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Silymarin as a Redox-Signalling and Proteostasis Modulator
 
 
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Correction

Correction: Lastra et al. Silymarin as a Redox-Signalling and Proteostasis Modulator. Nutraceuticals 2026, 6, 25

by
José Manuel Pérez de la Lastra
1,*,
Celia María Curieses Andrés
2,
Elena Bustamante Munguira
2,
Celia Andrés Juan
3 and
Eduardo Pérez Lebeña
4,*
1
Institute of Natural Products and Agrobiology, CSIC-Spanish Research Council, Avda. Astrofísico Fco. Sánchez, 3, 38206 La Laguna, Spain
2
Hospital Clínico Universitario de Valladolid, Avenida de Ramón y Cajal, 3, 47003 Valladolid, Spain
3
Department of Organic Chemistry, Cinquima Institute, Faculty of Sciences, Valladolid University, Paseo de Belén, 7, 47011 Valladolid, Spain
4
Sistemas de Biotecnología y Recursos Naturales, 47625 Valladolid, Spain
*
Authors to whom correspondence should be addressed.
Nutraceuticals 2026, 6(2), 26; https://doi.org/10.3390/nutraceuticals6020026
Submission received: 16 April 2026 / Accepted: 20 April 2026 / Published: 22 April 2026

Error in Figure

In the original publication, there was a mistake in Figure 12 as published [1]. The authors uploaded Figure 10 as Figure 12 by mistake. The corrected Figure 12 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.
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. Lastra, J.M.P.d.l.; Andrés, C.M.C.; Munguira, E.B.; Juan, C.A.; Pérez Lebeña, E. Silymarin as a Redox-Signalling and Proteostasis Modulator. Nutraceuticals 2026, 6, 25. [Google Scholar] [CrossRef]
Figure 12. Determinants of variability and precision use of silymarin. Interindividual response to silymarin arises from the interaction of formulation-dependent exposure, circadian timing, and gut–liver axis biology, including bile ecology, transporter topology, protein binding, and microbiome driven deconjugation.
Figure 12. Determinants of variability and precision use of silymarin. Interindividual response to silymarin arises from the interaction of formulation-dependent exposure, circadian timing, and gut–liver axis biology, including bile ecology, transporter topology, protein binding, and microbiome driven deconjugation.
Nutraceuticals 06 00026 g012
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MDPI and ACS Style

Lastra, J.M.P.d.l.; Andrés, C.M.C.; Munguira, E.B.; Juan, C.A.; Lebeña, E.P. Correction: Lastra et al. Silymarin as a Redox-Signalling and Proteostasis Modulator. Nutraceuticals 2026, 6, 25. Nutraceuticals 2026, 6, 26. https://doi.org/10.3390/nutraceuticals6020026

AMA Style

Lastra JMPdl, Andrés CMC, Munguira EB, Juan CA, Lebeña EP. Correction: Lastra et al. Silymarin as a Redox-Signalling and Proteostasis Modulator. Nutraceuticals 2026, 6, 25. Nutraceuticals. 2026; 6(2):26. https://doi.org/10.3390/nutraceuticals6020026

Chicago/Turabian Style

Lastra, José Manuel Pérez de la, Celia María Curieses Andrés, Elena Bustamante Munguira, Celia Andrés Juan, and Eduardo Pérez Lebeña. 2026. "Correction: Lastra et al. Silymarin as a Redox-Signalling and Proteostasis Modulator. Nutraceuticals 2026, 6, 25" Nutraceuticals 6, no. 2: 26. https://doi.org/10.3390/nutraceuticals6020026

APA Style

Lastra, J. M. P. d. l., Andrés, C. M. C., Munguira, E. B., Juan, C. A., & Lebeña, E. P. (2026). Correction: Lastra et al. Silymarin as a Redox-Signalling and Proteostasis Modulator. Nutraceuticals 2026, 6, 25. Nutraceuticals, 6(2), 26. https://doi.org/10.3390/nutraceuticals6020026

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