Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group. (Q34052581)

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English	Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group.	scientific article

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1 February 2020

Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group (English)

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acute myeloid leukemia

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childhood acute myeloid leukemia

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1

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Nyla A Heerema

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Rong Zeng

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Todd A Alonzo

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Robert B Gerbing

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Kristen L Miller

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Jessica A Pollard

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Derek L Stirewalt

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Susana C Raimondi

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Betsy Hirsch

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Janet L Franklin

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Beverly Lange

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Soheil Meshinchi

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22 April 2010

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702-710

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1 February 2020

Prevalence and prognostic significance of KIT mutations in pediatric patients with core binding factor AML enrolled on serial pediatric cooperative trials for de novo AML.

1 reference

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28 July 2018

WT1 expression at diagnosis does not predict survival in pediatric AML: a report from the Children's Oncology Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

Prevalence and prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group

1 reference

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28 July 2018

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

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28 July 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

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28 July 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

Cooperating gene mutations in acute myeloid leukemia: a review of the literature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

Outcomes in CCG-2961, a children's oncology group phase 3 trial for untreated pediatric acute myeloid leukemia: a report from the children's oncology group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

The incidence and clinical significance of nucleophosmin mutations in childhood AML.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

A tumor suppressor and oncogene: the WT1 story.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

Influence of new molecular prognostic markers in patients with karyotypically normal acute myeloid leukemia: recent advances

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

WT1 proteins: functions in growth and differentiation

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28 July 2018

Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia

1 reference

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28 July 2018

A clinical overview of WT1 gene mutations

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28 July 2018

Expression of the Wilms' tumor gene (WT1) in human leukemias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 July 2018

Prognostic impact of WT1 mutations in cytogenetically normal acute myeloid leukemia: a study of the German-Austrian AML Study Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 October 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918327

28 October 2018

Clinical implications of FLT3 mutations in pediatric AML.

1 reference

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28 October 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

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28 October 2018

Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.

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28 October 2018

Frequency and Heritability ofWT1Mutations in Nonsyndromic Wilms' Tumor Patients: A UK Children’s Cancer Study Group Study

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28 October 2018

The Wilms tumour (WT1) gene is mutated in a secondary leukaemia in a WAGR patient

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20413658

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/20413658

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20413658

12 December 2020

based on heuristic

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10.1182/BLOOD-2010-02-268953

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1 February 2020

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1 February 2020

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