O'Dell KM - Search Results

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. Toivonen JM, et al. Genetics. 2001 Sep;159(1):241-54. doi: 10.1093/genetics/159.1.241. Genetics. 2001. PMID: 11560901 Free PMC article.

2

Mitochondrial disease in flies.

Jacobs HT, Fernández-Ayala DJ, Manjiry S, Kemppainen E, Toivonen JM, O'Dell KM. Jacobs HT, et al. Biochim Biophys Acta. 2004 Dec 6;1659(2-3):190-6. doi: 10.1016/j.bbabio.2004.07.004. Biochim Biophys Acta. 2004. PMID: 15576051 Free article. Review.

3

Gene dosage and selective expression modify phenotype in a Drosophila model of human mitochondrial disease.

Toivonen JM, Manjiry S, Touraille S, Alziari S, O'Dell KM, Jacobs HT. Toivonen JM, et al. Mitochondrion. 2003 Oct;3(2):83-96. doi: 10.1016/S1567-7249(03)00077-1. Mitochondrion. 2003. PMID: 16120347

4

Gene expression in a Drosophila model of mitochondrial disease.

Fernández-Ayala DJ, Chen S, Kemppainen E, O'Dell KM, Jacobs HT. Fernández-Ayala DJ, et al. PLoS One. 2010 Jan 6;5(1):e8549. doi: 10.1371/journal.pone.0008549. PLoS One. 2010. PMID: 20066047 Free PMC article.

5

Metazoan nuclear genes for mitoribosomal protein S12.

Shah ZH, O'Dell KM, Miller SC, An X, Jacobs HT. Shah ZH, et al. Gene. 1997 Dec 19;204(1-2):55-62. doi: 10.1016/s0378-1119(97)00521-0. Gene. 1997. PMID: 9434165

6

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. Kemppainen E, et al. Mitochondrion. 2009 Sep;9(5):353-63. doi: 10.1016/j.mito.2009.07.002. Epub 2009 Jul 17. Mitochondrion. 2009. PMID: 19616644

7

Phenotypic rescue of a Drosophila model of mitochondrial ANT1 disease.

Vartiainen S, Chen S, George J, Tuomela T, Luoto KR, O'Dell KM, Jacobs HT. Vartiainen S, et al. Among authors: o dell km. Dis Model Mech. 2014 Jun;7(6):635-48. doi: 10.1242/dmm.016527. Epub 2014 May 8. Dis Model Mech. 2014. PMID: 24812436 Free PMC article.

8

The dominant cold-sensitive Out-cold mutants of Drosophila melanogaster have novel missense mutations in the voltage-gated sodium channel gene paralytic.

Lindsay HA, Baines R, ffrench-Constant R, Lilley K, Jacobs HT, O'Dell KM. Lindsay HA, et al. Genetics. 2008 Oct;180(2):873-84. doi: 10.1534/genetics.108.090951. Epub 2008 Aug 24. Genetics. 2008. PMID: 18723887 Free PMC article.

9

Expression of the Ciona intestinalis alternative oxidase (AOX) in Drosophila complements defects in mitochondrial oxidative phosphorylation.

Fernandez-Ayala DJ, Sanz A, Vartiainen S, Kemppainen KK, Babusiak M, Mustalahti E, Costa R, Tuomela T, Zeviani M, Chung J, O'Dell KM, Rustin P, Jacobs HT. Fernandez-Ayala DJ, et al. Cell Metab. 2009 May;9(5):449-60. doi: 10.1016/j.cmet.2009.03.004. Cell Metab. 2009. PMID: 19416715 Free article.

10

Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila.

Houseley JM, Wang Z, Brock GJ, Soloway J, Artero R, Perez-Alonso M, O'Dell KM, Monckton DG. Houseley JM, et al. Hum Mol Genet. 2005 Mar 15;14(6):873-83. doi: 10.1093/hmg/ddi080. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703191

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