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Journal Abstract Search
295 related items for PubMed ID: 29880640
1. Structural insight into the human mitochondrial tRNA purine N1-methyltransferase and ribonuclease P complexes. Oerum S, Roovers M, Rambo RP, Kopec J, Bailey HJ, Fitzpatrick F, Newman JA, Newman WG, Amberger A, Zschocke J, Droogmans L, Oppermann U, Yue WW. J Biol Chem; 2018 Aug 17; 293(33):12862-12876. PubMed ID: 29880640 [Abstract] [Full Text] [Related]
2. Novel patient missense mutations in the HSD17B10 gene affect dehydrogenase and mitochondrial tRNA modification functions of the encoded protein. Oerum S, Roovers M, Leichsenring M, Acquaviva-Bourdain C, Beermann F, Gemperle-Britschgi C, Fouilhoux A, Korwitz-Reichelt A, Bailey HJ, Droogmans L, Oppermann U, Sass JO, Yue WW. Biochim Biophys Acta Mol Basis Dis; 2017 Dec 17; 1863(12):3294-3302. PubMed ID: 28888424 [Abstract] [Full Text] [Related]
3. Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts. Deutschmann AJ, Amberger A, Zavadil C, Steinbeisser H, Mayr JA, Feichtinger RG, Oerum S, Yue WW, Zschocke J. Hum Mol Genet; 2014 Jul 01; 23(13):3618-28. PubMed ID: 24549042 [Abstract] [Full Text] [Related]
4. The MRPP1/MRPP2 complex is a tRNA-maturation platform in human mitochondria. Reinhard L, Sridhara S, Hällberg BM. Nucleic Acids Res; 2017 Dec 01; 45(21):12469-12480. PubMed ID: 29040705 [Abstract] [Full Text] [Related]
7. Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies. Metodiev MD, Thompson K, Alston CL, Morris AAM, He L, Assouline Z, Rio M, Bahi-Buisson N, Pyle A, Griffin H, Siira S, Filipovska A, Munnich A, Chinnery PF, McFarland R, Rötig A, Taylor RW. Am J Hum Genet; 2016 May 05; 98(5):993-1000. PubMed ID: 27132592 [Abstract] [Full Text] [Related]
13. Loss of the mitochondrial protein-only ribonuclease P complex causes aberrant tRNA processing and lethality in Drosophila. Sen A, Karasik A, Shanmuganathan A, Mirkovic E, Koutmos M, Cox RT. Nucleic Acids Res; 2016 Jul 27; 44(13):6409-22. PubMed ID: 27131785 [Abstract] [Full Text] [Related]
14. The amyloid-β-SDR5C1(ABAD) interaction does not mediate a specific inhibition of mitochondrial RNase P. Vilardo E, Rossmanith W. PLoS One; 2013 Jul 27; 8(6):e65609. PubMed ID: 23755257 [Abstract] [Full Text] [Related]
18. Cleavage kinetics of human mitochondrial RNase P and contribution of its non-nuclease subunits. Vilardo E, Toth U, Hazisllari E, Hartmann RK, Rossmanith W. Nucleic Acids Res; 2023 Oct 27; 51(19):10536-10550. PubMed ID: 37779095 [Abstract] [Full Text] [Related]
19. RNA processing in human mitochondria. Sanchez MI, Mercer TR, Davies SM, Shearwood AM, Nygård KK, Richman TR, Mattick JS, Rackham O, Filipovska A. Cell Cycle; 2011 Sep 01; 10(17):2904-16. PubMed ID: 21857155 [Abstract] [Full Text] [Related]
20. Mitochondrial ribonuclease P structure provides insight into the evolution of catalytic strategies for precursor-tRNA 5' processing. Howard MJ, Lim WH, Fierke CA, Koutmos M. Proc Natl Acad Sci U S A; 2012 Oct 02; 109(40):16149-54. PubMed ID: 22991464 [Abstract] [Full Text] [Related] Page: [Next] [New Search]