Succinate dehydrogenase/complex II is critical for metabolic and epigenetic regulation of T cell proliferation and inflammation.
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MITOCHONDRIA: Succinate dehydrogenase subunit B-associated phaeochromocytoma and paraganglioma.
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Int J Biochem Cell Biol. 2021 May;134:105949. doi: 10.1016/j.biocel.2021.105949. Epub 2021 Feb 17.
β-Cell Succinate Dehydrogenase Deficiency Triggers Metabolic Dysfunction and Insulinopenic Diabetes.
Lee S, Xu H, Van Vleck A, Mawla AM, Li AM, Ye J, Huising MO, Annes JP.
Diabetes. 2022 Jul 1;71(7):1439-1453. doi: 10.2337/db21-0834.
[Advanced GIST: Which treatments in 2022?].
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Bull Cancer. 2022 Oct;109(10):1082-1087. doi: 10.1016/j.bulcan.2022.06.009. Epub 2022 Aug 4.
The genetic basis of isolated mitochondrial complex II deficiency.
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Mol Genet Metab. 2020 Sep-Oct;131(1-2):53-65. doi: 10.1016/j.ymgme.2020.09.009. Epub 2020 Oct 3.
Two Patients Diagnosed as Succinate Dehydrogenase Deficiency: Case Report.
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Mol Syndromol. 2023 Apr;14(2):171-174. doi: 10.1159/000527538. Epub 2023 Jan 13.
Pyruvate transamination and NAD biosynthesis enable proliferation of succinate dehydrogenase-deficient cells by supporting aerobic glycolysis.
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Cell Death Dis. 2023 Jul 6;14(7):403. doi: 10.1038/s41419-023-05927-5.
SDHx mutation and pituitary adenoma: can in vivo 1H-MR spectroscopy unravel the link?
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A suppressor of dioxygenase inhibition in a yeast model of SDH deficiency.
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Endocr Relat Cancer. 2022 May 11;29(6):345-358. doi: 10.1530/ERC-21-0349.
Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literature.
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