(Q24305920)

positive regulation of transcription, DNA-templated

GOA release 2020-03-11

1 reference

congenital dyserythropoietic anemia

GOA release 2020-03-11

1 reference

inferred from title

author

Alexandre G de Brevern

object named as

Alexandre G de Brevern

10

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author name string

Lionel Arnaud

1

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Carole Saison

2

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Virginie Helias

3

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Nicole Lucien

4

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Dominique Steschenko

5

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Marie-Catherine Giarratana

6

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Claude Prehu

7

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Bernard Foliguet

8

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Lory Montout

9

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Alain Francina

11

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Pierre Ripoche

12

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Odile Fenneteau

13

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Lydie Da Costa

14

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Thierry Peyrard

15

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Gail Coghlan

16

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Niels Illum

17

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Henrik Birgens

18

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Hannah Tamary

19

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Achille Iolascon

20

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Jean Delaunay

21

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Gil Tchernia

22

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Jean-Pierre Cartron

American Journal of Human Genetics

23

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language of work or name

English

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publication date

12 November 2010

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published in

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volume

87

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issue

5

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page(s)

721-7

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cites work

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

A global role for EKLF in definitive and primitive erythropoiesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Structure of the Wilms tumor suppressor protein zinc finger domain bound to DNA

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

High-resolution structures of variant Zif268-DNA complexes: implications for understanding zinc finger-DNA recognition

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF gene

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

The erythroid phenotype of EKLF-null mice: defects in hemoglobin metabolism and membrane stability

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Advances in the understanding of haemoglobin switching

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

The congenital dyserythropoietic anemias

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Transcriptional control of erythropoiesis: emerging mechanisms and principles.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Multiple interactions between regulatory regions are required to stabilize an active chromatin hub.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

CD44 regulates hematopoietic progenitor distribution, granuloma formation, and tumorigenicity.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978953

[Congenital dyserythropoietic anemia]

29 November 2018

1 reference

12 December 2020

Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia

1 reference

12 December 2020

Analyses of beta-thalassemia mutant DNA interactions with erythroid Krüppel-like factor (EKLF), an erythroid cell-specific transcription factor

1 reference

12 December 2020

A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]

1 reference

12 December 2020