Cargando…

Determination of ETV6‐RUNX1 genomic breakpoint by next‐generation sequencing

The t(12;21)(p13;q22) ETV6‐RUNX1 gene fusion is one of the most common chromosomal translocation in childhood acute lymphoblastic leukemia (ALL). It is associated with favorable prognosis. The identification of the genomic sequence of the breakpoint flanking regions of the ETV6‐RUNX1 translocation s...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jin, Yanliang, Wang, Xingwei, Hu, Shaoyan, Tang, Jingyan, Li, Benshang, Chai, Yihuan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2015
Materias:	Cancer Biology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735785/ https://www.ncbi.nlm.nih.gov/pubmed/26711002 http://dx.doi.org/10.1002/cam4.579

Ejemplares similares

RAG1 co‐expression signature identifies ETV6‐RUNX1‐like B‐cell precursor acute lymphoblastic leukemia in children
por: Chen, Dongfeng, et al.
Publicado: (2021)

The Second Oncogenic Hit Determines the Cell Fate of ETV6-RUNX1 Positive Leukemia
por: Rodríguez-Hernández, Guillermo, et al.
Publicado: (2021)

Virome assembly and annotation in brain tissue based on next‐generation sequencing
por: Yuan, Zihao, et al.
Publicado: (2020)

Whole-Exome Sequencing of ETV6/RUNX1 in Four Childhood Acute Lymphoblastic Leukaemia Cases
por: Zakaria, Zubaidah, et al.
Publicado: (2017)

Detection of somatic BRCA1/2 mutations in ovarian cancer – next‐generation sequencing analysis of 100 cases
por: Koczkowska, Magdalena, et al.
Publicado: (2016)

Next‐generation sequencing of miRNAs in clinical samples of Epstein–Barr virus‐associated B‐cell lymphomas
por: Sakamoto, Kouta, et al.
Publicado: (2017)

Modeling the process of childhood ETV6-RUNX1 B-cell leukemias
por: Rodríguez-Hernández, Guillermo, et al.
Publicado: (2017)

Transcriptome analysis in primary colorectal cancer tissues from patients with and without liver metastases using next‐generation sequencing
por: Wang, Sen, et al.
Publicado: (2017)

Sequence determinants of breakpoint location during HIV-1 intersubtype recombination
por: Baird, Heather A., et al.
Publicado: (2006)

The CIC-ERF co-deletion underlies fusion-independent activation of ETS family member, ETV1, to drive prostate cancer progression
por: Gupta, Nehal, et al.
Publicado: (2022)

Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population
por: Mata-Rocha, Minerva, et al.
Publicado: (2022)

The role of EZH2 and DNA methylation in the silencing of the tumour suppressor RUNX3 in colorectal cancer
por: Kodach, Liudmila L., et al.
Publicado: (2010)

ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia
por: Gmidène, Abir, et al.
Publicado: (2009)

Evidence for a role of RUNX1 as recombinase cofactor for TCRβ rearrangements and pathological deletions in ETV6-RUNX1 ALL
por: Seitz, V., et al.
Publicado: (2020)

Blood-Based Next-Generation Sequencing in Adrenocortical Carcinoma
por: Nazha, Bassel, et al.
Publicado: (2022)

miR‐106b‐5p promotes aggressive progression of hepatocellular carcinoma via targeting RUNX3
por: Gu, Hao, et al.
Publicado: (2019)

Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
por: Ellinghaus, E, et al.
Publicado: (2012)

Prevalence of ETV6/RUNX1 Fusion Gene in Pediatric Patients with Acute Lymphoblastic Leukemia in Iran
por: Rahnemoon, Ahmad-Reza, et al.
Publicado: (2013)

Somatic drivers of B-ALL in a model of ETV6-RUNX1; Pax5(+/−) leukemia
por: van der Weyden, Louise, et al.
Publicado: (2015)

Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26
por: Homan, Claire C., et al.
Publicado: (2023)

Etoposide-induced DNA damage in a chromosomal breakpoint of RUNX1 gene is independent of RUNX1 expression
por: Schnake, Nicolás, et al.
Publicado: (2019)

Pathogenesis of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia and mechanisms underlying its relapse
por: Sun, Congcong, et al.
Publicado: (2017)

Cooperation of ETV6/RUNX1 and BCL2 enhances immunoglobulin production and accelerates glomerulonephritis in transgenic mice
por: Bauer, Eva, et al.
Publicado: (2016)

CD9 predicts ETV6-RUNX1 in childhood B-cell precursor acute lymphoblastic leukemia
por: Blunck, Caroline B., et al.
Publicado: (2019)

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
por: Fox, Alan J., et al.
Publicado: (2016)

Next-Generation Sequencing of Apoptotic DNA Breakpoints Reveals Association with Actively Transcribed Genes and Gene Translocations
por: Fullwood, Melissa J., et al.
Publicado: (2011)

Targeted Next-Generation Sequencing at Copy-Number Breakpoints for Personalized Analysis of Rearranged Ends in Solid Tumors
por: Kim, Hyun-Kyoung, et al.
Publicado: (2014)

First Case of ETV6–RUNX1 Fusion in Adult De Novo Acute Myeloid Leukemia Detected Using Targeted RNA Sequencing
por: Jeon, Seong-Jun, et al.
Publicado: (2023)

Space-Time Clustering of Childhood Leukemia: Evidence of an Association with ETV6-RUNX1 (TEL-AML1) Fusion
por: Kreis, Christian, et al.
Publicado: (2017)

Genome-wide repression of eRNA and target gene loci by the ETV6-RUNX1 fusion in acute leukemia
por: Teppo, Susanna, et al.
Publicado: (2016)

ETV6/RUNX1-positive childhood acute lymphoblastic leukemia in China: excellent prognosis with improved BFM protocol
por: Wang, Yu, et al.
Publicado: (2018)

The study of METTL3 and METTL14 expressions in childhood ETV6/RUNX1‐positive acute lymphoblastic leukemia
por: Sun, Congcong, et al.
Publicado: (2019)

A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins
por: Bang, Benedicte, et al.
Publicado: (2022)

Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations
por: Ovsyannikova, Galina S., et al.
Publicado: (2022)

Cytokine Hyperresponsiveness in Children With ETV6::RUNX1-positive Acute Lymphoblastic Leukemia After Challenge With Common Pathogens
por: Rüchel, Nadine, et al.
Publicado: (2023)

The Prognostic Effect of IKZF1 Deletions in ETV6::RUNX1 and High Hyperdiploid Childhood Acute Lymphoblastic Leukemia
por: Østergaard, Anna, et al.
Publicado: (2023)

Impact of pinworm infection on the development of murine B-cell leukemia/lymphoma in the presence and absence of ETV6::RUNX1
por: Fitch, Briana A., et al.
Publicado: (2023)

Identification of genes located at breakpoints of uncharacterized chromosomal translocations by the use of chromosomal microdissection and next generation DNA sequencing
por: Campregher, Paulo V, et al.
Publicado: (2013)

Emerging concepts in designing next-generation multifunctional nanomedicine for cancer treatment
por: Chakraborty, Kasturee, et al.
Publicado: (2022)

Next‐generation sequencing in precision oncology: Patient understanding and expectations
por: Roberts, J. Scott, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_21cpchnajrp0moj3psigs4md2l