Related Experiment Video

Updated: Aug 27, 2026

Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice
06:40

Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice

Published on: February 10, 2014

Correction to "mTOR Modulates the Endoplasmic Reticulum Stress-Induced CD4+ T Cell Apoptosis Mediated by ROS in

    Mediators of Inflammation
    |February 11, 2026
    PubMed

    Insights

    This study corrects a previous article DOI. The corrected DOI is 10.1155/2022/6077570, ensuring accurate citation and retrieval of scientific information.

    Area of Science:

    • Bibliometrics
    • Scientific Publishing

    Background:

    • Accurate citation is crucial for scientific integrity.
    • Digital Object Identifiers (DOIs) ensure reliable access to research articles.

    Purpose of the Study:

    • To provide the correct Digital Object Identifier (DOI) for a previously published article.
    • To ensure proper attribution and retrieval of scientific literature.

    Main Methods:

    • Cross-referencing publication records.
    • Verifying article metadata through publisher databases.

    Main Results:

    • The correct DOI for the article is 10.1155/2022/6077570.
    • This correction facilitates accurate citation and access to the research.

    Conclusions:

    • Ensuring DOI accuracy is essential for the scientific record.
    • Corrected DOIs maintain the traceability and impact of published research.

    More Related Videos

    Identification of Mediators of T-cell Receptor Signaling via the Screening of Chemical Inhibitor Libraries08:49

    Identification of Mediators of T-cell Receptor Signaling via the Screening of Chemical Inhibitor Libraries

    Published on: January 22, 2019

    Mechanistic Insight into the Development of TNBS-Mediated Intestinal Fibrosis and Evaluating the Inhibitory Effects of Rapamycin10:21

    Mechanistic Insight into the Development of TNBS-Mediated Intestinal Fibrosis and Evaluating the Inhibitory Effects of Rapamycin

    Published on: September 12, 2019

    Related Concept Videos

    mTOR Signaling and Cancer Progression03:03

    mTOR Signaling and Cancer Progression

    The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
    The mTOR pathway or the...
    PI3K/mTOR/AKT Signaling Pathway01:22

    PI3K/mTOR/AKT Signaling Pathway

    The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...