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 *

159 related articles for article (PubMed ID: 36983072)

  • 1. Mitochondrial Methionyl-tRNA Formyltransferase Deficiency Alleviates Metaflammation by Modulating Mitochondrial Activity in Mice.
    Sun X; Liu S; Cai J; Yang M; Li C; Tan M; He B
    Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36983072
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.
    Tucker EJ; Hershman SG; Köhrer C; Belcher-Timme CA; Patel J; Goldberger OA; Christodoulou J; Silberstein JM; McKenzie M; Ryan MT; Compton AG; Jaffe JD; Carr SA; Calvo SE; RajBhandary UL; Thorburn DR; Mootha VK
    Cell Metab; 2011 Sep; 14(3):428-34. PubMed ID: 21907147
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biochemical characterization of pathogenic mutations in human mitochondrial methionyl-tRNA formyltransferase.
    Sinha A; Köhrer C; Weber MH; Masuda I; Mootha VK; Hou YM; RajBhandary UL
    J Biol Chem; 2014 Nov; 289(47):32729-41. PubMed ID: 25288793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Improved lactate control with dichloroacetate in a case with severe neonatal lactic acidosis due to MTFMT mitochondrial translation disorder.
    Bennett J; Kerr M; Greenway SC; Friederich MW; Van Hove JLK; Hittel D; Khan A
    Mol Genet Metab Rep; 2020 Sep; 24():100616. PubMed ID: 32577402
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial methionyl
    Arguello T; Köhrer C; RajBhandary UL; Moraes CT
    J Biol Chem; 2018 Sep; 293(39):15021-15032. PubMed ID: 30087118
    [No Abstract]   [Full Text] [Related]  

  • 6. MTFMT deficiency correlates with reduced mitochondrial integrity and enhanced host susceptibility to intracellular infection.
    Seo JH; Hwang CS; Yoo JY
    Sci Rep; 2020 Jul; 10(1):11183. PubMed ID: 32636430
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Methionyl-tRNA Formyltransferase (MTFMT) Deficiency Mimicking Acquired Demyelinating Disease.
    Pena JA; Lotze T; Yang Y; Umana L; Walkiewicz M; Hunter JV; Scaglia F
    J Child Neurol; 2016 Feb; 31(2):215-9. PubMed ID: 26060307
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expression and characterization of bovine mitochondrial methionyl-tRNA transformylase.
    Takeuchi N; Ueda T; Watanabe K
    J Biochem; 1998 Dec; 124(6):1069-71. PubMed ID: 9832609
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leigh syndrome caused by mutations in
    Hayhurst H; de Coo IFM; Piekutowska-Abramczuk D; Alston CL; Sharma S; Thompson K; Rius R; He L; Hopton S; Ploski R; Ciara E; Lake NJ; Compton AG; Delatycki MB; Verrips A; Bonnen PE; Jones SA; Morris AA; Shakespeare D; Christodoulou J; Wesol-Kucharska D; Rokicki D; Smeets HJM; Pronicka E; Thorburn DR; Gorman GS; McFarland R; Taylor RW; Ng YS
    Ann Clin Transl Neurol; 2019 Mar; 6(3):515-524. PubMed ID: 30911575
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype.
    La Piana R; Weraarpachai W; Ospina LH; Tetreault M; Majewski J; ; Bruce Pike G; Decarie JC; Tampieri D; Brais B; Shoubridge EA
    Neurogenetics; 2017 Apr; 18(2):97-103. PubMed ID: 28058511
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Msc6p is required for mitochondrial translation initiation in the absence of formylated Met-tRNA
    Franco LVR; Moda BS; Soares MAKM; Barros MH
    FEBS J; 2019 Apr; 286(7):1407-1419. PubMed ID: 30767393
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mammalian mitochondrial methionyl-tRNA transformylase from bovine liver. Purification, characterization, and gene structure.
    Takeuchi N; Kawakami M; Omori A; Ueda T; Spremulli LL; Watanabe K
    J Biol Chem; 1998 Jun; 273(24):15085-90. PubMed ID: 9614118
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autonomic instability, arrhythmia and visual impairment in a new presentation of
    Howard C; Dev-Borman A; Stokes J; O'Rourke D; Gillespie C; Twomey E; Knerr I; Boruah R
    JIMD Rep; 2023 Mar; 64(2):150-155. PubMed ID: 36873085
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial Metabolic Reprogramming by CD36 Signaling Drives Macrophage Inflammatory Responses.
    Chen Y; Yang M; Huang W; Chen W; Zhao Y; Schulte ML; Volberding P; Gerbec Z; Zimmermann MT; Zeighami A; Demos W; Zhang J; Knaack DA; Smith BC; Cui W; Malarkannan S; Sodhi K; Shapiro JI; Xie Z; Sahoo D; Silverstein RL
    Circ Res; 2019 Dec; 125(12):1087-1102. PubMed ID: 31625810
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening.
    Haack TB; Gorza M; Danhauser K; Mayr JA; Haberberger B; Wieland T; Kremer L; Strecker V; Graf E; Memari Y; Ahting U; Kopajtich R; Wortmann SB; Rodenburg RJ; Kotzaeridou U; Hoffmann GF; Sperl W; Wittig I; Wilichowski E; Schottmann G; Schuelke M; Plecko B; Stephani U; Strom TM; Meitinger T; Prokisch H; Freisinger P
    Mol Genet Metab; 2014 Mar; 111(3):342-352. PubMed ID: 24461907
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial methionyl-tRNA transformylase from bovine liver.
    Takeuchi N; Kawakami M; Ueda T; Spremulli LL; Watanabe K
    Nucleic Acids Symp Ser; 1997; (37):195-6. PubMed ID: 9586066
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in
    Hemelsoet DM; Vanlander AV; Smet J; Vantroys E; Acou M; Goethals I; Sante T; Seneca S; Menten B; Van Coster R
    Neurol Genet; 2018 Dec; 4(6):e298. PubMed ID: 30569017
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.
    Hinttala R; Sasarman F; Nishimura T; Antonicka H; Brunel-Guitton C; Schwartzentruber J; Fahiminiya S; Majewski J; Faubert D; Ostergaard E; Smeitink JA; Shoubridge EA
    Hum Mol Genet; 2015 Jul; 24(14):4103-13. PubMed ID: 25911677
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial NAD-dependent methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase is essential for embryonic development.
    Di Pietro E; Sirois J; Tremblay ML; MacKenzie RE
    Mol Cell Biol; 2002 Jun; 22(12):4158-66. PubMed ID: 12024029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deficiency of mitophagy receptor FUNDC1 impairs mitochondrial quality and aggravates dietary-induced obesity and metabolic syndrome.
    Wu H; Wang Y; Li W; Chen H; Du L; Liu D; Wang X; Xu T; Liu L; Chen Q
    Autophagy; 2019 Nov; 15(11):1882-1898. PubMed ID: 30898010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.