Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: Syndrome and IDH2[original query] |
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Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas. The Journal of clinical endocrinology and metabolism 2010 Mar 95 (3): 1274-8. Gaal José, Burnichon Nelly, Korpershoek Esther, Roncelin Isabelle, Bertherat Jérôme, Plouin Pierre-François, de Krijger Ronald R, Gimenez-Roqueplo Anne-Paule, Dinjens Winand N |
IDH1 and IDH2 mutation analysis in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome. Annals of hematology 2012 Apr 91 (4): 519-25. Lin Jiang, Yao Dong-ming, Qian Jun, Chen Qin, Qian Wei, Li Yun, Yang Jing, Wang Cui-zhu, Chai Hai-yan, Qian Zhen, Xiao Gao-fei, Xu Wen-ro |
Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations. Haematologica 2014 Jan 99 (1): 28-36. Lin Tung-Liang, Nagata Yasunobu, Kao Hsiao-Wen, Sanada Masashi, Okuno Yusuke, Huang Chein-Fuang, Liang Der-Cherng, Kuo Ming-Chung, Lai Chang-Liang, Lee En-Hui, Shih Yu-Shu, Tanaka Hiroko, Shiraishi Yuichi, Chiba Kenichi, Lin Tung-Huei, Wu Jin-Hou, Miyano Satoru, Ogawa Seishi, Shih Lee-Yu |
Acquired somatic mutations of isocitrate dehydrogenases 1 and 2 (IDH1 and IDH2) in preleukemic disorders. Blood cells, molecules & diseases 2015 Mar 54 (3): 286-91. Chotirat Sadudee, Thongnoppakhun Wanna, Wanachiwanawin Wanchai, Auewarakul Chirayu |
[Relationship between clinical characteristics and myelodysplastic syndrome patients with isocitrate dehydrogenase gene mutations]. Zhonghua yi xue za zhi 2013 Oct 93 (40): 3180-4. Tong Hong-yan, Hu Chao, Yu Meng-xia, Ma Qiu-ling, Chen Fei-fei, Ye Li, Wei Ju-ying, Xu Gai-xiang, Mao Li-ping, Li Ying, Jin J |
Detection of Dual IDH1 and IDH2 Mutations by Targeted Next-Generation Sequencing in Acute Myeloid Leukemia and Myelodysplastic Syndromes. The Journal of molecular diagnostics : JMD 2015 Aug . Platt Mia Y, Fathi Amir T, Borger Darrell R, Brunner Andrew M, Hasserjian Robert P, Balaj Leonora, Lum Amy, Yip Stephen, Dias-Santagata Dora, Zheng Zongli, Le Long P, Graubert Timothy A, Iafrate A John, Nardi Valenti |
ATRX immunostaining predicts IDH and H3F3A status in gliomas. Acta neuropathologica communications 2016 4 (1): 60. Ebrahimi Azadeh, Skardelly Marco, Bonzheim Irina, Ott Ines, Mühleisen Helmut, Eckert Franziska, Tabatabai Ghazaleh, Schittenhelm Je |
RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features. Leukemia 2016 May . Gaidzik V I, Teleanu V, Papaemmanuil E, Weber D, Paschka P, Hahn J, Wallrabenstein T, Kolbinger B, Köhne C-H, Horst H A, Brossart P, Held G, Kündgen A, Ringhoffer M, Götze K, Rummel M, Gerstung M, Campbell P, Kraus J M, Kestler H A, Thol F, Heuser M, Schlegelberger B, Ganser A, Bullinger L, Schlenk R F, Döhner K, Döhner |
Splicing factor mutations predict poor prognosis in patients with de novo acute myeloid leukemia. Oncotarget 2016 Jan . Hou Hsin-An, Liu Chieh-Yu, Kuo Yuan-Yeh, Chou Wen-Chien, Tsai Cheng-Hong, Lin Chien-Chin, Lin Liang-In, Tseng Mei-Hsuan, Chiang Ying-Chieh, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Li Chi-Cheng, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Chen Chien-Yuan, Lin Chien-Ting, Wu Shang-Ju, Tsay Woei, Tien Hwei-Fa |
Individual outcome prediction for myelodysplastic syndrome (MDS) and secondary acute myeloid leukemia from MDS after allogeneic hematopoietic cell transplantation. Annals of hematology 2017 Jun . Heuser Michael, Gabdoulline Razif, Löffeld Patrick, Dobbernack Vera, Kreimeyer Henriette, Pankratz Mira, Flintrop Madita, Liebich Alessandro, Klesse Sabrina, Panagiota Victoria, Stadler Michael, Wichmann Martin, Shahswar Rabia, Platzbecker Uwe, Thiede Christian, Schroeder Thomas, Kobbe Guido, Geffers Robert, Schlegelberger Brigitte, Göhring Gudrun, Kreipe Hans-Heinrich, Germing Ulrich, Ganser Arnold, Kröger Nicolaus, Koenecke Christian, Thol Felicit |
Dynamics of DNMT3A mutation and prognostic relevance in patients with primary myelodysplastic syndrome. Clinical epigenetics 2018 4 10 42. Lin Ming-En, Hou Hsin-An, Tsai Cheng-Hong, Wu Shang-Ju, Kuo Yuan-Yeh, Tseng Mei-Hsuan, Liu Ming-Chih, Liu Chia-Wen, Chou Wen-Chien, Chen Chien-Yuan, Tang Jih-Luh, Yao Ming, Li Chi-Cheng, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Lin Chien-Ting, Tien Hwei-Fa |
Incorporation of mutations in five genes in the revised International Prognostic Scoring System can improve risk stratification in the patients with myelodysplastic syndrome. Blood cancer journal 2018 Apr 8 (4): 39. Hou Hsin-An, Tsai Cheng-Hong, Lin Chien-Chin, Chou Wen-Chien, Kuo Yuan-Yeh, Liu Chieh-Yu, Tseng Mei-Hsuan, Peng Yen-Ling, Liu Ming-Chih, Liu Chia-Wen, Liao Xiu-Wen, Lin Liang-In, Yao Ming, Tang Jih-Luh, Tien Hwei-Fa |
Mutations in the DNA methylation pathway and number of driver mutations predict response to azacitidine in myelodysplastic syndromes. Oncotarget 2018 1 8 (63): 106948-106961. Cedena M Teresa, Rapado Inmaculada, Santos-Lozano Alejandro, Ayala Rosa, Onecha Esther, Abaigar María, Such Esperanza, Ramos Fernando, Cervera José, Díez-Campelo María, Sanz Guillermo, Rivas Jesús Hernández, Lucía Alejandro, Martínez-López Joaqu |
Clinicopathologic and genetic characterization of nonacute NPM1-mutated myeloid neoplasms. Blood advances 2019 5 3 (9): 1540-1545. Patel Sanjay S, Ho Caleb, Ptashkin Ryan N, Sadigh Sam, Bagg Adam, Geyer Julia T, Xu Mina L, Prebet Thomas, Mason Emily F, Seegmiller Adam C, Morgan Elizabeth A, Steensma David P, Winer Eric S, Wong Waihay J, Hasserjian Robert P, Weinberg Olga |
The Clinical impact of PTPN11 mutations in adults with acute myeloid leukemia. Leukemia 2020 6 35 (3): 691-700. Alfayez Mansour, Issa Ghayas C, Patel Keyur P, Wang Feng, Wang Xuemei, Short Nicholas J, Cortes Jorge E, Kadia Tapan, Ravandi Farhad, Pierce Sherry, Assi Rita, Garcia-Manero Guillermo, DiNardo Courtney D, Daver Naval, Pemmaraju Naveen, Kantarjian Hagop, Borthakur Gaut |
[Analysis of RUNX1 Gene Mutation in Patients with Myelodysplastic Syndrome]. Zhongguo shi yan xue ye xue za zhi 2020 Feb 28 (1): 202-208. Cai Xiao-Hui, Chen Mei-Yu, Chao Hong-Ying, Jiang Nai-Ke, Lu Xu-Zhang, Han Wen-Min, Qin Wei, Jia Zhu-X |
Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis - A systematic analysis of 204 cases. Scientific reports 2020 Feb 10 (1): 3368. Trautmann Marcel, Rehkämper Jan, Gevensleben Heidrun, Becker Jessica, Wardelmann Eva, Hartmann Wolfgang, Grünewald Inga, Huss Sebasti |
Clinical, biological, and prognostic implications of SF3B1 co-occurrence mutations in very low/low- and intermediate-risk MDS patients. Annals of hematology 2021 Jan . Janusz Kamila, Izquierdo Marta Martín, Cadenas Félix López, Ramos Fernando, Sánchez Jesús María Hernández, Lumbreras Eva, Robledo Cristina, Del Real Javier Sánchez, Caballero Juan Carlos, Collado Rosa, Bernal Teresa, Pedro Carme, Insunza Andrés, de Paz Raquel, Xicoy Blanca, Salido Eduardo, García Joaquín Sánchez, Mínguez Sandra Santos, García Cristina Miguel, Muñoz Ana María Simón, Barba Mercedes Sánchez, Rivas Jesús María Hernández, Abáigar María, Campelo María Dí |
Clonal cytopenia of undetermined significance (CCUS) with dysplasia is enriched for MDS-type molecular findings compared to CCUS without dysplasia. European journal of haematology 2021 1 106 (4): 500-507. Jajosky Audrey N, Sadri Navid, Meyerson Howard J, Oduro Kwadwo A, Kelkar Ashwin, Fitzgerald Brynn, Tomlinson Benjamin, Moore Erika M, Beck Rose |
Effect of mutation allele frequency on the risk stratification of myelodysplastic syndrome patients. American journal of hematology 2022 9 97 (12): 1589-1598. Lee Wan-Hsuan, Lin Chien-Chin, Tsai Cheng-Hong, Tseng Mei-Hsuan, Kuo Yuan-Yeh, Liu Ming-Chih, Tang Jih-Luh, Sun Hsun-I, Chuang Yi-Kuang, Chou Wen-Chien, Hou Hsin-An, Tien Hwei-Fa |
[Analysis of Gene Mutation Characteristics and Prognosis of Elderly Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 Jun 30 (3): 755-759. Zhou Nai-Cen, Li Guo-Hui, Qin Wei-Wei, Wang Wen-Qing, Guo Huai-Peng, Liu Cong, Liu |
Genetic Characteristics According to Subgroup of Acute Myeloid Leukemia with Myelodysplasia-Related Changes. Journal of clinical medicine 2022 5 11 (9): . Kang Dain, Jung Jin, Park Silvia, Cho Byung-Sik, Kim Hee-Je, Kim Yeojae, Lee Jong-Mi, Kim Hoon Seok, Ahn Ari, Kim Myungshin, Kim Yongg |
DNMT3A R882 Mutations Confer Unique Clinicopathologic Features in MDS Including a High Risk of AML Transformation. Frontiers in oncology 2022 3 12 849376. Jawad Majd, Afkhami Michelle, Ding Yi, Zhang Xiaohui, Li Peng, Young Kim, Xu Mina Luqing, Cui Wei, Zhao Yiqing, Halene Stephanie, Al-Kali Aref, Viswanatha David, Chen Dong, He Rong, Zheng Ga |
Lab tests for MPN. International review of cell and molecular biology 2022 2 366 187-220. Moncada Alice, Pancrazzi Alessand |
Clinical and prognostic profile of SRSF2 and related spliceosome mutations in patients with acute myeloid leukemia. Molecular biology reports 2023 6 . Wenbo Jia, Xiaodong Guo, Yihong Wei, Jinting Liu, Can Can, Ruiqing Wang, Xinyu Yang, Chunyan Ji, Daoxin |
Liquid Biopsies for Circulating Tumor DNA Detection May Reveal Occult Hematologic Malignancies in Patients With Solid Tumors. JCO precision oncology 2023 3 7 e2200583. Aldea Mihaela, Tagliamento Marco, Bayle Arnaud, Vasseur Damien, Vergé Véronique, Marinello Arianna, Danlos François-Xavier, Blanc-Durand Felix, Bernard Elsa, Cerbone Luigi, Mosele Maria Fernanda, Renneville Aline, Hadoux Julien, Loriot Yohann, Sakkal Madona, Vozy Aurore, Sarkozy Clementine, Smolenschi Cristina, Nicotra Claudio, Martin-Romano Patricia, Boccon-Gibod Clementine, Habza Wafikaamira, Lazarovici Julien, Ponce Santiago, Hollebecque Antoine, Marzac Christophe, Lacroix Ludovic, Barlesi Fabrice, André Fabrice, Besse Benjamin, Rouleau Etienne, Italiano Antoine, Micol Jean-Baptis |
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