Terms: = Thyroid cancer AND SDHD, PGL1, 6392, ENSG00000204370, PGL, SDH4, CBT1, O14521
51 results:
1. Prospective Validation of ThyroSPEC Molecular Testing of Indeterminate thyroid Nodule Cytology Following Diagnostic Pathway Optimization.
Stewardson P; Eszlinger M; Wu J; Khalil M; Box A; Perizzolo M; Punjwani Z; Ziehr B; Sanyal R; Demetrick DJ; Paschke R
Thyroid; 2023 Dec; 33(12):1423-1433. PubMed ID: 37742115
[No Abstract] [Full Text] [Related]
2. Somatic IDH1 Hotspot Variants in Chinese Patients With Pheochromocytomas and Paragangliomas.
Li M; He Y; Pang Y; Zhang J; Feng Y; He Y; Xu X; Wei Y; Zhong D; Deng W; Wang L; Yan B; Jiang Y; Xu N; Cai H; Wen Y; Ning J; Liu Y; Gao X; Shan Z; Liu L; Teng X; Richter S; Jiang J
J Clin Endocrinol Metab; 2023 Apr; 108(5):1215-1223. PubMed ID: 36355572
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3. Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort.
Savatt JM; Ortiz NM; Thone GM; McDonald WS; Kelly MA; Berry ASF; Alvi MM; Hallquist MLG; Malinowski J; Purdy NC; Williams MS; Sturm AC; Buchanan AH
BMC Med; 2022 Jun; 20(1):205. PubMed ID: 35668420
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4. Long Noncoding RNA LOC554202 Predicts a Poor Prognosis and Correlates with Immune Infiltration in thyroid cancer.
Chen C; Qin L; Xiao MF
Comput Math Methods Med; 2022; 2022():3585626. PubMed ID: 35265169
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5. Identification of Dysregulated Expression of G Protein Coupled Receptors in Endocrine Tumors by Bioinformatics Analysis: Potential Drug Targets?
Suteau V; Munier M; Ben Boubaker R; Wery M; Henrion D; Rodien P; Briet C
Cells; 2022 Feb; 11(4):. PubMed ID: 35203352
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6. [Endocrine and neuroendocrine tumors].
Riss P; Scheuba K; Strobel O
Chirurg; 2021 Nov; 92(11):996-1002. PubMed ID: 34618164
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7. Non-medullary thyroid cancer Susceptibility Genes: Evidence and Disease Spectrum.
Zhou J; Singh P; Yin K; Wang J; Bao Y; Wu M; Pathak K; McKinley SK; Braun D; Lubitz CC; Hughes KS
Ann Surg Oncol; 2021 Oct; 28(11):6590-6600. PubMed ID: 33660127
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8. Carotid Body Tumor - radiological imaging and genetic assessment.
Berger G; Łukasiewicz A; Grinevych V; Tarasów E
Pol Przegl Chir; 2020 Nov; 92(6):39-44. PubMed ID: 33408267
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9. Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population.
Choi H; Kim KJ; Hong N; Shin S; Choi JR; Kang SW; Lee ST; Rhee Y
Endocrinol Metab (Seoul); 2020 Dec; 35(4):858-872. PubMed ID: 33397040
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10. Immunohistochemical distinction of paragangliomas from epithelial neuroendocrine tumors-gangliocytic duodenal and cauda equina paragangliomas align with epithelial neuroendocrine tumors.
Mamilla D; Manukyan I; Fetsch PA; Pacak K; Miettinen M
Hum Pathol; 2020 Sep; 103():72-82. PubMed ID: 32668278
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11. Pycnodysostosis with novel gene mutation and sporadic medullary thyroid carcinoma: A case report.
Shi X; Huang C; Xiao F; Liu W; Zeng J; Li X
Medicine (Baltimore); 2017 Dec; 96(50):e8730. PubMed ID: 29390266
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12.
Ashtekar A; Huk D; Magner A; La Perle K; Zhang X; Piruat JI; López-Barneo J; Jhiang SM; Kirschner LS
Endocr Relat Cancer; 2017 Nov; 24(11):579-591. PubMed ID: 28928232
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13. ATTITUDES TOWARD GENETIC COUNSELING AND TESTING IN PATIENTS WITH INHERITED ENDOCRINOPATHIES.
Gallagher TM; Bucciarelli M; Kavalukas SL; Baker MJ; Saunders BD
Endocr Pract; 2017 Sep; 23(9):1039-1044. PubMed ID: 28613942
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14. Cowden syndrome-associated germline succinate dehydrogenase complex subunit D (sdhd) variants cause PTEN-mediated down-regulation of autophagy in thyroid cancer cells.
Yu W; Ni Y; Saji M; Ringel MD; Jaini R; Eng C
Hum Mol Genet; 2017 Apr; 26(7):1365-1375. PubMed ID: 28164237
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15. A novel RET gene mutation in a patient with apparently sporadic pheochromocytoma.
Scollo C; Russo M; De Gregorio L; Terranova R; Mangione E; Castoro C; Squatrito S; Pellegriti G
Endocr J; 2016; 63(1):87-91. PubMed ID: 26497911
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16. Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis.
Bugalho MJ; Silva AL; Domingues R
Fam Cancer; 2015 Dec; 14(4):603-7. PubMed ID: 26071763
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17. A registry-based study of thyroid paraganglioma: histological and genetic characteristics.
von Dobschuetz E; Leijon H; Schalin-Jäntti C; Schiavi F; Brauckhoff M; Peczkowska M; Spiazzi G; Demattè S; Cecchini ME; Sartorato P; Krajewska J; Hasse-Lazar K; Roszkowska-Purska K; Taschin E; Malinoc A; Akslen LA; Arola J; Lange D; Fassina A; Pennelli G; Barbareschi M; Luettges J; Prejbisz A; Januszewicz A; Strate T; Bausch B; Castinetti F; Jarzab B; Opocher G; Eng C; Neumann HP
Endocr Relat Cancer; 2015 Apr; 22(2):191-204. PubMed ID: 25595276
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18. 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; 24(1):142-53. PubMed ID: 25149476
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19. Genetics, diagnosis, and management of medullary thyroid carcinoma and pheochromocytoma/paraganglioma.
Moraitis AG; Martucci VL; Pacak K
Endocr Pract; 2014 Feb; 20(2):176-87. PubMed ID: 24449662
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20. Non-pheochromocytoma (PCC)/paraganglioma (pgl) tumors in patients with succinate dehydrogenase-related PCC-pgl syndromes: a clinicopathological and molecular analysis.
Papathomas TG; Gaal J; Corssmit EP; Oudijk L; Korpershoek E; Heimdal K; Bayley JP; Morreau H; van Dooren M; Papaspyrou K; Schreiner T; Hansen T; Andresen PA; Restuccia DF; van Kessel I; van Leenders GJ; Kros JM; Looijenga LH; Hofland LJ; Mann W; van Nederveen FH; Mete O; Asa SL; de Krijger RR; Dinjens WN
Eur J Endocrinol; 2014 Jan; 170(1):1-12. PubMed ID: 24096523
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