J. B. Harrison - Concepedia

Concepedia

Author

J. B. Harrison

University of Cambridge

Also Known As

J B Harrison, J Harrison, J. B. Harrison, J. Barrie Harrison, J. HARRISON, J. Harrison, J.B Harrison, J.B. Harrison, J.Barrie Harrison, James Harrison

45

Publications

1.5K

Citations

23

H-Index

87

Concepts

All Affiliations

University of Cambridge Babraham Institute Biotechnology and Biological Sciences Research Council Medical Research Council

JB

About

J. B. Harrison is an author at University of Cambridge specializing in medicine, biology, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	781
2	Natural Sciences	4	4	162
3	Health Sciences	3	3	112
4	Public Health	1	1	13
5	Allergy	1	1	14

J. B. Harrison

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31

Publications

1.5K

Citations

22

H-Index

	Year	Citations
Mitochondrial DNA Damage Can Promote Atherosclerosis Independently of Reactive Oxygen Species Through Effects on Smooth Muscle Cells and Monocytes and Correlates With Higher-Risk Plaques in Humans Emma Yu, Patrick A. Calvert, John R. Mercer, Circulation	2013	270
An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome. A C Nicholls, Jane E. Oliver, Seamus McCarron, Journal of Medical Genetics	1996	99
A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II. Allan J. Richards, Sophie G. Martin, A C Nicholls, Journal of Medical Genetics Family MembersGeneticsGenetic EpidemiologyPathologyMolecular Genetics	1998	80
Immunocytochemical mapping of a C-terminus anti-peptide antibody to the GABA receptor subunit, RDL in the nervous system of Drosophila melanogaster J. B. Harrison, H. H. Chen, E. Sattelle, Cell and Tissue Research Drosophila MelanogasterMolecular NeuroscienceSignal TransductionC-terminus Anti-peptide AntibodyGaba Receptor Subunit	1996	78
A Point Mutation in an Intronic Branch Site Results in Aberrant Splicing of COL5A1 and in Ehlers-Danlos Syndrome Type II in Two British Families Nigel Burrows, A C Nicholls, Allan J. Richards, The American Journal of Human Genetics Aberrant SplicingGenetic DisorderGeneticsPathologyPoint Mutation	1998	77
An unusual cell surface modification: A double plasma membrane Nancy J. Lane, J. B. Harrison Journal of Cell Science BiologyConventional Thin SectionsMembrane StructureMembrane FormationOuter Membrane	1979	72
The permeability properties of septate junctions in Malpighian tubules of <i>Rhodnius</i> Hung V. Le, B. Skaer, S. H. P. Maddrell, Journal of Cell Science Higher PermeabilityCytoskeletonSeptate JunctionsCellular PhysiologyPolyethylene Glycol	1987	72
Drosophila nervous system muscarinic acetylcholine receptor: transient functional expression and localization by immunocytochemistry. Andrew Blake, Nicola M. Anthony, H H Chen, Molecular Pharmacology	1993	59
A reconsideration of the Poisson hypothesis for transmitter release at the crayfish neuromuscular junction George D. Bittner, J. B. Harrison The Journal of Physiology Compound Poisson HypothesisMuscle FunctionSynaptic TransmissionNeurotransmitterNeurotransmission	1970	54
ADRENOCORTICOTROPHIN (ACTH) DEFICIENCY UNDETECTED BY STANDARD DYNAMIC TESTS OF THE HYPOTHALAMIC‐PITUITARY‐ADRENAL AXIS Agathocles Tsatsoulis, S. M. SHALET, J. B. Harrison, Clinical Endocrinology Adrenal GlandExternal Pituitary IrradiationPituitary GlandPhysiologyAdrenal Health	1988	52

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