Christopher J. Danpure

Author

Also Known As

C DANPURE, C Danpure, C J Danpure, C. Danpure, C. J. DANPURE, C. J. Danpure, C.J Danpure, C.J. Danpure, CHRISTOPHER J. DANPURE, Christopher J Danpure

143

Publications

5.4K

Citations

H-Index

Concepts

All Affiliations

University College London MRC Clinical Trials Unit at UCL MRC Laboratory for Molecular Cell Biology University of Cambridge Medical Research Council

About

Christopher J. Danpure is an author at University College London specializing in medicine, biochemistry, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	34	2.7K
2	Natural Sciences	17	20	1.6K
3	Health Sciences	6	6	293
4	Engineering	1	1	22
5	Public Health	1	1	32

Christopher J. Danpure

Publications

4.2K

Citations

H-Index

Page 1

	Year	Citations
Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I Christopher J. Danpure, Patricia R. Jennings FEBS Letters Renal FunctionHepatologyBiochemistryPrimary HyperoxaluriaMedicine	1986	343
Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment Pierre Cochat, Sally A. Hulton, Cécile Acquaviva, Nephrology Dialysis Transplantation	2012	330
Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1. P. Edward Purdue, Yoshikazu Takada, Christopher J. Danpure The Journal of Cell Biology GeneticsMolecular BiologyMolecular GeneticsOxidative StressMitochondrial Biogenesis	1990	229
How can the products of a single gene be localized to more than one intracellular compartment? Christopher J. Danpure Trends in Cell Biology Intracellular CompartmentCell DivisionMedicineNatural SciencesMolecular Biology	1995	169
An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria. Christopher J. Danpure, P. J. Cooper, P. J. Wise, The Journal of Cell Biology GeneticsPathologyResidual Agt ActivityRedox BiologyOxidative Stress	1989	163
Functional Synergism between the Most Common Polymorphism in Human Alanine:Glyoxylate Aminotransferase and Four of the Most Common Disease-causing Mutations Michael J. Lumb, Christopher J. Danpure Journal of Biological Chemistry	2000	138
Crystal Structure of Alanine:Glyoxylate Aminotransferase and the Relationship Between Genotype and Enzymatic Phenotype in Primary Hyperoxaluria Type 1 Xiaoxuan Zhang, S. Mark Roe, Yanwen Hou, Journal of Molecular Biology Crystal StructureAldo-keto ReductaseCellular EnzymologyBiochemistryNatural Sciences	2003	136
Characterization and chromosomal mapping of a genomic clone encoding human alanine:Glyoxylate aminotransferase P. Edward Purdue, Michael J. Lumb, Margaret Fox, Genomics Genomic CloneBiochemistryChromosomal MappingGeneticsNatural Sciences	1991	135
Human peroxisomal <scp>l</scp>-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon Yoshikazu Takada, Naomi Kaneko, Hiroyasu Esumi, Biochemical Journal GeneticsMolecular BiologyMolecular GeneticsMitochondrial Signal SequenceRedox Biology	1990	110
Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1 Sonia Fargue, Gill Rumsby, Christopher J. Danpure Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease BiochemistryPrimary HyperoxaluriaMultiple MechanismsPhysiologyRenal Pathophysiology	2013	109

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