Atypical/unbalanced ETV6/NTRK3 rearrangement in salivary secretory carcinoma with a focus on the incidence, the patterns, and the clinical implications
J Sun, J Li, Z Tian, C Zhang, R Xia… - Journal of Oral Pathology …, 2022 - Wiley Online Library
Background Atypical/unbalanced rearrangement in salivary secretory carcinoma was
observed and its incidence, patterns, and clinical significance remain unknown. Methods …
observed and its incidence, patterns, and clinical significance remain unknown. Methods …
Clinical implications of additional chromosomal abnormalities in adult acute myeloid leukemia with inv (16)/t(16;16)/CBFB::MYH11
J Gao, L Santana‐Santos, L Fu, E Alvey… - European Journal of …, 2024 - Wiley Online Library
Objectives This study assesses the clinical significance of additional cytogenetic
abnormalities (ACAs) and/or the deletion of 3′ CBFB (3′ CBFB del) resulting in …
abnormalities (ACAs) and/or the deletion of 3′ CBFB (3′ CBFB del) resulting in …
3′CBFB deletion in CBFB-rearranged acute myeloid leukemia retains morphological features associated with inv(16), but patients have higher risk of relapse and …
Fluorescence in situ hybridization analysis (FISH) using a CBFB breakapart probe is widely
used to detect CBFB rearrangement (CBFB r) in cases of acute myeloid leukemia (AML) …
used to detect CBFB rearrangement (CBFB r) in cases of acute myeloid leukemia (AML) …
PPP1R7 Is a Novel Translocation Partner of CBFB via t(2;16)(q37;q22) in Acute Myeloid Leukemia
L Wang, W Wang, HC Beird, X Cheng, H Fang, G Tang… - Genes, 2022 - mdpi.com
In a subset of acute myeloid leukemia (AML) cases, the core binding factor beta subunit
gene (CBFB) was rearranged via inv (16)(p13. 1q22) or t (16; 16)(p13. 1; q22), in which the …
gene (CBFB) was rearranged via inv (16)(p13. 1q22) or t (16; 16)(p13. 1; q22), in which the …
Locating the Sry transgene and measuring estrous cycles in rats with manipulations of the testis-determining factor Sry
HR Schmidtke - 2024 - search.proquest.com
Abstract The Four Core Genotypes (FCG) transgenic mouse model allows us to investigate if
an observed sex difference in phenotype is caused by gonadal hormones, sex chromosome …
an observed sex difference in phenotype is caused by gonadal hormones, sex chromosome …
Alteraciones cromosómicas en pacientes con diagnóstico presuntivo de leucemia mieloide aguda. México, junio-diciembre 2019
DW Adriano Cadena - 2022 - repositorio.unprg.edu.pe
La Leucemia Mieloide Aguda (LMA) es una neoplasia hematológica heterogénea. Diversas
anomalías génicas y cromosómicas están involucradas en la progresión de la enfermedad; …
anomalías génicas y cromosómicas están involucradas en la progresión de la enfermedad; …
[PDF][PDF] Molecular Cytogenetic Characterization of a Structural Abnormal Chromosome 16 in a Patient with Acute Myeloid Leukemia Leading to Inversion Chromosome …
Acute myeloid leukemia (AML) presents as a heterogeneous blood cancer characterized by
the proliferation of immature myeloid cells. We present the case of an 18-year-old female …
the proliferation of immature myeloid cells. We present the case of an 18-year-old female …
Deletion 16q Involving Partial 3'Cbfbeta with an Additional Triple Trisomy; a Novel Finding in Aml M4 Eosinophilia; a Distinct Sub-Class
A Pais, PCP Ozturk - papers.ssrn.com
Del (16q) a rare and uncommon cytogenetic abnormality that occur in different types of
myeloid neoplasms. Here, we report del (16q) in an adult patient with acute myelomonocytic …
myeloid neoplasms. Here, we report del (16q) in an adult patient with acute myelomonocytic …