BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 34919756)

  • 21. Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice.
    Vrbacký M; Kovalčíková J; Chawengsaksophak K; Beck IM; Mráček T; Nůsková H; Sedmera D; Papoušek F; Kolář F; Sobol M; Hozák P; Sedlacek R; Houštěk J
    Hum Mol Genet; 2016 Nov; 25(21):4674-4685. PubMed ID: 28173120
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Polydatin and Nicotinamide Rescue the Cellular Phenotype of Mitochondrial Diseases by Mitochondrial Unfolded Protein Response (mtUPR) Activation.
    Cilleros-Holgado P; Gómez-Fernández D; Piñero-Pérez R; Romero Domínguez JM; Talaverón-Rey M; Reche-López D; Suárez-Rivero JM; Álvarez-Córdoba M; Romero-González A; López-Cabrera A; Oliveira MC; Rodríguez-Sacristan A; Sánchez-Alcázar JA
    Biomolecules; 2024 May; 14(5):. PubMed ID: 38786005
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs.
    Smeitink JA; Elpeleg O; Antonicka H; Diepstra H; Saada A; Smits P; Sasarman F; Vriend G; Jacob-Hirsch J; Shaag A; Rechavi G; Welling B; Horst J; Rodenburg RJ; van den Heuvel B; Shoubridge EA
    Am J Hum Genet; 2006 Nov; 79(5):869-77. PubMed ID: 17033963
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mitochondrial translation factors of Trypanosoma brucei: elongation factor-Tu has a unique subdomain that is essential for its function.
    Cristodero M; Mani J; Oeljeklaus S; Aeberhard L; Hashimi H; Ramrath DJ; Lukeš J; Warscheid B; Schneider A
    Mol Microbiol; 2013 Nov; 90(4):744-55. PubMed ID: 24033548
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1.
    Balasubramaniam S; Choy YS; Talib A; Norsiah MD; van den Heuvel LP; Rodenburg RJ
    JIMD Rep; 2012; 5():113-22. PubMed ID: 23430926
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy.
    Levéen P; Kotarsky H; Mörgelin M; Karikoski R; Elmér E; Fellman V
    Hepatology; 2011 Feb; 53(2):437-47. PubMed ID: 21274865
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4.
    Hershkovitz T; Kurolap A; Gonzaga-Jauregui C; Paperna T; Mory A; Wolf SE; ; Overton JD; Shuldiner AR; Saada A; Mandel H; Baris Feldman H
    J Hum Genet; 2019 Jun; 64(6):589-595. PubMed ID: 30903008
    [TBL] [Abstract][Full Text] [Related]  

  • 28. An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal function.
    Jin X; Zhang Z; Nie Z; Wang C; Meng F; Yi Q; Chen M; Sun J; Zou J; Jiang P; Guan MX
    J Biol Chem; 2021; 296():100437. PubMed ID: 33610547
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mitochondrial oxidative phosphorylation is impaired in TALLYHO mice, a new obesity and type 2 diabetes animal model.
    Hunter CA; Kartal F; Koc ZC; Murphy T; Kim JH; Denvir J; Koc EC
    Int J Biochem Cell Biol; 2019 Nov; 116():105616. PubMed ID: 31542429
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect.
    Janer A; Antonicka H; Lalonde E; Nishimura T; Sasarman F; Brown GK; Brown RM; Majewski J; Shoubridge EA
    Am J Hum Genet; 2012 Oct; 91(4):737-43. PubMed ID: 23022098
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and molecular findings in a family expressing a novel heterozygous variant of the G elongation factor mitochondrial 1 gene.
    Su C; Wang F
    Exp Ther Med; 2020 Dec; 20(6):173. PubMed ID: 33093908
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2.
    Yang H; Brosel S; Acin-Perez R; Slavkovich V; Nishino I; Khan R; Goldberg IJ; Graziano J; Manfredi G; Schon EA
    Hum Mol Genet; 2010 Jan; 19(1):170-80. PubMed ID: 19837698
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. The Drosophila mitochondrial translation elongation factor G1 contains a nuclear localization signal and inhibits growth and DPP signaling.
    Trivigno C; Haerry TE
    PLoS One; 2011 Feb; 6(2):e16799. PubMed ID: 21364917
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hepatic Mitochondrial Defects in a Nonalcoholic Fatty Liver Disease Mouse Model Are Associated with Increased Degradation of Oxidative Phosphorylation Subunits.
    Lee K; Haddad A; Osme A; Kim C; Borzou A; Ilchenko S; Allende D; Dasarathy S; McCullough A; Sadygov RG; Kasumov T
    Mol Cell Proteomics; 2018 Dec; 17(12):2371-2386. PubMed ID: 30171159
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ribosome-Targeting Antibiotics Impair T Cell Effector Function and Ameliorate Autoimmunity by Blocking Mitochondrial Protein Synthesis.
    Almeida L; Dhillon-LaBrooy A; Castro CN; Adossa N; Carriche GM; Guderian M; Lippens S; Dennerlein S; Hesse C; Lambrecht BN; Berod L; Schauser L; Blazar BR; Kalesse M; Müller R; Moita LF; Sparwasser T
    Immunity; 2021 Jan; 54(1):68-83.e6. PubMed ID: 33238133
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Adipocyte MTERF4 regulates non-shivering adaptive thermogenesis and sympathetic-dependent glucose homeostasis.
    Castillo A; Vilà M; Pedriza I; Pardo R; Cámara Y; Martín E; Beiroa D; Torres-Torronteras J; Oteo M; Morcillo MA; Martí R; Simó R; Nogueiras R; Villena JA
    Biochim Biophys Acta Mol Basis Dis; 2019 Jun; 1865(6):1298-1312. PubMed ID: 30690068
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Ribosome recycling defects modify the balance between the synthesis and assembly of specific subunits of the oxidative phosphorylation complexes in yeast mitochondria.
    Ostojić J; Panozzo C; Bourand-Plantefol A; Herbert CJ; Dujardin G; Bonnefoy N
    Nucleic Acids Res; 2016 Jul; 44(12):5785-97. PubMed ID: 27257059
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Compensatory upregulation of respiratory chain complexes III and IV in isolated deficiency of ATP synthase due to TMEM70 mutation.
    Havlíčková Karbanová V; Cížková Vrbacká A; Hejzlarová K; Nůsková H; Stránecký V; Potocká A; Kmoch S; Houštěk J
    Biochim Biophys Acta; 2012 Jul; 1817(7):1037-43. PubMed ID: 22433607
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.