HuGE Literature Finder
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Association of Pathway Mutations With Survival in Taiwanese Breast Cancers. Frontiers in oncology 2022 12 819555. Yang Po-Sheng, Chao Ying-Ting, Lung Chun-Fan, Liu Chien-Liang, Chang Yuan-Ching, Li Ker-Chau, Hsu Yi-Chiu |
Integrative study of EZH2 mutational status, copy number, protein expression and H3K27 trimethylation in AML/MDS patients. Clinical epigenetics 2021 Apr 13 (1): 77. Stomper Julia, Meier Ruth, Ma Tobias, Pfeifer Dietmar, Ihorst Gabriele, Blagitko-Dorfs Nadja, Greve Gabriele, Zimmer Dennis, Platzbecker Uwe, Hagemeijer Anne, Schmitt-Graeff Ingrid, Lübbert Micha |
Genetic profile and immunohistochemical study of clear cell renal carcinoma: Pathological-anatomical correlation and prognosis. Cancer treatment and research communications 2021 5 27 100374. Diez-Calzadilla N A, Noguera Salvá R, Soriano Sarrió P, Martínez-Jabaloyas J |
Clinicopathological Significance of RUNX1 in Non-Small Cell Lung Cancer. Journal of clinical medicine 2020 6 9 (6): . Kim Yujin, Lee Bo Bin, Kim Dongho, Um Sangwon, Cho Eun Yoon, Han Joungho, Shim Young Mog, Kim Duk-Hw |
Identification of Key Genes and Pathways Associated with RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis. Medical science monitor : international medical journal of experimental and clinical research 2018 Oct 24 7100-7108. Zhu Fangxiao, Huang Rui, Li Jing, Liao Xiwen, Huang Yumei, Lai Yongro |
Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AML. Leukemia 2018 2 32 (5): 1124-1134. Zampini Matteo, Tregnago Claudia, Bisio Valeria, Simula Luca, Borella Giulia, Manara Elena, Zanon Carlo, Zonta Francesca, Serafin Valentina, Accordi Benedetta, Campello Silvia, Buldini Barbara, Pession Andrea, Locatelli Franco, Basso Giuseppe, Pigazzi Marti |
Influence of TS (rs34743033) and RUNX1 (rs2014300) gene polymorphisms on survival outcomes of fluorouracil-based chemotherapy in Chinese advanced gastric cancer patients. Cancer management and research 2018 10 1429-1437. Han Rongbo, Wei Jingsun, Zhang Honghong, Su Xinyu, Chu Xia, Chen Yuetong, Gong Yang, Wang Xiujuan, Shi Junfeng, Chen Jinf |
Impact of genotype on leukaemic transformation in polycythaemia vera and essential thrombocythaemia. British journal of haematology 2017 09 178 (5): 764-771. Alvarez-Larrán Alberto, Senín Alicia, Fernández-Rodríguez Concepción, Pereira Arturo, Arellano-Rodrigo Eduardo, Gómez Montse, Ferrer-Marin Francisca, Martínez-López Joaquín, Camacho Laura, Colomer Dolors, Angona Anna, Navarro Blanca, Cervantes Francisco, Besses Carlos, Bellosillo Beatriz, Hernández-Boluda Juan Carl |
ASXL1 mutations in younger adult patients with acute myeloid leukemia: a study by the German-Austrian Acute Myeloid Leukemia Study Group. Haematologica 2015 Mar 100 (3): 324-30. Paschka Peter, Schlenk Richard F, Gaidzik Verena I, Herzig Julia K, Aulitzky Teresa, Bullinger Lars, Späth Daniela, Teleanu Veronika, Kündgen Andrea, Köhne Claus-Henning, Brossart Peter, Held Gerhard, Horst Heinz-A, Ringhoffer Mark, Götze Katharina, Nachbaur David, Kindler Thomas, Heuser Michael, Thol Felicitas, Ganser Arnold, Döhner Hartmut, Döhner Konstan |
Clinical impact of gene mutations and lesions detected by SNP-array karyotyping in acute myeloid leukemia patients in the context of gemtuzumab ozogamicin treatment: results of the ALFA-0701 trial. Oncotarget 2014 Feb 5 (4): 916-32. Renneville Aline, Abdelali Raouf Ben, Chevret Sylvie, Nibourel Olivier, Cheok Meyling, Pautas Cécile, Duléry Rémy, Boyer Thomas, Cayuela Jean-Michel, Hayette Sandrine, Raffoux Emmanuel, Farhat Hassan, Boissel Nicolas, Terre Christine, Dombret Hervé, Castaigne Sylvie, Preudhomme Clau |
Clinical effect of point mutations in myelodysplastic syndromes. The New England journal of medicine 2011 Jun 364 (26): 2496-506. Bejar Rafael, Stevenson Kristen, Abdel-Wahab Omar, Galili Naomi, Nilsson Björn, Garcia-Manero Guillermo, Kantarjian Hagop, Raza Azra, Levine Ross L, Neuberg Donna, Ebert Benjamin |
Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes. Tissue antigens 2003 Dec 62 (6): 492-7. Nielsen C, Hansen D, Husby S, Jacobsen B B, Lillevang S |
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nature genetics 2002 Dec 32 (4): 666-9. Prokunina Ludmila, Castillejo-López Casimiro, Oberg Fredrik, Gunnarsson Iva, Berg Louise, Magnusson Veronica, Brookes Anthony J, Tentler Dmitry, Kristjansdóttir Helga, Gröndal Gerdur, Bolstad Anne Isine, Svenungsson Elisabet, Lundberg Ingrid, Sturfelt Gunnar, Jönssen Andreas, Truedsson Lennart, Lima Guadalupe, Alcocer-Varela Jorge, Jonsson Roland, Gyllensten Ulf B, Harley John B, Alarcón-Segovia Donato, Steinsson Kristján, Alarcón-Riquelme Marta |
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