(Q81381430)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16239911%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations (English)

1 reference

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8 January 2020

1 reference

10

1 reference

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8 January 2020

author name string

Griffiths M

1

1 reference

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8 January 2020

Mason J

2

1 reference

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8 January 2020

Rindl M

3

1 reference

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8 January 2020

Akiki S

4

1 reference

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8 January 2020

McMullan D

5

1 reference

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8 January 2020

Stinton V

6

1 reference

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8 January 2020

Powell H

7

1 reference

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8 January 2020

Curtis A

8

1 reference

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8 January 2020

Bown N

9

1 reference

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8 January 2020

publication date

1 December 2005

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8 January 2020

1 reference

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8 January 2020

volume

19

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8 January 2020

page(s)

2355-2358

1 reference

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8 January 2020

issue

12

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2403988

8 January 2020

exact match

0 references

cites work

The role of FLT3 in haematopoietic malignancies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021

The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the Unite

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021

Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021

Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021

Genomic structure of human FLT3: implications for mutational analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021

Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403988

7 January 2021