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Biochemical and Biophysical Research Communications|December 3, 1999
Long-term analysis of differentiation in human myoblasts repopulated with mitochondria harboring mtDNA mutationsC Sobreira, M P King, M M Davidson, et al.Molecular Pathology : MP|August 26, 1998
Improved diagnosis of reactivated toxoplasmosisD Ashburn, M M Davidson, A W Joss, et al.Clinical Molecular Pathology|April 1, 1996
Improved serodiagnosis of Lyme diseaseM M Davidson, S M Chisholm, A D Wiseman, et al.Proceedings of the National Academy of Sciences of the United States of America|February 7, 1998
Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenesM Hirano, A Shtilbans, R Mayeux, et al.Journal of Medical Microbiology|January 27, 1999
Isolation of Borrelia burgdorferi from ticks in the Highlands of ScotlandM M Davidson, R Evans, C L Ling, et al.European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|September 11, 1999
Evidence-based diagnosis of Lyme diseaseM M Davidson, C L Ling, S M Chisholm, et al.The American Journal of Surgical Pathology|September 8, 2000
Primary cutaneous B-cell lymphoma and Borrelia burgdorferi infection in patients from the Highlands of ScotlandJ R Goodlad, M M Davidson, K Hollowood, et al.Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.Communications in Agricultural and Applied Biological Sciences|April 25, 2006
Evaluation of transgenic approaches for controlling tuber moth in potatoesS Meiyalaghan, M F G Takla, O Jaimess, et al.Nature Genetics|November 5, 1999
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneL C Papadopoulou, C M Sue, M M Davidson, et al.Pageof 7