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Correction for Oberleithner et al., J Cell Sci 119 (9) 1926-1932.
First published online July 2, 2007
doi: 10.1242/10.1242/jcs.017467


Journal of Cell Science 120, 2467 (2007)
Published by The Company of Biologists 2007
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Author Correction

Differential action of steroid hormones on human endothelium

Hans Oberleithner, Christoph Riethmüller, Thomas Ludwig, Victor Shahin, Christian Stock, Albrecht Schwab, Martin Hausberg, Kristina Kusche and Hermann Schillers


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Fig. 5. Identification of {alpha}ENaC in human endothelial cells (HUVEC; representative experiment). Membrane proteins were separated by SDS-PAGE and stained with Coomassie brilliant blue (lane 1). {alpha}ENaC was detected by using an anti-{alpha}ENaC antibody (lanes 2-4). The amount of {alpha}ENaC in the aldosterone-treated sample (A) is about twice that in the control (C) and about six times higher than that of aldosterone and spironolactone (A+S)-incubated HUVEC. As positive control (PC), we used ENaC-expressing oocytes. The molecular mass standard is given on the left. The upper band in the range of 95 kDa most likely represents a glycosylated form of ENaC.

 
There was an error published in J. Cell Sci. 119, 1926-1932.

A labelling error occurred in Fig. 5, showing a western blot with incorrect kDa values.

The correct Fig. 5 is shown below.

Owing to the labelling error, a sentence in the Results section (1926-1932, right column) refers to the incorrect kDa values: The {alpha}ENaC antibody recognises a specific band with an apparent molecular mass of about 67 kDa (Fig. 5), which is the same as that reported for the {alpha}ENaC subunit (Hughey et al., 2003).

The correct sentence is given below:

The {alpha}ENaC antibody recognises a specific band with an apparent molecular mass of about 95 kDa and a second band of about 55 kDa (Fig. 5), which is the same as that reported for the {alpha}ENaC subunit (Hughey et al., 2003).

This error appeared in both the print and the online versions of this article.

The authors apologise for this mistake.


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