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Computer Applications in the Biosciences : CABIOS|June 1, 1994
An algorithm based on graph theory for the assembly of contigs in physical mapping of DNAP Zhang, E A Schon, S G Fischer, 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.
Human Molecular Genetics|October 4, 2017
Low-dose rapamycin extends lifespan in a mouse model of mtDNA depletion syndromeStephanie E Siegmund, Hua Yang, Rohit Sharma, et al.
Neuromuscular Disorders : NMD|September 1, 1995
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding geneG Manfredi, E A Schon, C T Moraes, et al.
Human Reproduction (Oxford, England)|October 21, 2000
Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection?E A Schon, S H Kim, J C Ferreira, et al.
Gene|October 1, 1992
Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidaseG M Fabrizi, J Sadlock, M Hirano, et al.
The Biochemical Journal|April 5, 2002
Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutationsLeonardo Salviati, Evelyn Hernandez-Rosa, Winsome F Walker, et al.
The Journal of Biological Chemistry|July 10, 1980
The isolation of the beta A-, beta C-, and gamma-globin genes and a presumptive embryonic globin gene from a goat DNA recombinant libraryJ R Haynes, P Rosteck, E A Schon, et al.
The Journal of Biological Chemistry|January 22, 2005
Crystal structure of human SCO1: implications for redox signaling by a mitochondrial cytochrome c oxidase "assembly" proteinJohn C Williams, Carolyn Sue, Graham S Banting, et al.
American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.
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