(Q52126883)

22 April 2018

title

Spatial and temporal expression pattern of Runx3 (Aml2) and Runx1 (Aml1) indicates non-redundant functions during mouse embryogenesis. (English)

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22 April 2018

1 reference

Levanon D

1

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22 April 2018

Brenner O

2

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22 April 2018

Negreanu V

3

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22 April 2018

Bettoun D

4

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22 April 2018

Woolf E

5

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22 April 2018

Eilam R

6

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22 April 2018

Lotem J

7

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22 April 2018

Gat U

8

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22 April 2018

Otto F

9

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22 April 2018

Speck N

10

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22 April 2018

Groner Y

11

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22 April 2018

publication date

1 December 2001

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22 April 2018

Mechanisms of Development

published in

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22 April 2018

volume

109

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22 April 2018

page(s)

413-417

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22 April 2018

issue

2

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22 April 2018

Mapping of the mouse homolog of the human runt domain gene, AML2, to the distal region of mouse chromosome 4

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Cloning, mapping and expression of PEBP2 alpha C, a third gene encoding the mammalian Runt domain

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

The RUNX3 gene--sequence, structure and regulated expression

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Expression of AML1-d, a short human AML1 isoform, in embryonic stem cells suppresses in vivo tumor growth and differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Expression of the human acute myeloid leukemia gene AML1 is regulated by two promoter regions

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Molecular basis of tissue-specific gene expression mediated by the runt domain transcription factor PEBP2/CBF.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Cholinergic projection sites of the nucleus of tractus diagonalis

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Role of Cbfa1 in osteoblast differentiation and function

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Regulation of chondrocyte differentiation by Cbfa1

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Cbfa1 in bone development

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Regulation of AML2/CBFA3 in hematopoietic cells through the retinoic acid receptor alpha-dependent signaling pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

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/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Transcription-coupled translation control of AML1/RUNX1 is mediated by cap- and internal ribosome entry site-dependent mechanisms.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Expression of runt in the mouse embryo.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900537-8

7 January 2021

10.1016/S0925-4773(01)00537-8

Identifiers

DOI

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22 April 2018

PubMed ID

11731260

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22 April 2018