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197 related items for PubMed ID: 11560901
1. Technical knockout, a Drosophila model of mitochondrial deafness. Toivonen JM, O'Dell KM, Petit N, Irvine SC, Knight GK, Lehtonen M, Longmuir M, Luoto K, Touraille S, Wang Z, Alziari S, Shah ZH, Jacobs HT. Genetics; 2001 Sep; 159(1):241-54. PubMed ID: 11560901 [Abstract] [Full Text] [Related]
2. The alternative oxidase AOX does not rescue the phenotype of tko25t mutant flies. Kemppainen KK, Kemppainen E, Jacobs HT. G3 (Bethesda); 2014 Aug 21; 4(10):2013-21. PubMed ID: 25147191 [Abstract] [Full Text] [Related]
3. Phenotypic suppression of the Drosophila mitochondrial disease-like mutant tko(25t) by duplication of the mutant gene in its natural chromosomal context. Kemppainen E, Fernández-Ayala DJ, Galbraith LC, O'Dell KM, Jacobs HT. Mitochondrion; 2009 Sep 21; 9(5):353-63. PubMed ID: 19616644 [Abstract] [Full Text] [Related]
4. Lethal Interaction of Nuclear and Mitochondrial Genotypes in Drosophila melanogaster. Salminen TS, Cannino G, Oliveira MT, Lillsunde P, Jacobs HT, Kaguni LS. G3 (Bethesda); 2019 Jul 09; 9(7):2225-2234. PubMed ID: 31076384 [Abstract] [Full Text] [Related]
5. Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation. Guan MX, Fischel-Ghodsian N, Attardi G. Hum Mol Genet; 1996 Jul 09; 5(7):963-71. PubMed ID: 8817331 [Abstract] [Full Text] [Related]
6. Metazoan nuclear genes for mitoribosomal protein S12. Shah ZH, O'Dell KM, Miller SC, An X, Jacobs HT. Gene; 1997 Dec 19; 204(1-2):55-62. PubMed ID: 9434165 [Abstract] [Full Text] [Related]
7. Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation. Meng F, Cang X, Peng Y, Li R, Zhang Z, Li F, Fan Q, Guan AS, Fischel-Ghosian N, Zhao X, Guan MX. J Biol Chem; 2017 Feb 17; 292(7):2881-2892. PubMed ID: 28049726 [Abstract] [Full Text] [Related]
8. A cytoplasmic suppressor of a nuclear mutation affecting mitochondrial functions in Drosophila. Chen S, Oliveira MT, Sanz A, Kemppainen E, Fukuoh A, Schlicht B, Kaguni LS, Jacobs HT. Genetics; 2012 Oct 17; 192(2):483-93. PubMed ID: 22851652 [Abstract] [Full Text] [Related]
9. Gene expression in a Drosophila model of mitochondrial disease. Fernández-Ayala DJ, Chen S, Kemppainen E, O'Dell KM, Jacobs HT. PLoS One; 2010 Jan 06; 5(1):e8549. PubMed ID: 20066047 [Abstract] [Full Text] [Related]
10. Mitochondrial disease in flies. Jacobs HT, Fernández-Ayala DJ, Manjiry S, Kemppainen E, Toivonen JM, O'Dell KM. Biochim Biophys Acta; 2004 Dec 06; 1659(2-3):190-6. PubMed ID: 15576051 [Abstract] [Full Text] [Related]
11. The S12 ribosomal protein of Podospora anserina belongs to the S19 bacterial family and controls the mitochondrial genome integrity through cytoplasmic translation. Dequard-Chablat M, Sellem CH. J Biol Chem; 1994 May 27; 269(21):14951-6. PubMed ID: 8195128 [Abstract] [Full Text] [Related]
12. The tko locus, site of a behavioral mutation in D. melanogaster, codes for a protein homologous to prokaryotic ribosomal protein S12. Royden CS, Pirrotta V, Jan LY. Cell; 1987 Oct 23; 51(2):165-73. PubMed ID: 3117373 [Abstract] [Full Text] [Related]
13. Nuclear genetic background influences the phenotype of the Drosophila tko25t mitochondrial protein-synthesis mutant. Jacobs HT, Tuomela T, Lillsunde P. G3 (Bethesda); 2023 Jun 01; 13(6):. PubMed ID: 37017029 [Abstract] [Full Text] [Related]