BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 22490989)

  • 1. A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome.
    Giacché M; Panarotto A; Mori L; Daffini L; Tacchetti MC; Pirola I; Agabiti Rosei E; Castellano M
    J Endocrinol Invest; 2012 Feb; 35(2):124-8. PubMed ID: 22490989
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing.
    Kim BY; Park MH; Woo HM; Jo HY; Kim JH; Choi HJ; Koo SK
    BMC Med Genet; 2017 Oct; 18(1):106. PubMed ID: 28969599
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lack of MEN1 gene mutations in 27 sporadic insulinomas.
    Cupisti K; Höppner W; Dotzenrath C; Simon D; Berndt I; Röher HD; Goretzki PE
    Eur J Clin Invest; 2000 Apr; 30(4):325-9. PubMed ID: 10759881
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism.
    Alvelos MI; Vinagre J; Fonseca E; Barbosa E; Teixeira-Gomes J; Sobrinho-Simões M; Soares P
    Eur J Endocrinol; 2013 Feb; 168(2):119-28. PubMed ID: 23093699
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple endocrine neoplasia type 2-associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors.
    Willeke F; Hauer MP; Buchcik R; Gebert JF; Hahn M; Fitze G; Mechtersheimer G; Möller P; Saeger HD; Herfarth C; Schackert HK
    Surgery; 1998 Sep; 124(3):484-90. PubMed ID: 9736899
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expression.
    Zatelli MC; Tagliati F; Di Ruvo M; Castermans E; Cavazzini L; Daly AF; Ambrosio MR; Beckers A; degli Uberti E
    Fam Cancer; 2014 Jun; 13(2):273-80. PubMed ID: 24522746
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases.
    Tham E; Grandell U; Lindgren E; Toss G; Skogseid B; Nordenskjöld M
    J Clin Endocrinol Metab; 2007 Sep; 92(9):3389-95. PubMed ID: 17623761
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlation of mutant menin stability with clinical expression of multiple endocrine neoplasia type 1 and its incomplete forms.
    Shimazu S; Nagamura Y; Yaguchi H; Ohkura N; Tsukada T
    Cancer Sci; 2011 Nov; 102(11):2097-102. PubMed ID: 21819486
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation of the MENIN gene in sporadic pancreatic endocrine tumors.
    Wang EH; Ebrahimi SA; Wu AY; Kashefi C; Passaro E; Sawicki MP
    Cancer Res; 1998 Oct; 58(19):4417-20. PubMed ID: 9766672
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel MEN1 pathogenic variant in an Italian patient with multiple endocrine neoplasia type 1.
    Corsello A; Bruno C; Rizza R; Concolino P; Papi G; Pontecorvi A; Rindi G; Paragliola RM
    Mol Biol Rep; 2020 Sep; 47(9):7313-7316. PubMed ID: 32808116
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.
    Karges W; Jostarndt K; Maier S; Flemming A; Weitz M; Wissmann A; Feldmann B; Dralle H; Wagner P; Boehm BO
    J Endocrinol; 2000 Jul; 166(1):1-9. PubMed ID: 10856877
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.
    Klein RD; Salih S; Bessoni J; Bale AE
    Genet Med; 2005 Feb; 7(2):131-8. PubMed ID: 15714081
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype.
    Raef H; Zou M; Baitei EY; Al-Rijjal RA; Kaya N; Al-Hamed M; Monies D; Abu-Dheim NN; Al-Hindi H; Al-Ghamdi MH; Meyer BF; Shi Y
    Clin Endocrinol (Oxf); 2011 Dec; 75(6):791-800. PubMed ID: 21627674
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MEN1 gene mutations in 12 MEN1 families and their associated tumors.
    Bartsch D; Kopp I; Bergenfelz A; Rieder H; Münch K; Jäger K; Deiss Y; Schudy A; Barth P; Arnold R; Rothmund M; Simon B
    Eur J Endocrinol; 1998 Oct; 139(4):416-20. PubMed ID: 9820618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A germline c.1546dupC MEN1 mutation in an MEN1 family: A case report.
    Cho YY; Chung YJ
    Medicine (Baltimore); 2021 Jun; 100(25):e26382. PubMed ID: 34160414
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple endocrine neoplasia type 1.
    Marini F; Falchetti A; Del Monte F; Carbonell Sala S; Gozzini A; Luzi E; Brandi ML
    Orphanet J Rare Dis; 2006 Oct; 1():38. PubMed ID: 17014705
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Multiple Endocrine Neoplasia I (Wermers Syndrome), Forms of Clinical Manifestation, 5 Case Studies].
    Drbalová K; Herdová K; Krejčí P; Nývltová M; Solař S; Vedralová L; Záruba P; Netuka D; Bavor P
    Vnitr Lek; 2016; 62(9 Suppl 3):140-149. PubMed ID: 27734708
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas.
    Haven CJ; van Puijenbroek M; Tan MH; Teh BT; Fleuren GJ; van Wezel T; Morreau H
    Clin Endocrinol (Oxf); 2007 Sep; 67(3):370-6. PubMed ID: 17555500
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
    Lemos MC; Thakker RV
    Hum Mutat; 2008 Jan; 29(1):22-32. PubMed ID: 17879353
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.