Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Neoplasms and MYH11[original query] |
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Somatic mutation analysis of MYH11 in breast and prostate cancer. BMC cancer 2008 8 (1): 263. Alhopuro Pia, Karhu Auli, Winqvist Robert, Waltering Kati, Visakorpi Tapio, Aaltonen Lauri |
DNA methylation signatures identify biologically distinct subtypes in acute myeloid leukemia. Cancer cell 2010 1 17 (1): 13-27. Figueroa Maria E, Lugthart Sanne, Li Yushan, Erpelinck-Verschueren Claudia, Deng Xutao, Christos Paul J, Schifano Elizabeth, Booth James, van Putten Wim, Skrabanek Lucy, Campagne Fabien, Mazumdar Madhu, Greally John M, Valk Peter J M, Löwenberg Bob, Delwel Ruud, Melnick A |
[Genotyping and minimal residual disease study in children with acute myeloid leukemia: preliminary results]. Przegla?d lekarski 2010 67 (6): 371-4. Balwierz Walentyna, Pietrzyk Jacek J, Wator Gracjan, Stozek Karol, Klekawka Tomasz, Kwieci?ska Kinga, D?uzniewska Agnieszka, Matysiak Micha?, Malinowska Iwona, Sikorska-Fic Barbara, Balcerska Anna, Maciejka-Kapu?ci?ska Lucyna, So?ta-Jakimczyk Danuta, Tomaszewska Renata, Chybicka Alicja, Krawczuk-Rybak Maryna, Muszy?ska-Ros?an Katarzyna, M?ynarski Wojciech, Stolarska Ma?gorzata, Urasi?ski Tomasz, Kamie?ska Elzbieta, Sobol Grazyna, Wieczorek Maria, Karolczyk Grazyna, Wysocki Mariusz, Ko?tan Sylwia, Kowalczyk Jerzy R, Wójcik Beata, Ksiazek Teofila, Szewczyk Katarzy |
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients. Genes, chromosomes & cancer 2017 Jun . Busse Tracy M, Roth Jacquelyn J, Wilmoth Donna, Wainwright Luanne, Tooke Laura, Biegel Jaclyn |
Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development. Journal of molecular medicine (Berlin, Germany) 2017 Jan . Villacis Rolando A R, Basso Tatiane R, Canto Luisa M, Pinheiro Maísa, Santiago Karina M, Giacomazzi Juliana, de Paula Cláudia A A, Carraro Dirce M, Ashton-Prolla Patrícia, Achatz Maria I, Rogatto Silvia |
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 |
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 |
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- Page last updated:May 06, 2024
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