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Page 1
RNA Sequencing Analysis for the Identification of a PCM1/PDGFRB Fusion Gene Responsive to Imatinib.
Such E, Liquori A, Mora E, Marco-Ayala J, Avetisyan G, Regadera A, Ibañez F, Panadero J, Senent L, Llop M, Díaz A, Vicente A, Luna I, Ibáñez M, Barragán E, Sanz MA, Sanz G, Communidad Valenciana, Cervera J. Such E, et al. Among authors: liquori a. Acta Haematol. 2019;142(2):92-97. doi: 10.1159/000497348. Epub 2019 May 14. Acta Haematol. 2019. PMID: 31085913
The modular network structure of the mutational landscape of Acute Myeloid Leukemia.
Ibáñez M, Carbonell-Caballero J, Such E, García-Alonso L, Liquori A, López-Pavía M, Llop M, Alonso C, Barragán E, Gómez-Seguí I, Neef A, Hervás D, Montesinos P, Sanz G, Sanz MA, Dopazo J, Cervera J. Ibáñez M, et al. Among authors: liquori a. PLoS One. 2018 Oct 10;13(10):e0202926. doi: 10.1371/journal.pone.0202926. eCollection 2018. PLoS One. 2018. PMID: 30303964 Free PMC article.
Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype.
Ibáñez M, Such E, Onecha E, Gómez-Seguí I, Liquori A, Sellés J, Hervás-Marín D, Barragán E, Ayala R, LLop M, López-Pavía M, Rapado I, Neef A, Sanjuan-Pla A, Sargas C, Gonzalez-Romero E, Boluda-Navarro M, Andreu R, Senent L, Montesinos P, Martínez-López J, Angel Sanz M, Sanz G, Cervera J. Ibáñez M, et al. Among authors: liquori a. Sci Rep. 2020 Apr 3;10(1):5904. doi: 10.1038/s41598-020-61589-9. Sci Rep. 2020. PMID: 32246042 Free PMC article.
Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chédiak-Higashi Syndrome.
Boluda-Navarro M, Ibáñez M, Liquori A, Franco-Jarava C, Martínez-Gallo M, Rodríguez-Vega H, Teresa J, Carreras C, Such E, Zúñiga Á, Colobran R, Cervera JV. Boluda-Navarro M, et al. Among authors: liquori a. Front Immunol. 2021 Mar 31;12:625591. doi: 10.3389/fimmu.2021.625591. eCollection 2021. Front Immunol. 2021. PMID: 33868243 Free PMC article.
A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms.
Liquori A, Lesende I, Palomo L, Avetisyan G, Ibáñez M, González-Romero E, Boluda-Navarro M, Morote-Faubel M, Garcia-Ruiz C, Martinez-Valiente C, Santiago-Balsera M, Gomez-Seguí I, Sanjuan-Pla A, Sanz MA, Sanz G, Solé F, Such E, Cervera J. Liquori A, et al. Cancers (Basel). 2021 Apr 18;13(8):1947. doi: 10.3390/cancers13081947. Cancers (Basel). 2021. PMID: 33919541 Free PMC article.
Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients.
Ibáñez M, Such E, Liquori A, Avestisyan G, Andreu R, Vicente A, Macián MJ, Melendez MC, Morote-Faubel M, Asensi P, Lloret MP, Jarque I, Picón I, Pacios A, Donato E, Mas-Ochoa C, Alonso C, Cañigral C, Sempere A, Romero S, Santiago M, Sanz GF, de la Rubia J, Senent L, Luna I. Ibáñez M, et al. Among authors: liquori a. Diagnostics (Basel). 2022 Apr 11;12(4):953. doi: 10.3390/diagnostics12040953. Diagnostics (Basel). 2022. PMID: 35454001 Free PMC article.
55 results