(Q81890140)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18754024%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

title

Alterations of NFIA in chronic malignant myeloid diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18754024%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

9

1 reference

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13 January 2020

Daniel Birnbaum

13

1 reference

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13 January 2020

author name string

F Bernard

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18754024%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

V Gelsi-Boyer

2

1 reference

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13 January 2020

A Murati

3

1 reference

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13 January 2020

S Giraudier

4

1 reference

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13 January 2020

V Trouplin

5

1 reference

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13 January 2020

J Adélaïde

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18754024%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

J Rey

7

1 reference

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13 January 2020

S Olschwang

8

1 reference

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13 January 2020

M Chaffanet

10

1 reference

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13 January 2020

N Vey

11

1 reference

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13 January 2020

M J Mozziconacci

12

1 reference

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13 January 2020

publication date

28 August 2008

1 reference

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13 January 2020

1 reference

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13 January 2020

volume

23

1 reference

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13 January 2020

page(s)

583-585

1 reference

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13 January 2020

issue

3

1 reference

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https://scigraph.springernature.com/pub.10.1038/leu.2008.228

13 January 2020

exact match

0 references

cites work

Roles of the NFI/CTF gene family in transcription and development

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

Gene expression analysis of nuclear factor I-A deficient mice indicates delayed brain maturation

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

A minicircuitry comprised of microRNA-223 and transcription factors NFI-A and C/EBPalpha regulates human granulopoiesis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

The interplay between the master transcription factor PU.1 and miR-424 regulates human monocyte/macrophage differentiation.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

Suppression of the human erythropoietin gene expression by the TR2 orphan receptor, a member of the steroid receptor superfamily

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

Transcriptional regulation of the human TR2 orphan receptor gene by nuclear factor 1-A

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

The TR2 and TR4 orphan nuclear receptors repress Gata1 transcription

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

Integrated profiling of basal and luminal breast cancers.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

A cell-type-specific transcriptional network required for estrogen regulation of cyclin D1 and cell cycle progression in breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2008.228

7 January 2021