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Items where Person is "Enríquez-J-A"

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Number of items: 7.

2013

Marchis, F. and Vachier, F. and Ďurech, J. et al. (2013) Characteristics and large bulk density of the C-type main-belt triple asteroid (93) Minerva. Icarus, 224 (1). pp. 178-191. ISSN 0019-1035. https://resolver.caltech.edu/CaltechAUTHORS:20130610-092309109

2002

Attardi, Giuseppe and Enríquez, José A. and Cabezas-Herrera, Juan (2002) Inter-mitochondrial complementation of mtDNA mutations and nuclear context. Nature Genetics, 30 (4). p. 360. ISSN 1061-4036. https://resolver.caltech.edu/CaltechAUTHORS:20150408-121803968

2000

Chomyn, Anne and Enríquez, José Antonio and Micol, Vicente et al. (2000) The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes. Journal of Biological Chemistry, 275 (25). pp. 19198-19209. ISSN 0021-9258. https://resolver.caltech.edu/CaltechAUTHORS:CHOjbc00

Enríquez, José A. and Cabezas-Herrera, Juan and Bayona-Bafaluy, M. Pilar et al. (2000) Very Rare Complementation between Mitochondria Carrying Different Mitochondrial DNA Mutations Points to Intrinsic Genetic Autonomy of the Organelles in Cultured Human Cells. Journal of Biological Chemistry, 275 (15). pp. 11207-11215. ISSN 0021-9258. https://resolver.caltech.edu/CaltechAUTHORS:ENRjbc00

1998

Guan, Min-Xin and Enriquez, José Antonio and Fischel-Ghodsian, Nathan et al. (1998) The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNASer(UCN) Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression. Molecular and Cellular Biology, 18 (10). pp. 5868-5879. ISSN 0270-7306. https://resolver.caltech.edu/CaltechAUTHORS:GUAmcb98

1996

Enríquez, José A. and Attardi, Giuseppe (1996) Evidence for aminoacylation-induced conformational changes in human mitochondrial tRNAs. Proceedings of the National Academy of Sciences of the United States of America, 93 (16). pp. 8300-8305. ISSN 0027-8424. PMCID PMC38665. https://resolver.caltech.edu/CaltechAUTHORS:ENRpnas96

1995

Enriquez, José Antonio and Chomyn, Anne and Attardi, Giuseppe (1995) MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA^(Lys) and premature translation termination. Nature Genetics, 10 (1). pp. 47-55. ISSN 1061-4036. https://resolver.caltech.edu/CaltechAUTHORS:20150624-150439462

This list was generated on Thu Aug 6 00:42:46 2020 PDT.