Correction Volume 16, Issue 3 pp 3043—3044
Correction for: RNA-seq analysis of the key long noncoding RNAs and mRNAs related to cognitive impairment after cardiac arrest and cardiopulmonary resuscitation
- 1 Department of Anesthesiology, Laboratory of Anesthesia and Critical Care Medicine, Translational Neuroscience Center, West China Hospital, Sichuan University and The Research Units of West China, Chinese Academy of Medical Sciences, Chengdu, Sichuan, China
- 2 Department of Emergency Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China
Received: February 5, 2024 Accepted: February 13, 2024 Published: February 15, 2024
https://doi.org/10.18632/aging.205612How to Cite
Copyright: © 2024 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This article has been corrected: The authors recently found an error in Figure 4B, “In situ hybridization of lncRNA and mRNA in neuron cells.” The image of the hippocampal CA1 region in the Sham group depicting colocalization of lncRNA with MAP-2-labeled neuronal cells was inadvertently substituted with an image from the CA/CPR group from the same experiment. That incorrect image was replaced with the correct Sham group image from the initial set of experiments. The authors stated that this alteration does not affect the results or conclusion of this work and apologize for any inconvenience.
The corrected Figure 4 is presented below.
Figure 4. In situ hybridization of lncRNA and mRNA in neuron cells. (A) Biotin-labeled lncRNA and digoxigenin-labeled mRNA probes are shown in green and red, respectively. LncRNA and mRNA are co-expressed in CA1 of the hippocampus. (B, C) The colocation effect of LncRNA (B) or mRNA (C) with MAP-2 labeled neuron cells indicated these correlations mainly happened in neuron cells of the hippocampus. LncRNA and mRNA were labeled by red fluorescent probes, and the neuron cells were marked using anti-MAP2 antibody and Alexa 488 conjugated anti-rabbit IgG. Scale bar: 50 μm.