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Volume 14
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Correction to Biomolecules 2024, 14(3), 267.
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Correction

Correction: Yi et al. An Innovative Inducer of Platelet Production, Isochlorogenic Acid A, Is Uncovered through the Application of Deep Neural Networks. Biomolecules 2024, 14, 267

by
Taian Yi
1,†,
Jiesi Luo
2,†,
Ruixue Liao
3,
Long Wang
3,
Anguo Wu
3,
Yueyue Li
1,
Ling Zhou
3,
Chengyang Ni
3,
Kai Wang
3,
Xiaoqin Tang
3,
Wenjun Zou
1,* and
Jianming Wu
2,3,4,*
1
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China
2
Department of Chemistry, School of Basic Medical Sciences, Southwest Medical University, Luzhou 646000, China
3
Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou 646000, China
4
The Institute of Cardiovascular Research, Key Laboratory of Medical Electrophysiology of Ministry of Education, Luzhou 646000, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Biomolecules 2024, 14(6), 655; https://doi.org/10.3390/biom14060655
Submission received: 10 May 2024 / Accepted: 13 May 2024 / Published: 4 June 2024
Browse Figure
Versions Notes
  • Error in Figure
In the original publication [1], there was a mistake in Figure 5 as published. The ICGA-A (10 μM) group of K562 cells in Figure 5A was incorrectly placed. The corrected Figure 5 appears below.
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

Reference

  1. Yi, T.; Luo, J.; Liao, R.; Wang, L.; Wu, A.; Li, Y.; Zhou, L.; Ni, C.; Wang, K.; Tang, X.; et al. An Innovative Inducer of Platelet Production, Isochlorogenic Acid A, Is Uncovered through the Application of Deep Neural Networks. Biomolecules 2024, 14, 267. [Google Scholar] [CrossRef] [PubMed]
Biomolecules 14 00655 g005
Figure 5. ICGA-A induces MK differentiation of Meg-01 and K562 cells. (A) Microscope photographs of Meg-01 and K562 cells treated with or without ICGA-A (5, 10 and 20 μM) for 5 days. Scale bar: 100 µm. (B) Giemsa staining of Meg-01 and K562 cells with or without ICGA-A (5, 10 and 20 μM) treatment for 5 days. Scale bar: 50 µm. (C,D) Phalloidin staining of Meg-01 and K562 cells with or without ICGA-A (5, 10 and 20 μM) treatment for 5 days. Scale bar: 100 μm. (E,G) CD41 and CD42b expression on Meg-01 and K562 cells with or without ICGA-A (5, 10 and 20 μM) treatment for 5 days. (F,H) The proportion of CD41+CD42b+ cells of Meg-01 and K562 cells in control- and ICGA-A-treated groups. Data are presented as mean ± SD (n = 3). (I,J) Detection of LDH activity of Meg-01 and K562 cells after treatment with or without ICGA-A (5, 10 and 20 μM) for 2, 4 and 6 days. Maximum LDH control represents the total amount of LDH present in the cells. Data are presented as mean ± SD (n = 3, ANOVA). * p < 0.05, *** p < 0.001 vs. the control group.
Figure 5. ICGA-A induces MK differentiation of Meg-01 and K562 cells. (A) Microscope photographs of Meg-01 and K562 cells treated with or without ICGA-A (5, 10 and 20 μM) for 5 days. Scale bar: 100 µm. (B) Giemsa staining of Meg-01 and K562 cells with or without ICGA-A (5, 10 and 20 μM) treatment for 5 days. Scale bar: 50 µm. (C,D) Phalloidin staining of Meg-01 and K562 cells with or without ICGA-A (5, 10 and 20 μM) treatment for 5 days. Scale bar: 100 μm. (E,G) CD41 and CD42b expression on Meg-01 and K562 cells with or without ICGA-A (5, 10 and 20 μM) treatment for 5 days. (F,H) The proportion of CD41+CD42b+ cells of Meg-01 and K562 cells in control- and ICGA-A-treated groups. Data are presented as mean ± SD (n = 3). (I,J) Detection of LDH activity of Meg-01 and K562 cells after treatment with or without ICGA-A (5, 10 and 20 μM) for 2, 4 and 6 days. Maximum LDH control represents the total amount of LDH present in the cells. Data are presented as mean ± SD (n = 3, ANOVA). * p < 0.05, *** p < 0.001 vs. the control group.
Biomolecules 14 00655 g005
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MDPI and ACS Style

Yi, T.; Luo, J.; Liao, R.; Wang, L.; Wu, A.; Li, Y.; Zhou, L.; Ni, C.; Wang, K.; Tang, X.; et al. Correction: Yi et al. An Innovative Inducer of Platelet Production, Isochlorogenic Acid A, Is Uncovered through the Application of Deep Neural Networks. Biomolecules 2024, 14, 267. Biomolecules 2024, 14, 655. https://doi.org/10.3390/biom14060655

AMA Style

Yi T, Luo J, Liao R, Wang L, Wu A, Li Y, Zhou L, Ni C, Wang K, Tang X, et al. Correction: Yi et al. An Innovative Inducer of Platelet Production, Isochlorogenic Acid A, Is Uncovered through the Application of Deep Neural Networks. Biomolecules 2024, 14, 267. Biomolecules. 2024; 14(6):655. https://doi.org/10.3390/biom14060655

Chicago/Turabian Style

Yi, Taian, Jiesi Luo, Ruixue Liao, Long Wang, Anguo Wu, Yueyue Li, Ling Zhou, Chengyang Ni, Kai Wang, Xiaoqin Tang, and et al. 2024. "Correction: Yi et al. An Innovative Inducer of Platelet Production, Isochlorogenic Acid A, Is Uncovered through the Application of Deep Neural Networks. Biomolecules 2024, 14, 267" Biomolecules 14, no. 6: 655. https://doi.org/10.3390/biom14060655

APA Style

Yi, T., Luo, J., Liao, R., Wang, L., Wu, A., Li, Y., Zhou, L., Ni, C., Wang, K., Tang, X., Zou, W., & Wu, J. (2024). Correction: Yi et al. An Innovative Inducer of Platelet Production, Isochlorogenic Acid A, Is Uncovered through the Application of Deep Neural Networks. Biomolecules 2024, 14, 267. Biomolecules, 14(6), 655. https://doi.org/10.3390/biom14060655

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