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Records 1-10

Query Trace: Parathyroid Neoplasms and MEN1[orginal query]

Comprehensive Genomic Characterization of Parathyroid Cancer Identifies Novel Candidate Driver Mutations and Core Pathways. Journal of the Endocrine Society 2019 Mar 3 (3): 544-559. Clarke Callisia N, Katsonis Panagiotis, Hsu Teng-Kuei, Koire Amanda M, Silva-Figueroa Angelica, Christakis Ioannis, Williams Michelle D, Kutahyalioglu Merve, Kwatampora Lily, Xi Yuanxin, Lee Jeffrey E, Koptez E Scott, Busaidy Naifa L, Perrier Nancy D, Lichtarge Olivi Similar articles in PubMed
Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas. Endocrinology 2018 Jul . Wei Zhe, Sun Bin, Wang Zong-Ping, He Jin-Wei, Fu Wen-Zhen, Fan You-Ben, Zhang Zhen-L Similar articles in PubMed
EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms. Endocrine 2016 Feb . Sanpaolo E, Miroballo M, Corbetta S, Verdelli C, Baorda F, Balsamo T, Graziano P, Fabrizio F P, Cinque L, Scillitani A, Muscarella L A, Guarnieri Vi Similar articles in PubMed
Unravelling the intra-familial correlations and heritability of tumor types in MEN1, a GTE study. European journal of endocrinology / European Federation of Endocrine Societies 2015 Sep . Thevenon Julien, Bourredjem Abderrahmane, Faivre Laurence, Bauters Catherine, Calender Alain, Lebras Maelle, Giraud Sophie, Niccoli Patricia, Odou Marie-Françoise, Borson-Chazot Francoise, Barlier Anne, Lombard-Bohas Catherine, Clauser Eric, Tabarin Antoine, Pasmant Eric, Chabre Olivier, Castermans Emilie, Ruszniewski Philippe, Bertherat Jerôme, Delemer Brigitte, Christin-Maitre Sophie, Beckers Albert, Guilhem Isabelle, Rohmer Vincent, Goichot Bernard, Caron Philippe, Baudin Eric, Chanson Philippe, Groussin Lionel, Du Boullay Helene, Weryha Georges, Lecomte Pierre, Schillo Franck, Bihan Helene, Archambeaud Francoise, Kerlan Veronique, Bourcigaux Nathalie, Kuhn Jean-Marc, Vergès Bruno, Rodier Michel, Renard Michel, Sadoul Jean Louis, Binquet Christine, Goudet Pier Similar articles in PubMed
Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas. The Journal of clinical endocrinology and metabolism 2013 Jul 98 (7): 2800-10. Pardi Elena, Marcocci Claudio, Borsari Simona, Saponaro Federica, Torregrossa Liborio, Tancredi Mariella, Raspini Benedetta, Basolo Fulvio, Cetani Filome Similar articles in PubMed
MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism. European journal of endocrinology / European Federation of Endocrine Societies 2013 Feb 168 (2): 119-28. Alvelos Maria Inês, Vinagre João, Fonseca Elsa, Barbosa Eva, Teixeira-Gomes José, Sobrinho-Simões Manuel, Soares Pau Similar articles in PubMed
Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition. Journal of endocrinological investigation 2009 Jun 32 (6): 512-8. Vierimaa O, Villablanca A, Alimov A, Georgitsi M, Raitila A, Vahteristo P, Larsson C, Ruokonen A, Eloranta E, Ebeling T M L, Ignatius J, Aaltonen L A, Leisti J, Salmela P Similar articles in PubMed
Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases. The Journal of clinical endocrinology and metabolism 2007 Sep 92 (9): 3389-95. Tham Emma, Grandell Ulla, Lindgren Eva, Toss Göran, Skogseid Britt, Nordenskjöld Magn Similar articles in PubMed
Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas. Clinical endocrinology 2007 Sep 67 (3): 370-6. Haven C J, van Puijenbroek M, Tan M H, Teh B T, Fleuren G J, van Wezel T, Morreau Similar articles in PubMed
Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics. Journal of endocrinological investigation 2004 Dec 27 (11): 1015-21. Scarpelli D, D'Aloiso L, Arturi F, Scillitani A, Presta I, Bisceglia M, Cristofaro C, Russo D, Filetti Similar articles in PubMed

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