Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies. (Q47268104)

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10 February 2020

title

Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies (English)

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10 February 2020

6

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10 February 2020

Claude Preudhomme

11

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10 February 2020

Hélène Cavé

12

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10 February 2020

author name string

A Renneville

1

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10 February 2020

S Kaltenbach

2

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10 February 2020

E Clappier

3

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10 February 2020

S Collette

4

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10 February 2020

J-B Micol

5

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10 February 2020

P Lepelley

7

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10 February 2020

N Dastugue

8

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Y Benoît

9

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10 February 2020

Y Bertrand

10

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10 February 2020

publication date

22 October 2009

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10 February 2020

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10 February 2020

volume

24

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10 February 2020

issue

2

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10 February 2020

page(s)

476-480

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Wilms' tumor 1 gene mutations independently predict poor outcome in adults with cytogenetically normal acute myeloid leukemia: a cancer and leukemia group B study

10 February 2020

cites work

1 reference

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Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia: a study from the Acute Leukemia French Association

21 January 2018

1 reference

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Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party

21 January 2018

1 reference

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Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951

21 January 2018

1 reference

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The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children.

21 January 2018

1 reference

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The SCFFBW7 ubiquitin ligase complex as a tumor suppressor in T cell leukemia

21 January 2018

1 reference

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Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia

21 January 2018

1 reference

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Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome

21 January 2018

1 reference

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21 January 2018

WT1 mutations in T-ALL

1 reference

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Real-time quantitative polymerase chain reaction detection of minimal residual disease by standardized WT1 assay to enhance risk stratification in acute myeloid leukemia: a European LeukemiaNet study.

21 January 2018

1 reference

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