RAS mutation is associated with hyperdiploidy and parental characteristics in pediatric acute lymphoblastic leukemia (Q46519927)

22 December 2017

title

RAS mutation is associated with hyperdiploidy and parental characteristics in pediatric acute lymphoblastic leukemia (English)

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22 December 2017

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Wiemels JL

1

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22 December 2017

Zhang Y

2

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22 December 2017

Chang J

3

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22 December 2017

Zheng S

4

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22 December 2017

Metayer C

5

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22 December 2017

Zhang L

6

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22 December 2017

Smith MT

7

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22 December 2017

Ma X

8

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22 December 2017

Selvin S

9

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22 December 2017

Buffler PA

10

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22 December 2017

Wiencke JK

11

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22 December 2017

publication date

1 March 2005

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22 December 2017

published in

Leukemia

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22 December 2017

volume

19

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22 December 2017

issue

3

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22 December 2017

page(s)

415-419

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22 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.leu.2403641

exact match

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Hypermethylation of the 5' CpG island of the FHIT gene is associated with hyperdiploid and translocation-negative subtypes of pediatric leukemia

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Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia

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Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis.

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FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy

21 January 2018

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Activating mutations of RTK/ras signal transduction pathway in pediatric acute myeloid leukemia

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ras Oncogene Activation and Occupational Exposures in Acute Myeloid Leukemia

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A tobacco-specific carcinogen in the fetus

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Identifiers

DOI

10.1038/SJ.LEU.2403641

1 reference

22 December 2017

PubMed ID

15674422

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22 December 2017