ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia (Q42011641)

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English	ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

title

ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia (English)

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

main subject

lymphoblastic leukemia

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based on heuristic

inferred from title

author name string

Abir Gmidène

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1

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

Hatem Elghezal

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2

1 reference

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

Hlima Sennana

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3

1 reference

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

Yosra Ben Youssef

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4

1 reference

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

Balkiss Meddeb

series ordinal

5

1 reference

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

Moez Elloumi

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6

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Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

Abderrahim Khlif

series ordinal

7

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Europe PubMed Central

PMC publication ID

2799269

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15 October 2017

Ali Saad

series ordinal

8

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stated in

Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

publication date

22 December 2009

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stated in

Europe PubMed Central

PMC publication ID

2799269

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15 October 2017

published in

Advances in Hematology

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Europe PubMed Central

PMC publication ID

2799269

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15 October 2017

volume

2009

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stated in

Europe PubMed Central

PMC publication ID

2799269

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15 October 2017

page(s)

924301

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stated in

Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

copyright license

Creative Commons Attribution 3.0 Unported

start time

1 January 2009

1 reference

stated in

April 2022 Public Data File from Crossref

copyright status

copyrighted

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stated in

April 2022 Public Data File from Crossref

cites work

Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature.

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

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5 June 2018

Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

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5 June 2018

AML1 gene over-expression in childhood acute lymphoblastic leukemia

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

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5 June 2018

The TEL-AML1 fusion accompanied by loss of the untranslocated TEL allele in B-precursor acute lymphoblastic leukaemia of childhood

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

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5 June 2018

Cytogenetics and molecular genetics of childhood leukemia

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Associazione Italiana Ematologia Oncologia Pediatrica and the Berlin-Frankfurt-Mün

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

Current status of cytogenetic research in childhood acute lymphoblastic leukemia

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

t(12;21): a new recurrent translocation in acute lymphoblastic leukemia.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

5 June 2018

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

17 August 2018

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799269

retrieved

17 August 2018

Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in Spain

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TEL-AML1 frequency in multi-ethnic Malaysian pediatric acute lymphoblastic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of t(12;21) in childhood acute lymphoblastic leukemia by fluorescence in situ hybridization

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TEL is one of the targets for deletion on 12p in many cases of childhood B-lineage acute lymphoblastic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of t(12;21)(p13;q22) in children with acute lymphoblastic leukemia and known clinical outcome in southern Brazil

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A fluorescence in situ hybridization study of TEL-AML1 fusion gene in B-cell acute lymphoblastic leukemia (1984-2001)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification of AML1 gene is present in childhood acute lymphoblastic leukemia but not in adult, and is not associated with AML1 gene mutation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization analysis of the cryptic t(12;21) (p13;q22) in childhood B-lineage acute lymphoblastic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization study of TEL/AML1 fusion and other abnormalities involving TEL and AML1 genes. Correlation with cytogenetic findings and prognostic value in children with acute lymphocytic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of additional genetic events in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion: a molecular cytogenetics study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification of AML1 in childhood acute lymphoblastic leukemias

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AML1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20049174

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1155/2009/924301

1 reference

stated in

Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

PMC publication ID

2799269

1 reference

stated in

Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

PubMed publication ID

20049174

1 reference

stated in

Europe PubMed Central

PMC publication ID

2799269

retrieved

15 October 2017

ResearchGate publication ID

40848048

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