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Items: 19


Renal cell carcinoma with angioleiomyoma-like stroma and clear cell papillary renal cell carcinoma: exploring SDHB protein immunohistochemistry and the relationship to tuberous sclerosis complex.

Williamson SR, Hornick JL, Eble JN, Gupta NS, Rogers CG, True L, Grignon DJ, Cheng L.

Hum Pathol. 2018 May;75:10-15. doi: 10.1016/j.humpath.2017.11.013. Epub 2017 Nov 24.


Orbital Paraganglioma and Succinate Dehydrogenase Staining for Genetic Testing Triage and Prognosis.

Salinas-La Rosa CM.

Ocul Oncol Pathol. 2015 Sep;2(1):36-9. doi: 10.1159/000436973. Epub 2015 Jul 15.


Renal Cell Carcinoma Occurring in Patients With Prior Neuroblastoma: A Heterogenous Group of Neoplasms.

Falzarano SM, McKenney JK, Montironi R, Eble JN, Osunkoya AO, Guo J, Zhou S, Xiao H, Dhanasekaran SM, Shukla S, Mehra R, Magi-Galluzzi C.

Am J Surg Pathol. 2016 Jul;40(7):989-97. doi: 10.1097/PAS.0000000000000632.


SDHD immunohistochemistry: a new tool to validate SDHx mutations in pheochromocytoma/paraganglioma.

Menara M, Oudijk L, Badoual C, Bertherat J, Lepoutre-Lussey C, Amar L, Iturrioz X, Sibony M, Zinzindohoué F, de Krijger R, Gimenez-Roqueplo AP, Favier J.

J Clin Endocrinol Metab. 2015 Feb;100(2):E287-91. doi: 10.1210/jc.2014-1870. Epub 2014 Nov 18.


Succinate dehydrogenase-deficient renal cell carcinoma: detailed characterization of 11 tumors defining a unique subtype of renal cell carcinoma.

Williamson SR, Eble JN, Amin MB, Gupta NS, Smith SC, Sholl LM, Montironi R, Hirsch MS, Hornick JL.

Mod Pathol. 2015 Jan;28(1):80-94. doi: 10.1038/modpathol.2014.86. Epub 2014 Jul 18.


Renal cell carcinoma in tuberous sclerosis complex.

Yang P, Cornejo KM, Sadow PM, Cheng L, Wang M, Xiao Y, Jiang Z, Oliva E, Jozwiak S, Nussbaum RL, Feldman AS, Paul E, Thiele EA, Yu JJ, Henske EP, Kwiatkowski DJ, Young RH, Wu CL.

Am J Surg Pathol. 2014 Jul;38(7):895-909. doi: 10.1097/PAS.0000000000000237.


Green tea epigallocatechin gallate binds to and inhibits respiratory complexes in swelling but not normal rat hepatic mitochondria.

Weng Z, Zhou P, Salminen WF, Yang X, Harrill AH, Cao Z, Mattes WB, Mendrick DL, Shi Q.

Biochem Biophys Res Commun. 2014 Jan 17;443(3):1097-104. doi: 10.1016/j.bbrc.2013.12.110. Epub 2013 Dec 31.


Phospho-mTOR is not upregulated in metastatic SDHB paragangliomas.

Ghayee HK, Giubellino A, Click A, Kapur P, Christie A, Xie XJ, Martucci V, Shay JW, Souza RF, Pacak K.

Eur J Clin Invest. 2013 Sep;43(9):970-7. doi: 10.1111/eci.12127. Epub 2013 Jul 26.


Succinate dehydrogenase expression in breast cancer.

Kim S, Kim DH, Jung WH, Koo JS.

Springerplus. 2013 Jul 3;2(1):299. doi: 10.1186/2193-1801-2-299. Print 2013 Dec.


Rationale for anti-angiogenic therapy in pheochromocytoma and paraganglioma.

Favier J, Igaz P, Burnichon N, Amar L, Libé R, Badoual C, Tissier F, Bertherat J, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP.

Endocr Pathol. 2012 Mar;23(1):34-42. doi: 10.1007/s12022-011-9189-0.


Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells.

Cervera AM, Bayley JP, Devilee P, McCreath KJ.

Mol Cancer. 2009 Oct 22;8:89. doi: 10.1186/1476-4598-8-89.


Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors.

Matyakhina L, Bei TA, McWhinney SR, Pasini B, Cameron S, Gunawan B, Stergiopoulos SG, Boikos S, Muchow M, Dutra A, Pak E, Campo E, Cid MC, Gomez F, Gaillard RC, Assie G, Füzesi L, Baysal BE, Eng C, Carney JA, Stratakis CA.

J Clin Endocrinol Metab. 2007 Aug;92(8):2938-43. Epub 2007 May 29.


Functioning paraganglioma and gastrointestinal stromal tumor of the jejunum in three women: syndrome or coincidence.

Perry CG, Young WF Jr, McWhinney SR, Bei T, Stergiopoulos S, Knudson RA, Ketterling RP, Eng C, Stratakis CA, Carney JA.

Am J Surg Pathol. 2006 Jan;30(1):42-9.


Active succinate dehydrogenase (SDH) and lack of SDHD mutations in sporadic paragangliomas.

Braun S, Riemann K, Kupka S, Leistenschneider P, Sotlar K, Schmid H, Blin N.

Anticancer Res. 2005 Jul-Aug;25(4):2809-14.


Evidence of increased microvessel density and activation of the hypoxia pathway in tumours from the hereditary leiomyomatosis and renal cell cancer syndrome.

Pollard P, Wortham N, Barclay E, Alam A, Elia G, Manek S, Poulsom R, Tomlinson I.

J Pathol. 2005 Jan;205(1):41-9.


Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.

Hensen EF, Jordanova ES, van Minderhout IJ, Hogendoorn PC, Taschner PE, van der Mey AG, Devilee P, Cornelisse CJ.

Oncogene. 2004 May 20;23(23):4076-83.


Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma.

Gimenez-Roqueplo AP, Favier J, Rustin P, Rieubland C, Kerlan V, Plouin PF, Rötig A, Jeunemaitre X.

J Clin Endocrinol Metab. 2002 Oct;87(10):4771-4.


The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway.

Gimenez-Roqueplo AP, Favier J, Rustin P, Mourad JJ, Plouin PF, Corvol P, Rötig A, Jeunemaitre X.

Am J Hum Genet. 2001 Dec;69(6):1186-97. Epub 2001 Oct 16.


Characterization of the human SDHC gene encoding of the integral membrane proteins of succinate-quinone oxidoreductase in mitochondria.

Elbehti-Green A, Au HC, Mascarello JT, Ream-Robinson D, Scheffler IE.

Gene. 1998 Jun 15;213(1-2):133-40.


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