Correction to “potential role of heat shock proteins in neural differentiation of murine embryonal carcinoma stem cells (P19)”

IF 3.3 3区 生物学 Q3 CELL BIOLOGY Cell Biology International Pub Date : 2024-06-30 DOI:10.1002/cbin.12193
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Abstract

Afzal E, Ebrahimi M, Najafi SM, Daryadel A, Baharvand H. Potential role of heat shock proteins in neural differentiation of murine embryonal carcinoma stem cells (P19). Cell Biol Int. 2011 Jul;35(7):713-20. doi: 10.1042/CBI20100457.

We regret to acknowledge a non-intentional human error related to data placement/handling during the preparation of the representative images of Figures 2d and 4. We, therefore, corrected them. A replacement to figures is included below:

In Figure 4, the left column is the control group as demonstrated in Figure 2 (first row). At that time, we did this to compare the results and help the readers to have a better understanding of the story. It could be deleted without any changes in results and conclusion.

These image displacement by no means change our conclusions, since the aim was to show the expression of HSC70 in non-heat treated (first row) with the heat treated (second row). As mentioned in the paper the expression of HSC70 did not change pre- and post-heated.

The authors would like to apologize for any inconvenience caused.

Abstract Image

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更正 "热休克蛋白在小鼠胚胎癌干细胞(P19)神经分化中的潜在作用"。
Afzal E, Ebrahimi M, Najafi SM, Daryadel A, Baharvand H. 热休克蛋白在小鼠胚胎癌干细胞(P19)神经分化中的潜在作用。Doi: 10.1042/CBI20100457.我们很遗憾地承认,在准备图 2d 和图 4 的代表性图像时,在数据放置/处理方面出现了非故意的人为错误。因此,我们对其进行了更正。替换图如下:在图 4 中,左列是图 2(第一行)中所示的对照组。当时,我们这样做是为了比较结果,帮助读者更好地理解故事。这些图像位移绝对不会改变我们的结论,因为我们的目的是显示 HSC70 在未热处理组(第一行)和热处理组(第二行)中的表达情况。正如论文中提到的,加热前后 HSC70 的表达没有变化。
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来源期刊
Cell Biology International
Cell Biology International 生物-细胞生物学
CiteScore
7.60
自引率
0.00%
发文量
208
审稿时长
1 months
期刊介绍: Each month, the journal publishes easy-to-assimilate, up-to-the minute reports of experimental findings by researchers using a wide range of the latest techniques. Promoting the aims of cell biologists worldwide, papers reporting on structure and function - especially where they relate to the physiology of the whole cell - are strongly encouraged. Molecular biology is welcome, as long as articles report findings that are seen in the wider context of cell biology. In covering all areas of the cell, the journal is both appealing and accessible to a broad audience. Authors whose papers do not appeal to cell biologists in general because their topic is too specialized (e.g. infectious microbes, protozoology) are recommended to send them to more relevant journals. Papers reporting whole animal studies or work more suited to a medical journal, e.g. histopathological studies or clinical immunology, are unlikely to be accepted, unless they are fully focused on some important cellular aspect. These last remarks extend particularly to papers on cancer. Unless firmly based on some deeper cellular or molecular biological principle, papers that are highly specialized in this field, with limited appeal to cell biologists at large, should be directed towards journals devoted to cancer, there being very many from which to choose.
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