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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

735 related items for PubMed ID: 24576561

  • 61.
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  • 63. Coenzyme Q10 a mitochondrial restorer for various brain disorders.
    Pradhan N, Singh C, Singh A.
    Naunyn Schmiedebergs Arch Pharmacol; 2021 Nov; 394(11):2197-2222. PubMed ID: 34596729
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  • 65. 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 28; 33(1):165-170. PubMed ID: 31821167
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  • 67. Suppression of coenzyme Q₁₀ levels and the induction of multiple PDSS and COQ genes in human cells following oligomycin treatment.
    Yen HC, Liu CC, Kan CC, Chen CS, Wei HR.
    Free Radic Res; 2014 Sep 28; 48(9):1125-34. PubMed ID: 25002068
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  • 68. Design of High-Throughput Screening of Natural Extracts to Identify Molecules Bypassing Primary Coenzyme Q Deficiency in Saccharomyces cerevisiae.
    Berenguel Hernández AM, de la Cruz M, Alcázar-Fabra M, Prieto-Rodríguez A, Sánchez-Cuesta A, Martin J, Tormo JR, Rodríguez-Aguilera JC, Cortés-Rodríguez AB, Navas P, Reyes F, Vicente F, Genilloud O, Santos-Ocaña C.
    SLAS Discov; 2020 Mar 28; 25(3):299-309. PubMed ID: 31751168
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  • 69. Coenzyme Q10 Assessment and the Establishment of a Neuronal Cell Model of CoQ10 Deficiency.
    Heaton R, Duberley K, Hargreaves IP.
    Methods Mol Biol; 2020 Mar 28; 2138():277-287. PubMed ID: 32219756
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  • 74. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
    Lalani SR, Vladutiu GD, Plunkett K, Lotze TE, Adesina AM, Scaglia F.
    Arch Neurol; 2005 Feb 28; 62(2):317-20. PubMed ID: 15710863
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  • 76. The Influence of Atorvastatin, Amlodipine and Ethoxidol on Ubiquinol and Ubiquinone Endogenous Plasma Concentrations in Patients with Chronic Heart Failure.
    Zozina VI, Kondratenko SN, Shikh EV, Krasnykh LM, Melnikov ES, Kukes VG.
    Curr Drug Metab; 2023 Feb 28; 24(9):635-644. PubMed ID: 37711113
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  • 77. Clinical spectrum in multiple families with primary COQ10 deficiency.
    Hashemi SS, Zare-Abdollahi D, Bakhshandeh MK, Vafaee A, Abolhasani S, Inanloo Rahatloo K, DanaeeFard F, Farboodi N, Rohani M, Alavi A.
    Am J Med Genet A; 2021 Feb 28; 185(2):440-452. PubMed ID: 33215859
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  • 78. 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 28; 9(1):78-95. PubMed ID: 27856619
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  • 79.
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  • 80. Coenzyme Q10 deficiency in children: frequent type 2C muscle fibers with normal morphology.
    Sommerville RB, Zaidman CM, Pestronk A.
    Muscle Nerve; 2013 Nov 28; 48(5):722-6. PubMed ID: 23494902
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