Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Multiple Endocrine Neoplasia Type 2a and RET[original query] |
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| Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A. Cancer research 2006 1 66 (2): 1177-80. Lesueur Fabienne, Cebrian Arancha, Robledo Mercedes, Niccoli-Sire Patricia, Svensson Karl-Axel, Pinson Stephane, Leyland Jean, Whittaker Joanne, Pharoah Paul D, Ponder Bruce A |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Is new American Thyroid Association risk classification for hereditary medullary thyroid carcinoma applicable to Chinese patients? A single-center study. Chinese journal of cancer research = Chung-kuo yen cheng yen chiu 2017 7 29 (3): 223-230. Zhang Xiwei, Yan Dangui, Wang Junyi, Wan Hanfeng, Zhang Yongxia, Zhang Yabing, He Yuqin, Liu Wensheng, Zhang B |
| Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families. Medicine 2017 1 96 (3): e5967. Liu Qiuli, Tong Dali, Yuan Wenqiang, Liu Gaolei, Yuan Gang, Lan Weihua, Zhang Dianzheng, Zhang Jun, Huang Zaoming, Zhang Yao, Jiang J |
| The Clinical Spectrum of Multiple Endocrine Neoplasia Type 2A with Cutaneous Lichen Amyloidosis in Ethnic Han Chinese. Cancer investigation 2018 2 36 (2): 141-151. Qi Xiao-Ping, Zhao Jian-Qiang, Cao Zhi-Lie, Fu Er, Li Feng, Zhao Yi-Hua, Wang Guang-Ping, Li Peng-Fei, Ma Wo-Long, Guo Jian, Jia Ho |
| Clinical utility of genetic diagnosis for sporadic and hereditary medullary thyroid carcinoma. Annales d'endocrinologie 2019 5 80 (3): 187-190. Elisei Rossella, Bottici Valeria, Cappagli Virginia, Ramone Teresa, Tacito Alessia, Ciampi Raffaele, Romei Cristi |
| Variability in Medullary Thyroid Carcinoma in RET L790F Carriers: A Case Comparison Study of Index Patients. Frontiers in endocrinology 2020 5 11 251. Mathiesen Jes Sloth, Nielsen Søren Grønlund, Rasmussen Åse Krogh, Kiss Katalin, Wadt Karin, Hermann Anne Pernille, Nielsen Morten Frost, Larsen Stine Rosenkilde, Brusgaard Klaus, Frederiksen Anja Lisbeth, Godballe Christian, Rossing Mar |
| Medullary thyroid cancer with RET V804M mutation: more indolent than expected? Surgery 2022 9 173 (1): 260-267. Frisco Nicholas A, Gunn Alexander H, Thomas Samantha M, Stang Michael T, Scheri Randall P, Kazaure Hadiza |
| Pheochromocytoma recurrence in hereditary disease: does a cortical-sparing technique increase recurrence rate? Surgery 2022 10 173 (1): 26-34. Shirali Aditya S, Clemente-Gutierrez Uriel, Huang Bernice L, Lui Michael S, Chiang Yi-Ju, Jimenez Camilo, Fisher Sarah B, Graham Paul H, Lee Jeffrey E, Grubbs Elizabeth G, Perrier Nancy |
| Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families. European journal of endocrinology 2023 9 189 (3): 402-408. Axelle Vuylsteke, Laurens Hannes, Hilde Brems, Koen Devis, Marleen Renard, Anne Uyttebroeck, Eric Legius, Brigitte Decallon |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 18, 2023
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