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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

320 related items for PubMed ID: 20200222

  • 21.
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  • 22. The leucine-rich pentatricopeptide repeat-containing protein (LRPPRC) does not activate transcription in mammalian mitochondria.
    Harmel J, Ruzzenente B, Terzioglu M, Spåhr H, Falkenberg M, Larsson NG.
    J Biol Chem; 2013 May 31; 288(22):15510-9. PubMed ID: 23599432
    [Abstract] [Full Text] [Related]

  • 23. SLIRP stabilizes LRPPRC via an RRM-PPR protein interface.
    Spåhr H, Rozanska A, Li X, Atanassov I, Lightowlers RN, Chrzanowska-Lightowlers ZM, Rackham O, Larsson NG.
    Nucleic Acids Res; 2016 Aug 19; 44(14):6868-82. PubMed ID: 27353330
    [Abstract] [Full Text] [Related]

  • 24. Structural basis of LRPPRC-SLIRP-dependent translation by the mitoribosome.
    Singh V, Moran JC, Itoh Y, Soto IC, Fontanesi F, Couvillion M, Huynen MA, Churchman LS, Barrientos A, Amunts A.
    Nat Struct Mol Biol; 2024 Dec 19; 31(12):1838-1847. PubMed ID: 39134711
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  • 25. CircPTEN-MT from PTEN regulates mitochondrial energy metabolism.
    Ruan D, Xu J, Liu Y, Luo J, Zhao X, Li Y, Wang G, Feng J, Liang H, Yin Y, Luo J, Yin Y.
    J Genet Genomics; 2024 May 19; 51(5):531-542. PubMed ID: 38184105
    [Abstract] [Full Text] [Related]

  • 26. Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations.
    Kovářová N, Cížková Vrbacká A, Pecina P, Stránecký V, Pronicka E, Kmoch S, Houštěk J.
    Biochim Biophys Acta; 2012 Jul 19; 1822(7):1114-24. PubMed ID: 22465034
    [Abstract] [Full Text] [Related]

  • 27. A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression.
    Wilson WC, Hornig-Do HT, Bruni F, Chang JH, Jourdain AA, Martinou JC, Falkenberg M, Spåhr H, Larsson NG, Lewis RJ, Hewitt L, Baslé A, Cross HE, Tong L, Lebel RR, Crosby AH, Chrzanowska-Lightowlers ZM, Lightowlers RN.
    Hum Mol Genet; 2014 Dec 01; 23(23):6345-55. PubMed ID: 25008111
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  • 28.
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  • 29. Isolation of an mRNA binding protein homologue that is expressed in nociceptors.
    Eilers H, Trilk SL, Lee SY, Xue Q, Jong BE, Moff I, Levine JD, Schumacher MA.
    Eur J Neurosci; 2004 Nov 01; 20(9):2283-93. PubMed ID: 15525270
    [Abstract] [Full Text] [Related]

  • 30. The mitochondrial mRNA-stabilizing protein SLIRP regulates skeletal muscle mitochondrial structure and respiration by exercise-recoverable mechanisms.
    Pham TCP, Raun SH, Havula E, Henriquez-Olguín C, Rubalcava-Gracia D, Frank E, Fritzen AM, Jannig PR, Andersen NR, Kruse R, Ali MS, Irazoki A, Halling JF, Ringholm S, Needham EJ, Hansen S, Lemminger AK, Schjerling P, Petersen MH, de Almeida ME, Jensen TE, Kiens B, Hostrup M, Larsen S, Ørtenblad N, Højlund K, Kjær M, Ruas JL, Trifunovic A, Wojtaszewski JFP, Nielsen J, Qvortrup K, Pilegaard H, Richter EA, Sylow L.
    Nat Commun; 2024 Nov 13; 15(1):9826. PubMed ID: 39537626
    [Abstract] [Full Text] [Related]

  • 31. Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants.
    Tiranti V, Munaro M, Sandonà D, Lamantea E, Rimoldi M, DiDonato S, Bisson R, Zeviani M.
    Hum Mol Genet; 1995 Nov 13; 4(11):2017-23. PubMed ID: 8589677
    [Abstract] [Full Text] [Related]

  • 32. LRPPRC-mediated folding of the mitochondrial transcriptome.
    Siira SJ, Spåhr H, Shearwood AJ, Ruzzenente B, Larsson NG, Rackham O, Filipovska A.
    Nat Commun; 2017 Nov 16; 8(1):1532. PubMed ID: 29146908
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  • 33.
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  • 36. Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome.
    Lake NJ, Webb BD, Stroud DA, Richman TR, Ruzzenente B, Compton AG, Mountford HS, Pulman J, Zangarelli C, Rio M, Boddaert N, Assouline Z, Sherpa MD, Schadt EE, Houten SM, Byrnes J, McCormick EM, Zolkipli-Cunningham Z, Haude K, Zhang Z, Retterer K, Bai R, Calvo SE, Mootha VK, Christodoulou J, Rötig A, Filipovska A, Cristian I, Falk MJ, Metodiev MD, Thorburn DR.
    Am J Hum Genet; 2017 Aug 03; 101(2):239-254. PubMed ID: 28777931
    [Abstract] [Full Text] [Related]

  • 37. A novel neurofibromin (NF1) interaction with the leucine-rich pentatricopeptide repeat motif-containing protein links neurofibromatosis type 1 and the French Canadian variant of Leigh's syndrome in a common molecular complex.
    Arun V, Wiley JC, Kaur H, Kaplan DR, Guha A.
    J Neurosci Res; 2013 Apr 03; 91(4):494-505. PubMed ID: 23361976
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  • 38.
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