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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 6, 2023. (Total: 223792Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hyperparathyroidism and CTNNB1[original query]
Evidence of a stabilizing mutation of ß-catenin encoded by CTNNB1 exon 3 in a large series of sporadic parathyroid adenomas.
Endocrine 2012 Dec 42 (3): 612-5.
Starker Lee F, Fonseca Annabelle L, Fonseca Annabelle, Akerström Göran, Björklund Peyman, Westin Gunnar, Carling Tobi
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
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
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