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Boon, W, Petkovic-Duran, K, White, K, Tucker, E, Albiston, A, Manasseh, R, Horne, MK, Aumann, TD.
Acoustic microstreaming increases the efficiency of reverse transcription reactions comprising single-cell quantities of RNA.
BioTechniques
50(2)
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116 -119
2011
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Tucker, EJ, Compton, AG, Calvo, SE, Thorburn, DR.
The molecular basis of human complex I deficiency.
IUBMB Life
63(9)
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669 -677
2011
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Calvo, SE, Tucker, EJ, Compton, AG, Kirby, DM, Crawford, G, Burtt, NP, Rivas, M, Guiducci, C, Bruno, DL, Goldberger, OA, et al.
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
Nature Genetics
42(10)
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851 -858
2010
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Tucker, EJ, Compton, AG, Thorburn, DR.
Recent Advances in the Genetics of Mitochondrial Encephalopathies.
Current Neurology and Neuroscience Reports
10(4)
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277 -285
2010
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Tucker, E, Compton, A, McKenzie, M, Calvo, S, Pagliarini, D, Mootha, V, Ryan, M, Thorburn, D.
74 A splice-site mutation in C8orf38 causes impaired Complex I assembly due to a defect in translation or integration of ND1 into an early assembly intermediate.
Mitochondrion
10(2)
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221
2010
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