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FEBS Letters|May 3, 2005
A 5' intronic splice site polymorphism leads to a null allele of the P2X7 gene in 1-2% of the Caucasian populationKristen K Skarratt, Stephen J Fuller, Ronald Sluyter, et al.
Journal of Visualized Experiments : Jove|April 23, 2019
Real-time Live-cell Flow Cytometry to Investigate Calcium Influx, Pore Formation, and Phagocytosis by P2X7 Receptors in Adult Neural Progenitor CellsHannah C Leeson, Tailoi Chan-Ling, Michael D Lovelace, et al.
Neural Regeneration Research|June 7, 2019
P2X7 receptor signaling during adult hippocampal neurogenesisHannah C Leeson, Tailoi Chan-Ling, Michael D Lovelace, et al.
Cellular and Molecular Life Sciences : CMLS|October 28, 2021
Genomics of Alzheimer's disease implicates the innate and adaptive immune systemsYihan Li, Simon M Laws, Luke A Miles, et al.
Arthritis Research & Therapy|July 4, 2013
Epistasis with HLA DR3 implicates the P2X7 receptor in the pathogenesis of primary Sjögren's syndromeSusan Lester, Leanne Stokes, Kristen K Skarratt, et al.
Stem Cells (Dayton, Ohio)|October 23, 2014
P2X7 receptors mediate innate phagocytosis by human neural precursor cells and neuroblastsMichael D Lovelace, Ben J Gu, Steven S Eamegdool, et al.
Hypertension (Dallas, Tex. : 1979)|November 10, 2011
A loss-of-function polymorphism in the human P2X4 receptor is associated with increased pulse pressureLeanne Stokes, Katrina Scurrah, Justine A Ellis, et al.
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