Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Hyperplasia and RET[original query] |
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| [Hereditary medullary thyroid carcinoma--genotype-phenotype characterization]. Deutsche medizinische Wochenschrift (1946) 2003 Sep 128 (39): 1998-2002. Frank-Raue K, Heimbach C, Rondot S, Usadel K-H, Meng W, Varma C, Fuchs-Hammoser R, Höppner W, Schulze E, Raue |
| Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations. Surgery 2003 Sep 134 (3): 425-31. Machens Andreas, Holzhausen Hans-Jürgen, Thanh Phuong Nguyen, Dralle Henni |
| Succinate dehydrogenase D variants do not constitute a risk factor for developing C cell hyperplasia or sporadic medullary thyroid carcinoma. The Journal of clinical endocrinology and metabolism 2005 Apr 90 (4): 2127-30. Cascon Alberto, Cebrian Arancha, Pollan Marina, Ruiz-Llorente Sergio, Montero-Conde Cristina, Leton Rocio, Gutierrez Ruth, Lesueur Fabienne, Milne Roger L, Gonzalez-Albarran Olga, Lucas-Morante Tomas, Benitez Javier, Ponder Bruce A J, Robledo Merced |
| Long-term follow up of a "sporadic" unilateral pheochromocytoma revealing multiple endocrine neoplasia MEN2A-2 in an elderly woman. Endocrine pathology 2004 1 14 (4): 375-82. Weinhäusel Andreas, Behmel Annemarie, Ponder Bruce A J, Haas Oskar A, Niederle Bruno, Gessl Alois, Vierhapper Heinrich, Pfragner Roswit |
| Clinical case seminar: in vivo and in vitro characterization of a novel germline RET mutation associated with low-penetrant nonaggressive familial medullary thyroid carcinoma. The Journal of clinical endocrinology and metabolism 2005 12 91 (3): 754-9. D'Aloiso Leonardo, Carlomagno Francesca, Bisceglia Michele, Anaganti Suresh, Ferretti Elisabetta, Verrienti Antonella, Arturi Franco, Scarpelli Daniela, Russo Diego, Santoro Massimo, Filetti Sebastia |
| RET polymorphisms and sporadic medullary thyroid carcinoma in a Portuguese population. Endocrine 2005 Aug 27 (3): 239-43. Costa Patrícia, Domingues Rita, Sobrinho Luís G, Bugalho Maria Jo |
| Exon 5 of the RET proto-oncogene: a newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg. Journal of endocrinological investigation 2006 1 28 (10): 905-9. Dvorakova S, Vaclavikova E, Duskova J, Vlcek P, Ryska A, Bendlova |
| Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma? Clinical endocrinology 2008 Sep 69 (3): 506-10. Cardot-Bauters C, Leteurtre E, Leclerc L, Vantyghem M-C, Do Cao C, Wemeau J-L, d'Herbomez M, Carnaille B, Barbu V, Pinson S, Pigny P, |
| The influence of gender, age, and RET polymorphisms on C-cell hyperplasia and medullary thyroid carcinoma. Thyroid : official journal of the American Thyroid Association 2008 Dec 18 (12): 1269-76. Weinhaeusel Andreas, Scheuba Christian, Lauss Martin, Kriegner Albert, Kaserer Klaus, Vierlinger Klemens, Haas Oskar A, Niederle Bru |
| 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 |
| MicroRNA profiles in familial and sporadic medullary thyroid carcinoma: preliminary relationships with RET status and outcome. Thyroid : official journal of the American Thyroid Association 2012 Sep 22 (9): 890-6. Mian Caterina, Pennelli Gianmaria, Fassan Matteo, Balistreri Mariangela, Barollo Susi, Cavedon Elisabetta, Galuppini Francesca, Pizzi Marco, Vianello Federica, Pelizzo Maria Rosa, Girelli Maria Elisa, Rugge Massimo, Opocher Giusep |
| C-Cell Neoplasia in Asymptomatic Carriers of RET Mutation in Extracellular Cysteine-Rich and Intracellular Tyrosine Kinase Domain. Human pathology 2015 Aug 46 (8): 1121-8. Abi-Raad Rita, Virk Renu K, Dinauer Catherine A, Prasad A, Morotti Raffaella A, Breuer Christopher K, Sosa Julie A, Udelsman Robert, Rivkees Scott A, Prasad Manju |
| A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors. BMC cancer 2015 15 157. Evangelisti Cecilia, de Biase Dario, Kurelac Ivana, Ceccarelli Claudio, Prokisch Holger, Meitinger Thomas, Caria Paola, Vanni Roberta, Romeo Giovanni, Tallini Giovanni, Gasparre Giuseppe, Bonora Ele |
| 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 |
| Expression of Tenascin C, EGFR, E-Cadherin, and TTF-1 in Medullary Thyroid Carcinoma and the Correlation with RET Mutation Status. International journal of molecular sciences 2016 17 (7): . Steiner Florian, Hauser-Kronberger Cornelia, Rendl Gundula, Rodrigues Margarida, Pirich Christi |
| M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds. Endocrine-related cancer 2016 Dec 23 (12): 909-920. Martins-Costa M Cecília, Cunha Lucas L, Lindsey Susan C, Camacho Cleber P, Dotto Renata P, Furuzawa Gilberto K, Sousa M Sharmila A, Kasamatsu Teresa S, Kunii Ilda S, Martins Márcio M, Machado Alberto L, Martins João R M, Dias-da-Silva Magnus R, Maciel Rui M |
| 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 |
| Medullary Thyroid Carcinoma Associated with Germline RET Mutation. Thyroid : official journal of the American Thyroid Association 2016 Sep . Xu Jian Yu, Grubbs Elizabeth G, Waguespack Steven G, Jimenez Camilo, Gagel Robert F, Sosa Julie Ann, Vassilopoulou-Sellin Rena, Dadu Ramona, Hu Mimi I, Trotter Chardria S, Jackson Michelle, Rich Thereasa A, Hyde Samuel M, Sherman Steven I, Cote Gilbert |
| 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 |
| [Prophylactic thyroidectomy in RET proto-oncogen mutation]. Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica 2017 9 30 (2): 100-104. Rodríguez Caraballo L, Gómez-Chacón Villalba J, Rodríguez Iglesias P, Cortés Sáez J, Moreno Macián F, Marco Macián A, Vila Carbó J |
| 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 |
| Molecular Testing for Oncogenic Gene Alterations in Pediatric Thyroid Lesions. Thyroid : official journal of the American Thyroid Association 2017 Nov . Mostoufi-Moab Sogol, Labourier Emmanuel, Sullivan Lisa, LiVolsi Virginia, Li Yimei, Xiao Rui, Beaudenon-Huibregtse Sylvie, Kazahaya Ken, Adzick N Scott, Baloch Zubair, Bauer Andrew |
| Genotype-specific progression of hereditary medullary thyroid cancer. Human mutation 2018 4 39 (6): 860-869. Machens Andreas, Lorenz Kerstin, Weber Frank, Dralle Henni |
| p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy. Human mutation 2019 3 40 (7): 926-937. Giacché Mara, Panarotto Alessandra, Tacchetti Maria Chiara, Tosini Rossella, Campana Federica, Mori Luigi, Cappelli Carlo, Pirola Ilenia, Lombardi Davide, Pezzola Diego Cesare, Casella Claudio, Castellano Mauriz |
| Revisiting the genotype-phenotype correlation in children with medullary thyroid carcinoma: A report from the GPOH-MET registry. Pediatric blood & cancer 2020 1 67 (4): e28171. Kuhlen Michaela, Frühwald Michael C, Dunstheimer Désirée P A, Vorwerk Peter, Redlich Ant |
| 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 |
| Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 . An Song, Yi Yang, Yue Jiang, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wa |
| [Hereditary medullary thyroid cancer]. Chirurgie (Heidelberg, Germany) 2023 2 . Fendrich V, Zahn |
| Genomic Landscape Features of Minimally Invasive Adenocarcinoma and Invasive Lung Adenocarcinoma. Global medical genetics 2024 11 11 (4): 312-318. Wei Zhang, Hui Xu, Ning Tang, Shuang Han, Hongyan S |
- Page last reviewed:Feb 1, 2024
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