Rossmanith W - Search Results

1

A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression.

Falk MJ, Gai X, Shigematsu M, Vilardo E, Takase R, McCormick E, Christian T, Place E, Pierce EA, Consugar M, Gamper HB, Rossmanith W, Hou YM. Falk MJ, et al. Among authors: rossmanith w. RNA Biol. 2016 May 3;13(5):477-85. doi: 10.1080/15476286.2016.1159381. Epub 2016 Mar 7. RNA Biol. 2016. PMID: 26950678 Free PMC article.

2

RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme.

Holzmann J, Frank P, Löffler E, Bennett KL, Gerner C, Rossmanith W. Holzmann J, et al. Among authors: rossmanith w. Cell. 2008 Oct 31;135(3):462-74. doi: 10.1016/j.cell.2008.09.013. Cell. 2008. PMID: 18984158 Free article.

3

tRNA recognition, processing, and disease: hypotheses around an unorthodox type of RNase P in human mitochondria.

Holzmann J, Rossmanith W. Holzmann J, et al. Among authors: rossmanith w. Mitochondrion. 2009 Jul;9(4):284-8. doi: 10.1016/j.mito.2009.03.008. Epub 2009 Apr 17. Mitochondrion. 2009. PMID: 19376274 Review.

4

Of P and Z: mitochondrial tRNA processing enzymes.

Rossmanith W. Rossmanith W. Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):1017-26. doi: 10.1016/j.bbagrm.2011.11.003. Epub 2011 Nov 23. Biochim Biophys Acta. 2012. PMID: 22137969 Free PMC article. Review.

5

A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase--extensive moonlighting in mitochondrial tRNA biogenesis.

Vilardo E, Nachbagauer C, Buzet A, Taschner A, Holzmann J, Rossmanith W. Vilardo E, et al. Among authors: rossmanith w. Nucleic Acids Res. 2012 Dec;40(22):11583-93. doi: 10.1093/nar/gks910. Epub 2012 Oct 5. Nucleic Acids Res. 2012. PMID: 23042678 Free PMC article.

6

The amyloid-β-SDR5C1(ABAD) interaction does not mediate a specific inhibition of mitochondrial RNase P.

Vilardo E, Rossmanith W. Vilardo E, et al. Among authors: rossmanith w. PLoS One. 2013 Jun 5;8(6):e65609. doi: 10.1371/journal.pone.0065609. Print 2013. PLoS One. 2013. PMID: 23755257 Free PMC article.

7

Molecular insights into HSD10 disease: impact of SDR5C1 mutations on the human mitochondrial RNase P complex.

Vilardo E, Rossmanith W. Vilardo E, et al. Among authors: rossmanith w. Nucleic Acids Res. 2015 May 26;43(10):5112-9. doi: 10.1093/nar/gkv408. Epub 2015 Apr 29. Nucleic Acids Res. 2015. PMID: 25925575 Free PMC article.

8

Molecular insights into HSD10 disease: impact of SDR5C1 mutations on the human mitochondrial RNase P complex.

Vilardo E, Rossmanith W. Vilardo E, et al. Among authors: rossmanith w. Nucleic Acids Res. 2015 Jul 27;43(13):6649. doi: 10.1093/nar/gkv658. Epub 2015 Jun 19. Nucleic Acids Res. 2015. PMID: 26092698 Free PMC article. No abstract available.

9

Repairing tRNA termini: News from the 3' end.

Rammelt C, Rossmanith W. Rammelt C, et al. Among authors: rossmanith w. RNA Biol. 2016 Dec;13(12):1182-1188. doi: 10.1080/15476286.2016.1239007. Epub 2016 Sep 23. RNA Biol. 2016. PMID: 27661287 Free PMC article.

10

Functional characterization of the human tRNA methyltransferases TRMT10A and TRMT10B.

Vilardo E, Amman F, Toth U, Kotter A, Helm M, Rossmanith W. Vilardo E, et al. Among authors: rossmanith w. Nucleic Acids Res. 2020 Jun 19;48(11):6157-6169. doi: 10.1093/nar/gkaa353. Nucleic Acids Res. 2020. PMID: 32392304 Free PMC article.

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