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Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function.

Floyd BJ, Wilkerson EM, Veling MT, Minogue CE, Xia C, Beebe ET, Wrobel RL, Cho H, Kremer LS, Alston CL, Gromek KA, Dolan BK, Ulbrich A, Stefely JA, Bohl SL, Werner KM, Jochem A, Westphall MS, Rensvold JW, Taylor RW, Prokisch H, Kim JJ, Coon JJ, Pagliarini DJ.

Mol Cell. 2016 Aug 18;63(4):621-32. doi: 10.1016/j.molcel.2016.06.033. Epub 2016 Aug 4.


Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.

Yang X, Coulombe-Huntington J, Kang S, Sheynkman GM, Hao T, Richardson A, Sun S, Yang F, Shen YA, Murray RR, Spirohn K, Begg BE, Duran-Frigola M, MacWilliams A, Pevzner SJ, Zhong Q, Trigg SA, Tam S, Ghamsari L, Sahni N, Yi S, Rodriguez MD, Balcha D, Tan G, Costanzo M, Andrews B, Boone C, Zhou XJ, Salehi-Ashtiani K, Charloteaux B, Chen AA, Calderwood MA, Aloy P, Roth FP, Hill DE, Iakoucheva LM, Xia Y, Vidal M.

Cell. 2016 Feb 11;164(4):805-17. doi: 10.1016/j.cell.2016.01.029.


[Hereditary pheochromocytoma-associated syndromes. Part 1].

Yukina MY, Troshina EA, Beltsevich DG.

Ter Arkh. 2015;87(9):102-5. Review. Russian.


Loss of succinate dehydrogenase activity results in dependency on pyruvate carboxylation for cellular anabolism.

Lussey-Lepoutre C, Hollinshead KE, Ludwig C, Menara M, Morin A, Castro-Vega LJ, Parker SJ, Janin M, Martinelli C, Ottolenghi C, Metallo C, Gimenez-Roqueplo AP, Favier J, Tennant DA.

Nat Commun. 2015 Nov 2;6:8784. doi: 10.1038/ncomms9784.


In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma.

Lussey-Lepoutre C, Bellucci A, Morin A, Buffet A, Amar L, Janin M, Ottolenghi C, Zinzindohoué F, Autret G, Burnichon N, Robidel E, Banting B, Fontaine S, Cuenod CA, Benit P, Rustin P, Halimi P, Fournier L, Gimenez-Roqueplo AP, Favier J, Tavitian B.

Clin Cancer Res. 2016 Mar 1;22(5):1120-9. doi: 10.1158/1078-0432.CCR-15-1576. Epub 2015 Oct 21.


Genetic variations in genes of metabolic enzymes predict postoperational prognosis of patients with colorectal cancer.

Dong G, He X, Chen Y, Cao H, Wang J, Liu X, Wang S, Wan S, Xing J.

Mol Cancer. 2015 Sep 17;14:171. doi: 10.1186/s12943-015-0442-x.


Analysis of SDHD promoter mutations in various types of melanoma.

Scholz SL, Horn S, Murali R, Möller I, Sucker A, Sondermann W, Stiller M, Schilling B, Livingstone E, Zimmer L, Reis H, Metz CH, Zeschnigk M, Paschen A, Steuhl KP, Schadendorf D, Westekemper H, Griewank KG.

Oncotarget. 2015 Sep 22;6(28):25868-82. doi: 10.18632/oncotarget.4665.


Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.

Niemeijer ND, Papathomas TG, Korpershoek E, de Krijger RR, Oudijk L, Morreau H, Bayley JP, Hes FJ, Jansen JC, Dinjens WN, Corssmit EP.

J Clin Endocrinol Metab. 2015 Oct;100(10):E1386-93. doi: 10.1210/jc.2015-2689. Epub 2015 Aug 10.


15 YEARS OF PARAGANGLIOMA: Genetics and mechanism of pheochromocytoma-paraganglioma syndromes characterized by germline SDHB and SDHD mutations.

Baysal BE, Maher ER.

Endocr Relat Cancer. 2015 Aug;22(4):T71-82. doi: 10.1530/ERC-15-0226. Epub 2015 Jun 25. Review.


A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency.

Alston CL, Ceccatelli Berti C, Blakely EL, Oláhová M, He L, McMahon CJ, Olpin SE, Hargreaves IP, Nolli C, McFarland R, Goffrini P, O'Sullivan MJ, Taylor RW.

Hum Genet. 2015 Aug;134(8):869-79. doi: 10.1007/s00439-015-1568-z. Epub 2015 May 26.


Role of miR-101 in pheochromocytoma patients with SDHD mutation.

Zong L, Meng L, Shi R.

Int J Clin Exp Pathol. 2015 Feb 1;8(2):1545-54. eCollection 2015.


Malignant phenotype and two SDHD mutations in a family with paraganglioma syndrome type 1.

Leidenz FB, Bastos-Rodrigues L, Oliveira M, Mamede M, Sarquis M, Friedman E, de Marco L.

Genet Res (Camb). 2015 Mar 30;97:e3. doi: 10.1017/S0016672315000063.


No evidence for increased mortality in SDHD variant carriers compared with the general population.

van Hulsteijn LT, Heesterman B, Jansen JC, Bayley JP, Hes FJ, Corssmit EP, Dekkers OM.

Eur J Hum Genet. 2015 Dec;23(12):1713-6. doi: 10.1038/ejhg.2015.36. Epub 2015 Mar 11.


Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay.

Yelavarthi K, Cabral H, Wilson GN, Rohena L, Risheg H, Penton A, Schleede J, Burnside RD.

Am J Med Genet A. 2015 Apr;167A(4):695-700. doi: 10.1002/ajmg.a.36956. Epub 2015 Mar 3.


Germline and somatic SDHx alterations in apparently sporadic differentiated thyroid cancer.

Ni Y, Seballos S, Ganapathi S, Gurin D, Fletcher B, Ngeow J, Nagy R, Kloos RT, Ringel MD, LaFramboise T, Eng C.

Endocr Relat Cancer. 2015 Apr;22(2):121-30. doi: 10.1530/ERC-14-0537.


Instability of succinate dehydrogenase in SDHD polymorphism connects reactive oxygen species production to nuclear and mitochondrial genomic mutations in yeast.

Chang YL, Hsieh MH, Chang WW, Wang HY, Lin MC, Wang CP, Lou PJ, Teng SC.

Antioxid Redox Signal. 2015 Mar 1;22(7):587-602. doi: 10.1089/ars.2014.5966. Epub 2015 Jan 13.


Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

Bayley JP, Oldenburg RA, Nuk J, Hoekstra AS, van der Meer CA, Korpershoek E, McGillivray B, Corssmit EP, Dinjens WN, de Krijger RR, Devilee P, Jansen JC, Hes FJ.

BMC Med Genet. 2014 Oct 10;15:111. doi: 10.1186/s12881-014-0111-8.


Cowden syndrome-associated germline SDHD variants alter PTEN nuclear translocation through SRC-induced PTEN oxidation.

Yu W, He X, Ni Y, Ngeow J, Eng C.

Hum Mol Genet. 2015 Jan 1;24(1):142-53. doi: 10.1093/hmg/ddu425. Epub 2014 Aug 22.

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