(Q35545539)

English

Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A

scientific article published on 24 April 2015

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scholarly article

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Europe PubMed Central

PubMed publication ID

8 August 2017

Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

lymphoblastic leukemia

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based on heuristic

inferred from title

T-cell acute lymphoblastic leukemia

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based on heuristic

inferred from title

9

object named as

Kajsa Paulsson

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Europe PubMed Central

PubMed publication ID

8 August 2017

object named as

Thoas Fioretos

8

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author name string

Kristina Karrman

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Anders Castor

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Mikael Behrendtz

3

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Erik Forestier

4

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Linda Olsson

5

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Mats Ehinger

6

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Andrea Biloglav

7

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Europe PubMed Central

PubMed publication ID

8 August 2017

Bertil Johansson

10

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Europe PubMed Central

PubMed publication ID

8 August 2017

publication date

24 April 2015

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Europe PubMed Central

PubMed publication ID

8 August 2017

Journal of Hematology & Oncology

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Europe PubMed Central

PubMed publication ID

8 August 2017

8

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Europe PubMed Central

PubMed publication ID

8 August 2017

42

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Europe PubMed Central

PubMed publication ID

8 August 2017

copyright license

Creative Commons Attribution 4.0 International

24 April 2015

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April 2022 Public Data File from Crossref

copyright status

0 references

Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens

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Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia

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Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.

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Notch signaling expands a pre-malignant pool of T-cell acute lymphoblastic leukemia clones without affecting leukemia-propagating cell frequency

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Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia

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The BCL11B tumor suppressor is mutated across the major molecular subtypes of T-cell acute lymphoblastic leukemia

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Clonal selection in xenografted human T cell acute lymphoblastic leukemia recapitulates gain of malignancy at relapse

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Massive genomic rearrangement acquired in a single catastrophic event during cancer development

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Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

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Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia

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12 July 2018

PHF6 mutations in T-cell acute lymphoblastic leukemia

1 reference

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12 July 2018

Inactivation of LEF1 in T-cell acute lymphoblastic leukemia

1 reference

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Long-term results of NOPHO ALL-92 and ALL-2000 studies of childhood acute lymphoblastic leukemia

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WT1 mutations in T-ALL

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Fast and accurate short read alignment with Burrows-Wheeler transform

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12 July 2018

High hyperdiploid childhood acute lymphoblastic leukemia

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12 July 2018

Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia.

1 reference

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12 July 2018

NOTCH is a key regulator of human T-cell acute leukemia initiating cell activity

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12 July 2018

A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.

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12 July 2018

Molecular-genetic insights in paediatric T-cell acute lymphoblastic leukaemia

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12 July 2018

Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia

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12 July 2018

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

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Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

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Telomeric IGH losses detectable by fluorescence in situ hybridization in chronic lymphocytic leukemia reflect somatic VH recombination events.

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Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCRbeta locus rearrangements and putative new T-cell oncogenes

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Genes contributing to minimal residual disease in childhood acute lymphoblastic leukemia: prognostic significance of CASP8AP2

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Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia

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Alterations of the p53, p21, p16, p15 and RAS genes in childhood T-cell acute lymphoblastic leukemia

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Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011.

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Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia.

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Extensive molecular mapping of TCRα/δ- and TCRβ-involved chromosomal translocations reveals distinct mechanisms of oncogene activation in T-ALL.

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The tumor suppressor gene hCDC4 is frequently mutated in human T-cell acute lymphoblastic leukemia with functional consequences for Notch signaling.

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10.1186/S13045-015-0138-0

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Europe PubMed Central

PubMed publication ID

8 August 2017

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

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