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Journal Abstract Search
328 related items for PubMed ID: 33380464
1. Disease-associated mutations in mitochondrial precursor tRNAs affect binding, m1R9 methylation, and tRNA processing by mtRNase P. Karasik A, Wilhelm CA, Fierke CA, Koutmos M. RNA; 2021 Apr; 27(4):420-432. PubMed ID: 33380464 [Abstract] [Full Text] [Related]
2. Interplay between substrate recognition, 5' end tRNA processing and methylation activity of human mitochondrial RNase P. Karasik A, Fierke CA, Koutmos M. RNA; 2019 Dec; 25(12):1646-1660. PubMed ID: 31455609 [Abstract] [Full Text] [Related]
3. Structural basis for human mitochondrial tRNA maturation. Meynier V, Hardwick SW, Catala M, Roske JJ, Oerum S, Chirgadze DY, Barraud P, Yue WW, Luisi BF, Tisné C. Nat Commun; 2024 Jun 01; 15(1):4683. PubMed ID: 38824131 [Abstract] [Full Text] [Related]
4. 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]
6. Loss of Individual Mitochondrial Ribonuclease P Complex Proteins Differentially Affects Mitochondrial tRNA Processing In Vivo. Saoji M, Sen A, Cox RT. Int J Mol Sci; 2021 Jun 04; 22(11):. PubMed ID: 34199774 [Abstract] [Full Text] [Related]
10. Complete chemical structures of human mitochondrial tRNAs. Suzuki T, Yashiro Y, Kikuchi I, Ishigami Y, Saito H, Matsuzawa I, Okada S, Mito M, Iwasaki S, Ma D, Zhao X, Asano K, Lin H, Kirino Y, Sakaguchi Y, Suzuki T. Nat Commun; 2020 Aug 28; 11(1):4269. PubMed ID: 32859890 [Abstract] [Full Text] [Related]
12. Pathogenesis-related mutations in the T-loops of human mitochondrial tRNAs affect 3' end processing and tRNA structure. Levinger L, Serjanov D. RNA Biol; 2012 Mar 28; 9(3):283-91. PubMed ID: 22336717 [Abstract] [Full Text] [Related]
14. 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]
15. Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations. Hochberg I, Demain LAM, Richer J, Thompson K, Urquhart JE, Rea A, Pagarkar W, Rodríguez-Palmero A, Schlüter A, Verdura E, Pujol A, Quijada-Fraile P, Amberger A, Deutschmann AJ, Demetz S, Gillespie M, Belyantseva IA, McMillan HJ, Barzik M, Beaman GM, Motha R, Ng KY, O'Sullivan J, Williams SG, Bhaskar SS, Lawrence IR, Jenkinson EM, Zambonin JL, Blumenfeld Z, Yalonetsky S, Oerum S, Rossmanith W, Genomics England Research Consortium, Yue WW, Zschocke J, Munro KJ, Battersby BJ, Friedman TB, Taylor RW, O'Keefe RT, Newman WG. Am J Hum Genet; 2021 Nov 04; 108(11):2195-2204. PubMed ID: 34715011 [Abstract] [Full Text] [Related]
16. Human mitochondrial diseases associated with tRNA wobble modification deficiency. Kirino Y, Suzuki T. RNA Biol; 2005 Apr 04; 2(2):41-4. PubMed ID: 17132941 [Abstract] [Full Text] [Related]
17. 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. Nucleic Acids Res; 2012 Dec 04; 40(22):11583-93. PubMed ID: 23042678 [Abstract] [Full Text] [Related]
18. Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs. Schöller E, Marks J, Marchand V, Bruckmann A, Powell CA, Reichold M, Mutti CD, Dettmer K, Feederle R, Hüttelmaier S, Helm M, Oefner P, Minczuk M, Motorin Y, Hafner M, Meister G. Mol Cell; 2021 Dec 02; 81(23):4810-4825.e12. PubMed ID: 34774131 [Abstract] [Full Text] [Related]