Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Multiple Sclerosis and P2RX7[original query] |
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A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human molecular genetics 2015 Oct 24 (19): 5644-54. Gu Ben J, Field Judith, Dutertre Sébastien, Ou Amber, Kilpatrick Trevor J, Lechner-Scott Jeannette, Scott Rodney, Lea Rodney, Taylor Bruce V, Stankovich Jim, Butzkueven Helmut, Gresle Melissa, Laws Simon M, Petrou Steven, Hoffjan Sabine, Akkad Denis A, Graham Colin A, Hawkins Stanley, Glaser Anna, Bedri Sahl Khalid, Hillert Jan, Matute Carlos, Antiguedad Alfredo, , Wiley James |
P2X7 as a scavenger receptor for innate phagocytosis in the brain. British journal of pharmacology 2018 8 175 (22): 4195-4208. Gu Ben J, Wiley James |
Exonic variants of the P2RX7 gene in familial multiple sclerosis. Neurologia 2022 12 . Gómez-Pinedo U, Torre-Fuentes L, Matías-Guiu J A, Pytel V, Ojeda-Hernández D D, Selma-Calvo B, Montero-Escribano P, Vidorreta-Ballesteros L, Matías-Guiu |
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- Page last updated:May 22, 2023
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