Exonic variants of the P2RX7 gene in familial multiple sclerosis-Reference-Cited by-同舟云学术

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Exonic variants of the P2RX7 gene in familial multiple sclerosis

Published:2022-12 Issue: Volume: Page:
ISSN:2173-5808
Container-title:Neurología (English Edition)
language:en
Short-container-title:Neurología (English Edition)

Author:

Gómez-Pinedo U.^ORCID,Torre-Fuentes L.^ORCID,Matías-Guiu J.A.^ORCID,Pytel V.^ORCID,Ojeda-Hernández D.D.^ORCID,Selma-Calvo B.^ORCID,Montero-Escribano P.^ORCID,Vidorreta-Ballesteros L.^ORCID,Matías-Guiu J.^ORCID

Publisher

Elsevier BV

Subject

General Materials Science

Reference92 articles.

1. Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity;Sorge;Nat Med,2012

2. Gain and loss of function of P2X7 receptors: mechanisms, pharmacology and relevance to diabetic neuropathic pain;Ursu;Mol Pain,2014

3. Immune cell regulation by autocrine purinergic signalling;Junger;Nat Rev Immunol,2011

4. The P2X7 receptor in infection and inflamation;Vigilio;Inmunity,2017

5. Autocrine regulation of T-cell activation by ATP release and P2X7 receptors;Yip;Faseb J,2009

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