215 related articles for article (PubMed ID: 37262072)
1. Mitochondrial-Encoded Complex I Impairment Induces a Targetable Dependency on Aerobic Fermentation in Hürthle Cell Carcinoma of the Thyroid.
Frank AR; Li V; Shelton SD; Kim J; Stott GM; Neckers LM; Xie Y; Williams NS; Mishra P; McFadden DG
Cancer Discov; 2023 Aug; 13(8):1884-1903. PubMed ID: 37262072
[TBL] [Abstract][Full Text] [Related]
2. Forward Genetic Screens Identify Mechanisms of Resistance to Small-Molecule Lactate Dehydrogenase Inhibitors.
Frank AR; Vandiver F; McFadden DG
ACS Chem Biol; 2024 Feb; 19(2):471-482. PubMed ID: 38270591
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors.
Máximo V; Soares P; Lima J; Cameselle-Teijeiro J; Sobrinho-Simões M
Am J Pathol; 2002 May; 160(5):1857-65. PubMed ID: 12000737
[TBL] [Abstract][Full Text] [Related]
4. Forward genetic screens identify mechanisms of resistance to small molecule lactate dehydrogenase inhibitors.
Frank AR; Vandiver F; McFadden DG
bioRxiv; 2023 Sep; ():. PubMed ID: 37808702
[TBL] [Abstract][Full Text] [Related]
5. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
6. Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.
Mayr JA; Meierhofer D; Zimmermann F; Feichtinger R; Kögler C; Ratschek M; Schmeller N; Sperl W; Kofler B
Clin Cancer Res; 2008 Apr; 14(8):2270-5. PubMed ID: 18413815
[TBL] [Abstract][Full Text] [Related]
7. Short Review: Genomic Alterations in Hürthle Cell Carcinoma.
Ganly I; McFadden DG
Thyroid; 2019 Apr; 29(4):471-479. PubMed ID: 30848171
[TBL] [Abstract][Full Text] [Related]
8. Hürthle (oncocytic) cell tumors of thyroid: etiopathogenesis, diagnosis and clinical significance.
Sobrinho-Simões M; Máximo V; Castro IV; Fonseca E; Soares P; Garcia-Rostan G; Oliveira MC
Int J Surg Pathol; 2005 Jan; 13(1):29-35. PubMed ID: 15735852
[TBL] [Abstract][Full Text] [Related]
9. The biology and the genetics of Hurthle cell tumors of the thyroid.
Máximo V; Lima J; Prazeres H; Soares P; Sobrinho-Simões M
Endocr Relat Cancer; 2012 Aug; 19(4):R131-47. PubMed ID: 22514109
[TBL] [Abstract][Full Text] [Related]
10. Effectors Enabling Adaptation to Mitochondrial Complex I Loss in Hürthle Cell Carcinoma.
Gopal RK; Vantaku VR; Panda A; Reimer B; Rath S; To TL; Fisch AS; Cetinbas M; Livneh M; Calcaterra MJ; Gigliotti BJ; Pierce KA; Clish CB; Dias-Santagata D; Sadow PM; Wirth LJ; Daniels GH; Sadreyev RI; Calvo SE; Parangi S; Mootha VK
Cancer Discov; 2023 Aug; 13(8):1904-1921. PubMed ID: 37262067
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA "common deletion" in post-fine needle aspiration infarcted oncocytic thyroid tumors.
Conti L; Vatrano S; Bertero L; Masu L; Pacchioni D; Daniele L; De Rosa G; Cassoni P; Volante M; Papotti M
Hum Pathol; 2017 Nov; 69():23-30. PubMed ID: 28962946
[TBL] [Abstract][Full Text] [Related]
12. Core I gene is overexpressed in Hürthle and non-Hürthle cell microfollicular adenomas and follicular carcinomas of the thyroid.
Máximo V; Preto A; Crespo A; Rocha AS; Machado JC; Soares P; Sobrinho-Simões M
BMC Cancer; 2004 Mar; 4():12. PubMed ID: 15043758
[TBL] [Abstract][Full Text] [Related]
13. Clinical utility of EZH1 mutations in the diagnosis of follicular-patterned thyroid tumors.
Jung CK; Kim Y; Jeon S; Jo K; Lee S; Bae JS
Hum Pathol; 2018 Nov; 81():9-17. PubMed ID: 29723601
[TBL] [Abstract][Full Text] [Related]
14. Hürthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance.
Máximo V; Sobrinho-Simões M
Virchows Arch; 2000 Aug; 437(2):107-15. PubMed ID: 10993269
[TBL] [Abstract][Full Text] [Related]
15. Somatic and germline mutation in GRIM-19, a dual function gene involved in mitochondrial metabolism and cell death, is linked to mitochondrion-rich (Hurthle cell) tumours of the thyroid.
Máximo V; Botelho T; Capela J; Soares P; Lima J; Taveira A; Amaro T; Barbosa AP; Preto A; Harach HR; Williams D; Sobrinho-Simões M
Br J Cancer; 2005 May; 92(10):1892-8. PubMed ID: 15841082
[TBL] [Abstract][Full Text] [Related]
16. The Molecular Landscape of Hürthle Cell Thyroid Cancer Is Associated with Altered Mitochondrial Function-A Comprehensive Review.
Kumari S; Adewale R; Klubo-Gwiezdzinska J
Cells; 2020 Jun; 9(7):. PubMed ID: 32605113
[TBL] [Abstract][Full Text] [Related]
17. EIF1AX Mutation in a Patient with Hürthle Cell Carcinoma.
Topf MC; Wang ZX; Furlong K; Miller JL; Tuluc M; Pribitkin EA
Endocr Pathol; 2018 Mar; 29(1):27-29. PubMed ID: 28965201
[TBL] [Abstract][Full Text] [Related]
18. Papillary thyroid carcinoma tall cell variant shares accumulation of mitochondria, mitochondrial DNA mutations, and loss of oxidative phosphorylation complex I integrity with oncocytic tumors.
Tsybrovskyy O; De Luise M; de Biase D; Caporali L; Fiorini C; Gasparre G; Carelli V; Hackl D; Imamovic L; Haim S; Sobrinho-Simões M; Tallini G
J Pathol Clin Res; 2022 Mar; 8(2):155-168. PubMed ID: 34792302
[TBL] [Abstract][Full Text] [Related]
19. Widespread Chromosomal Losses and Mitochondrial DNA Alterations as Genetic Drivers in Hürthle Cell Carcinoma.
Gopal RK; Kübler K; Calvo SE; Polak P; Livitz D; Rosebrock D; Sadow PM; Campbell B; Donovan SE; Amin S; Gigliotti BJ; Grabarek Z; Hess JM; Stewart C; Braunstein LZ; Arndt PF; Mordecai S; Shih AR; Chaves F; Zhan T; Lubitz CC; Kim J; Iafrate AJ; Wirth L; Parangi S; Leshchiner I; Daniels GH; Mootha VK; Dias-Santagata D; Getz G; McFadden DG
Cancer Cell; 2018 Aug; 34(2):242-255.e5. PubMed ID: 30107175
[TBL] [Abstract][Full Text] [Related]
20. Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma.
Gasparre G; Hervouet E; de Laplanche E; Demont J; Pennisi LF; Colombel M; Mège-Lechevallier F; Scoazec JY; Bonora E; Smeets R; Smeitink J; Lazar V; Lespinasse J; Giraud S; Godinot C; Romeo G; Simonnet H
Hum Mol Genet; 2008 Apr; 17(7):986-95. PubMed ID: 18156159
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
