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  1. 1
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 2658 other entries.

  2. 2
    "Lysine acetylation targets protein complexes and co-regulates major cellular functions."
    Choudhary C., Kumar C., Gnad F., Nielsen M.L., Rehman M., Walther T.C., Olsen J.V., Mann M.
    Science 325:834-840(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 3088 other entries.

  3. 3
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 18092 other entries.

  4. 4
    Ensembl
    Submitted (JUL-2011) to UniProtKB
    Cited for: IDENTIFICATION.
    Source: UniProtKB/TrEMBL (unreviewed).
  5. 5
    "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."
    Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D., Wang L., Ye M., Zou H.
    J. Proteomics 96:253-262(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 11535 other entries.

  6. 6
    "N-terminome analysis of the human mitochondrial proteome."
    Vaca Jacome A.S., Rabilloud T., Schaeffer-Reiss C., Rompais M., Ayoub D., Lane L., Bairoch A., Van Dorsselaer A., Carapito C.
    Proteomics 15:2519-2524(2015) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 6356 other entries.

  7. 7
    "A role for mitochondrial enzymes in inherited neoplasia and beyond."
    Eng C., Kiuru M., Fernandez M.J., Aaltonen L.A.
    Nat. Rev. Cancer 3:193-202(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: Review. Succinate dehydrogenase catalyses a step in the Krebs tricarboxylic-acid cycle. Inherited heterozygous mutations in the gene encoding this enzyme causes a predisposition to inherited neoplasia syndromes.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 28 other entries.

  8. 8
    "Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis."
    Bonache S., Martinez J., Fernandez M., Bassas L., Larriba S.
    Int. J. Androl. 30:144-152(2007) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 20 other entries.

  9. 9
    "Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA."
    Baysal B.E., Lawrence E.C., Ferrell R.E.
    BMC Biol. 5:12-12(2007) [PubMed] [Europe PMC] [Abstract]
    Annotation: The SDHA variants that have increased in frequency during human evolution might by influencing the regulation of cellular oxygen homeostasis confer protection against certain environmental toxins or pathogens that are prevalent in Africa.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  10. 10
    "Polymorphisms in mitochondrial genes and prostate cancer risk."
    Wang L., McDonnell S.K., Hebbring S.J., Cunningham J.M., St Sauver J., Cerhan J.R., Isaya G., Schaid D.J., Thibodeau S.N.
    Cancer Epidemiol. Biomarkers Prev. 17:3558-3566(2008) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 287 other entries.

  11. 11
    "Regulation of succinate-ubiquinone reductase and fumarate reductase activities in human complex II by phosphorylation of its flavoprotein subunit."
    Tomitsuka E., Kita K., Esumi H.
    Proc. Jpn. Acad., Ser. B, Phys. Biol. Sci. 85:258-265(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: Phosphorylation of flavoprotein subunit ofsuccinate-ubiquinone reductase might be important for maintaining mitochondrial energy metabolism within the tumor microenvironment.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  12. 12
    "Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation."
    Korsten A., de Coo I.F., Spruijt L., de Wit L.E., Smeets H.J., Sluiter W.
    Biochim. Biophys. Acta 1797:197-203(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: Mutations in electron Transport Complex II is associated with Leber hereditary optic neuropathy failing to compensate for impaired oxidative phosphorylation.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 11 other entries.

  13. 13
    "Mitochondrial respiratory chain in the colonic mucosal of patients with ulcerative colitis."
    Sifroni K.G., Damiani C.R., Stoffel C., Cardoso M.R., Ferreira G.K., Jeremias I.C., Rezin G.T., Scaini G., Schuck P.F., Dal-Pizzol F., Streck E.L.
    Mol. Cell. Biochem. 342:111-115(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: Decreased electron Transport Complex II activity is associated with ulcerative colitis.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 10 other entries.

  14. 14
    "Calcium signalling-dependent mitochondrial dysfunction and bioenergetics regulation in respiratory chain Complex II deficiency."
    Mbaya E., Oules B., Caspersen C., Tacine R., Massinet H., Pennuto M., Chretien D., Munnich A., Rotig A., Rizzuto R., Rutter G.A., Paterlini-Brechot P., Chami M.
    Cell Death Differ. 17:1855-1866(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: Cells with Complex II defect may undergo a progressive mitochondrial dysfunction characterized by Dcmit loss Calcium overload and increased ROS eventually leading to cell death.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  15. 15
    "Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase."
    Levitas A., Muhammad E., Harel G., Saada A., Caspi V.C., Manor E., Beck J.C., Sheffield V., Parvari R.
    Eur. J. Hum. Genet. 18:1160-1165(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: study presents the association of a mutation in the SDHA gene with recessive neonatal isolated dilated cardiomyopathy in 15 patients of two large consanguineous Bedouin familiesImported.
    Source: GeneRIF:6389.

    This publication is mapped to 5 other entries.

  16. 16
    "Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."
    Hendrickson S.L., Lautenberger J.A., Chinn L.W., Malasky M., Sezgin E., Kingsley L.A., Goedert J.J., Kirk G.D., Gomperts E.D., Buchbinder S.P., Troyer J.L., O'Brien S.J.
    PLoS ONE 5:e12862-e12862(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 3038 other entries.

  17. 17
    "SDHA loss-of-function mutations in KIT-PDGFRA wild-type gastrointestinal stromal tumors identified by massively parallel sequencing."
    Pantaleo M.A., Astolfi A., Indio V., Moore R., Thiessen N., Heinrich M.C., Gnocchi C., Santini D., Catena F., Formica S., Martelli P.L., Casadio R., Pession A., Biasco G.
    J. Natl. Cancer Inst. 103:983-987(2011) [PubMed] [Europe PMC] [Abstract]
    Annotation: First report describing germline and somatic loss-of-function mutations in SDHA that are linked to the development of sporadic KIT/PDGFRA wild-type GISTs.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  18. 18
    "Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degeneration."
    Martins-de-Souza D., Guest P.C., Mann D.M., Roeber S., Rahmoune H., Bauder C., Kretzschmar H., Volk B., Baborie A., Bahn S.
    J. Proteome Res. 11:2533-2543(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: A protein encoded by this locus was found to be differentially expressed in postmortem brains from patients with atypical frontotemporal lobar degeneration.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 424 other entries.

  19. 19
    "Inhibition of alpha-KG-dependent histone and DNA demethylases by fumarate and succinate that are accumulated in mutations of FH and SDH tumor suppressors."
    Xiao M., Yang H., Xu W., Ma S., Lin H., Zhu H., Liu L., Liu Y., Yang C., Xu Y., Zhao S., Ye D., Xiong Y., Guan K.L.
    Genes Dev. 26:1326-1338(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: Tumor-derived FH and SDH mutations accumulate fumarate and succinate leading to enzymatic inhibition of multiple alpha-KG-dependent dioxygenases and consequent alterations of genome-wide histone and DNA methylation.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 18 other entries.

  20. 20
    "Loss of expression of SDHA predicts SDHA mutations in gastrointestinal stromal tumors."
    Wagner A.J., Remillard S.P., Zhang Y.X., Doyle L.A., George S., Hornick J.L.
    Mod. Pathol. 26:289-294(2013) [PubMed] [Europe PMC] [Abstract]
    Annotation: Loss of SDHA expression in gastrointestinal stromal tumor (GIST) reliably predicts the presence of SDHA mutations which represent a relatively common cause of SDH-deficient GIST in adults.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  21. 21
    "Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency."
    Alston C.L., Davison J.E., Meloni F., van der Westhuizen F.H., He L., Hornig-Do H.T., Peet A.C., Gissen P., Goffrini P., Ferrero I., Wassmer E., McFarland R., Taylor R.W.
    J. Med. Genet. 49:569-577(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: This report represents the first example of SDHB mutation as a cause of inherited mitochondrial respiratory chain disease and extends the SDHA mutation spectrum in patients with isolated complex II deficiency.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 9 other entries.

  22. 22
    "SDHA loss of function mutations in a subset of young adult wild-type gastrointestinal stromal tumors."
    Italiano A., Chen C.L., Sung Y.S., Singer S., DeMatteo R.P., LaQuaglia M.P., Besmer P., Socci N., Antonescu C.R.
    BMC Cancer 12:408-408(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: A germline p.Arg31X nonsense SDHA mutation was identified in one of the six wild-type gastrointestinal stromal tumors cases. An additional SDHA missense mutation was identified in the extended KIT/PDGFRA WT GIST patients cohort.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  23. 23
    "Respiratory chain complex II as general sensor for apoptosis."
    Grimm S.
    Biochim. Biophys. Acta 1827:565-572(2013) [PubMed] [Europe PMC] [Abstract]
    Annotation: Studies indicate that the pH change leads to the dissociation of SDHA and SDHB subunits from the remaining membrane-anchored subunits and the consequent block of enzymatic succinate-ubiquinone reductase (SQR) activity.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 8 other entries.

  24. 24
    "Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors."
    Dwight T., Benn D.E., Clarkson A., Vilain R., Lipton L., Robinson B.G., Clifton-Bligh R.J., Gill A.J.
    Am. J. Surg. Pathol. 37:226-233(2013) [PubMed] [Europe PMC] [Abstract]
    Annotation: Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 6 other entries.

  25. 25
    "Overexpression of insulin-like growth factor 1 receptor and frequent mutational inactivation of SDHA in wild-type SDHB-negative gastrointestinal stromal tumors."
    Belinsky M.G., Rink L., Flieder D.B., Jahromi M.S., Schiffman J.D., Godwin A.K., Mehren M.v.
    Genes Chromosomes Cancer 52:214-224(2013) [PubMed] [Europe PMC] [Abstract]
    Annotation: Data indicate that SDHB-deficiency was tightly associated with overexpression of IGF1R protein and transcript and Biallelic inactivation of the SDHA gene was identified in 5 of 11 SDHB-negative gastrointestinal stromal tumors.Imported.
    Source: GeneRIF:6389.

    This publication is mapped to 8 other entries.

1 to 25 of 50  Show

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