Terms: = Germ cell tumor AND TMEM127, FLJ20507, 55654, ENSG00000135956, O75204, FLJ22257
94 results:
1. tmem127 suppresses tumor development by promoting RET ubiquitination, positioning, and degradation.
Guo Q; Cheng ZM; Gonzalez-Cantú H; Rotondi M; Huelgas-Morales G; Ethiraj P; Qiu Z; Lefkowitz J; Song W; Landry BN; Lopez H; Estrada-Zuniga CM; Goyal S; Khan MA; Walker TJ; Wang E; Li F; Ding Y; Mulligan LM; Aguiar RCT; Dahia PLM
Cell Rep; 2023 Sep; 42(9):113070. PubMed ID: 37659079
[TBL] [Abstract] [Full Text] [Related]
2. [Bilateral pheochromocytoma associates with tmem127 gene mutation. Report of one case].
Delgado JF; Pérez E MJ; Delgado D; Lagos C; Baudrand R; Uslar T
Rev Med Chil; 2022 Aug; 150(8):1115-1118. PubMed ID: 37358160
[TBL] [Abstract] [Full Text] [Related]
3. 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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4. 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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5. 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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6. 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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7. Genetics of pheochromocytoma and paraganglioma.
Wachtel H; Fishbein L
Curr Opin Endocrinol Diabetes Obes; 2021 Jun; 28(3):283-290. PubMed ID: 33764930
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8. 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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9. Recent Advances in Histopathological and Molecular Diagnosis in Pheochromocytoma and Paraganglioma: Challenges for Predicting Metastasis in Individual Patients.
Yamazaki Y; Gao X; Pecori A; Nakamura Y; Tezuka Y; Omata K; Ono Y; Morimoto R; Satoh F; Sasano H
Front Endocrinol (Lausanne); 2020; 11():587769. PubMed ID: 33193100
[TBL] [Abstract] [Full Text] [Related]
10. Genotype-Phenotype Features of germline Variants of the tmem127 Pheochromocytoma Susceptibility Gene: A 10-Year Update.
Armaiz-Pena G; Flores SK; Cheng ZM; Zhang X; Esquivel E; Poullard N; Vaidyanathan A; Liu Q; Michalek J; Santillan-Gomez AA; Liss M; Ahmadi S; Katselnik D; Maldonado E; Salgado SA; Jimenez C; Fishbein L; Hamidi O; Else T; Lechan R; Tischler AS; Benn DE; Dwight T; Clifton-Bligh R; Sanso G; Barontini M; Vincent D; Aronin N; Biondi B; Koops M; Bowhay-Carnes E; Gimenez-Roqueplo AP; Alvarez-Eslava A; Bruder JM; Kitano M; Burnichon N; Ding Y; Dahia PLM
J Clin Endocrinol Metab; 2021 Jan; 106(1):e350-e364. PubMed ID: 33051659
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11. Functional Characterization of tmem127 Variants Reveals Novel Insights into Its Membrane Topology and Trafficking.
Flores SK; Deng Y; Cheng Z; Zhang X; Tao S; Saliba A; Chu I; Burnichon N; Gimenez-Roqueplo AP; Wang E; Aguiar RCT; Dahia PLM
J Clin Endocrinol Metab; 2020 Sep; 105(9):e3142-56. PubMed ID: 32575117
[TBL] [Abstract] [Full Text] [Related]
12. A Novel MAX Gene Mutation Variant in a Patient With Multiple and "Composite" Neuroendocrine-Neuroblastic tumors.
Pozza C; Sesti F; Di Dato C; Sbardella E; Pofi R; Schiavi F; Bonifacio V; Isidori AM; Faggiano A; Lenzi A; Giannetta E
Front Endocrinol (Lausanne); 2020; 11():234. PubMed ID: 32508744
[No Abstract] [Full Text] [Related]
13. An overview of 20 years of genetic studies in pheochromocytoma and paraganglioma.
Buffet A; Burnichon N; Favier J; Gimenez-Roqueplo AP
Best Pract Res Clin Endocrinol Metab; 2020 Mar; 34(2):101416. PubMed ID: 32295730
[TBL] [Abstract] [Full Text] [Related]
14. Malignant Intrarenal/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations.
Irwin T; Konnick EQ; Tretiakova MS
Endocr Pathol; 2019 Dec; 30(4):270-275. PubMed ID: 31705439
[TBL] [Abstract] [Full Text] [Related]
15. A systematic review on the genetic analysis of paragangliomas: primarily focused on head and neck paragangliomas.
Guha A; Musil Z; Vicha A; Zelinka T; Pacak K; Astl J; Chovanec M
Neoplasma; 2019 Sep; 66(5):671-680. PubMed ID: 31307198
[TBL] [Abstract] [Full Text] [Related]
16. A Full Phenotype of Paraganglioma Linked to a germline SDHB Mosaic Mutation.
Cardot-Bauters C; Carnaille B; Aubert S; Crépin M; Boury S; Burnichon N; Pigny P
J Clin Endocrinol Metab; 2019 Aug; 104(8):3362-3366. PubMed ID: 31046099
[TBL] [Abstract] [Full Text] [Related]
17. Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma.
Muth A; Crona J; Gimm O; Elmgren A; Filipsson K; Stenmark Askmalm M; Sandstedt J; Tengvar M; Tham E
J Intern Med; 2019 Feb; 285(2):187-204. PubMed ID: 30536464
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18. [Genetics of pheochromocytoma and the relevance in surgery].
von Dobschütz E; Neumann HPH
Chirurg; 2019 Jan; 90(1):15-22. PubMed ID: 30306232
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19. [Hereditary pheochromocytoma and paraganglioma: screening and follow-up strategies in asymptomatic mutation carriers].
Vermalle M; Tabarin A; Castinetti F
Ann Endocrinol (Paris); 2018 Sep; 79 Suppl 1():S10-S21. PubMed ID: 30213301
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20. Frequency of germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma.
Panou V; Gadiraju M; Wolin A; Weipert CM; Skarda E; Husain AN; Patel JD; Rose B; Zhang SR; Weatherly M; Nelakuditi V; Knight Johnson A; Helgeson M; Fischer D; Desai A; Sulai N; Ritterhouse L; Røe OD; Turaga KK; Huo D; Segal J; Kadri S; Li Z; Kindler HL; Churpek JE
J Clin Oncol; 2018 Oct; 36(28):2863-2871. PubMed ID: 30113886
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