These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 23877644)

  • 1. Neurodegenerative disease: defective mitochondrial dynamics in the hot seat-a therapeutic target common to many neurological disorders?
    Malpass K
    Nat Rev Neurol; 2013 Aug; 9(8):417. PubMed ID: 23877644
    [No Abstract]   [Full Text] [Related]  

  • 2. Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency.
    Boczonadi V; Smith PM; Pyle A; Gomez-Duran A; Schara U; Tulinius M; Chinnery PF; Horvath R
    Hum Mol Genet; 2013 Nov; 22(22):4602-15. PubMed ID: 23814040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Recent topics in mitochondrial translation systems].
    Watanabe K; Ohtsuki T; Suzuki T
    Tanpakushitsu Kakusan Koso; 2003 Mar; 48(4 Suppl):365-74. PubMed ID: 12696143
    [No Abstract]   [Full Text] [Related]  

  • 4. Mitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases.
    Umeda N; Suzuki T; Yukawa M; Ohya Y; Shindo H; Watanabe K; Suzuki T
    J Biol Chem; 2005 Jan; 280(2):1613-24. PubMed ID: 15509579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the Caenorhabditis elegans orthologs of human genes required for mitochondrial tRNA modification cause similar electron transport chain defects but different nuclear responses.
    Navarro-González C; Moukadiri I; Villarroya M; López-Pascual E; Tuck S; Armengod ME
    PLoS Genet; 2017 Jul; 13(7):e1006921. PubMed ID: 28732077
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
    Guan MX; Yan Q; Li X; Bykhovskaya Y; Gallo-Teran J; Hajek P; Umeda N; Zhao H; Garrido G; Mengesha E; Suzuki T; del Castillo I; Peters JL; Li R; Qian Y; Wang X; Ballana E; Shohat M; Lu J; Estivill X; Watanabe K; Fischel-Ghodsian N
    Am J Hum Genet; 2006 Aug; 79(2):291-302. PubMed ID: 16826519
    [TBL] [Abstract][Full Text] [Related]  

  • 7. METTLing in the right place: METTL8 is a mitochondrial tRNA-specific methyltransferase.
    Kowalinski E; Alfonzo JD
    Mol Cell; 2021 Dec; 81(23):4765-4767. PubMed ID: 34861186
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Modifying mitochondrial tRNAs: delivering what the cell needs.
    Horvath R; Chinnery PF
    Cell Metab; 2015 Mar; 21(3):351-2. PubMed ID: 25738451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Child With Ichthyosis and Liver Failure.
    Indolfi G; Iascone M; Remaschi G; Donati MA; Nesti C; Rubegni A; Pezzoli L; Buccoliero AM; Santorelli FM; Resti M
    J Pediatr Gastroenterol Nutr; 2017 Sep; 65(3):e70-e73. PubMed ID: 28562522
    [No Abstract]   [Full Text] [Related]  

  • 10. Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.
    Meng F; Cang X; Peng Y; Li R; Zhang Z; Li F; Fan Q; Guan AS; Fischel-Ghosian N; Zhao X; Guan MX
    J Biol Chem; 2017 Feb; 292(7):2881-2892. PubMed ID: 28049726
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analyzing the suppression of respiratory defects in the yeast model of human mitochondrial tRNA diseases.
    Montanari A; Zhou YF; D'Orsi MF; Bolotin-Fukuhara M; Frontali L; Francisci S
    Gene; 2013 Sep; 527(1):1-9. PubMed ID: 23727608
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mitochondrial liver disease caused by TRMU gene mutation].
    Zhang ZH; Ma XP; Guo HM
    Zhonghua Er Ke Za Zhi; 2020 Jul; 58(7):602-604. PubMed ID: 32605348
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Acute infantile liver failure due to mutations in the TRMU gene.
    Zeharia A; Shaag A; Pappo O; Mager-Heckel AM; Saada A; Beinat M; Karicheva O; Mandel H; Ofek N; Segel R; Marom D; Rötig A; Tarassov I; Elpeleg O
    Am J Hum Genet; 2009 Sep; 85(3):401-7. PubMed ID: 19732863
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial diseases: Yeast as a model for the study of suppressors.
    Francisci S; Montanari A
    Biochim Biophys Acta Mol Cell Res; 2017 Apr; 1864(4):666-673. PubMed ID: 28089773
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nuclear genes and mitochondrial translation: a new class of genetic disease.
    Jacobs HT; Turnbull DM
    Trends Genet; 2005 Jun; 21(6):312-4. PubMed ID: 15922826
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation.
    Garcia-Diaz B; Barros MH; Sanna-Cherchi S; Emmanuele V; Akman HO; Ferreiro-Barros CC; Horvath R; Tadesse S; El Gharaby N; DiMauro S; De Vivo DC; Shokr A; Hirano M; Quinzii CM
    Am J Hum Genet; 2012 Oct; 91(4):729-36. PubMed ID: 23022099
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The m1A landscape on cytosolic and mitochondrial mRNA at single-base resolution.
    Safra M; Sas-Chen A; Nir R; Winkler R; Nachshon A; Bar-Yaacov D; Erlacher M; Rossmanith W; Stern-Ginossar N; Schwartz S
    Nature; 2017 Nov; 551(7679):251-255. PubMed ID: 29072297
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of the MTO2 gene related to tRNA modification causes a failure in mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae.
    Wang X; Yan Q; Guan MX
    FEBS Lett; 2007 Sep; 581(22):4228-34. PubMed ID: 17706197
    [TBL] [Abstract][Full Text] [Related]  

  • 19. It's a mod mod tRNA world.
    Maraia RJ; Blewett NH; Bayfield MA
    Nat Chem Biol; 2008 Mar; 4(3):162-4. PubMed ID: 18277975
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification and characterization of mouse TRMU gene encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase.
    Yan Q; Guan MX
    Biochim Biophys Acta; 2004 Jan; 1676(2):119-26. PubMed ID: 14746906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.