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Orly Elpeleg, Avraham Shaag, Ronen Spiegel, Ann Saada, Jonatan Halvardson, Devorah Soiferman, Simon Edvardson, Yoseph Horovitz, Morad Khayat, Stavit A Shalev, Lars Feuk

European journal of human genetics : EJHG 2015;22(7):902-6

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Coenzyme Q-dependent mitochondrial respiratory chain activity in granulosa cells is reduced with aging.

Assaf Ben-Meir, Shlomi Yahalomi, Brit Moshe, Yoel Shufaro, Benjamin Reubinoff, Ann Saada

Fertility and sterility 2015;104(3):724-7

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Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literature.

Katta Mohan Girisha, Parneet Kaur, Anju Shukla, Suvasini Sharma, Rajagopal Kadavigere

Annals of human genetics 2021;84(4):345-351

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Variation in proton donor/acceptor pathways in succinate:quinone oxidoreductases.

Gary Cecchini, Elena Maklashina, Victoria Yankovskaya, Tina M Iverson, So Iwata

FEBS letters 2003;545(1):31-8

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The di-heme family of respiratory complex II enzymes.

C Roy D Lancaster

Biochimica et biophysica acta 2013;1827(5):679-87

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Results for ""Electron Transport Complex II""[mesh_terms]

Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II.

Mitochondrial Ca(2+) influx targets cardiolipin to disintegrate respiratory chain complex II for cell death induction.

Physiological consequences of complex II inhibition for aging, disease, and the mKATP channel.

Pathology of mitochondrial encephalomyopathies.

Complex II deficiency--a case report and review of the literature.

Computational and experimental insight into the molecular mechanism of carboxamide inhibitors of succinate-ubquinone oxidoreductase.

The quinone-binding and catalytic site of complex II.

Differential effects of complex II on mitochondrial ROS production and their relation to cardioprotective pre- and postconditioning.

A novel de novo heterozygous pathogenic variant in the SDHA gene results in childhood onset bilateral optic atrophy and cognitive impairment.

Hereditary paraganglioma targets diverse paraganglia.

Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.

Coenzyme Q-dependent mitochondrial respiratory chain activity in granulosa cells is reduced with aging.

Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literature.

Variation in proton donor/acceptor pathways in succinate:quinone oxidoreductases.

The di-heme family of respiratory complex II enzymes.

Results for
""Electron Transport Complex II""[mesh_terms]