HuGE Literature Finder
Records
1
-
11
| The RET E616Q Variant is a Gain of Function Mutation Present in a Family with Features of Multiple Endocrine Neoplasia 2A. Endocrine pathology 2016 Oct . Grey William, Hulse Rosaline, Yakovleva Anna, Genkova Dilyana, Whitelaw Benjamin, Solomon Ellen, Diaz-Cano Salvador J, Izatt Loui |
| A Nationwide Study of Multiple Endocrine Neoplasia Type 2A in Norway: Predictive and Prognostic Factors for the Clinical Course of Medullary Thyroid Carcinoma. Thyroid : official journal of the American Thyroid Association 2016 Jul . Opsahl Else Marie, Schlichting Ellen, Helset Kristin, Svartberg Johan, Brauckhoff Katrin, Mæhle Lovise, Engebretsen Lars Fredrik, Sigstad Eva, Grøholt Krystyna, Akslen Lars Andreas, Jørgensen Lars Hilmar, Varhaug Jan Erik, Bjøro Tri |
| Clinical significance of RET mutation screening in a pedigree of multiple endocrine neoplasia type 2A. Molecular medicine reports 2016 Jun . Ying Rongbiao, Feng J |
| Presence of the RET Cys634Tyr mutation and Gly691Ser functional polymorphism in Iranian families with multiple endocrine neoplasia type 2A. Hormones (Athens, Greece) 2016 Jan . Aghdam Maryam Nasiri, Abbaszadegan Mohammad Reza, Tafazoli JAlireza, Aslzare Mohammad, Mosavi Zohr |
| Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives. Familial cancer 2015 Aug . Wang Junyi, Zhang Bin, Liu Wensheng, Zhang Yongxia, Di Xuebing, Yang Yanmei, Yan Dang |
| Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Jul 36 (7): 5225-31. Zarif Yeganeh Marjan, Sheikholeslami Sara, Dehbashi Behbahani Golnoush, Farashi Samaneh, Hedayati Meh |
| Genetic screening of patients with medullary thyroid cancer in a referral center in Greece during the past two decades. European journal of endocrinology / European Federation of Endocrine Societies 2015 Apr 172 (4): 501-9. Sarika H-L, Papathoma A, Garofalaki M, Saltiki K, Pappa T, Pazaitou-Panayiotou K, Anastasiou E, Alevizaki |
| Exome sequencing reveals mutant genes with low penetrance involved in MEN2A-associated tumorigenesis. Endocrine-related cancer 2015 Feb 22 (1): 23-33. Cai Jie, Li Lin, Ye Lei, Jiang Xiaohua, Shen Liyun, Gao Zhibo, Fang Weiyuan, Huang Fengjiao, Su Tingwei, Zhou Yulin, Wang Weiqing, Ning Gua |
| Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation 2011 Jan 32 (1): 51-8. Frank-Raue Karin, Rybicki Lisa A, Erlic Zoran, Schweizer Heiko, Winter Aurelia, Milos Ioana, Toledo Sergio P A, Toledo Rodrigo A, Tavares Marcos R, Alevizaki Maria, Mian Caterina, Siggelkow Heide, Hüfner Michael, Wohllk Nelson, Opocher Giuseppe, Dvo?áková Sárka, Bendlova Bela, Czetwertynska Ma?gorzata, Skasko El?bieta, Barontini Marta, Sanso Gabriela, Vorländer Christian, Maia Ana Luiza, Patocs Attila, Links Thera P, de Groot Jan Willem, Kerstens Michiel N, Valk Gerlof D, Miehle Konstanze, Musholt Thomas J, Biarnes Josefina, Damjanovic Svetozar, Muresan Mihaela, Wüster Christian, Fassnacht Martin, Peczkowska Mariola, Fauth Christine, Golcher Henriette, Walter Martin A, Pichl Josef, Raue Friedhelm, Eng Charis, Neumann Hartmut P H, |
| The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A. The Journal of clinical endocrinology and metabolism 2010 Sep 95 (9): E92-7. Schulte Klaus-Martin, Machens Andreas, Fugazzola Laura, McGregor Alan, Diaz-Cano Salvador, Izatt Louise, Aylwin Simon, Talat Nadia, Beck-Peccoz Paolo, Dralle Henni |
| Germline RET mutations in exons 10 and 11: an Iranian survey of 57 medullary thyroid carcinoma cases. The Medical journal of Malaysia 2006 Dec 61 (5): 564-9. Hedayati M, Nabipour I, Rezaei-Ghaleh N, Azizi |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 28, 2022
- Content source: