Grant Scotland - Concepedia

Author

Grant Scotland

University of Glasgow

Also Known As

G Scotland, G. Scotland, Grant SCOTLAND, Grant Scotland

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

University of Glasgow University of Utah Huntsman Cancer Institute University of Birmingham

About

Grant Scotland is an author at University of Glasgow specializing in medicine, biochemistry, and signal transduction.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	798
2	Biochemistry	7	7	798
3	Natural Sciences	6	6	714
4	Cell Biology	1	1	114
5	Cellular Physiology	1	1	159

Grant Scotland

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
The RACK1 Signaling Scaffold Protein Selectively Interacts with the cAMP-specific Phosphodiesterase PDE4D5 Isoform Stephen J. Yarwood, Michael R. Steele, Grant Scotland, Journal of Biological Chemistry Protein FunctionSignal TransductionMolecular PhysiologyBiochemistryG Protein-coupled Receptor	1999	306
Characterization of five different proteins produced by alternatively spliced mRNAs from the human cAMP-specific phosphodiesterase PDE4D gene B. Graeme BOLGER, Suat Erdoğan, Eleanor Jones, Biochemical Journal	1997	185
TAPAS-1, a Novel Microdomain within the Unique N-terminal Region of the PDE4A1 cAMP-specific Phosphodiesterase That Allows Rapid, Ca2+-triggered Membrane Association with Selectivity for Interaction with Phosphatidic Acid George S. Baillie, Elaine Huston, Grant Scotland, Journal of Biological Chemistry Proteinlipid InteractionProtein SecretionBilayer InsertionProtein AssemblyCa2+-triggered Membrane Association	2002	159
Association with the SRC Family Tyrosyl Kinase LYN Triggers a Conformational Change in the Catalytic Region of Human cAMP-specific Phosphodiesterase HSPDE4A4B Ian McPhee, Stephen J. Yarwood, Grant Scotland, Journal of Biological Chemistry Src KinaseProtein FunctionSignal TransductionCatalytic RegionBiochemistry	1999	114
The Human Cyclic AMP-specific Phosphodiesterase PDE-46 (HSPDE4A4B) Expressed in Transfected COS7 Cells Occurs as Both Particulate and Cytosolic Species That Exhibit Distinct Kinetics of Inhibition by the Antidepressant Rolipram Elaine Huston, L Pooley, Pascale Julien, Journal of Biological Chemistry	1996	101
Altered Expression of PDE1 and PDE4 Cyclic Nucleotide Phosphodiesterase Isoforms in 7-oxo-prostacyclin-preconditioned Rat Heart Milena Kostić, Suat Erdoğan, Graham Rena, Journal of Molecular and Cellular Cardiology 7-Oxo-prostacyclin-preconditioned Rat HeartMolecular PharmacologyCardiac MuscleHeart FailureAltered Expression	1997	84
Chimeric constructs show that the unique N-terminal domain of the cyclic AMP phosphodiesterase RD1 (RNPDE4A1A; rPDE-IVA1) can confer membrane association upon the normally cytosolic protein chloramphenicol acetyltransferase Grant Scotland, Miles D. Houslay Biochemical Journal Cat ActivityProteinlipid InteractionMolecular BiologyMembrane AssociationProtein Synthesis	1995	71
Determination of the Structure of the N-terminal Splice Region of the Cyclic AMP-specific Phosphodiesterase RD1 (RNPDE4A1) by 1H NMR and Identification of the Membrane Association Domain Using Chimeric Constructs K. John Smith, Grant Scotland, James Beattie, Journal of Biological Chemistry	1996	62
In addition to the SH3 binding region, multiple regions within the N-terminal noncatalytic portion of the cAMP-specific phosphodiesterase, PDE4A5, contribute to its intracellular targeting Matthew Beard, Elaine Huston, Lachlan Campbell, Cellular Signalling Intracellular TargetingProtein FunctionSignal TransductionBiochemistryNatural Sciences	2002	52
The cAMP-specific Phosphodiesterase PDE4A5 Is Cleaved Downstream of Its SH3 Interaction Domain by Caspase-3 Elaine Huston, Matthew Beard, Fraser McCallum, Journal of Biological Chemistry	2000	52

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