Reverse engineering of TLX oncogenic transcriptional networks identifies RUNX1 as tumor suppressor in T-ALL. (Q35816648)

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24 January 2020

title

Reverse engineering of TLX oncogenic transcriptional networks identifies RUNX1 as tumor suppressor in T-ALL (English)

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24 January 2020

7

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24 January 2020

Xavier Solé

8

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24 January 2020

Jules P Meijerink

14

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15

Andrea Califano

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10

Elisabeth Paietta

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24 January 2020

12

Peter H Wiernik

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24 January 2020

author name string

Giusy Della Gatta

1

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24 January 2020

Teresa Palomero

2

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24 January 2020

Arianne Perez-Garcia

3

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24 January 2020

Mukesh Bansal

5

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24 January 2020

Zachary W Carpenter

6

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24 January 2020

Luyao Xu

9

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24 January 2020

Janis Racevskis

11

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24 January 2020

Jacob M Rowe

13

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24 January 2020

Adolfo A Ferrando

16

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24 January 2020

Alberto Ambesi-Impiombato

4

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24 January 2020

language of work or name

English

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publication date

26 February 2012

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24 January 2020

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24 January 2020

volume

18

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24 January 2020

issue

3

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24 January 2020

page(s)

436-440

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https://scigraph.springernature.com/pub.10.1038/nm.2610

24 January 2020

exact match

0 references

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11 July 2018

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Various types of rearrangements target TLX3 locus in T-cell acute lymphoblastic leukemia

11 July 2018

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Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia

11 July 2018

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Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia

11 July 2018

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11 July 2018

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A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.

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https://api.crossref.org/works/10.1038%2FNM.2610

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia

21 January 2018

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Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/22366949

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

AML1 mutation and its coexistence with different transcription factor gene families in de novo acute myeloid leukemia (AML): redundancy or synergism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22366949

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22366949

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NM.2610

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22366949%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22366949%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22366949%20AND%20SRC:MED&resulttype=core&format=json