Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Carcinoma and EIF1AX[original query] |
---|
Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes. Oncotarget 2015 Oct . Hunter Sally M, Anglesio Michael S, Ryland Georgina L, Sharma Raghwa, Chiew Yoke-Eng, Rowley Simone M, Doyle Maria A, Li Jason, Gilks C Blake, Moss Phillip, Allan Prue E, Stephens Andrew N, Huntsman David G, deFazio Anna, Bowtell David D, , Gorringe Kylie L, Campbell Ian |
Prevalence and phenotypic correlations of EIF1AX mutations in thyroid nodules. Endocrine-related cancer 2016 Apr 23 (4): 295-301. Karunamurthy Arivarasan, Panebianco Federica, J Hsiao Susan, Vorhauer Jennie, Nikiforova Marina N, Chiosea Simion, Nikiforov Yuri |
Identification of somatic TERT promoter mutations in familial nonmedullary thyroid carcinomas. Clinical endocrinology 2017 May . Marques Inês J, Moura Margarida M, Cabrera Rafael, Pinto António E, Simões-Pereira Joana, Santos Catarina, Menezes Francisco D, Montezuma Diana, Henrique Rui, Teixeira Manuel R, Leite Valeriano, Cavaco Branca |
EIF1AX Mutation in a Patient with Hürthle Cell Carcinoma. Endocrine pathology 2017 10 29 (1): 27-29. Topf Michael C, Wang Zi-Xuan, Furlong Kevin, Miller Jeffrey L, Tuluc Madalina, Pribitkin Edmund |
Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology. The Journal of clinical endocrinology and metabolism 2018 07 103 (7): 2640-2650. Nicolson Norman G, Murtha Timothy D, Dong Weilai, Paulsson Johan O, Choi Jungmin, Barbieri Andrea L, Brown Taylor C, Kunstman John W, Larsson Catharina, Prasad Manju L, Korah Reju, Lifton Richard P, Juhlin C Christofer, Carling Tobi |
Clinical utility of EZH1 mutations in the diagnosis of follicular-patterned thyroid tumors. Human pathology 2018 Apr . Jung Chan Kwon, Kim Yourha, Jeon Sora, Jo Kwanhoon, Lee Sohee, Bae Ja Seo |
Mutation profiles of follicular thyroid tumors by targeted sequencing. Diagnostic pathology 2019 May 14 (1): 39. Duan Huanli, Liu Xiaoding, Ren Xinyu, Zhang Hui, Wu Huanwen, Liang Zhiyo |
EIF1AX c.338-2A>T splice site mutation in a patient with trabecular adenoma and cytological indeterminate lesion. Archives of endocrinology and metabolism 2020 4 64 (2): 185-189. Castagna Maria Grazia, Pilli Tania, Maino Fabio, Marzocchi Carlotta, Cairano Giovanni Di, Cantara Silv |
High Prevalence of DICER1 Mutations and Low Frequency of Gene Fusions in Pediatric Follicular-Patterned Tumors of the Thyroid. Endocrine pathology 2021 7 32 (3): 336-346. Bae Ja-Seong, Jung Seung-Hyun, Hirokawa Mitsuyoshi, Bychkov Andrey, Miyauchi Akira, Lee Sohee, Chung Yeun-Jun, Jung Chan Kw |
Characterization and Clinical Significance of EIF1AX Mutations and Co-Mutations in Cytologically Indeterminate Thyroid Nodules: A 5-Year Retrospective Analysis. Acta medica academica 2021 6 50 (1): 4-12. Gargano Stacey M, Badjatia Nitika, Nikolaus Yanina, Peiper Stephen C, Wang Zi-Xu |
A thyroid EIF1AX story: how clinical, cytologic, and molecular surveillance led to appropriate management. Journal of the American Society of Cytopathology 2022 12 . Geisler Daniel L, Karslioglu French Esra, Yip Linwah, Nikiforova Marina N, Nikiforov Yuri E, Schoedel Karen E, Seethala Raja R, Ohori N Pa |
EIF1AX mutation in thyroid tumors: a retrospective analysis of cytology, histopathology and co-mutation profiles. Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale 2022 11 51 (1): 43. Elsherbini Noha, Kim Dong Hyun, Payne Richard J, Hudson Thomas, Forest Véronique-Isabelle, Hier Michael P, Payne Alexandra E, Pusztaszeri Marc |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 18, 2024
- Content source: