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CPE-mediated pro-protein processing in tumor cells and its differentiated cells or tissues” [Mol. Cell. Endocrinol. 303 (2009) 43–49]
Molecular and Cellular Endocrinology 309 (2009) 117–119
Contents lists available at ScienceDirect
Molecular and Cellular Endocrinology journal homepage: www.elsevier.com/locate/mce
Corrigendum
Corrigendum to “PC2/CPE-mediated pro-protein processing in tumor cells and its differentiated cells or tissues” [Mol. Cell. Endocrinol. 303 (2009) 43–49] Song-Shan Tang a,∗ , Juan-Hui Zhang b , Huan-Xin Liu c , Hong-Zhi Li d a
Department of Biochemistry, School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou 510006, China Department of Obstetrics & Gynecology, Guangdong Armed Police Hospital, Guangzhou, China Department of Pathology, Guangdong Armed Police Hospital, Guangzhou, China d Department of Biology, School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou, China b c
The Authors regret that when the above referenced paper was published an error occurred in author affiliations. The above author list and affiliations are the corrected versions. The authors also regret that Figs. 1–4 and 9 were published incorrectly. The correct Figs. 1–4 and 9 are below. The Authors would like to apologise for any inconvenience this may have caused to the readers of the journal.
Fig. 1. Differentiation of NS20Y or RGC-5 cell (Mag.15 × 10 times). (A) Undifferentiated cells; (B) differentiated cells.
DOI of original article:10.1016/j.mce.2009.01.020. ∗ Corresponding author at: No. 104, Building 7, Tianhe District, 268 Yanling Road, Guangzhou 510507, China. Tel.: +86 20 61627623; fax: +86 20 39352187. E-mail address: [email protected] (S.-S. Tang). 0303-7207/$ – see front matter. Published by Elsevier Ireland Ltd. doi:10.1016/j.mce.2009.04.007
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S.-S. Tang et al. / Molecular and Cellular Endocrinology 309 (2009) 117–119
Fig. 2. PC2 fluorescent ICC analyses of the cultured cells (Merged, Mag. 40 × 10 times). (A) Undifferentiated cells; (B) differentiated cells. White arrowheads indicate positive portion in cell (red portion).
Fig. 3. CPE fluorescent ICC analyses of the cultured cells (Merged, Mag. 40 × 10 times). (A) Undifferentiated cells; (B) differentiated cells. White arrowheads indicate positive portion in cell (red portion).
Fig. 4. preproNPY fluorescent ICC analyses of the cultured cells (Merged, Mag. 40 × 10 times). (A) Undifferentiated cells; (B) differentiated cells. White arrowheads indicate positive portion in cell (red portion).
S.-S. Tang et al. / Molecular and Cellular Endocrinology 309 (2009) 117–119
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Fig. 9. Western blot analyses of PC2, CPE and preproNPY proteins. (A) Expression in NS20Y or RGC-5 cells. BD: undifferentiated cells; D: differentiated cells. (B) Expression in mature retina or brain cortex tissue. Protein markers 14.4–97 kDa or 3.5–45 kDa were used for PC2 and CPE or preproNPY analysis.
Contents lists available at ScienceDirect
Molecular and Cellular Endocrinology journal homepage: www.elsevier.com/locate/mce
Corrigendum
Corrigendum to “PC2/CPE-mediated pro-protein processing in tumor cells and its differentiated cells or tissues” [Mol. Cell. Endocrinol. 303 (2009) 43–49] Song-Shan Tang a,∗ , Juan-Hui Zhang b , Huan-Xin Liu c , Hong-Zhi Li d a
Department of Biochemistry, School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou 510006, China Department of Obstetrics & Gynecology, Guangdong Armed Police Hospital, Guangzhou, China Department of Pathology, Guangdong Armed Police Hospital, Guangzhou, China d Department of Biology, School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou, China b c
The Authors regret that when the above referenced paper was published an error occurred in author affiliations. The above author list and affiliations are the corrected versions. The authors also regret that Figs. 1–4 and 9 were published incorrectly. The correct Figs. 1–4 and 9 are below. The Authors would like to apologise for any inconvenience this may have caused to the readers of the journal.
Fig. 1. Differentiation of NS20Y or RGC-5 cell (Mag.15 × 10 times). (A) Undifferentiated cells; (B) differentiated cells.
DOI of original article:10.1016/j.mce.2009.01.020. ∗ Corresponding author at: No. 104, Building 7, Tianhe District, 268 Yanling Road, Guangzhou 510507, China. Tel.: +86 20 61627623; fax: +86 20 39352187. E-mail address: [email protected] (S.-S. Tang). 0303-7207/$ – see front matter. Published by Elsevier Ireland Ltd. doi:10.1016/j.mce.2009.04.007
118
S.-S. Tang et al. / Molecular and Cellular Endocrinology 309 (2009) 117–119
Fig. 2. PC2 fluorescent ICC analyses of the cultured cells (Merged, Mag. 40 × 10 times). (A) Undifferentiated cells; (B) differentiated cells. White arrowheads indicate positive portion in cell (red portion).
Fig. 3. CPE fluorescent ICC analyses of the cultured cells (Merged, Mag. 40 × 10 times). (A) Undifferentiated cells; (B) differentiated cells. White arrowheads indicate positive portion in cell (red portion).
Fig. 4. preproNPY fluorescent ICC analyses of the cultured cells (Merged, Mag. 40 × 10 times). (A) Undifferentiated cells; (B) differentiated cells. White arrowheads indicate positive portion in cell (red portion).
S.-S. Tang et al. / Molecular and Cellular Endocrinology 309 (2009) 117–119
119
Fig. 9. Western blot analyses of PC2, CPE and preproNPY proteins. (A) Expression in NS20Y or RGC-5 cells. BD: undifferentiated cells; D: differentiated cells. (B) Expression in mature retina or brain cortex tissue. Protein markers 14.4–97 kDa or 3.5–45 kDa were used for PC2 and CPE or preproNPY analysis.