(Q39992358)

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Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study.

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19322206%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19322206%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

multicenter clinical trial

0 references

childhood acute myeloid leukemia

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

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24 January 2020

Gisbert Schneider

5

1 reference

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24 January 2020

author name string

B Gruhn

2

1 reference

Europe PubMed Central

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24 January 2020

T Coliva

3

1 reference

Europe PubMed Central

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24 January 2020

M Kalinova

4

1 reference

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24 January 2020

H Kreyenberg

6

1 reference

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24 January 2020

D Steinbach

7

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24 January 2020

G Weber

8

1 reference

Europe PubMed Central

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24 January 2020

I H I M Hollink

9

1 reference

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24 January 2020

C M Zwaan

10

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24 January 2020

A Biondi

11

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24 January 2020

V H J van der Velden

12

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24 January 2020

D Reinhardt

13

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24 January 2020

G Cazzaniga

14

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24 January 2020

P Bader

15

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24 January 2020

J Trka

16

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Europe PubMed Central

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24 January 2020

European Study Group on WT1 Expression in Childhood AML

17

1 reference

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24 January 2020

publication date

26 March 2009

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24 January 2020

1 reference

Europe PubMed Central

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24 January 2020

23

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24 January 2020

8

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24 January 2020

1472-1479

1 reference

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24 January 2020

https://scigraph.springernature.com/pub.10.1038/leu.2009.51

0 references

WT1 as a universal marker for minimal residual disease detection and quantification in myeloid leukemias and in myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

High WT1 expression after induction therapy predicts high risk of relapse and death in pediatric acute myeloid leukemia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Prognostic impact of RT-PCR-based quantification of WT1 gene expression during MRD monitoring of acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Identification of a set of seven genes for the monitoring of minimal residual disease in pediatric acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Wilms' tumour gene 1 (WT1) in human neoplasia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

WT1 gene expression: an excellent tool for monitoring minimal residual disease in 70% of acute myeloid leukaemia patients - results from a single-centre study

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

WT1 gene expression: useful marker for minimal residual disease in childhood myelodysplastic syndromes and juvenile myelo-monocytic leukemia?

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Significant correlation between the degree of WT1 expression and the International Prognostic Scoring System Score in patients with myelodysplastic syndromes.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Wilms tumour gene 1 overexpression in bone marrow as a marker for minimal residual disease in acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Wilms' tumor gene 1 (WT1) expression in childhood acute lymphoblastic leukemia: a wide range of WT1 expression levels, its impact on prognosis and minimal residual disease monitoring.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Wilms' tumour 1 mutations are associated with FLT3-ITD and failure of standard induction chemotherapy in patients with normal karyotype AML.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Prognostic implications of gene mutations in acute myeloid leukemia with normal cytogenetics

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Evaluation of candidate control genes for diagnosis and residual disease detection in leukemic patients using 'real-time' quantitative reverse-transcriptase polymerase chain reaction (RQ-PCR) - a Europe against cancer program.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - a Europe Against Cancer program.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual disease. Report of the BIOMED-1 Concerted Action: investigation of minimal residual disease in acute leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Detection of minimal residual disease in hematologic malignancies by real-time quantitative PCR: principles, approaches, and laboratory aspects.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

What do we mean by sensitivity when we talk about detecting minimal residual disease?

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Wilms' tumor 1 mutation accumulated during therapy in acute myeloid leukemia: biological and clinical implications

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

21 January 2018

Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

A tumor suppressor and oncogene: the WT1 story.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

Real-time quantitative PCR detection of WT1 gene expression in children with AML: prognostic significance, correlation with disease status and residual disease detection by flow cytometry

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

Quantitative assessment of WT1 expression by real time quantitative PCR may be a useful tool for monitoring minimal residual disease in acute leukemia patients

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

Elevated levels of WT1 transcripts in bone marrow harvests are associated with a high relapse risk in patients autografted for acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

The Wilms' tumor gene WT1 is a good marker for diagnosis of disease progression of myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

Fluorescent 5'-exonuclease assay for the absolute quantification of Wilms' tumour gene (WT1) mRNA: implications for monitoring human leukaemias

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.51

7 January 2021

based on heuristic

inferred from DOI database lookup

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