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Rebuttal to: In Vivo Studies Should Take Priority When Defining Mechanisms of Intestinal Crypt Morphogenesis.对《在定义肠道隐窝形态发生机制时体内研究应优先考虑》的反驳
Cell Mol Gastroenterol Hepatol. 2022;13(1):5. doi: 10.1016/j.jcmgh.2021.09.010. Epub 2021 Oct 10.
2
In Vivo Studies Should Take Priority When Defining Mechanisms of Intestinal Crypt Morphogenesis.在定义肠道隐窝形态发生机制时,体内研究应优先进行。
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Characterization of rat epimorphin/syntaxin 2 expression suggests a role in crypt-villus morphogenesis.大鼠表皮形态发生素/ syntaxin 2表达的特征表明其在隐窝-绒毛形态发生中起作用。
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Selection of multipotent stem cells during morphogenesis of small intestinal crypts of Lieberkuhn is perturbed by stimulation of Lef-1/beta-catenin signaling.在利伯库恩小肠隐窝形态发生过程中,多能干细胞的选择受到Lef-1/β-连环蛋白信号通路刺激的干扰。
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引用本文的文献

1
Morphological alterations in C57BL/6 mouse intestinal organoids as a tool for predicting chemical-induced toxicity.C57BL/6 小鼠肠类器官形态改变作为预测化学物诱导毒性的工具。
Arch Toxicol. 2023 Apr;97(4):1133-1146. doi: 10.1007/s00204-023-03451-1. Epub 2023 Feb 20.

Rebuttal to: In Vivo Studies Should Take Priority When Defining Mechanisms of Intestinal Crypt Morphogenesis.

作者信息

Sugimoto Shinya, Sato Toshiro

机构信息

Department of Organoid Medicine, Keio University School of Medicine, Tokyo, Japan; Department of Gastroenterology, Keio University School of Medicine, Tokyo, Japan.

Department of Organoid Medicine, Keio University School of Medicine, Tokyo, Japan; Department of Gastroenterology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Cell Mol Gastroenterol Hepatol. 2022;13(1):5. doi: 10.1016/j.jcmgh.2021.09.010. Epub 2021 Oct 10.

DOI:10.1016/j.jcmgh.2021.09.010
PMID:34644540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8600056/
Abstract
摘要