Cargando…

Identification of Two Critically Deleted Regions within Chromosome Segment 7q35-q36 in EVI1 Deregulated Myeloid Leukemia Cell Lines

Chromosomal rearrangements involving the EVI1 proto-oncogene are a recurrent finding in myeloid leukemias and are indicative of a poor prognosis. Rearrangements of the EVI1 locus are often associated with monosomy 7 or cytogenetic detectable deletions of part of 7q. As EVI1 overexpression alone is n...

Descripción completa

Detalles Bibliográficos
Autores principales:	De Weer, An, Poppe, Bruce, Vergult, Sarah, Van Vlierberghe, Pieter, Petrick, Marjan, De Bock, Robrecht, Benoit, Yves, Noens, Lucien, De Paepe, Anne, Van Roy, Nadine, Menten, Björn, Speleman, Frank
Formato:	Texto
Lenguaje:	English
Publicado:	Public Library of Science 2010
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800774/ https://www.ncbi.nlm.nih.gov/pubmed/20084277 http://dx.doi.org/10.1371/journal.pone.0008676

Ejemplares similares

EVI1 activation in blast crisis CML due to juxtaposition to the rare 17q22 partner region as part of a 4-way variant translocation t(9;22)
por: De Weer, An, et al.
Publicado: (2008)

A novel and universal method for microRNA RT-qPCR data normalization
por: Mestdagh, Pieter, et al.
Publicado: (2009)

Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report
por: Ruiz-Botero, Felipe, et al.
Publicado: (2016)

qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
por: Hellemans, Jan, et al.
Publicado: (2007)

Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C
por: Tosca, Lucie, et al.
Publicado: (2021)

Establishment of an Undifferentiated Leukemia Cell Line (Kasumi‐3) with t(3;7)(q27;q22) and Activation of the EVI1 Gene
por: Asou, Hiroya, et al.
Publicado: (1996)

EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome
por: Li, Chuan, et al.
Publicado: (2015)

Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription
por: Di Stolfo, Giuseppe, et al.
Publicado: (2019)

Radial excitations of $\overline{q}q$ mesons and non-$\overline{q}q$ candidates
por: Montanet, Lucien
Publicado: (1999)

A Constitutional Translocation t(1;17)(p36.2;q11.2) in a Neuroblastoma Patient Disrupts the Human NBPF1 and ACCN1 Genes
por: Vandepoele, Karl, et al.
Publicado: (2008)

RNA pre-amplification enables large-scale RT-qPCR gene-expression studies on limiting sample amounts
por: Vermeulen, Joëlle, et al.
Publicado: (2009)

Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 Deletion
por: Fan, Liang-Liang, et al.
Publicado: (2021)

A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization
por: Kjeldsen, Eigil
Publicado: (2014)

Expressed Repeat Elements Improve RT-qPCR Normalization across a Wide Range of Zebrafish Gene Expression Studies
por: Vanhauwaert, Suzanne, et al.
Publicado: (2014)

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
por: Vandesompele, Jo, et al.
Publicado: (2002)

Aberrant EVI1 splicing contributes to EVI1-rearranged leukemia
por: Tanaka, Atsushi, et al.
Publicado: (2022)

Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2)
por: Bodega, Beatrice, et al.
Publicado: (2007)

Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia
por: Roberts, Aedan, et al.
Publicado: (2010)

CADM1 is a strong neuroblastoma candidate gene that maps within a 3.72 Mb critical region of loss on 11q23
por: Michels, Evi, et al.
Publicado: (2008)

Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2
por: Schlaweck, Annika E., et al.
Publicado: (2019)

Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation
por: Mohamed, A. M., et al.
Publicado: (2018)

Uptake of a web-based oncology protocol system: how do cancer clinicians use eviQ cancer treatments online?
por: Langton, Julia M, et al.
Publicado: (2013)

Combined subtractive cDNA cloning and array CGH: an efficient approach for identification of overexpressed genes in DNA amplicons
por: De Preter, Katleen, et al.
Publicado: (2004)

ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation
por: Sante, Tom, et al.
Publicado: (2014)

Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice
por: Renard, Marjolijn, et al.
Publicado: (2018)

A Novel Acquired t(2;4)(q36.1;q24) with a Concurrent Submicroscopic del(4)(q23q24) in An Adult with Polycythemia Vera
por: Kjeldsen, Eigil
Publicado: (2018)

Unexplained Pancytopenia in a Patient with 5q35.2-q35.3 Microduplication Encompassing NSD1: A Case Report
por: Park, Sungwoo, et al.
Publicado: (2018)

Delineation of 2q32q35 Deletion Phenotypes: Two Apparent “Proximal” and “Distal” Syndromes
por: Mc Cormack, Adrian, et al.
Publicado: (2013)

Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat
por: Meza-Espinoza, Juan Pablo, et al.
Publicado: (2020)

Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
por: Choi, Asayeon, et al.
Publicado: (2017)

Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
por: Xiao, Gefei, et al.
Publicado: (2021)

7q36 deletion and 9p22 duplication: effects of a double imbalance
por: Pelegrino, Karla de Oliveira, et al.
Publicado: (2013)

Use of a Neural Network for the determination of the $e^{+}e^{-} \rightarrow W^{+}W^{-} \rightarrow q \overline{q} q \overline{q}$ production cross-section at 189 GeV
por: Van den Boeck, W, et al.
Publicado: (2001)

EVI1, a target gene for amplification at 3q26, antagonizes transforming growth factor-β-mediated growth inhibition in hepatocellular carcinoma
por: Yasui, Kohichiroh, et al.
Publicado: (2015)

Interstitial deletion of 5q33.3q35.1 in a boy with severe mental retardation
por: Lee, Jin Hwan, et al.
Publicado: (2016)

Deletion of 7q33-q35 in a Patient with Intellectual Disability and Dysmorphic Features: Further Characterization of 7q Interstitial Deletion Syndrome
por: Dilzell, Kristen, et al.
Publicado: (2015)

Risk of malignancy in 22q11.2 deletion syndrome
por: Stevens, Toer, et al.
Publicado: (2017)

Haploinsufficiency of RPS14 in 5q− syndrome is associated with deregulation of ribosomal- and translation-related genes
por: Pellagatti, Andrea, et al.
Publicado: (2008)

A novel t (5; 17) (q35; q21) associated with t (8; 21) (q22; q22) in a patient with acute myeloid leukemia: case report and review of literature
por: Zahra, Kmira, et al.
Publicado: (2023)

On the nonleading $q\overline{q}$ and q g contributions in Drell-Yan processes
por: Humpert, Benedikt, et al.
Publicado: (1979)

Cannot write session to /tmp/vufind_sessions/sess_8cck7h5e4nmt457s2ditg11j8f