Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: Syndrome and SRSF2[original query] |
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Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression. American journal of hematology 2014 Feb 89 (2): 181-6. Hou Hsin-An, Kuo Yuan-Yeh, Tang Jih-Luh, Chou Wen-Chien, Yao Ming, Lai Yan-Jun, Lin Chien-Chin, Chen Chien-Yuan, Liu Chieh-Yu, Tseng Mei-Hsuan, Huang Chi-Fei, Chiang Ying-Chieh, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Huang Shang-Yi, Ko Bor-Sheng, Wu Shang-Ju, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
Detection of SRSF2-P95 mutation by high-resolution melting curve analysis and its effect on prognosis in myelodysplastic syndrome. PloS one 2014 9 (12): e115693. Lin Jiang, Yang Jing, Wen Xiang-Mei, Yang Lei, Deng Zhao-Qun, Qian Zhen, Ma Ji-Chun, Guo Hong, Zhang Ying-Ying, Qian Wei, Qian J |
Preferential occurrence of spliceosome mutations in acute myeloid leukemia with preceding myelodysplastic syndrome and/or myelodysplasia morphology. Leukemia & lymphoma 2015 Jan 1-8. Cho Young-Uk, Jang Seongsoo, Seo Eul-Ju, Park Chan-Jeoung, Chi Hyun-Sook, Kim Dae-Young, Lee Jung-Hee, Lee Je-Hwan, Lee Kyoo-Hyung, Koh Kyung-Nam, Im Ho-Joon, Seo Jong Jin, Park Sang Hyuk, Park Young-Mi, Lee Jong-Ke |
Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome. Blood cancer journal 2014 4 e177. Chen T-C, Hou H-A, Chou W-C, Tang J-L, Kuo Y-Y, Chen C-Y, Tseng M-H, Huang C-F, Lai Y-J, Chiang Y-C, Lee F-Y, Liu M-C, Liu C-W, Liu C-Y, Yao M, Huang S-Y, Ko B-S, Hsu S-C, Wu S-J, Tsay W, Chen Y-C, Tien H |
Impact of TET2, SRSF2, ASXL1 and SETBP1 mutations on survival of patients with chronic myelomonocytic leukemia. Experimental hematology & oncology 2015 4 14. Cui Yajuan, Tong Hongyan, Du Xin, Li Bing, Gale Robert Peter, Qin Tiejun, Liu Jinqin, Xu Zefeng, Zhang Yue, Huang Gang, Jin Jie, Fang Liwei, Zhang Hongli, Pan Lijuan, Hu Naibo, Qu Shiqiang, Xiao Zhiji |
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 |
The high frequency of the U2AF1 S34Y mutation and its association with isolated trisomy 8 in myelodysplastic syndrome in Asians, but not in Caucasians. Leukemia research 2017 9 61 96-103. Kim Seon Young, Kim Kwantae, Hwang Byungjin, Im Kyongok, Park Si Nae, Kim Jung-Ah, Hwang Sang Mee, Bang Duhee, Lee Dong So |
Prognostic significance of SRSF2 mutations in myelodysplastic syndromes and chronic myelomonocytic leukemia: a meta-analysis. Hematology (Amsterdam, Netherlands) 2018 May 1-7. Arbab Jafari Pourya, Ayatollahi Hossein, Sadeghi Ramin, Sheikhi Maryam, Asghari Am |
SETBP1 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome. Pathology, research and practice 2018 Mar . Yao Xin-Yu, Zhou Jing-Dong, Yang Jing, Zhang Wei, Ma Ji-Chun, Wen Xiang-Mei, Yao Dong-Ming, Xu Zi-Jun, Wu De-Hong, He Pin-Fang, Qian Jun, Lin Jia |
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 |
Machine learning demonstrates that somatic mutations imprint invariant morphologic features in myelodysplastic syndromes. Blood 2020 9 136 (20): 2249-2262. Nagata Yasunobu, Zhao Ran, Awada Hassan, Kerr Cassandra M, Mirzaev Inom, Kongkiatkamon Sunisa, Nazha Aziz, Makishima Hideki, Radivoyevitch Tomas, Scott Jacob G, Sekeres Mikkael A, Hobbs Brian P, Maciejewski Jaroslaw |
Juvenile myelomonocytic leukemia - A bona fide RASopathy syndrome. Best practice & research. Clinical haematology 2020 5 33 (2): 101171. Lasho Terra, Patnaik Mrinal |
Sex-Related Differences in Chronic Myeloid Neoplasms: From the Clinical Observation to the Underlying Biology. International journal of molecular sciences 2021 Mar 22 (5): . Karantanos Theodoros, Jain Tania, Moliterno Alison R, Jones Richard J, DeZern Amy |
Genetic alterations in Thai adult patients with acute myeloid leukemia and myelodysplastic syndrome-excess blasts detected by next-generation sequencing technique. Annals of hematology 2021 Apr . Owattanapanich Weerapat, Herzig Julia, Jahn Nikolaus, Panina Ekaterina, Ruchutrakool Theera, Kungwankiattichai Smith, Issaragrisil Surapol, Döhner Hartmut, Döhner Konstan |
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 |
Bioinformatics analysis of high frequency mutations in myelodysplastic syndrome-related patients. Annals of translational medicine 2021 11 9 (19): 1491. Wu Kun, Nie Bo, Li Liyin, Yang Xin, Yang Jinrong, He Zhenxin, Li Yanhong, Cheng Shenju, Shi Mingxia, Zeng Y |
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 |
Cardiovascular Disease Among Patients With AML and CHIP-Related Mutations. JACC. CardioOncology 2022 Mar 4 (1): 38-49. Calvillo-Argüelles Oscar, Schoffel Alice, Capo-Chichi José-Mario, Abdel-Qadir Husam, Schuh Andre, Carrillo-Estrada Montserrat, Liu Shiying, Gupta Vikas, Schimmer Aaron D, Yee Karen, Shlush Liran I, Natarajan Pradeep, Thavendiranathan Paaladine |
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 |
Therapy-related myeloid neoplasms with normal karyotype show distinct genomic and clinical characteristics compared to their counterparts with abnormal karyotype. British journal of haematology 2022 3 197 (6): 736-744. Tariq Hamza, Barnea Slonim Liron, Coty Fattal Zachary, Alikhan Mir B, Segal Jeremy, Gurbuxani Sandeep, Helenowski Irene B, Zhang Hui, Sukhanova Madina, Lu Xinyan, Altman Jessica K, Chen Qing C, Behdad Am |
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 |
Higher RUNX1 expression levels are associated with worse overall and leukaemia-free survival in myelodysplastic syndrome patients. EJHaem 2022 12 3 (4): 1209-1219. Wang Yu-Hung, Yao Chi-Yuan, Lin Chien-Chin, Chen Chi-Ling, Hsu Chia-Lang, Tsai Cheng-Hong, Hou Hsin-An, Chou Wen-Chien, Tien Hwei-Fa |
Allogeneic Hematopoietic Cell Transplantation Improves Outcome in Myelodysplastic Syndrome Across High-Risk Genetic Subgroups: Genetic Analysis of the Blood and Marrow Transplant Clinical Trials Network 1102 Study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2023 8 JCO2300866. Jurjen Versluis, Wael Saber, Harrison K Tsai, Christopher J Gibson, Laura W Dillon, Asmita Mishra, Joseph McGuirk, Richard T Maziarz, Peter Westervelt, Pranay Hegde, Devdeep Mukherjee, Michael J Martens, Brent Logan, Mary Horowitz, Christopher S Hourigan, Ryotaro Nakamura, Corey Cutler, R Coleman Lindsley, |
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 |
The clinical and molecular spectrum of ETV6 mutated myeloid neoplasms. British journal of haematology 2023 5 . Mark Gurney, Ismahene Chekkaf, Anmol Baranwal, Rami Basmaci, Bahga Katamesh, Patricia Greipp, James M Foran, Talha Badar, Abhishek A Mangaonkar, Kebede H Begna, Naseema Gangat, Mrinal M Patnaik, Mark R Litzow, Mithun V Shah, David S Viswanatha, Rong He, Hassan B Alkhateeb, Aref Al-Ka |
Wilms' tumor 1 expression combined with genetic mutations for prognostic assessment in MDS. Leukemia & lymphoma 2023 3 1-9. Pan Danqi, Zhao Wenshu, Jiang Qianli, Yin Changxin, He Han, Liao Libin, Ye Jieyu, Dai M |
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 |
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- Page last updated:Apr 22, 2024
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