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 *

172 related articles for article (PubMed ID: 30087118)

  • 61. N-terminal formylmethionine as a novel initiator and N-degron of eukaryotic proteins.
    Kim JM
    BMB Rep; 2019 Mar; 52(3):163-164. PubMed ID: 30885288
    [TBL] [Abstract][Full Text] [Related]  

  • 62. The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1.
    Sasarman F; Thiffault I; Weraarpachai W; Salomon S; Maftei C; Gauthier J; Ellazam B; Webb N; Antonicka H; Janer A; Brunel-Guitton C; Elpeleg O; Mitchell G; Shoubridge EA
    Hum Mol Genet; 2015 May; 24(10):2841-7. PubMed ID: 25652405
    [TBL] [Abstract][Full Text] [Related]  

  • 63. A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome.
    Duff RM; Shearwood AM; Ermer J; Rossetti G; Gooding R; Richman TR; Balasubramaniam S; Thorburn DR; Rackham O; Lamont PJ; Filipovska A
    Mitochondrion; 2015 Nov; 25():113-9. PubMed ID: 26524491
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Structure of crystalline Escherichia coli methionyl-tRNA(f)Met formyltransferase: comparison with glycinamide ribonucleotide formyltransferase.
    Schmitt E; Blanquet S; Mechulam Y
    EMBO J; 1996 Sep; 15(17):4749-58. PubMed ID: 8887566
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Striking effects of coupling mutations in the acceptor stem on recognition of tRNAs by Escherichia coli Met-tRNA synthetase and Met-tRNA transformylase.
    Lee CP; Dyson MR; Mandal N; Varshney U; Bahramian B; RajBhandary UL
    Proc Natl Acad Sci U S A; 1992 Oct; 89(19):9262-6. PubMed ID: 1409632
    [TBL] [Abstract][Full Text] [Related]  

  • 66. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P; Jin X; Peng Y; Wang M; Liu H; Liu X; Zhang Z; Ji Y; Zhang J; Liang M; Zhao F; Sun YH; Zhang M; Zhou X; Chen Y; Mo JQ; Huang T; Qu J; Guan MX
    Hum Mol Genet; 2016 Feb; 25(3):584-96. PubMed ID: 26647310
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I.
    Lazarou M; McKenzie M; Ohtake A; Thorburn DR; Ryan MT
    Mol Cell Biol; 2007 Jun; 27(12):4228-37. PubMed ID: 17438127
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Metabolic rescue in pluripotent cells from patients with mtDNA disease.
    Ma H; Folmes CD; Wu J; Morey R; Mora-Castilla S; Ocampo A; Ma L; Poulton J; Wang X; Ahmed R; Kang E; Lee Y; Hayama T; Li Y; Van Dyken C; Gutierrez NM; Tippner-Hedges R; Koski A; Mitalipov N; Amato P; Wolf DP; Huang T; Terzic A; Laurent LC; Izpisua Belmonte JC; Mitalipov S
    Nature; 2015 Aug; 524(7564):234-8. PubMed ID: 26176921
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Induced fit of a peptide loop of methionyl-tRNA formyltransferase triggered by the initiator tRNA substrate.
    Ramesh V; Mayer C; Dyson MR; Gite S; RajBhandary UL
    Proc Natl Acad Sci U S A; 1999 Feb; 96(3):875-80. PubMed ID: 9927661
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Mitochondrial protein synthesis in HeLa cells.
    Galper JB
    J Cell Biol; 1974 Mar; 60(3):755-63. PubMed ID: 4824294
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Oxidative phosphorylation: synthesis of mitochondrially encoded proteins and assembly of individual structural subunits into functional holoenzyme complexes.
    Leary SC; Sasarman F
    Methods Mol Biol; 2009; 554():143-62. PubMed ID: 19513673
    [TBL] [Abstract][Full Text] [Related]  

  • 72. CRIF1 is essential for the synthesis and insertion of oxidative phosphorylation polypeptides in the mammalian mitochondrial membrane.
    Kim SJ; Kwon MC; Ryu MJ; Chung HK; Tadi S; Kim YK; Kim JM; Lee SH; Park JH; Kweon GR; Ryu SW; Jo YS; Lee CH; Hatakeyama H; Goto Y; Yim YH; Chung J; Kong YY; Shong M
    Cell Metab; 2012 Aug; 16(2):274-83. PubMed ID: 22819524
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Toward an understanding of the formylation of initiator tRNA methionine in prokaryotic protein synthesis. I. In vitro studies of the 30S and 70S ribosomal-tRNA complex.
    Petersen HU; Danchin A; Grunberg-Manago M
    Biochemistry; 1976 Apr; 15(7):1357-62. PubMed ID: 769821
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Methionine as translation start signal: a review of the enzymes of the pathway in Escherichia coli.
    Meinnel T; Mechulam Y; Blanquet S
    Biochimie; 1993; 75(12):1061-75. PubMed ID: 8199241
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Deficient methylation and formylation of mt-tRNA(Met) wobble cytosine in a patient carrying mutations in NSUN3.
    Van Haute L; Dietmann S; Kremer L; Hussain S; Pearce SF; Powell CA; Rorbach J; Lantaff R; Blanco S; Sauer S; Kotzaeridou U; Hoffmann GF; Memari Y; Kolb-Kokocinski A; Durbin R; Mayr JA; Frye M; Prokisch H; Minczuk M
    Nat Commun; 2016 Jun; 7():12039. PubMed ID: 27356879
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Disrupted in schizophrenia 1 (DISC1) is a constituent of the mammalian mitochondrial contact site and cristae organizing system (MICOS) complex, and is essential for oxidative phosphorylation.
    Piñero-Martos E; Ortega-Vila B; Pol-Fuster J; Cisneros-Barroso E; Ruiz-Guerra L; Medina-Dols A; Heine-Suñer D; Lladó J; Olmos G; Vives-Bauzà C
    Hum Mol Genet; 2016 Oct; 25(19):4157-4169. PubMed ID: 27466199
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Eukaryotic-type elongator tRNAMet of Trypanosoma brucei becomes formylated after import into mitochondria.
    Tan TH; Bochud-Allemann N; Horn EK; Schneider A
    Proc Natl Acad Sci U S A; 2002 Feb; 99(3):1152-7. PubMed ID: 11792845
    [TBL] [Abstract][Full Text] [Related]  

  • 78. MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination.
    Enriquez JA; Chomyn A; Attardi G
    Nat Genet; 1995 May; 10(1):47-55. PubMed ID: 7647790
    [TBL] [Abstract][Full Text] [Related]  

  • 79. 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; 1822(7):1114-24. PubMed ID: 22465034
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A Drosophila model for mito-nuclear diseases generated by an incompatible interaction between tRNA and tRNA synthetase.
    Holmbeck MA; Donner JR; Villa-Cuesta E; Rand DM
    Dis Model Mech; 2015 Aug; 8(8):843-54. PubMed ID: 26035388
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.