[HTML][HTML] Drug resistance biomarkers and their clinical applications in childhood acute lymphoblastic leukemia

N Aberuyi, S Rahgozar, ES Ghodousi… - Frontiers in oncology, 2020 - frontiersin.org
Biomarkers are biological molecules found in body fluids or tissues, which can be
considered as indications of a normal or abnormal process, or of a condition or disease …

[HTML][HTML] Molecular basis and clinical significance of genetic aberrations in B-cell precursor acute lymphoblastic leukemia

F Ghazavi, T Lammens, N Van Roy, B Poppe… - Experimental …, 2015 - Elsevier
Highlights•B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is currently treated by
risk-adapted intensive chemotherapy•Genome-wide genomic analyses have uncovered the …

[HTML][HTML] Characterization of leukemias with ETV6-ABL1 fusion

M Zaliova, AV Moorman, G Cazzaniga, M Stanulla… - …, 2016 - ncbi.nlm.nih.gov
To characterize the incidence, clinical features and genetics of ETV6-ABL1 leukemias,
representing targetable kinase-activating lesions, we analyzed 44 new and published cases …

[HTML][HTML] Cancer drivers and clonal dynamics in acute lymphoblastic leukaemia subtypes

JB Studd, AJ Cornish, PH Hoang, P Law… - Blood Cancer …, 2021 - nature.com
To obtain a comprehensive picture of composite genetic driver events and clonal dynamics
in subtypes of paediatric acute lymphoblastic leukaemia (ALL) we analysed tumour-normal …

[HTML][HTML] Digital multiplex ligation-dependent probe amplification for detection of key copy number alterations in T-and B-cell lymphoblastic leukemia

A Benard-Slagter, I Zondervan, K de Groot… - The Journal of Molecular …, 2017 - Elsevier
Recurrent and clonal genetic alterations are characteristic of different subtypes of T-and B-
cell lymphoblastic leukemia (ALL), and several subtypes are strong independent predictors …

HVEM network signaling in cancer

JR Šedý, P Ramezani-Rad - Advances in Cancer Research, 2019 - Elsevier
Somatic mutations in cancer cells may influence tumor growth, survival, or immune
interactions in their microenvironment. The tumor necrosis factor receptor family member …

[HTML][HTML] Intragenic Variations in BTLA Gene Influence mRNA Expression of BTLA Gene in Chronic Lymphocytic Leukemia Patients and Confer Susceptibility to …

L Karabon, A Partyka, M Jasek… - Archivum Immunologiae …, 2016 - Springer
The aim of this study was to determine the association between polymorphisms in gene
encoding B-and T-lymphocyte attenuator (BTLA) and susceptibility to chronic lymphocytic …

[HTML][HTML] Development of a fluorescence in situ hybridization probe for detecting IKZF1 deletion mutations in patients with acute lymphoblastic leukemia

J Hashiguchi, M Onozawa, S Oguri, S Fujisawa… - The Journal of Molecular …, 2018 - Elsevier
Intragenic deletion of IKZF1 is a recurrent genomic alteration in acute lymphoblastic
leukemia. The deletions are mediated by illegitimate variable (diversity) joining …

[图书][B] Implicación de las alteraciones en el número de copias en el pronóstico y progresión de la leucemia aguda linfoblástica de línea B del adulto

J Ribera Salas - 2017 - ddd.uab.cat
El 75% de los pacientes con leucemia aguda linfoblástica (LAL) tiene alteraciones
cromosómicas recurrentes (numéricas o estructurales). Dichas anomalías (alteraciones …

[图书][B] Secondary Somatic Mutations in ETV6-RUNX1 Acute Lymphoblastic Leukemia Pathogenesis

M Leon - 2016 - search.proquest.com
Abstract ETV6-RUNX1, also known as TEL-AML1, is the most frequent chromosomal
translocation in childhood Acute Lymphoblastic Leukemia (ALL) with an incidence of …