-org.brum.beds.ac.uk/10.3390/biom6040040

AMA Style

Pennisi R, Ascenzi P, Di Masi A. Correction: Pennisi, R., et al. Hsp90: A New Player in DNA Repair? Biomolecules 2015, 5, 2589–2618. Biomolecules. 2016; 6(4):40. https://0-doi-org.brum.beds.ac.uk/10.3390/biom6040040

Chicago/Turabian Style

Pennisi, Rosa, Paolo Ascenzi, and Alessandra Di Masi. 2016. "Correction: Pennisi, R., et al. Hsp90: A New Player in DNA Repair? Biomolecules 2015, 5, 2589–2618" Biomolecules 6, no. 4: 40. https://0-doi-org.brum.beds.ac.uk/10.3390/biom6040040

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop