Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 57 Records) |
Query Trace: MYH11[original query] |
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CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia. Cancer 2018 Jun . Zhang Yang, Wang Fang, Chen Xue, Zhang Yu, Wang Mingyu, Liu Hong, Cao Panxiang, Ma Xiaoli, Wang Tong, Zhang Jianping, Zhang Xian, Lu Peihua, Liu Hongxi |
Clinical and biological implications of mutational spectrum in acute myeloid leukemia of FAB subtypes M4 and M5. Cancer gene therapy 2018 Feb . Cheng Zhiheng, Hu Kai, Tian Lei, Dai Yifeng, Pang Yifan, Cui Wei, Zhao Hongmian, Qin Tong, Han Yu, Hu Ning, Chen Li, Wang Chao, Zhang Yijie, Wu Depei, Ke Xiaoyan, Shi Jinlong, Fu L |
Dasatinib overrides the differentiation blockage in a patient with mutant-KIT D816V positive CBF?-MYH11 leukemia. Oncotarget 2018 3 9 (14): 11876-11882. Kampa-Schittenhelm Kerstin M, Vogel Wichard, Bonzheim Irina, Fend Falko, Horger Marius, Kanz Lothar, Soekler Martin, Schittenhelm Marcus |
Distinct genetic alteration profiles of acute myeloid leukemia between Caucasian and Eastern Asian population. Journal of hematology & oncology 2018 Feb 11 (1): 18. Wei Hui, Wang Ying, Zhou Chunlin, Lin Dong, Liu Bingcheng, Liu Kaiqi, Qiu Shaowei, Gong Benfa, Li Yan, Zhang Guangji, Wei Shuning, Gong Xiaoyuan, Liu Yuntao, Zhao Xingli, Gu Runxia, Mi Yingchang, Wang Jianxia |
[Characterization of mutational pattern of patients with core-binding factor acute myeloid leukemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 Jul 36 (7): 657-661. He Jinyuan, Chao Hongying, Zhou Min, Lu Xuzhang, Chen Tao, Yang Jianhe, Jiang Naike, Zhang |
Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
Genetic basis of hereditary thoracic aortic aneurysms and dissections. Journal of cardiology 2019 4 74 (2): 136-143. Takeda Norifumi, Komuro Iss |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jan . Renner Sina, Schüler Helke, Alawi Malik, Kolbe Verena, Rybczynski Meike, Woitschach Rixa, Sheikhzadeh Sara, Stark Veronika C, Olfe Jakob, Roser Elke, Seggewies Friederike Sophia, Mahlmann Adrian, Hempel Maja, Hartmann Melanie J, Hillebrand Mathias, Wieczorek Dagmar, Volk Alexander Erich, Kloth Katja, Koch-Hogrebe Margarete, Abou Jamra Rami, Mitter Diana, Altmüller Janine, Wey-Fabrizius Alexandra, Petersen Christine, Rau Isabella, Borck Guntram, Kubisch Christian, Mir Thomas S, von Kodolitsch Yskert, Kutsche Kerstin, Rosenberger Geo |
Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 9 17 (2): 215-225. Blue Elizabeth E, Thornton Timothy A, Kooperberg Charles, Liu Simin, Wactawski-Wende Jean, Manson JoAnn, Kuller Lew, Hayden Kathleen, Reiner Alexander |
[Analysis of Genomic Landscape in Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2020 6 28 (3): 797-801. Wang Sheng-Mei, Zheng Hong-Jun, Tian Ying, Zhang Jian-Mei, Yao Jin-H |
[The prognostic value of cloned genetic mutations in patients with CBF?-MYH11 fusion-positive acute myeloid leukemia receiving intensive consolidation therapy]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2020 11 41 (10): 853-857. Wang J, Xue S L, Li Z, Yu J Q, Wang C, Chu X L, Han R, Tao T, Wu T M, Wang B R, Wan C L, Qiu Q C, Bao X B, Wu D |
99-Case Study of Sporadic Aortic Dissection by Whole Exome Sequencing Indicated Novel Disease-Associated Genes and Variants in Chinese Population. BioMed research international 2020 2020 7857043. Wang Zanxin, Zhuang Xianmian, Chen Bailang, Wen Junmin, Peng Fang, Liu Xiling, Wei Minx |
Prospective evaluation of prognostic impact of KIT mutations on acute myeloid leukemia with RUNX1-RUNX1T1 and CBFB-MYH11. Blood advances 2020 Jan 4 (1): 66-75. Ishikawa Yuichi, Kawashima Naomi, Atsuta Yoshiko, Sugiura Isamu, Sawa Masashi, Dobashi Nobuaki, Yokoyama Hisayuki, Doki Noriko, Tomita Akihiro, Kiguchi Toru, Koh Shiro, Kanamori Heiwa, Iriyama Noriyoshi, Kohno Akio, Moriuchi Yukiyoshi, Asada Noboru, Hirano Daiki, Togitani Kazuto, Sakura Toru, Hagihara Maki, Tomikawa Tatsuki, Yokoyama Yasuhisa, Asou Norio, Ohtake Shigeki, Matsumura Itaru, Miyazaki Yasushi, Naoe Tomoki, Kiyoi Hitos |
CBFB-MYH11 fusion transcripts distinguish acute myeloid leukemias with distinct molecular landscapes and outcomes. Blood advances 2021 Sep . Huang Benjamin J, Smith Jenny L, Wang Yi-Cheng, Taghizadeh Kassra, Leonti Amanda R, Ries Rhonda E, Liu Yanling, Kolekar Pandurang, Tarlock Katherine, Gerbing Robert, Crowgey Erin, Furlan Scott N, Shaw Timothy I, Hagiwara Kohei, Wei Lisa, Cooper Todd M, Gamis Alan S, Aplenc Richard, Kolb E Anders, Farrar Jason E, Triche Timothy, Alonzo Todd A, Ma Xiaotu, Meshinchi Sohe |
Prognostic values of D816V KIT mutation and peri-transplant CBFB-MYH11 MRD monitoring on acute myeloid leukemia with CBFB-MYH11. Bone marrow transplantation 2021 Jun . Cho Byung-Sik, Min Gi-June, Park Sung-Soo, Park Silvia, Jeon Young-Woo, Shin Seung-Hwan, Yahng Seung-Ah, Yoon Jae-Ho, Lee Sung-Eun, Eom Ki-Seong, Kim Yoo-Jin, Lee Seok, Min Chang-Ki, Cho Seok-Goo, Kim Dong-Wook, Lee Jong Wook, Kim Myungshin, Kim Yonggoo, Kim Hee- |
Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China. American journal of translational research 2021 6 13 (5): 4281-4295. Li Ying, Fang Miaoxian, Yang Jue, Yu Changjiang, Kuang Juntao, Sun Tucheng, Fan Ruix |
[The Prognostic Factors for AML Children with CBF?/MYH11 Positive]. Zhongguo shi yan xue ye xue za zhi 2021 4 29 (2): 369-373. Yan Min, Song Fu-Xing, Lu J |
Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia. Haematologica 2021 Mar . Kaburagi Taeko, Yamato Genki, Shiba Norio, Yoshida Kenichi, Hara Yusuke, Tabuchi Ken, Shiraishi Yuichi, Ohki Kentaro, Sotomatsu Manabu, Arakawa Hirokazu, Matsuo Hidemasa, Shimada Akira, Taki Tomohiko, Kiyokawa Nobutaka, Tomizawa Daisuke, Horibe Keizo, Miyano Satoru, Taga Takashi, Adachi Souichi, Ogawa Seishi, Hayashi Yasuhi |
Association of gene polymorphisms in MYH11 and TGF-? signaling with the susceptibility and clinical outcomes of DeBakey type III aortic dissection. Mammalian genome : official journal of the International Mammalian Genome Society 2021 Nov . Chang Yafei, Yuan Qinghua, Jiang Peipei, Sun Ling, Ma Yitong, Ma Xia |
Impact of KMT2A Rearrangement and CSPG4 Expression in Pediatric Acute Myeloid Leukemia. Cancers 2021 10 13 (19): . Hoffmeister Lina Marie, Orhan Eser, Walter Christiane, Niktoreh Naghmeh, Hanenberg Helmut, von Neuhoff Nils, Reinhardt Dirk, Schneider Mark |
Both the subtypes of KIT mutation and minimal residual disease are associated with prognosis in core binding factor acute myeloid leukemia: a retrospective clinical cohort study in single center. Annals of hematology 2021 Jan . Duan Wenbing, Liu Xiaohong, Zhao Xiaosu, Jia Jinsong, Wang Jing, Gong Lizhong, Jiang Qian, Zhao Ting, Wang Yu, Zhang Xiaohui, Xu Lanping, Shi Hongxia, Chang Yingjun, Liu Kaiyan, Huang Xiaojun, Qin Yazhen, Jiang H |
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
Molecular dissection of a hyper-aggressive CBFB-MYH11/FLT3-ITD-positive acute myeloid leukemia. Journal of translational medicine 2022 7 20 (1): 311. Lo Iudice Gabriele, De Bellis Eleonora, Savi Arianna, Guarnera Luca, Massacci Alice, De Nicola Francesca, Goeman Frauke, Ottone Tiziana, Divona Mariadomenica, Pallocca Matteo, Fanciulli Maurizio, Voso Maria Teresa, Ciliberto Genna |
Comprehensive Mutation Profile in Acute Myeloid Leukemia Patients with RUNX1-RUNX1T1 or CBFB-MYH11 Fusions. Turkish journal of haematology : official journal of Turkish Society of Haematology 2022 4 39 (2): 84-93. Qin Wei, Chen Xiayu, Shen Hong Jie, Wang Zheng, Cai Xiaohui, Jiang Naike, Hua Haiyi |
[Molecular Genetic Characteristics of Acute Myeloid Leukemia Patients with CBF?-MYH11 Positive]. Zhongguo shi yan xue ye xue za zhi 2022 12 30 (6): 1661-1667. Jiang Yu, Chao Hong-Ying, Lu Xu-Zhang, Wu Pin, Sun Xiao-Ch |
Core-binding factor abnormalities involving chromosome 16 in acute myeloid leukaemia: prognostic and therapeutic implications. BMJ case reports 2023 8 16 (8): . Chinmayee Panigrahi, Nakul Tikare, Prabodha Kumar Das, Somanath Pad |
TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia. Genes, chromosomes & cancer 2023 4 . Yusuke Hara, Norio Shiba, Kenichi Yoshida, Genki Yamato, Taeko Kaburagi, Yuichi Shiraishi, Kentaro Ohki, Yusuke Shiozawa, Machiko Kawamura, Hirohide Kawasaki, Manabu Sotomatsu, Takumi Takizawa, Hidemasa Matsuo, Akira Shimada, Nobutaka Kiyokawa, Daisuke Tomizawa, Takashi Taga, Etsuro Ito, Keizo Horibe, Satoru Miyano, Souichi Adachi, Tomohiko Taki, Seishi Ogawa, Yasuhide Hayas |
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis. Journal of the American Society of Nephrology : JASN 2023 3 . Ahram Dina F, Lim Tze Y, Ke Juntao, Jin Gina, Verbitsky Miguel, Bodria Monica, Kil Byum Hee, Chatterjee Debanjana, Piva Stacy E, Marasa Maddalena, Zhang Jun Y, Cocchi Enrico, Caridi Gianluca, Gucev Zoran, Lozanovski Vladimir J, Pisani Isabella, Izzi Claudia, Savoldi Gianfranco, Gnutti Barbara, Capone Valentina P, Morello William, Guarino Stefano, Esposito Pasquale, Lambert Sarah, Radhakrishnan Jai, Appel Gerald B, Uy Natalie S, Rao Maya K, Canetta Pietro A, Bomback Andrew S, Nestor Jordan G, Hays Thomas, Cohen David J, Finale Na Carolina, van Wijk Joanna A E, La Scola Claudio, Baraldi Olga, Tondolo Francesco, Di Renzo Dacia, Jamry-Dziurla Anna, Pezzutto Alessandro, Manca Valeria, Mitrotti Adele, Santoro Domenico, Conti Giovanni, Martino Marida, Giordano Mario, Gesualdo Loreto, Zibar Lada, Masnata Giuseppe, Bonomini Mario, Alberti Daniele, La Manna Gaetano, Caliskan Yasar, Ranghino Andrea, Marzuillo Pierluigi, Kiryluk Krzysztof, Krzemie? Gra?yna, Miklaszewska Monika, Lin Fangming, Montini Giovanni, Scolari Francesco, Fiaccadori Enrico, Arapovi? Adela, Saraga Marijan, McKiernan James, Alam Shumyle, Zaniew Marcin, Szczepa?ska Maria, Szmigielska Agnieszka, Sikora Przemys?aw, Dro?d? Dorota, Mizerska-Wasiak Malgorzata, Mane Shrikant, Lifton Richard P, Tasic Velibor, Latos-Bielenska Anna, Gharavi Ali G, Ghiggeri Gian Marco, Materna-Kiryluk Anna, Westland Rik, Sanna-Cherchi Simo |
A comprehensive analysis of cytogenetics, molecular profile, and survival among pediatric acute myeloid leukemia: a prospective study from a tertiary referral center. American journal of blood research 2023 2 12 (6): 177-189. Meena Jagdish Prasad, Makkar Harshita, Gupta Aditya Kumar, Bakhshi Sameer, Gupta Ritu, Thakral Deepshi, Chopra Anita, Tanwar Pranay, Upadhyay Ashish Datt, Pathak Nivedita, Seth Rach |
KIT exon 17 mutations are predictive of inferior outcome in pediatric acute myeloid leukemia with RUNX1::RUNX1T1. Pediatric blood & cancer 2023 11 e30791. Shyam Srinivasan, Chetan Dhamne, Nikhil Patkar, Gaurav Chatterjee, Nirmalya Roy Moulik, Akanksha Chichra, Aneeta Pallath, Prashant Tembhare, Dhanalaxmi Shetty, P G Subramanian, Gaurav Narula, Shripad Banava |
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- Page last updated:Apr 16, 2024
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