Chrzanowska-Lightowlers ZM - Search Results

1

Defective mitochondrial mRNA maturation is associated with spastic ataxia.

Crosby AH, Patel H, Chioza BA, Proukakis C, Gurtz K, Patton MA, Sharifi R, Harlalka G, Simpson MA, Dick K, Reed JA, Al-Memar A, Chrzanowska-Lightowlers ZM, Cross HE, Lightowlers RN. Crosby AH, et al. Am J Hum Genet. 2010 Nov 12;87(5):655-60. doi: 10.1016/j.ajhg.2010.09.013. Epub 2010 Oct 21. Am J Hum Genet. 2010. PMID: 20970105 Free PMC article.

2

Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria.

Temperley RJ, Seneca SH, Tonska K, Bartnik E, Bindoff LA, Lightowlers RN, Chrzanowska-Lightowlers ZM. Temperley RJ, et al. Hum Mol Genet. 2003 Sep 15;12(18):2341-8. doi: 10.1093/hmg/ddg238. Epub 2003 Jul 22. Hum Mol Genet. 2003. PMID: 12915481

3

Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons.

Chrzanowska-Lightowlers ZM, Temperley RJ, Smith PM, Seneca SH, Lightowlers RN. Chrzanowska-Lightowlers ZM, et al. Biochem J. 2004 Feb 1;377(Pt 3):725-31. doi: 10.1042/BJ20031556. Biochem J. 2004. PMID: 14585098 Free PMC article.

4

Messenger RNA stability in mitochondria: different means to an end.

Gagliardi D, Stepien PP, Temperley RJ, Lightowlers RN, Chrzanowska-Lightowlers ZM. Gagliardi D, et al. Trends Genet. 2004 Jun;20(6):260-7. doi: 10.1016/j.tig.2004.04.006. Trends Genet. 2004. PMID: 15145579 Review.

5

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.

Bidooki S, Jackson MJ, Johnson MA, Chrzanowska-Lightowlers ZM, Taylor RW, Venables G, Lightowlers RN, Turnbull DM, Bindoff LA. Bidooki S, et al. Neuromuscul Disord. 2004 Jul;14(7):417-20. doi: 10.1016/j.nmd.2004.03.004. Neuromuscul Disord. 2004. PMID: 15210164

6

Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.

Kolesnikova OA, Entelis NS, Jacquin-Becker C, Goltzene F, Chrzanowska-Lightowlers ZM, Lightowlers RN, Martin RP, Tarassov I. Kolesnikova OA, et al. Hum Mol Genet. 2004 Oct 15;13(20):2519-34. doi: 10.1093/hmg/ddh267. Epub 2004 Aug 18. Hum Mol Genet. 2004. PMID: 15317755

7

Serum-deprivation stimulates cap-binding by PARN at the expense of eIF4E, consistent with the observed decrease in mRNA stability.

Seal R, Temperley R, Wilusz J, Lightowlers RN, Chrzanowska-Lightowlers ZM. Seal R, et al. Nucleic Acids Res. 2005 Jan 14;33(1):376-87. doi: 10.1093/nar/gki169. Print 2005. Nucleic Acids Res. 2005. PMID: 15653638 Free PMC article.

8

Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants.

Pye D, Kyriakouli DS, Taylor GA, Johnson R, Elstner M, Meunier B, Chrzanowska-Lightowlers ZM, Taylor RW, Turnbull DM, Lightowlers RN. Pye D, et al. Nucleic Acids Res. 2006 Aug 2;34(13):e95. doi: 10.1093/nar/gkl516. Nucleic Acids Res. 2006. PMID: 16885236 Free PMC article.

9

How do mammalian mitochondria synthesize proteins?

Rorbach J, Soleimanpour-Lichaei R, Lightowlers RN, Chrzanowska-Lightowlers ZM. Rorbach J, et al. Biochem Soc Trans. 2007 Nov;35(Pt 5):1290-1. doi: 10.1042/BST0351290. Biochem Soc Trans. 2007. PMID: 17956332 Review.

10

Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation.

Rorbach J, Yusoff AA, Tuppen H, Abg-Kamaludin DP, Chrzanowska-Lightowlers ZM, Taylor RW, Turnbull DM, McFarland R, Lightowlers RN. Rorbach J, et al. Nucleic Acids Res. 2008 May;36(9):3065-74. doi: 10.1093/nar/gkn147. Epub 2008 Apr 8. Nucleic Acids Res. 2008. PMID: 18400783 Free PMC article.

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