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Journal Abstract Search

234 related items for PubMed ID: 34571904

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  • 29. Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome.
    Xu B, Li X, Du M, Zhou C, Fang H, Lyu J, Yang Y.
    J Hum Genet; 2017 Feb; 62(2):291-297. PubMed ID: 27761019
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  • 32. mRNA Reprogramming of T8993G Leigh's Syndrome Fibroblast Cells to Create Induced Pluripotent Stem Cell Models for Mitochondrial Disorders.
    Grace HE, Galdun P, Lesnefsky EJ, West FD, Iyer S.
    Stem Cells Dev; 2019 Jul 01; 28(13):846-859. PubMed ID: 31017045
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  • 33. [Mitochondrial ND5 as the causative gene of Leight syndrome].
    Wang K, Yan CZ, Wang GX, Jiao JS, Jin M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec 01; 27(6):616-9. PubMed ID: 21154318
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  • 37. Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene.
    Martín MA, Blázquez A, Gutierrez-Solana LG, Fernández-Moreira D, Briones P, Andreu AL, Garesse R, Campos Y, Arenas J.
    Arch Neurol; 2005 Apr 01; 62(4):659-61. PubMed ID: 15824269
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  • 38. Abnormal calcium homeostasis in fibroblasts from patients with Leigh disease.
    Wasniewska M, Karczmarewicz E, Pronicki M, Piekutowska-Abramczuk D, Zablocki K, Popowska E, Pronicka E, Duszyński J.
    Biochem Biophys Res Commun; 2001 May 11; 283(3):687-93. PubMed ID: 11341780
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  • 39. Cell-Permeable Succinate Rescues Mitochondrial Respiration in Cellular Models of Amiodarone Toxicity.
    Bețiu AM, Chamkha I, Gustafsson E, Meijer E, Avram VF, Åsander Frostner E, Ehinger JK, Petrescu L, Muntean DM, Elmér E.
    Int J Mol Sci; 2021 Oct 29; 22(21):. PubMed ID: 34769217
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  • 40. α-Lactalbumin-oleic acid complex kills tumor cells by inducing excess energy metabolism but inhibiting mRNA expression of the related enzymes.
    Fang B, Zhang M, Ge KS, Xing HZ, Ren FZ.
    J Dairy Sci; 2018 Jun 29; 101(6):4853-4863. PubMed ID: 29550120
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