(Q34448183)

2 August 2017

1 reference

title

Point mutations of the RUNx1/AML1 gene in sporadic and familial myeloid leukemias (English)

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2 August 2017

Osato M

1

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2 August 2017

Yanagida M

series ordinal

2

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2 August 2017

Shigesada K

series ordinal

3

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2 August 2017

Ito Y

series ordinal

4

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2 August 2017

publication date

1 October 2001

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International Journal of Hematology

2 August 2017

published in

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2 August 2017

volume

74

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2 August 2017

issue

3

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2 August 2017

page(s)

245-251

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https://scigraph.springernature.com/pub.10.1007/bf02982056

2 August 2017

exact match

0 references

cites work

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

1 reference

12 December 2020

Down syndrome and leukemia, an update

1 reference

12 December 2020

CBFA2, frequently rearranged in leukemia, is not responsible for a familial leukemia syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

CBFA2(AML1) translocations with novel partner chromosomes in myeloid leukemias: association with prior therapy

1 reference

12 December 2020

Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia

1 reference

12 December 2020

Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2

1 reference

12 December 2020

Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2.

1 reference

12 December 2020

Functional mutagenesis of AML1/RUNX1 and PEBP2 beta/CBF beta define distinct, non-overlapping sites for DNA recognition and heterodimerization by the Runt domain

1 reference

12 December 2020

Immunoglobulin motif DNA recognition and heterodimerization of the PEBP2/CBF Runt domain

1 reference

12 December 2020

Dimerization with PEBP2beta protects RUNX1/AML1 from ubiquitin-proteasome-mediated degradation

1 reference

12 December 2020

High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21

1 reference

12 December 2020

Embryonic lethality and impairment of haematopoiesis in mice heterozygous for an AML1-ETO fusion gene.

1 reference

12 December 2020

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

12 December 2020

Mutations of the AML1 gene in myelodysplastic syndrome and their functional implications in leukemogenesis

1 reference

12 December 2020

Structural analyses of DNA recognition by the AML1/Runx-1 Runt domain and its allosteric control by CBFbeta

1 reference

12 December 2020

Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias

1 reference

12 December 2020

The fusion gene Cbfb-MYH11 blocks myeloid differentiation and predisposes mice to acute myelomonocytic leukaemia

1 reference

12 December 2020

Inherited platelet-storage pool deficiency associated with a high incidence of acute myeloid leukaemia

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02982056

1 reference

Dimensions Publication ID

2 August 2017

1010293046

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1 reference