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Items where Person is "Hurko-O"

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Jump to: 1996 | 1992
Number of items: 4.

1996

Hofhaus, Götz and Johns, Donald R. and Hurko, Orest et al. (1996) Respiration and Growth Defects in Transmitochondrial Cell Lines Carrying the 11778 Mutation Associated with Leber’s Hereditary Optic Neuropathy. Journal of Biological Chemistry, 271 (22). pp. 13155-13161. ISSN 0021-9258. https://resolver.caltech.edu/CaltechAUTHORS:HOFjbc96

1992

Yoneda, Makoto and Chomyn, Anne and Martinuzzi, Andrea et al. (1992) Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. Proceedings of the National Academy of Sciences of the United States of America, 89 (23). pp. 11164-11168. ISSN 0027-8424. PMCID PMC50510. https://resolver.caltech.edu/CaltechAUTHORS:YONpnas92

Lunardi, Joël and Hurko, Orest and Engel, W. King et al. (1992) The multiple ADP/ATP translocase genes are differentially expressed during human muscle development. Journal of Biological Chemistry, 267 (22). pp. 15267-15270. ISSN 0021-9258. https://resolver.caltech.edu/CaltechAUTHORS:LUNjbc92

Chomyn, A. and Martinuzzi, A. and Yoneda, M. et al. (1992) MELAS Mutation in mtDNA Binding Site for Transcription Termination Factor Causes Defects in Protein Synthesis and in Respiration but no Change in Levels of Upstream and Downstream Mature Transcripts. Proceedings of the National Academy of Sciences of the United States of America, 89 (10). pp. 4221-4225. ISSN 0027-8424. PMCID PMC49053. https://resolver.caltech.edu/CaltechAUTHORS:20120309-160913724

This list was generated on Tue Oct 27 09:01:08 2020 PDT.