Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: Syndrome and IDH1[original query] |
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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 |
Persistence of DNMT3A mutations at long-term remission in adult patients with AML. British journal of haematology 2014 Nov 167 (4): 478-86. Pløen Gro G, Nederby Line, Guldberg Per, Hansen Maria, Ebbesen Lene H, Jensen Uffe Birk, Hokland Peter, Aggerholm An |
[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 |
IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association. Oncotarget 2015 Oct . Debarri Houria, Lebon Delphine, Roumier Christophe, Cheok Meyling, Marceau-Renaut Alice, Nibourel Olivier, Geffroy Sandrine, Helevaut Nathalie, Rousselot Philippe, Gruson Bérengère, Gardin Claude, Chretien Marie-Lorraine, Sebda Shéhérazade, Figeac Martin, Berthon Céline, Quesnel Bruno, Boissel Nicolas, Castaigne Sylvie, Dombret Hervé, Renneville Aline, Preudhomme Clau |
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 |
Prognostic significance of histomolecular subgroups of adult anaplastic (WHO Grade III) gliomas: applying the 'integrated' diagnosis approach. Journal of clinical pathology 2016 Jan . Rajmohan K S, Sugur Harsha S, Shwetha S D, Ramesh Arvind, Thennarasu Kandavel, Pandey Paritosh, Arivazhagan Arimappamagan, Santosh Va |
Clinical Outcomes and Co-Occurring Mutations in Patients with RUNX1-Mutated Acute Myeloid Leukemia. International journal of molecular sciences 2017 Jul 18 (8): . Khan Maliha, Cortes Jorge, Kadia Tapan, Naqvi Kiran, Brandt Mark, Pierce Sherry, Patel Keyur P, Borthakur Gautam, Ravandi Farhad, Konopleva Marina, Kornblau Steven, Kantarjian Hagop, Bhalla Kapil, DiNardo Courtney |
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 |
ATRX status correlates with 11 C-methionine uptake in WHO grade II and III gliomas with IDH1 mutations. Brain tumor pathology 2017 Mar . Ogishima Takahiro, Tamura Kaoru, Kobayashi Daisuke, Inaji Motoki, Hayashi Shihori, Tamura Reina, Nariai Tadashi, Ishii Kenji, Maehara Taketos |
Durable Remissions with Ivosidenib in IDH1-Mutated Relapsed or Refractory AML. The New England journal of medicine 2018 6 378 (25): 2386-2398. DiNardo Courtney D, Stein Eytan M, de Botton Stéphane, Roboz Gail J, Altman Jessica K, Mims Alice S, Swords Ronan, Collins Robert H, Mannis Gabriel N, Pollyea Daniel A, Donnellan Will, Fathi Amir T, Pigneux Arnaud, Erba Harry P, Prince Gabrielle T, Stein Anthony S, Uy Geoffrey L, Foran James M, Traer Elie, Stuart Robert K, Arellano Martha L, Slack James L, Sekeres Mikkael A, Willekens Christophe, Choe Sung, Wang Hongfang, Zhang Vickie, Yen Katharine E, Kapsalis Stephanie M, Yang Hua, Dai David, Fan Bin, Goldwasser Meredith, Liu Hua, Agresta Sam, Wu Bin, Attar Eyal C, Tallman Martin S, Stone Richard M, Kantarjian Hagop |
Ivosidenib Deemed Safe, Effective in AML. Cancer discovery 2018 6 8 (8): OF1. Authors are not available |
Clinical relevance of IDH1/2 mutant allele burden during follow-up in acute myeloid leukemia. A study by the French ALFA group. Haematologica 2018 2 103 (5): 822-829. Ferret Yann, Boissel Nicolas, Helevaut Nathalie, Madic Jordan, Nibourel Olivier, Marceau-Renaut Alice, Bucci Maxime, Geffroy Sandrine, Celli-Lebras Karine, Castaigne Sylvie, Thomas Xavier, Terré Christine, Dombret Hervé, Preudhomme Claude, Renneville Ali |
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 |
[Analysis of ASXL1 gene variant in patients with myelodysplastic syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Feb 37 (2): 110-115. Chen Meiyu, Liu Jie, Chao Hongying, Qin Wei, Jiang Naike, Lu Xuzhang, Cen Ling, Jiang Yu, Cai Xiaohui, Zhang Ri, Wang Qi |
[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 |
Incidence of biomarkers in high-grade gliomas and their impact on survival in a diverse SouthEast Asian cohort - a population-based study. BMC cancer 2020 2 20 (1): 79. Ang Samantha Ya Lyn, Lee Lester, See Angela An Qi, Ang Ting Yao, Ang Beng Ti, King Nicolas Kon K |
Panel gene profiling of small bowel adenocarcinoma: Results from the NADEGE prospective cohort. International journal of cancer 2020 Nov . Aparicio Thomas, Svrcek Magali, Henriques Julie, Afchain Pauline, Lièvre Astrid, Tougeron David, Gagniere Johan, Terrebonne Eric, Piessen Guillaume, Legoux Jean-Louis, Lecaille Cédric, Pocard Marc, Gornet Jean-Marc, Zaanan Aziz, Lavau-Denes Sandrine, Lecomte Thierry, Deutsch David, Vernerey Dewi, Puig Pierre Laure |
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome. Blood advances 2021 9 6 (3): 793-807. West Robert R, Calvo Katherine R, Embree Lisa J, Wang Weixin, Tuschong Laura M, Bauer Thomas R, Tillo Desiree, Lack Justin, Droll Stephenie, Hsu Amy P, Holland Steven M, Hickstein Dennis |
High mutation burden in the checkpoint and micro-RNA processing genes in myelodysplastic syndrome. PloS one 2021 3 16 (3): e0248430. Moiseev Ivan Sergeevich, Tcvetkov Nikolay Yurevich, Barkhatov Ildar Munerovich, Barabanshikova Maria Vladimirovna, Bug Dmitrii Sergeevich, Petuhova Natalya Vitalievna, Tishkov Artem Valerievich, Bakin Evgenyi Alexandrovich, Izmailova Ekaterina Andreevna, Shakirova Alena Igorevna, Kulagin Alexandr Dmitrievich, Morozova Elena Vladislavov |
Glioma Imaging by O-(2-18F-Fluoroethyl)-L-Tyrosine PET and Diffusion-Weighted MRI and Correlation With Molecular Phenotypes, Validated by PET/MR-Guided Biopsies. Frontiers in oncology 2021 12 11 743655. Cheng Ye, Song Shuangshuang, Wei Yukui, Xu Geng, An Yang, Ma Jie, Yang Hongwei, Qi Zhigang, Xiao Xinru, Bai Jie, Xu Lixin, Hu Zeliang, Sun Tingting, Wang Leiming, Lu Jie, Lin Qingta |
BRAF Frequently Co-occurs With IDH1/2, TP53, and ATRX Mutations in Adult Patients With Gliomas and Is Associated With Poorer Survival Than That of Patients Harboring BRAF . Frontiers in oncology 2021 1 10 531968. Da Rong, Wang Maode, Jiang Haitao, Wang Tuo, Wang W |
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 |
Ivosidenib and Azacitidine in IDH1-Mutated Acute Myeloid Leukemia. The New England journal of medicine 2022 4 386 (16): 1519-1531. Montesinos Pau, Recher Christian, Vives Susana, Zarzycka Ewa, Wang Jianxiang, Bertani Giambattista, Heuser Michael, Calado Rodrigo T, Schuh Andre C, Yeh Su-Peng, Daigle Scott R, Hui Jianan, Pandya Shuchi S, Gianolio Diego A, de Botton Stephane, Döhner Hartm |
Lab tests for MPN. International review of cell and molecular biology 2022 2 366 187-220. Moncada Alice, Pancrazzi Alessand |
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 |
Gene mutation analysis using next-generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi-center study from China. Cancer medicine 2023 2 . Li Junnan, Pei Li, Liang Simin, Xu Shuangnian, Wang Yi, Wang Xiao, Liao Yi, Zhan Qian, Cheng Wei, Yang Zesong, Tang Xiaoqiong, Zhang Hongbin, Xiao Qing, Chen Jianbin, Liu Lin, Wang |
Pediatric-type high-grade gliomas with PDGFRA amplification in adult patients with Li-Fraumeni syndrome: clinical and molecular characterization of three cases. Acta neuropathologica communications 2024 4 12 (1): 57. Yuji Kibe, Fumiharu Ohka, Kosuke Aoki, Junya Yamaguchi, Kazuya Motomura, Eiji Ito, Kazuhito Takeuchi, Yuichi Nagata, Satoshi Ito, Nobuhiko Mizutani, Yoshiki Shiba, Sachi Maeda, Tomohide Nishikawa, Hiroki Shimizu, Ryuta Sai |
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- Page last updated:Apr 22, 2024
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