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3. Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas. Yao L; Schiavi F; Cascon A; Qin Y; Inglada-Pérez L; King EE; Toledo RA; Ercolino T; Rapizzi E; Ricketts CJ; Mori L; Giacchè M; Mendola A; Taschin E; Boaretto F; Loli P; Iacobone M; Rossi GP; Biondi B; Lima-Junior JV; Kater CE; Bex M; Vikkula M; Grossman AB; Gruber SB; Barontini M; Persu A; Castellano M; Toledo SP; Maher ER; Mannelli M; Opocher G; Robledo M; Dahia PL JAMA; 2010 Dec; 304(23):2611-9. PubMed ID: 21156949 [TBL] [Abstract][Full Text] [Related]
4. A novel TMEM127 mutation in a patient with familial bilateral pheochromocytoma. Burnichon N; Lepoutre-Lussey C; Laffaire J; Gadessaud N; Molinié V; Hernigou A; Plouin PF; Jeunemaitre X; Favier J; Gimenez-Roqueplo AP Eur J Endocrinol; 2011 Jan; 164(1):141-5. PubMed ID: 20923864 [TBL] [Abstract][Full Text] [Related]
5. 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 [TBL] [Abstract][Full Text] [Related]
6. Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome. Patócs A; Lendvai NK; Butz H; Liko I; Sapi Z; Szucs N; Toth G; Grolmusz VK; Igaz P; Toth M; Rácz K Pathol Oncol Res; 2016 Oct; 22(4):673-9. PubMed ID: 26960314 [TBL] [Abstract][Full Text] [Related]
7. Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites. Neumann HP; Sullivan M; Winter A; Malinoc A; Hoffmann MM; Boedeker CC; Bertz H; Walz MK; Moeller LC; Schmid KW; Eng C J Clin Endocrinol Metab; 2011 Aug; 96(8):E1279-82. PubMed ID: 21613359 [TBL] [Abstract][Full Text] [Related]
8. Homozygous TMEM127 mutations in 2 patients with bilateral pheochromocytomas. Eijkelenkamp K; Olderode-Berends MJW; van der Luijt RB; Robledo M; van Dooren M; Feelders RA; de Vries J; Kerstens MN; Links TP; van der Horst-Schrivers ANA Clin Genet; 2018 May; 93(5):1049-1056. PubMed ID: 29282712 [TBL] [Abstract][Full Text] [Related]
9. Penetrance and clinical features of pheochromocytoma in a six-generation family carrying a germline TMEM127 mutation. Toledo SP; Lourenço DM; Sekiya T; Lucon AM; Baena ME; Castro CC; Bortolotto LA; Zerbini MC; Siqueira SA; Toledo RA; Dahia PL J Clin Endocrinol Metab; 2015 Feb; 100(2):E308-18. PubMed ID: 25389632 [TBL] [Abstract][Full Text] [Related]
10. Identical germline mutations in the TMEM127 gene in two unrelated Japanese patients with bilateral pheochromocytoma. Takeichi N; Midorikawa S; Watanabe A; Naing BT; Tamura H; Wakakuri-Kano T; Ishizaki A; Sugihara H; Nissato S; Saito Y; Aita Y; Ishii KA; Igarashi T; Kawakami Y; Hara H; Ikeda T; Shimizu K; Suzuki S; Shimano H; Kawamoto M; Shimada T; Watanabe T; Oikawa S; Takekoshi K Clin Endocrinol (Oxf); 2012 Nov; 77(5):707-14. PubMed ID: 22541004 [TBL] [Abstract][Full Text] [Related]
11. TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma. Abermil N; Guillaud-Bataille M; Burnichon N; Venisse A; Manivet P; Guignat L; Drui D; Chupin M; Josseaume C; Affres H; Plouin PF; Bertherat J; Jeunemaître X; Gimenez-Roqueplo AP J Clin Endocrinol Metab; 2012 May; 97(5):E805-9. PubMed ID: 22419703 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas. Welander J; Larsson C; Bäckdahl M; Hareni N; Sivlér T; Brauckhoff M; Söderkvist P; Gimm O Hum Mol Genet; 2012 Dec; 21(26):5406-16. PubMed ID: 23010473 [TBL] [Abstract][Full Text] [Related]
16. Primary Renal Paragangliomas and Renal Neoplasia Associated with Pheochromocytoma/Paraganglioma: Analysis of von Hippel-Lindau (VHL), Succinate Dehydrogenase (SDHX) and Transmembrane Protein 127 (TMEM127). Gupta S; Zhang J; Milosevic D; Mills JR; Grebe SK; Smith SC; Erickson LA Endocr Pathol; 2017 Sep; 28(3):253-268. PubMed ID: 28646318 [TBL] [Abstract][Full Text] [Related]
17. Integrity of the pheochromocytoma susceptibility TMEM127 gene in patients with pediatric malignancies. King EE; Qin Y; Toledo RA; Luo A; Ball E; Faucz FR; Janeway KA; Stratakis CA; Tomlinson GE; Dahia PL Endocr Relat Cancer; 2015 Jun; 22(3):L5-7. PubMed ID: 25770152 [No Abstract] [Full Text] [Related]
18. Minireview: the busy road to pheochromocytomas and paragangliomas has a new member, TMEM127. Jiang S; Dahia PL Endocrinology; 2011 Jun; 152(6):2133-40. PubMed ID: 21447639 [TBL] [Abstract][Full Text] [Related]
19. [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]