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 *

380 related articles for article (PubMed ID: 25802402)

  • 1. The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene.
    Luna-Sánchez M; Díaz-Casado E; Barca E; Tejada MÁ; Montilla-García Á; Cobos EJ; Escames G; Acuña-Castroviejo D; Quinzii CM; López LC
    EMBO Mol Med; 2015 May; 7(5):670-87. PubMed ID: 25802402
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dysfunctional Coq9 protein causes predominant encephalomyopathy associated with CoQ deficiency.
    García-Corzo L; Luna-Sánchez M; Doerrier C; García JA; Guarás A; Acín-Pérez R; Bullejos-Peregrín J; López A; Escames G; Enríquez JA; Acuña-Castroviejo D; López LC
    Hum Mol Genet; 2013 Mar; 22(6):1233-48. PubMed ID: 23255162
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of 6-demethoxyubiquinone in CoQ
    Herebian D; Seibt A; Smits SHJ; Bünning G; Freyer C; Prokisch H; Karall D; Wredenberg A; Wedell A; López LC; Mayatepek E; Distelmaier F
    Mol Genet Metab; 2017 Jul; 121(3):216-223. PubMed ID: 28552678
    [TBL] [Abstract][Full Text] [Related]  

  • 4. β-RA reduces DMQ/CoQ ratio and rescues the encephalopathic phenotype in
    Hidalgo-Gutiérrez A; Barriocanal-Casado E; Bakkali M; Díaz-Casado ME; Sánchez-Maldonado L; Romero M; Sayed RK; Prehn C; Escames G; Duarte J; Acuña-Castroviejo D; López LC
    EMBO Mol Med; 2019 Jan; 11(1):. PubMed ID: 30482867
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q
    Romero-Moya D; Santos-Ocaña C; Castaño J; Garrabou G; Rodríguez-Gómez JA; Ruiz-Bonilla V; Bueno C; González-Rodríguez P; Giorgetti A; Perdiguero E; Prieto C; Moren-Nuñez C; Fernández-Ayala DJ; Victoria Cascajo M; Velasco I; Canals JM; Montero R; Yubero D; Jou C; López-Barneo J; Cardellach F; Muñoz-Cánoves P; Artuch R; Navas P; Menendez P
    Stem Cells; 2017 Jul; 35(7):1687-1703. PubMed ID: 28472853
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Disruption of the human COQ5-containing protein complex is associated with diminished coenzyme Q10 levels under two different conditions of mitochondrial energy deficiency.
    Yen HC; Liu YC; Kan CC; Wei HJ; Lee SH; Wei YH; Feng YH; Chen CW; Huang CC
    Biochim Biophys Acta; 2016 Sep; 1860(9):1864-76. PubMed ID: 27155576
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ubiquinol-10 ameliorates mitochondrial encephalopathy associated with CoQ deficiency.
    García-Corzo L; Luna-Sánchez M; Doerrier C; Ortiz F; Escames G; Acuña-Castroviejo D; López LC
    Biochim Biophys Acta; 2014 Jul; 1842(7):893-901. PubMed ID: 24576561
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency.
    Desbats MA; Lunardi G; Doimo M; Trevisson E; Salviati L
    J Inherit Metab Dis; 2015 Jan; 38(1):145-56. PubMed ID: 25091424
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Coenzyme Q biosynthesis in health and disease.
    Acosta MJ; Vazquez Fonseca L; Desbats MA; Cerqua C; Zordan R; Trevisson E; Salviati L
    Biochim Biophys Acta; 2016 Aug; 1857(8):1079-1085. PubMed ID: 27060254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bypassing human CoQ
    Herebian D; López LC; Distelmaier F
    Mol Genet Metab; 2018 Mar; 123(3):289-291. PubMed ID: 29246431
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Muscle coenzyme Q: a potential test for mitochondrial activity and redox status.
    Miles L; Miles MV; Tang PH; Horn PS; Wong BL; DeGrauw TJ; Morehart PJ; Bove KE
    Pediatr Neurol; 2005 May; 32(5):318-24. PubMed ID: 15866432
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation.
    Olgac A; Öztoprak Ü; Kasapkara ÇS; Kılıç M; Yüksel D; Derinkuyu EB; Taşçı Yıldız Y; Ceylaner S; Ezgu FS
    J Pediatr Endocrinol Metab; 2020 Jan; 33(1):165-170. PubMed ID: 31821167
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The COQ2 genotype predicts the severity of coenzyme Q10 deficiency.
    Desbats MA; Morbidoni V; Silic-Benussi M; Doimo M; Ciminale V; Cassina M; Sacconi S; Hirano M; Basso G; Pierrel F; Navas P; Salviati L; Trevisson E
    Hum Mol Genet; 2016 Oct; 25(19):4256-4265. PubMed ID: 27493029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family segregating lethal neonatal coenzyme Q
    Smith AC; Ito Y; Ahmed A; Schwartzentruber JA; Beaulieu CL; Aberg E; Majewski J; Bulman DE; Horsting-Wethly K; Koning DV; ; Rodenburg RJ; Boycott KM; Penney LS
    J Inherit Metab Dis; 2018 Jul; 41(4):719-729. PubMed ID: 29560582
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency.
    Doimo M; Trevisson E; Airik R; Bergdoll M; Santos-Ocaña C; Hildebrandt F; Navas P; Pierrel F; Salviati L
    Biochim Biophys Acta; 2014 Jan; 1842(1):1-6. PubMed ID: 24140869
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated with this syndrome.
    Luna-Sánchez M; Hidalgo-Gutiérrez A; Hildebrandt TM; Chaves-Serrano J; Barriocanal-Casado E; Santos-Fandila Á; Romero M; Sayed RK; Duarte J; Prokisch H; Schuelke M; Distelmaier F; Escames G; Acuña-Castroviejo D; López LC
    EMBO Mol Med; 2017 Jan; 9(1):78-95. PubMed ID: 27856619
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cellular Models for Primary CoQ Deficiency Pathogenesis Study.
    Santos-Ocaña C; Cascajo MV; Alcázar-Fabra M; Staiano C; López-Lluch G; Brea-Calvo G; Navas P
    Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638552
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Coenzyme Q
    Awad AM; Bradley MC; Fernández-Del-Río L; Nag A; Tsui HS; Clarke CF
    Essays Biochem; 2018 Jul; 62(3):361-376. PubMed ID: 29980630
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular diagnosis of coenzyme Q10 deficiency.
    Yubero D; Montero R; Armstrong J; Espinós C; Palau F; Santos-Ocaña C; Salviati L; Navas P; Artuch R
    Expert Rev Mol Diagn; 2015; 15(8):1049-59. PubMed ID: 26144946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum.
    Barca E; Kleiner G; Tang G; Ziosi M; Tadesse S; Masliah E; Louis ED; Faust P; Kang UJ; Torres J; Cortes EP; Vonsattel JP; Kuo SH; Quinzii CM
    J Neuropathol Exp Neurol; 2016 Jul; 75(7):663-72. PubMed ID: 27235405
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.