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Published in 2019 at "Bioelectromagnetics"
DOI: 10.1002/bem.22193
Abstract: Exposure to extremely low-frequency magnetic fields (ELF-MFs) has been classified by the International Agency for Research on Cancer (IARC) as "possibly carcinogenic to humans," based on limited scientific evidence concerning childhood leukemia. This assessment emphasized…
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Keywords:
etv6 runx1;
runx1;
study;
leukemia ... See more keywords
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Published in 2019 at "Experimental hematology"
DOI: 10.1016/j.exphem.2019.03.004
Abstract: The most frequently occurring genetic abnormality in pediatric B-lymphocyte-lineage acute lymphoblastic leukemia is the t(12;21) chromosomal translocation that results in a ETV6-RUNX1 (also known as TEL-AML1) fusion gene. Expression of ETV6-RUNX1 induces a preleukemic condition…
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Keywords:
etv6 runx1;
expression;
cell;
gene expression ... See more keywords
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Published in 2017 at "International Journal of Laboratory Hematology"
DOI: 10.1111/ijlh.12593
Abstract: The translocation t(12;21)(p13;q22) resulting in the fusion gene ETV6–RUNX1, is the most frequent gene fusion in childhood B lymphoblastic leukemia. In the Nordic Society of Paediatric Haematology and Oncology ALL‐2008 treatment protocol, treatment stratification in…
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Keywords:
etv6 runx1;
minimal residual;
p13 q22;
lymphoblastic leukemia ... See more keywords
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Published in 2023 at "Cancer Research"
DOI: 10.1158/1538-7445.am2023-2992
Abstract: Tumor-specific antigens can be targeted by T cells and cancer immunotherapies directed against these neoantigens have resulted in regression across several cancer types. Both missense mutations and gene fusions can serve as targets for cytotoxic…
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Keywords:
fusion;
hla;
missense mutations;
etv6 runx1 ... See more keywords
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2
Published in 2022 at "Blood Advances"
DOI: 10.1182/bloodadvances.2021005703
Abstract: Key Points A somatic UBA2 deletion preceded the well-established leukemia initiating event ETV6-RUNX1 fusion in monozygotic twins with BCP-ALL. A shared complex rearrangement created an ETV6-RUNX1 fusion and provided evidence of a common clonal in…
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Keywords:
somatic uba2;
etv6 runx1;
variant preceded;
monozygotic twins ... See more keywords
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0
Published in 2021 at "PLoS ONE"
DOI: 10.1371/journal.pone.0253012
Abstract: ETV6/RUNX1 gene fusion is the most common chromosomal translocation abnormality occurred in pediatric B-cell acute lymphoblastic leukemia (B-ALL). Compared with ETV6-RUNX1-negative patients, ETV6-RUNX1-positive patients possess more improved treatment strategies but higher risk to relapse. In…
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Keywords:
etv6 runx1;
runx1 positive;
lncrna mrna;
expression ... See more keywords
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Published in 2019 at "Haematologica"
DOI: 10.3324/haematol.2018.205849
Abstract: Today, most children with acute lymphoblastic leukemia (ALL) can be cured by treatment regimens consisting of combination chemotherapy supplemented in certain patient populations with preventive or therapeutic cranial irradiation (CI) and/or an allogeneic hematopoietic stem…
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Keywords:
etv6 runx1;
treatment;
lymphoblastic leukemia;
tp53 etv6 ... See more keywords
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1
Published in 2021 at "Frontiers in Oncology"
DOI: 10.3389/fonc.2021.588101
Abstract: Around 85% of childhood Acute Lymphoblastic Leukemia (ALL) are of B-cell origin and characterized by the presence of different translocations including BCR-ABL1, ETV6-RUNX1, E2A-PBX1, and MLL fusion proteins. The current clinical investigations used to identify…
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Keywords:
etv6 runx1;
utility;
lymphoblastic leukemia;
acute lymphoblastic ... See more keywords