TOP

Corrigendum

Split Viewer

Mol. Cells 2023; 46(4): 256-257

Published online April 6, 2023

https://doi.org/10.14348/molcells.2022.0029.e

© The Korean Society for Molecular and Cellular Biology

Corrigendum to: Modification of ERα by UFM1 Increases Its Stability and Transactivity for Breast Cancer Development

Hee Min Yoo1,2,3,*, Jong Ho Park1, Jae Yeon Kim1, and Chin Ha Chung1,4,*

1School of Biological Sciences, Seoul National University, Seoul 08826, Korea, 2Biometrology Group, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, Korea, 3Department of Precision Measurement, University of Science & Technology (UST), Daejeon 34113, Korea, 4The Second Division of Natural Sciences, Korea National Academy of Sciences, Seoul 06579, Korea

Correspondence to : hmy@kriss.re.kr (HMY); chchung@snu.ac.kr (CHC)

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.

Corrigendum to: Mol. Cells 2022; 45(6): 425-434

https://doi.org/10.14348/molcells.2022.0029

In the article by Yoo et al. that appeared in the journal, the panel A in Fig. 1, the panel C in Fig. 6, and Fig. 6C legend have been corrected by the authors as shown below because the authors made image duplications during the arrangement of the images and typo errors in Fig. 6C legend. This correction will not affect the conclusions of this article.

The online version of the original article can be found under Mol. Cells 2022; 45(6): 425-434.

Fig. 6C

legend

(C) Normal and ERα-positive tumor tissues were subjected to immunohistochemical analysis. The large boxes (scale bar = 500 µm) show the magnified view of the small boxes (scale bar = 100 µm).


Article

Corrigendum

Mol. Cells 2023; 46(4): 256-257

Published online April 30, 2023 https://doi.org/10.14348/molcells.2022.0029.e

Copyright © The Korean Society for Molecular and Cellular Biology.

Corrigendum to: Modification of ERα by UFM1 Increases Its Stability and Transactivity for Breast Cancer Development

Hee Min Yoo1,2,3,*, Jong Ho Park1, Jae Yeon Kim1, and Chin Ha Chung1,4,*

1School of Biological Sciences, Seoul National University, Seoul 08826, Korea, 2Biometrology Group, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, Korea, 3Department of Precision Measurement, University of Science & Technology (UST), Daejeon 34113, Korea, 4The Second Division of Natural Sciences, Korea National Academy of Sciences, Seoul 06579, Korea

Correspondence to:hmy@kriss.re.kr (HMY); chchung@snu.ac.kr (CHC)

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.

Body

Corrigendum to: Mol. Cells 2022; 45(6): 425-434

https://doi.org/10.14348/molcells.2022.0029

In the article by Yoo et al. that appeared in the journal, the panel A in Fig. 1, the panel C in Fig. 6, and Fig. 6C legend have been corrected by the authors as shown below because the authors made image duplications during the arrangement of the images and typo errors in Fig. 6C legend. This correction will not affect the conclusions of this article.

The online version of the original article can be found under Mol. Cells 2022; 45(6): 425-434.

Fig 1.

Figure 1.Fig. 1
Molecules and Cells 2023; 46: 256-257https://doi.org/10.14348/molcells.2022.0029.e

Fig 2.

Figure 2.

Fig. 6C legend

(C) Normal and ERα-positive tumor tissues were subjected to immunohistochemical analysis. The large boxes (scale bar = 500 µm) show the magnified view of the small boxes (scale bar = 100 µm).

Molecules and Cells 2023; 46: 256-257https://doi.org/10.14348/molcells.2022.0029.e
Mol. Cells
Dec 31, 2023 Vol.46 No.12, pp. 727~777
COVER PICTURE
Lee et al. (pp. 757-763), show that disruption of ANKS1A promotes the entry of intraflagellar transport trains into cilia, increasing protein transport and forming extracellular vesicles (ECVs). This figure illustrates the abundance of ECVs along the cilia of primary ependymal cells derived from ANKS1A KO mice.

Share this article on

  • line

Molecules and Cells

eISSN 0219-1032
qr-code Download