Simulation of Different Truncated p16INK4a Forms and In Silico Study of Interaction with Cdk4
Author:
Affiliation:
1. Department of Medical Biotechnology, Biotechnology Research Center, Pasteur Institute, Tehran, Iran 13164.
2. Department of Pharmacology–Toxicology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Publisher
SAGE Publications
Subject
Cancer Research,Oncology
Link
http://journals.sagepub.com/doi/pdf/10.4137/CIN.S878
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Unraveling Potential Candidate Targets Associated with Expression of p16INK4a or p16 Truncated Fragment by Comparative Proteomics Analysis;Current Proteomics;2021-07-28
2. Analysis of the putative tumor suppressor gene cdkn2ab in pigment cells and melanoma of Xiphophorus and medaka;Pigment Cell & Melanoma Research;2018-09-06
3. Huperzine A attenuates nonalcoholic fatty liver disease by regulating hepatocyte senescence and apoptosis: an in vitro study;PeerJ;2018-06-26
4. C-terminal domain of p16INK4a is adequate in inducing cell cycle arrest, growth inhibition and CDK4/6 interaction similar to the full length protein in HT-1080 fibrosarcoma cells;Journal of Cellular Biochemistry;2010-11-29
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