BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Brain cancer AND SDHC, CYBL, 6391, ENSG00000143252, SDH3, PGL3, QPS1, CYB560
22 results:

  • 1. Pituitary tumours: molecular and genetic aspects.
    De Sousa SMC; Lenders NF; Lamb LS; Inder WJ; McCormack A
    J Endocrinol; 2023 Jun; 257(3):. PubMed ID: 36951812
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Succinate dehydrogenase complex subunit C: Role in cellular physiology and disease.
    Wang Q; Li M; Zeng N; Zhou Y; Yan J
    Exp Biol Med (Maywood); 2023 Feb; 248(3):263-270. PubMed ID: 36691338
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Computed tomography scan radiation and brain cancer incidence.
    Smoll NR; Brady Z; Scurrah KJ; Lee C; Berrington de González A; Mathews JD
    Neuro Oncol; 2023 Jul; 25(7):1368-1376. PubMed ID: 36638155
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  • 4. Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours.
    Loughrey PB; Roncaroli F; Healy E; Weir P; Basetti M; Casey RT; Hunter SJ; Korbonits M
    Endocr Relat Cancer; 2022 Oct; 29(10):R157-R172. PubMed ID: 35938916
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  • 5. Alternative Promoters of
    Zhawar VK; Kandpal RP; Athwal RS
    Genes (Basel); 2022 Mar; 13(3):. PubMed ID: 35328043
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  • 6. Germinal defects of SDHx genes in patients with isolated pituitary adenoma.
    Mougel G; Lagarde A; Albarel F; Essamet W; Luigi P; Mouly C; Vialon M; Cuny T; Castinetti F; Saveanu A; Brue T; Barlier A; Romanet P
    Eur J Endocrinol; 2020 Oct; 183(4):369-379. PubMed ID: 32621582
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  • 7. Pheochromocytoma, paragangliomas, and pituitary adenoma: An unusual association in a patient with an SDHD mutation. Case report.
    Lemelin A; Lapoirie M; Abeillon J; Lasolle H; Giraud S; Philouze P; Ceruse P; Raverot G; Vighetto A; Borson-Chazot F
    Medicine (Baltimore); 2019 Jul; 98(30):e16594. PubMed ID: 31348302
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  • 8. Stereotactic radiosurgery to surgical cavity post resection of brain metastases: Local recurrence and overall survival rates. A single-centre experience.
    Higgins MJ; Burke O; Fitzpatrick D; Nugent KG; Skourou C; Dunne M; Javadpour M; Faul C
    J Med Imaging Radiat Oncol; 2018 Oct; 62(5):726-733. PubMed ID: 30044047
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma.
    Capasso M; McDaniel LD; Cimmino F; Cirino A; Formicola D; Russell MR; Raman P; Cole KA; Diskin SJ
    J Cell Mol Med; 2017 Dec; 21(12):3224-3230. PubMed ID: 28667701
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours.
    De Sousa SMC; McCabe MJ; Wu K; Roscioli T; Gayevskiy V; Brook K; Rawlings L; Scott HS; Thompson TJ; Earls P; Gill AJ; Cowley MJ; Dinger ME; McCormack AI
    Eur J Endocrinol; 2017 May; 176(5):635-644. PubMed ID: 28220018
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  • 11. Conventional Risk Stratification Fails to Predict Progression of Succinate Dehydrogenase-deficient Gastrointestinal Stromal Tumors: A Clinicopathologic Study of 76 Cases.
    Mason EF; Hornick JL
    Am J Surg Pathol; 2016 Dec; 40(12):1616-1621. PubMed ID: 27340750
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  • 12. 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. PubMed ID: 26259135
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  • 13. R-MPV followed by high-dose chemotherapy with TBC and autologous stem-cell transplant for newly diagnosed primary CNS lymphoma.
    Omuro A; Correa DD; DeAngelis LM; Moskowitz CH; Matasar MJ; Kaley TJ; Gavrilovic IT; Nolan C; Pentsova E; Grommes CC; Panageas KS; Baser RE; Faivre G; Abrey LE; Sauter CS
    Blood; 2015 Feb; 125(9):1403-10. PubMed ID: 25568347
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.
    Dénes J; Swords F; Rattenberry E; Stals K; Owens M; Cranston T; Xekouki P; Moran L; Kumar A; Wassif C; Fersht N; Baldeweg SE; Morris D; Lightman S; Agha A; Rees A; Grieve J; Powell M; Boguszewski CL; Dutta P; Thakker RV; Srirangalingam U; Thompson CJ; Druce M; Higham C; Davis J; Eeles R; Stevenson M; O'Sullivan B; Taniere P; Skordilis K; Gabrovska P; Barlier A; Webb SM; Aulinas A; Drake WM; Bevan JS; Preda C; Dalantaeva N; Ribeiro-Oliveira A; Garcia IT; Yordanova G; Iotova V; Evanson J; Grossman AB; Trouillas J; Ellard S; Stratakis CA; Maher ER; Roncaroli F; Korbonits M
    J Clin Endocrinol Metab; 2015 Mar; 100(3):E531-41. PubMed ID: 25494863
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  • 15. Succinate dehydrogenase deficiency is rare in pituitary adenomas.
    Gill AJ; Toon CW; Clarkson A; Sioson L; Chou A; Winship I; Robinson BG; Benn DE; Clifton-Bligh RJ; Dwight T
    Am J Surg Pathol; 2014 Apr; 38(4):560-6. PubMed ID: 24625421
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  • 16. Hyperacetylation of histone H3K9 involved in the promotion of abnormally high transcription of the gdnf gene in glioma cells.
    Yu ZQ; Zhang BL; Ni HB; Liu ZH; Wang JC; Ren QX; Mo JB; Xiong Y; Yao RQ; Gao DS
    Mol Neurobiol; 2014 Dec; 50(3):914-22. PubMed ID: 24619502
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Unusual case of Cowden-like syndrome, neck paraganglioma, and pituitary adenoma.
    Efstathiadou ZA; Sapranidis M; Anagnostis P; Kita MD
    Head Neck; 2014 Jan; 36(1):E12-6. PubMed ID: 23804288
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  • 18. Connecting molecular pathways to hereditary cancer risk syndromes.
    Testa JR; Malkin D; Schiffman JD
    Am Soc Clin Oncol Educ Book; 2013; ():81-90. PubMed ID: 23714463
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  • 19. Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma.
    Dwight T; Mann K; Benn DE; Robinson BG; McKelvie P; Gill AJ; Winship I; Clifton-Bligh RJ
    J Clin Endocrinol Metab; 2013 Jun; 98(6):E1103-8. PubMed ID: 23633203
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency.
    Alston CL; Davison JE; Meloni F; van der Westhuizen FH; He L; Hornig-Do HT; Peet AC; Gissen P; Goffrini P; Ferrero I; Wassmer E; McFarland R; Taylor RW
    J Med Genet; 2012 Sep; 49(9):569-77. PubMed ID: 22972948
    [TBL] [Abstract] [Full Text] [Related]  


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