Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Abnormalities and CD34[original query] |
---|
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. The New England journal of medicine 2005 1 352 (3): 254-66. Falini Brunangelo, Mecucci Cristina, Tiacci Enrico, Alcalay Myriam, Rosati Roberto, Pasqualucci Laura, La Starza Roberta, Diverio Daniela, Colombo Emanuela, Santucci Antonella, Bigerna Barbara, Pacini Roberta, Pucciarini Alessandra, Liso Arcangelo, Vignetti Marco, Fazi Paola, Meani Natalia, Pettirossi Valentina, Saglio Giuseppe, Mandelli Franco, Lo-Coco Francesco, Pelicci Pier-Giuseppe, Martelli Massimo F, |
Analysis of NPM1 gene mutations in Chinese adults with acute myeloid leukemia. International journal of hematology 2007 Aug 86 (2): 143-6. Yan Lingzhi, Chen Suning, Liang Jianying, Feng Yufeng, Cen Jiannong, He Jun, Chang Weirong, Zhu Ziling, Pan Jinlan, Wu Yafang, Xue Yongquan, Wu Dep |
Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis. PloS one 2009 4 (2): e4583. Graubert Timothy A, Payton Michelle A, Shao Jin, Walgren Richard A, Monahan Ryan S, Frater John L, Walshauser Mark A, Martin Mike G, Kasai Yumi, Walter Matthew |
ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events. Genes, chromosomes & cancer 2012 Apr 51 (4): 328-37. Haferlach Claudia, Bacher Ulrike, Schnittger Susanne, Alpermann Tamara, Zenger Melanie, Kern Wolfgang, Haferlach Torst |
Next-generation sequencing and FISH studies reveal the appearance of gene mutations and chromosomal abnormalities in hematopoietic progenitors in chronic lymphocytic leukemia. Journal of hematology & oncology 2017 Apr 10 (1): 83. Quijada-Álamo Miguel, Hernández-Sánchez María, Robledo Cristina, Hernández-Sánchez Jesús-María, Benito Rocío, Montaño Adrián, Rodríguez-Vicente Ana E, Quwaider Dalia, Martín Ana-África, García-Álvarez María, Vidal-Manceñido María Jesús, Ferrer-Garrido Gonzalo, Delgado-Beltrán María-Pilar, Galende Josefina, Rodríguez Juan-Nicolás, Martín-Núñez Guillermo, Alonso José-María, García de Coca Alfonso, Queizán José A, Sierra Magdalena, Aguilar Carlos, Kohlmann Alexander, Hernández José-Ángel, González Marcos, Hernández-Rivas Jesús-Mar |
Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY): Molecular Profiling Confirms Frequent MAPK Pathway Activation. Journal of neuropathology and experimental neurology 2021 8 80 (9): 821-829. Ida Cristiane M, Johnson Derek R, Nair Asha A, Davila Jaime, Kollmeyer Thomas M, Minn Kay, Fadra Numrah M, Balcom Jessica R, Fung Kar-Ming A, Kim Dong Kun, Kaufmann Timothy J, Kipp Benjamin R, Halling Kevin C, Jenkins Robert B, Giannini Cateri |
Analysis of RAS gene mutations in cytogenetically normal de novo acute myeloid leukemia patients reveals some novel alterations. Saudi journal of biological sciences 2021 Jul 28 (7): 3735-3740. Akram Afia Muhammad, Chaudhary Asma, Kausar Humera, Althobaiti Fayez, Abbas Afshan Syed, Hussain Zawar, Fatima Naz, Zafar Erum, Asif Wajiha, Afzal Umair, Yousaf Zoufishan, Zafar Amjad, Harakeh Steve M, Qamer Sami |
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes. Nature medicine 2021 10 27 (10): 1806-1817. Sahoo Sushree S, Pastor Victor B, Goodings Charnise, Voss Rebecca K, Kozyra Emilia J, Szvetnik Amina, Noellke Peter, Dworzak Michael, Starý Jan, Locatelli Franco, Masetti Riccardo, Schmugge Markus, De Moerloose Barbara, Catala Albert, Kállay Krisztián, Turkiewicz Dominik, Hasle Henrik, Buechner Jochen, Jahnukainen Kirsi, Ussowicz Marek, Polychronopoulou Sophia, Smith Owen P, Fabri Oksana, Barzilai Shlomit, de Haas Valerie, Baumann Irith, Schwarz-Furlan Stephan, , Niewisch Marena R, Sauer Martin G, Burkhardt Birgit, Lang Peter, Bader Peter, Beier Rita, Müller Ingo, Albert Michael H, Meisel Roland, Schulz Ansgar, Cario Gunnar, Panda Pritam K, Wehrle Julius, Hirabayashi Shinsuke, Derecka Marta, Durruthy-Durruthy Robert, Göhring Gudrun, Yoshimi-Noellke Ayami, Ku Manching, Lebrecht Dirk, Erlacher Miriam, Flotho Christian, Strahm Brigitte, Niemeyer Charlotte M, Wlodarski Marcin |
Morphologic, immunophenotypic, and molecular genetic comparison study in patients with clonal cytopenia of undetermined significance, myelodysplastic syndrome, and acute myeloid leukemia with myelodysplasia-related changes: A single institution experience. International journal of laboratory hematology 2022 3 44 (4): 738-749. Gao Linlin, Hyter Stephen, Zhang Da, Kelting Sarah, Woodroof Janet, Abdallah Al-Ola, Yacoub Abdulraheem, McGuirk Joseph, Abdelhakim Haitham, Godwin Andrew K, Cui W |
[Association of Next Generation Sequencing Based Genotypic Profiling with MICM Characteristics in NPM1 Mutated Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 2 30 (1): 56-60. Wang Biao, Ling Yun, Dai Li, Gu Wei-Ying, Zhang Xiu-Wen, Xing Shan-Shan, Li Hai-Qi |
Integrated clinical genotype-phenotype characteristics of early T-cell precursor acute lymphoblastic leukemia. Cancer 2022 Oct . Ye Matthew T, Wang Yi, Zuo Zhuang, Calin Steliana, He Hua, Tang Zhenya, Jabbour Elias J, Borthakur Gautam, Zhang Yizhuo, Yang Yaling, You M Jam |
Abnormalities by Multicolor Flow Cytometry for Detection of Minimal Residual Disease in Recipients of Allo-HSCT Originating from Donors: A Cohort Study. Turkish journal of haematology : official journal of Turkish Society of Haematology 2023 1 40 (1): 18-27. Wang Hui, Wang Aixian, Chen Man, Gong Meiwei, Wu Xueying, Zhen Junyi, Lu Y |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
- Content source: