MicroRNA miR-181a/b-1 controls MAIT cell development-Reference-Cited by-同舟云学术

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MicroRNA miR-181a/b-1 controls MAIT cell development

Published:2018-11-12 Issue:2 Volume:97 Page:190-202
ISSN:0818-9641
Container-title:Immunology and Cell Biology
language:en
Short-container-title:Immunol Cell Biol

Author:

Winter Samantha J¹,Kunze-Schumacher Heike¹,Imelmann Esther¹,Grewers Zoe¹,Osthues Tabea¹,Krueger Andreas¹^ORCID

Affiliation:

1. Institute for Molecular Medicine; Goethe University Frankfurt; Frankfurt Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Cell Biology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/imcb.12211/fullpdf

Reference42 articles.

1. Selection of evolutionarily conserved mucosal-associated invariant T cells by MR1;Treiner;Nature,2003

2. T-cell activation by transitory neo-antigens derived from distinct microbial pathways;Corbett;Nature,2014

3. MR1 presents microbial vitamin B metabolites to MAIT cells;Kjer-Nielsen;Nature,2012

4. An invariant T cell receptor alpha chain defines a novel TAP-independent major histocompatibility complex class Ib-restricted alpha/beta T cell subpopulation in mammals;Tilloy;J Exp Med,1999

5. Diversity of T cells restricted by the MHC class I-related molecule MR1 facilitates differential antigen recognition;Gherardin;Immunity,2016

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1. A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match;Nucleic Acids Research;2024-05-23

2. A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match;2023-09-12

3. Classic costimulatory interactions in MAIT cell responses: from gene expression to immune regulation;Clinical and Experimental Immunology;2023-06-03

4. Mucosal‐associated invariant T cells in digestive tract: Local guardians or destroyers?;Immunology;2023-05-02

5. Mucosal-associated invariant T cells for cancer immunotherapy;Molecular Therapy;2023-03

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