Frequent cases of RAS-mutated Down syndrome acute lymphoblastic leukaemia lack JAK2 mutations. (Q36334267)

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12 March 2020

title

Frequent cases of RAS-mutated Down syndrome acute lymphoblastic leukaemia lack JAK2 mutations (English)

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12 March 2020

1 reference

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Stilianos Antonarakis

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12 March 2020

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12 March 2020

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12 March 2020

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12 March 2020

Michel Guipponi

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12 March 2020

Sergey I Nikolaev

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12 March 2020

Marco Garieri

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12 March 2020

Emilie Falconnet

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12 March 2020

Pascale Ribaux

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12 March 2020

Jürgen Groet

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12 March 2020

Emanuela Giarin

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12 March 2020

Dean Nizetic

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12 March 2020

language of work or name

English

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publication date

8 August 2014

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12 March 2020

published in

Nature Communications

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volume

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12 March 2020

page(s)

4654

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RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia

12 March 2020

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Down syndrome childhood acute lymphoblastic leukemia has a unique spectrum of sentinel cytogenetic lesions that influences treatment outcome: a report from the Children's Oncology Group

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Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group

30 September 2017

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Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia

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Insights into the manifestations, outcomes, and mechanisms of leukemogenesis in Down syndrome

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Hyperactive Ras in developmental disorders and cancer

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Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome

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Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder

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Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

21 January 2018

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Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia.

21 January 2018

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Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome.

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High incidence of RAS signalling pathway mutations in MLL-rearranged acute myeloid leukemia

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Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemia.

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Different drug sensitivity profiles of acute myeloid and lymphoblastic leukemia and normal peripheral blood mononuclear cells in children with and without Down syndrome

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A Single-Nucleotide Substitution Mutator Phenotype Revealed by Exome Sequencing of Human Colon Adenomas

21 January 2018

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BTG1 deletions do not predict outcome in Down syndrome acute lymphoblastic leukemia

21 January 2018

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Simultaneous occurrence of mongolism and leukemia; report of a nationwide survey

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PubMed

https://pubmed.ncbi.nlm.nih.gov/25105841

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Tumorigenesis in Down's syndrome: big lessons from a small chromosome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25105841

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NCOMMS5654

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25105841%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

0 references

1 reference

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12 March 2020

PubMed publication ID

25105841

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25105841%20AND%20SRC:MED&resulttype=core&format=json