Zobrazeno 1 - 10
of 57
pro vyhledávání: '"John COADWELL"'
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1791:889-897
Phospholipase D (PLD) catalyses the hydrolysis of phosphatidylcholine to generate phosphatidic acid and choline. Historically, much PLD work has been conducted in mammalian settings although genes encoding enzymes of this family have been identified
Autor:
Maureen Hamon, Michael J. Osborn, John Coadwell, Louise S. Matheson, Daniel Corcos, Marianne Brüggemann, Rima Chaouaf, David Oxley, Geoff Morgan, Jennifer A. Smith
Publikováno v:
International Immunology. 21:957-966
Recently, we identified that diverse heavy chain (H-chain)-only IgG is spontaneously produced in light chain (L-chain)-deficient mice (L(-/-) with silenced kappa and lambda loci) despite a block in B cell development. In murine H-chain IgG, the first
Publikováno v:
FEBS Journal. 276:1208-1220
Endoplasmic reticulum (ER)-associated degradation (ERAD) is a cell-autonomous process that eliminates large quantities of misfolded, newly synthesized protein, and is thus essential for the survival of any basic eukaryotic cell. Accordingly, the prot
Publikováno v:
Biology of Reproduction. 79:421-431
The equatorial subsegment (EqSS) was originally identified by atomic force microscopy as a discrete region within the equatorial segment of Artiodactyl spermatozoa. In this investigation, we show that the EqSS is enriched in tyrosine phosphorylated p
Autor:
Carine Dion, Geoffrey W. Butcher, Christine Carter, Margaret Graham, J. Ross Miller, Geoffrey Morgan, Silke Schnell, W. John Coadwell, Heinz Jacobs, John C. Pascall, Lucy Hepburn, Amanda Hutchings
Publikováno v:
Scopus-Elsevier
The Gimap/IAN family of GTPases has been implicated in the regulation of cell survival, particularly in lymphomyeloid cells. Prosurvival and prodeath properties have been described for different family members. We generated novel serological reagents
Autor:
Martin R Turner, G. John Ferguson, Hervé Guillou, Alison M. Condliffe, Len R. Stephens, Edwin R. Chilvers, Phillip T. Hawkins, Keith Davidson, John Coadwell, Sabine Suire, Chris D. Ellson, Heidi C.E. Welch
Publikováno v:
Nature Cell Biology. 8:1303-1309
Through their ability to regulate production of the key lipid messenger PtdIns(3,4,5)P(3), the class I phosphatidylinositol-3-OH kinases (PI(3)Ks) support many critical cell responses. They, in turn, can be regulated by cell-surface receptors through
Autor:
Nicholas Pugh, Daniela Rossi, W. John Coadwell, Alan J. Williams, Vincenzo Sorrentino, Fiona C. Mead-Savery
Publikováno v:
Biochemical and Biophysical Research Communications. 337:1072-1079
In this study, we have investigated block of potassium (K(+)) current by neomycin, a large polycation, from the luminal face of the type 3 ryanodine receptor (RyR3). Previous studies have shown that neomycin is an open channel blocker of RyR2 that in
Autor:
Gareth E. Jones, G. John Ferguson, W. John Coadwell, Louise M. C. Webb, Phillip T. Hawkins, Kirsti Hill, Marcus Thelen, Len R. Stephens, Laura Milne, Klaus Okkenhaug, Alison M. Condliffe, Simon Andrews, Heidi C.E. Welch
Publikováno v:
Current Biology. 15(20):1867-1873
SummaryRac GTPases regulate cytoskeletal structure, gene expression, and reactive oxygen species (ROS) production [1, 2]. Rac2-deficient neutrophils cannot chemotax, produce ROS, or degranulate upon G protein-coupled receptor (GPCR) activation [3–1
Autor:
John Coadwell, G. John Ferguson, Phillip T. Hawkins, Keith Davidson, Len R. Stephens, Sabine Suire
Publikováno v:
Current Biology. 15:566-570
Summary A variety of genetic and inhibitor studies have shown that phosphoinositide 3-kinase γ (PI3Kγ) plays an essential role in a number of physiological responses, including neutrophil chemotaxis, mast cell degranulation, and cardiac function [1
Autor:
Simon Andrews, Sarah Donald, Heidi C.E. Welch, Kirsti Hill, Simon Walker, Charlotte Lécureuil, Romain Barnouin, Sonja Krugmann, Len R. Stephens, Phillip T. Hawkins, W. John Coadwell
Publikováno v:
FEBS Letters. 572:172-176
We have identified a new guanine-nucleotide exchange factor, P-Rex2, and cloned it from human skeletal muscle and brain libraries. It has widespread tissue distribution but is not expressed in neutrophils. P-Rex2 is a 183 kDa protein that activates t