Terms: = Germ cell tumor AND SDHC, CYBL, 6391, ENSG00000143252, SDH3, PGL3, QPS1, CYB560
312 results:
1. Genotype-phenotype associations in paragangliomas of the temporal bone in a multi-ethnic cohort.
Angeli SI; Chiossone K JA; Goncalves S; Telischi FF
Acta Otolaryngol; 2023; 143(7):551-557. PubMed ID: 37354038
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2. Abdominal nonfunctional paraganglioma in which succinate dehydrogenase subunit B (SDHB) immunostaining was performed: a case report.
Tanaka T; Joraku A; Ishibashi S; Endo K; Emura M; Kikuchi Y; Shikama A; Kimura N; Shimazui T
J Med Case Rep; 2023 Mar; 17(1):106. PubMed ID: 36945070
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3. Back to Biochemistry: Evaluation for and Prognostic Significance of SDH Mutations in Paragangliomas and Pheochromocytomas.
Gupta S; Erickson LA
Surg Pathol Clin; 2023 Mar; 16(1):119-129. PubMed ID: 36739159
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4. Kidney tumors associated with germline mutations of FH and SDHB show a CpG island methylator phenotype (CIMP).
Ricketts CJ; Killian JK; Vocke CD; Wang Y; Merino MJ; Meltzer PS; Linehan WM
PLoS One; 2022; 17(12):e0278108. PubMed ID: 36455002
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5. Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases.
Araujo PB; Carvallo MS; Vidal AP; Nascimento JB; Wo JM; Naliato EO; Cunha Neto SH; Conceição FL; Fontes R; de Lima VV; Carvalho DP; Soares P; Lima J; Lourenço DM; Violante AHD
Front Endocrinol (Lausanne); 2022; 13():903085. PubMed ID: 36187102
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6. Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas.
Bayley JP; Rebel HG; Scheurwater K; Duesman D; Zhang J; Schiavi F; Korpershoek E; Jansen JC; Schepers A; Devilee P
PLoS One; 2022; 17(9):e0274478. PubMed ID: 36178902
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7. Novel germline
Provenzano A; Chetta M; De Filpo G; Cantini G; La Barbera A; Nesi G; Santi R; Martinelli S; Rapizzi E; Luconi M; Maggi M; Mannelli M; Ercolino T; Canu L
Medicina (Kaunas); 2022 Aug; 58(8):. PubMed ID: 36013579
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8. Succinate: A Serum Biomarker of SDHB-Mutated Paragangliomas and Pheochromocytomas.
Lamy C; Tissot H; Faron M; Baudin E; Lamartina L; Pradon C; Al Ghuzlan A; Leboulleux S; Perfettini JL; Paci A; Hadoux J; Broutin S
J Clin Endocrinol Metab; 2022 Sep; 107(10):2801-2810. PubMed ID: 35948272
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9. 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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10. Serum fatty acid profiling in patients with SDHx mutations: New advances on cellular metabolism in SDH deficiency.
Vamecq J; Masso V; Bancel LP; Jannin A; Dessein AF; Cardot-Bauters C; Pigny P
Biochimie; 2022 Oct; 201():196-203. PubMed ID: 35870552
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11. An exploration in pitfalls in interpreting SDHB immunohistochemistry.
Ding CC; Chan S; Mak J; Umetsu SE; Simko JP; Ruiz-Cordero R; Saunders T; Chan E
Histopathology; 2022 Aug; 81(2):264-269. PubMed ID: 35546442
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12. SDHB and SDHD silenced pheochromocytoma spheroids respond differently to tumour microenvironment and their aggressiveness is inhibited by impairing stroma metabolism.
Martinelli S; Riverso M; Mello T; Amore F; Parri M; Simeone I; Mannelli M; Maggi M; Rapizzi E
Mol Cell Endocrinol; 2022 May; 547():111594. PubMed ID: 35149119
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13. Universal germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield.
Horton C; LaDuca H; Deckman A; Durda K; Jackson M; Richardson ME; Tian Y; Yussuf A; Jasperson K; Else T
J Clin Endocrinol Metab; 2022 Apr; 107(5):e1917-e1923. PubMed ID: 35026032
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14. sdhc phaeochromocytoma and paraganglioma: A UK-wide case series.
Williams ST; Chatzikyriakou P; Carroll PV; McGowan BM; Velusamy A; White G; Obholzer R; Akker S; Tufton N; Casey RT; Maher ER; Park SM; Porteous M; Dyer R; Tan T; Wernig F; Brady AF; Kosicka-Slawinska M; Whitelaw BC; Dorkins H; Lalloo F; Brennan P; Carlow J; Martin R; Mitchell AL; Harrison R; Hawkes L; Newell-Price J; Kelsall A; Igbokwe R; Adlard J; Schirwani S; Davidson R; Morrison PJ; Chung TT; Bowles C; Izatt L
Clin Endocrinol (Oxf); 2022 Apr; 96(4):499-512. PubMed ID: 34558728
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15. Substance P containing peptide gene delivery vectors for specifically transfecting glioma cells mediated by a neurokinin-1 receptor.
Ding G; Wang T; Han Z; Tian L; Cheng Q; Luo L; Zhao B; Wang C; Feng S; Wang L; Meng Z; Meng Q
J Mater Chem B; 2021 Aug; 9(32):6347-6356. PubMed ID: 34251002
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16. Carney Triad, Carney-Stratakis Syndrome, 3PAS and Other tumors Due to SDH Deficiency.
Pitsava G; Settas N; Faucz FR; Stratakis CA
Front Endocrinol (Lausanne); 2021; 12():680609. PubMed ID: 34012423
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17. The emerging clinical relevance of genomic profiling in neuroendocrine tumours.
Burak GI; Ozge S; Cem M; Gulgun B; Zeynep DY; Atil B
BMC Cancer; 2021 Mar; 21(1):234. PubMed ID: 33676450
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18. sdhc Methylation Pattern in Patients With Carney Triad.
Daumova M; Svajdler M; Fabian P; Kren L; Babankova I; Jezova M; Sedivcova M; Vanecek T; Behenska K; Michal M; Daum O
Appl Immunohistochem Mol Morphol; 2021 Sep; 29(8):599-605. PubMed ID: 33624983
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19. Genetic and Clinical Profiles of Pheochromocytoma and Paraganglioma: A Single Center Study.
Ma X; Li M; Tong A; Wang F; Cui Y; Zhang X; Zhang Y; Chen S; Li Y
Front Endocrinol (Lausanne); 2020; 11():574662. PubMed ID: 33362715
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20. Head and neck paragangliomas in Norway, importance of genetics, updated diagnostic workup and treatment.
Rana MU; Østhus AA; Heimdal K; Jebsen P; Revheim MR; Osnes TA
Acta Otolaryngol; 2021 Mar; 141(3):303-308. PubMed ID: 33320715
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