Correction: Costanzo, V.; Costanzo, M. Intravital Imaging with Two-Photon Microscopy: A Look into the Kidney. Photonics 2022, 9, 294
1
Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna AlmaMater Studiorum, 40126 Bologna, Italy
2
Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy
3
CEINGE–Biotecnologie Avanzate S.C.R.L., 80145 Naples, Italy
*
Author to whom correspondence should be addressed.
Photonics 2022, 9(10), 759; https://doi.org/10.3390/photonics9100759
Submission received: 26 July 2022
/
Accepted: 29 July 2022
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Published: 12 October 2022
(This article belongs to the Special Issue Multiphoton Microscopy)
Error in Figure
In the original publication [1], there was a mistake in Figure 2 as published. The figure reported a representative image of the renal cortex acquired in vivo by two-photon microscopy for other purposes than this review. Consequently, the image was removed and the figure legend was modified. The corrected Figure 2 and its legend appear below.
In the original publication [1], there was a mistake in Figure 3 as published. The figure reported representative images of a linescan-based experiment acquired for other purposes than this review. Consequently, Figure 3, its legend, and its mention into the text were removed.
The authors apologize for any inconvenience caused and state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.
Reference
- Costanzo, V.; Costanzo, M. Intravital Imaging with Two-Photon Microscopy: A Look into the Kidney. Photonics 2022, 9, 294. [Google Scholar] [CrossRef]
Figure 2.
Schematic representation of the renal structures identified with 2PM. The nephron segments that are visible with confocal and 2PM are shown. As indicated by the vertical arrows, 2PM allows the renal structures to be imaged about 3 times deeper compared to confocal microscopy. G = glomerulus; S1 = S1 proximal convoluted tubule; S2 = S2 proximal convoluted tubule; DT = distal tubule. This figure was drawn adapting the vector image from the Servier Medical Art bank (http://smart.servier.com/; last accessed on 22 February 2022).
Figure 2.
Schematic representation of the renal structures identified with 2PM. The nephron segments that are visible with confocal and 2PM are shown. As indicated by the vertical arrows, 2PM allows the renal structures to be imaged about 3 times deeper compared to confocal microscopy. G = glomerulus; S1 = S1 proximal convoluted tubule; S2 = S2 proximal convoluted tubule; DT = distal tubule. This figure was drawn adapting the vector image from the Servier Medical Art bank (http://smart.servier.com/; last accessed on 22 February 2022).
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MDPI and ACS Style
Costanzo, V.; Costanzo, M. Correction: Costanzo, V.; Costanzo, M. Intravital Imaging with Two-Photon Microscopy: A Look into the Kidney. Photonics 2022, 9, 294. Photonics 2022, 9, 759. https://doi.org/10.3390/photonics9100759
AMA Style
Costanzo V, Costanzo M. Correction: Costanzo, V.; Costanzo, M. Intravital Imaging with Two-Photon Microscopy: A Look into the Kidney. Photonics 2022, 9, 294. Photonics. 2022; 9(10):759. https://doi.org/10.3390/photonics9100759
Chicago/Turabian StyleCostanzo, Vincenzo, and Michele Costanzo. 2022. "Correction: Costanzo, V.; Costanzo, M. Intravital Imaging with Two-Photon Microscopy: A Look into the Kidney. Photonics 2022, 9, 294" Photonics 9, no. 10: 759. https://doi.org/10.3390/photonics9100759
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