Next Article in Journal
Naturally-Occurring Rare Mutations Cause Mild to Catastrophic Effects in the Multifunctional and Cancer-Associated NQO1 Protein
Next Article in Special Issue
A Novel Kindred with Familial Gastrointestinal Stromal Tumors Caused by a Rare KIT Germline Mutation (N655K): Clinico-Pathological Presentation and TKI Sensitivity
Previous Article in Journal
Analysis of miRNA Expression in Patients with Rheumatoid Arthritis during Olokizumab Treatment
Previous Article in Special Issue
Efficacy of Incremental Next-Generation ALK Inhibitor Treatment in Oncogene-Addicted, ALK-Positive, TP53-Mutant NSCLC
 
 
Review

Article Versions Notes

J. Pers. Med. 2020, 10(4), 206; https://doi.org/10.3390/jpm10040206
Action Date Notes Link
article xml file uploaded 1 November 2020 08:23 CET Original file -
article xml uploaded. 1 November 2020 08:23 CET Update -
article pdf uploaded. 1 November 2020 08:23 CET Version of Record https://www.mdpi.com/2075-4426/10/4/206/pdf-vor
article html file updated 1 November 2020 08:24 CET Original file -
article xml file uploaded 6 November 2020 09:17 CET Update -
article xml uploaded. 6 November 2020 09:17 CET Update https://www.mdpi.com/2075-4426/10/4/206/xml
article pdf uploaded. 6 November 2020 09:17 CET Updated version of record https://www.mdpi.com/2075-4426/10/4/206/pdf
article html file updated 6 November 2020 09:18 CET Update -
article html file updated 22 July 2022 23:28 CEST Update https://www.mdpi.com/2075-4426/10/4/206/html
Back to TopTop