(Q54763872)

English

AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.

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scholarly article

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies. (English)

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

1 reference

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8

object named as

Atsushi Manabe

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

author name string

Takeshi Taketani

1

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Tomohiko Taki

2

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Junko Takita

3

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Masahiro Tsuchida

4

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Ryoji Hanada

5

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Teruaki Hongo

6

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Takashi Kaneko

7

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Kohmei Ida

9

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Yasuhide Hayashi

10

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

publication date

1 September 2003

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Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Genes, Chromosomes and Cancer

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Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

38

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

1

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

1-7

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

Proposal for the recognition of minimally differentiated acute myeloid leukaemia (AML-MO)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

The expression pattern of the AML1 gene in non-Hodgkin's B-cell lymphomas and normal B lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Coduplication of the MLL and FLT3 genes in patients with acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the AML1 gene in acute myeloid leukemia of FAB types M0 and M7.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

A large variety of alternatively spliced and differentially expressed mRNAs are encoded by the human acute myeloid leukemia gene AML1.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Generation of the AML1-EVI-1 fusion gene in the t(3;21)(q26;q22) causes blastic crisis in chronic myelocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

RUNX1/AML1: a central player in hematopoiesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the transcription factor AML1/CBA2 are uncommon in blastic transformation of chronic myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of the AML1/RUNX1 gene in a transient myeloproliferative disorder patient with Down syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic imbalance on chromosome 2q and alterations of the caspase 8 gene in neuroblastoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

An acute myeloid leukemia gene, AML1, regulates hemopoietic myeloid cell differentiation and transcriptional activation antagonistically by two alternative spliced forms.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term follow-up of childhood acute lymphoblastic leukemia in Tokyo Children's Cancer Study Group 1981-1995

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

C/EBP-beta, C/EBP-delta, PU.1, AML1 genes: mutational analysis in 381 samples of hematopoietic and solid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural basis for the heterodimeric interaction between the acute leukaemia-associated transcription factors AML1 and CBFbeta

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10246

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.10246

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12874780

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