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Tucker, EJ, Hershman, SG, Köhrer, C, Belcher-Timme, CA, Patel, J, Goldberger, OA, Christodoulou, J, Silberstein, JM, McKenzie, M, Ryan, MT, et al.
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation..
Cell Metab
14(3)
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428 -434
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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Swalwell, H, Kirby, DM, Blakely, EL, Mitchell, A, Salemi, R, Sugiana, C, Compton, AG, Tucker, EJ, Ke, B-X, Lamont, PJ, et al.
Respiratory chain complex I deficiency caused by mitochondrial DNA mutations..
Eur J Hum Genet
19(7)
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769 -775
2011
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Taylor, RW, Swalwell, H, Kirby, DM, Blakely, EL, Mitchell, A, Salemi, R, Sugiana, C, Compton, AG, Tucker, EJ, Ke, B-X, et al.
P59 Respiratory chain complex I deficiency caused by mitochondrial DNA mutations.
Neuromuscular Disorders
21:
s23
2011
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Boon, WC, 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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