These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
221 related articles for article (PubMed ID: 26184857)
21. Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors. Molatore S; Kiermaier E; Jung CB; Lee M; Pulz E; Höfler H; Atkinson MJ; Pellegata NS Mol Cancer; 2010 May; 9():116. PubMed ID: 20492666 [TBL] [Abstract][Full Text] [Related]
22. RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B. Zhou Y; Zhao Y; Cui B; Gu L; Zhu S; Li J; Liu J; Yin M; Zhao T; Yin Z; Yu C; Chen C; Wang L; Xiao B; Hong J; Zhang Y; Tang Z; Wang S; Li X; Ning G Clin Endocrinol (Oxf); 2007 Oct; 67(4):570-6. PubMed ID: 17573899 [TBL] [Abstract][Full Text] [Related]
23. Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review. Chevalier B; Coppin L; Romanet P; Cuny T; Maïza JC; Abeillon J; Forestier J; Walter T; Gilly O; Le Bras M; Smati S; Nunes ML; Geslot A; Grunenwald S; Mouly C; Arnault G; Wagner K; Koumakis E; Cortet-Rudelli C; Merlen É; Jannin A; Espiard S; Morange I; Baudin É; Cavaille M; Tauveron I; Teissier MP; Borson-Chazot F; Mirebeau-Prunier D; Savagner F; Pasmant É; Giraud S; Vantyghem MC; Goudet P; Barlier A; Cardot-Bauters C; Odou MF J Clin Endocrinol Metab; 2024 Jun; 109(7):e1482-e1493. PubMed ID: 38288531 [TBL] [Abstract][Full Text] [Related]
24. Coincidence of multiple endocrine neoplasia types 1 and 2: mutations in the RET protooncogene and MEN1 tumor suppressor gene in a family presenting with recurrent primary hyperparathyroidism. Frank-Raue K; Rondot S; Hoeppner W; Goretzki P; Raue F; Meng W J Clin Endocrinol Metab; 2005 Jul; 90(7):4063-7. PubMed ID: 15870131 [TBL] [Abstract][Full Text] [Related]
25. Mutational analysis of p27 (CDKN1B) and p18 (CDKN2C) in sporadic pancreatic endocrine tumors argues against tumor-suppressor function. Lindberg D; Akerström G; Westin G Neoplasia; 2007 Jul; 9(7):533-5. PubMed ID: 17710155 [TBL] [Abstract][Full Text] [Related]
26. Multiple endocrine neoplasms. Falchetti A; Marini F; Luzi E; Tonelli F; Brandi ML Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):149-63. PubMed ID: 18328987 [TBL] [Abstract][Full Text] [Related]
27. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. Longuini VC; Lourenço DM; Sekiya T; Meirelles O; Goncalves TD; Coutinho FL; Francisco G; Osaki LH; Chammas R; Alves VA; Siqueira SA; Schlesinger D; Naslavsky MS; Zatz M; Duarte YA; Lebrão ML; Gama P; Lee M; Molatore S; Pereira MA; Jallad RS; Bronstein MD; Cunha-Neto MB; Liberman B; Fragoso MC; Toledo SP; Pellegata NS; Toledo RA Eur J Endocrinol; 2014 Sep; 171(3):335-42. PubMed ID: 24920291 [TBL] [Abstract][Full Text] [Related]
28. [Genetics of multiple endocrine neoplasies: clinical implications]. Igaz P; Gaillard RC Rev Med Suisse; 2005 Feb; 1(6):408-13. PubMed ID: 15786644 [TBL] [Abstract][Full Text] [Related]
29. Case Report: New CDKN1B Mutation in Multiple Endocrine Neoplasia Type 4 and Brief Literature Review on Clinical Management. Lavezzi E; Brunetti A; Smiroldo V; Nappo G; Pedicini V; Vitali E; Trivellin G; Mazziotti G; Lania A Front Endocrinol (Lausanne); 2022; 13():773143. PubMed ID: 35355569 [TBL] [Abstract][Full Text] [Related]
30. MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations. Georgitsi M Best Pract Res Clin Endocrinol Metab; 2010 Jun; 24(3):425-37. PubMed ID: 20833334 [TBL] [Abstract][Full Text] [Related]
31. Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations. Igreja S; Chahal HS; Akker SA; Gueorguiev M; Popovic V; Damjanovic S; Burman P; Wass JA; Quinton R; Grossman AB; Korbonits M Clin Endocrinol (Oxf); 2009 Feb; 70(2):259-64. PubMed ID: 18710468 [TBL] [Abstract][Full Text] [Related]
32. Clinical Features of Multiple Endocrine Neoplasia Type 4: Novel Pathogenic Variant and Review of Published Cases. Frederiksen A; Rossing M; Hermann P; Ejersted C; Thakker RV; Frost M J Clin Endocrinol Metab; 2019 Sep; 104(9):3637-3646. PubMed ID: 30990521 [TBL] [Abstract][Full Text] [Related]
33. Functional characterization of a rare germline mutation in the gene encoding the cyclin-dependent kinase inhibitor p27Kip1 (CDKN1B) in a Spanish patient with multiple endocrine neoplasia-like phenotype. Malanga D; De Gisi S; Riccardi M; Scrima M; De Marco C; Robledo M; Viglietto G Eur J Endocrinol; 2012 Mar; 166(3):551-60. PubMed ID: 22129891 [TBL] [Abstract][Full Text] [Related]
34. Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas. Borsari S; Pardi E; Pellegata NS; Lee M; Saponaro F; Torregrossa L; Basolo F; Paltrinieri E; Zatelli MC; Materazzi G; Miccoli P; Marcocci C; Cetani F Endocrine; 2017 Feb; 55(2):386-397. PubMed ID: 27038812 [TBL] [Abstract][Full Text] [Related]
35. Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias. Marx SJ; Agarwal SK; Kester MB; Heppner C; Kim YS; Skarulis MC; James LA; Goldsmith PK; Saggar SK; Park SY; Spiegel AM; Burns AL; Debelenko LV; Zhuang Z; Lubensky IA; Liotta LA; Emmert-Buck MR; Guru SC; Manickam P; Crabtree J; Erdos MR; Collins FS; Chandrasekharappa SC Recent Prog Horm Res; 1999; 54():397-438; discussion 438-9. PubMed ID: 10548885 [TBL] [Abstract][Full Text] [Related]
36. Recessive transmission of a multiple endocrine neoplasia syndrome in the rat. Fritz A; Walch A; Piotrowska K; Rosemann M; Schäffer E; Weber K; Timper A; Wildner G; Graw J; Höfler H; Atkinson MJ Cancer Res; 2002 Jun; 62(11):3048-51. PubMed ID: 12036912 [TBL] [Abstract][Full Text] [Related]
37. Occurrence of the Cys611Tyr mutation and a novel Arg886Trp substitution in the RET proto-oncogene in multiple endocrine neoplasia type 2 families and sporadic medullary thyroid carcinoma cases originating from the central region of Portugal. Prazeres HJ; Rodrigues F; Figueiredo P; Naidenov P; Soares P; Bugalho MJ; Lacerda M; Campos B; Martins TC Clin Endocrinol (Oxf); 2006 Jun; 64(6):659-66. PubMed ID: 16712668 [TBL] [Abstract][Full Text] [Related]