Enriquez JA - Search Results

1

Inter-mitochondrial complementation of mtDNA mutations and nuclear context.

Attardi G, Enriquez JA, Cabezas-Herrera J. Attardi G, et al. Among authors: enriquez ja. Nat Genet. 2002 Apr;30(4):360; author reply 361. doi: 10.1038/ng0402-360. Nat Genet. 2002. PMID: 11925561 No abstract available.

2

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination.

Enriquez JA, Chomyn A, Attardi G. Enriquez JA, et al. Nat Genet. 1995 May;10(1):47-55. doi: 10.1038/ng0595-47. Nat Genet. 1995. PMID: 7647790

3

Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells.

Enríquez JA, Cabezas-Herrera J, Bayona-Bafaluy MP, Attardi G. Enríquez JA, et al. J Biol Chem. 2000 Apr 14;275(15):11207-15. doi: 10.1074/jbc.275.15.11207. J Biol Chem. 2000. PMID: 10753928 Free article.

4

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.

Chomyn A, Enriquez JA, Micol V, Fernandez-Silva P, Attardi G. Chomyn A, et al. Among authors: enriquez ja. J Biol Chem. 2000 Jun 23;275(25):19198-209. doi: 10.1074/jbc.M908734199. J Biol Chem. 2000. PMID: 10858457 Free article.

5

Analysis of aminoacylation of human mitochondrial tRNAs.

Enríquez JA, Attardi G. Enríquez JA, et al. Methods Enzymol. 1996;264:183-96. doi: 10.1016/s0076-6879(96)64019-1. Methods Enzymol. 1996. PMID: 8965692 No abstract available.

6

Evidence for aminoacylation-induced conformational changes in human mitochondrial tRNAs.

Enríquez JA, Attardi G. Enríquez JA, et al. Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8300-5. doi: 10.1073/pnas.93.16.8300. Proc Natl Acad Sci U S A. 1996. PMID: 8710865 Free PMC article.

7

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.

Guan MX, Enriquez JA, Fischel-Ghodsian N, Puranam RS, Lin CP, Maw MA, Attardi G. Guan MX, et al. Among authors: enriquez ja. Mol Cell Biol. 1998 Oct;18(10):5868-79. doi: 10.1128/MCB.18.10.5868. Mol Cell Biol. 1998. PMID: 9742104 Free PMC article.

8

Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing.

Latorre-Pellicer A, Moreno-Loshuertos R, Lechuga-Vieco AV, Sánchez-Cabo F, Torroja C, Acín-Pérez R, Calvo E, Aix E, González-Guerra A, Logan A, Bernad-Miana ML, Romanos E, Cruz R, Cogliati S, Sobrino B, Carracedo Á, Pérez-Martos A, Fernández-Silva P, Ruíz-Cabello J, Murphy MP, Flores I, Vázquez J, Enríquez JA. Latorre-Pellicer A, et al. Among authors: enriquez ja. Nature. 2016 Jul 28;535(7613):561-5. doi: 10.1038/nature18618. Epub 2016 Jul 6. Nature. 2016. PMID: 27383793

9

Human mtDNA haplogroups associated with high or reduced spermatozoa motility.

Ruiz-Pesini E, Lapeña AC, Díez-Sánchez C, Pérez-Martos A, Montoya J, Alvarez E, Díaz M, Urriés A, Montoro L, López-Pérez MJ, Enríquez JA. Ruiz-Pesini E, et al. Among authors: enriquez ja. Am J Hum Genet. 2000 Sep;67(3):682-96. doi: 10.1086/303040. Epub 2000 Aug 9. Am J Hum Genet. 2000. PMID: 10936107 Free PMC article.

10

Implications of mitochondrial DNA mutations in human induced pluripotent stem cells.

Carelli V, Hirano M, Enríquez JA, Chinnery PF. Carelli V, et al. Among authors: enriquez ja. Nat Rev Genet. 2022 Feb;23(2):69-70. doi: 10.1038/s41576-021-00430-z. Nat Rev Genet. 2022. PMID: 34728812 Free PMC article.

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