(Q55671562)

Michael A Simpson

2

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Pia Ostergaard

Pia Ostergaard

1

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Dimitra Dafou

Dimitra Dafou

7

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Colin Steward

Colin G Steward

4

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Richard C Trembath

Richard C Trembath

19

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Shirley Hodgson

12

Shirley Hodgson

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author name string

Fiona C Connell

3

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Glen Brice

5

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Wesley J Woollard

6

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Tatjana Kilo

8

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Sarah Smithson

9

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Peter Lunt

10

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Victoria A Murday

11

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Russell Keenan

13

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Daniela T Pilz

14

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Taija Makinen

16

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Peter S Mortimer

17

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Steve Jeffery

18

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Sahar Mansour

https://scigraph.springernature.com/pub.10.1038/ng.923

20

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language of work or name

English

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publication date

4 September 2011

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published in

Nature Genetics

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volume

43

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page(s)

929-31

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issue

10

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exact match

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cites work

Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia

1 reference

12 December 2020

Mutation of CEBPA in familial acute myeloid leukemia

1 reference

12 December 2020

GATA-2 regulates granulocyte-macrophage progenitor cell function

1 reference

12 December 2020

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

1 reference

12 December 2020

GATA Transcription Factors and Cancer

1 reference

12 December 2020

Emberger syndrome-Primary lymphedema with myelodysplasia: Report of seven new cases

1 reference

12 December 2020

An early haematopoietic defect in mice lacking the transcription factor GATA-2

1 reference

12 December 2020

Interaction between GATA and the C/EBP family of transcription factors is critical in GATA-mediated suppression of adipocyte differentiation

1 reference

12 December 2020

Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.

1 reference

12 December 2020

Gata2 is required for the development of inner ear semicircular ducts and the surrounding perilymphatic space

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

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.

1 reference

12 December 2020

Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia

1 reference

12 December 2020

Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia

1 reference

12 December 2020

A Gata2 intronic enhancer confers its pan-endothelia-specific regulation.

1 reference

12 December 2020