Zebrafish as a model for leukemia and other hematopoietic disorders
P Rasighaemi, F Basheer, C Liongue… - Journal of hematology & …, 2015 - Springer
Zebrafish is an established model for the study of vertebrate development, and is especially
amenable for investigating hematopoiesis, where there is strong conservation of key …
amenable for investigating hematopoiesis, where there is strong conservation of key …
ETV6 and ETV7: Siblings in hematopoiesis and its disruption in disease
P Rasighaemi, AC Ward - Critical reviews in oncology/hematology, 2017 - Elsevier
Abstract ETV6 (TEL1) and ETV7 (TEL2) are closely-related members of the ETS family of
transcriptional regulators. Both ETV6 and ETV7 have been demonstrated to play key roles in …
transcriptional regulators. Both ETV6 and ETV7 have been demonstrated to play key roles in …
Study of inherited thrombocytopenia resulting from mutations in ETV6 or RUNX1 using a human pluripotent stem cell model
Inherited thrombocytopenia results in low platelet counts and increased bleeding. Subsets of
these patients have monoallelic germline mutations in ETV6 or RUNX1 and a heightened …
these patients have monoallelic germline mutations in ETV6 or RUNX1 and a heightened …
Neoplasia-associated chromosome translocations resulting in gene truncation
I Panagopoulos, S Heim - Cancer Genomics & Proteomics, 2022 - cgp.iiarjournals.org
Chromosomal translocations in cancer as well as benign neoplasias typically lead to the
formation of fusion genes. Such genes may encode chimeric proteins when two protein …
formation of fusion genes. Such genes may encode chimeric proteins when two protein …
A novel ETV6-miR-429-CRKL regulatory circuitry contributes to aggressiveness of hepatocellular carcinoma
C Guo, C Gao, D Zhao, J Li, J Wang, X Sun… - Journal of Experimental …, 2020 - Springer
Background Tumor metastasis is one of the main causes of the high mortality of
hepatocellular carcinoma (HCC). E-Twenty Six variant gene 6 (ETV6) is a strong …
hepatocellular carcinoma (HCC). E-Twenty Six variant gene 6 (ETV6) is a strong …
[HTML][HTML] Clinical Validation of FusionPlex RNA Sequencing and Its Utility in the Diagnosis and Classification of Hematologic Neoplasms
X Chen, W Wang, J Yeh, Y Wu, VG Oehler… - The Journal of Molecular …, 2023 - Elsevier
Recurrent gene rearrangements result in gene fusions that encode chimeric proteins, driving
the pathogenesis of many hematologic neoplasms. The fifth edition World Health …
the pathogenesis of many hematologic neoplasms. The fifth edition World Health …
Rearrangement of the chromatin organizer special AT-rich binding protein 1 gene, SATB1, resulting from at (3; 5)(p24; q14) chromosomal translocation in acute …
S Torkildsen, M Brunetti, L Gorunova… - Anticancer …, 2017 - ar.iiarjournals.org
Background/Aim: New chromosomal aberrations continue to be reported in acute myeloid
leukemias (AML). The addition of more cases with the same genetic characteristics would …
leukemias (AML). The addition of more cases with the same genetic characteristics would …
Survivin downregulation using siRNA nanoliposomes inhibits cell proliferation and promotes the apoptosis of MHCC-97H hepatic cancer cells: An in vitro and in vivo …
Z Liu, T Wang, Z Zhang, S Tang, S Feng… - Oncology …, 2017 - spandidos-publications.com
At present, survivin is one of the most cancer-specific proteins that has been identified. The
present study aimed to investigate the antitumor effects of novel survivin small interfering …
present study aimed to investigate the antitumor effects of novel survivin small interfering …
PAN3–PSMA2 fusion resulting from a novel t(7;13)(p14;q12) chromosome translocation in a myelodysplastic syndrome that evolved into acute myeloid leukemia
I Panagopoulos, L Gorunova, HK Andersen… - … Hematology & Oncology, 2018 - Springer
Background Acquired primary chromosomal changes in cancer are sometimes found as
sole karyotypic abnormalities. They are specifically associated with particular types of …
sole karyotypic abnormalities. They are specifically associated with particular types of …
FAM53B truncation caused by t (10; 19)(q26; q13) chromosome translocation in acute lymphoblastic leukemia
I Panagopoulos, L Gorunova… - Oncology …, 2017 - spandidos-publications.com
RNA-sequencing of the patient's bone marrow detected fusion transcripts in which the
coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from …
coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from …