Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts (Q24294499)

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24 January 2020

title

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21364188%20AND%20SRC:MED&resulttype=core&format=json

SEC23 homolog B, COPII coat complex component

24 January 2020

main subject

congenital disorder

0 references

1 reference

GOA release 2020-03-11

Codanin 1

1 reference

Congenital dyserythropoietic anemia, type I (human)

GOA release 2020-03-11

1 reference

congenital dyserythropoietic anemia

GOA release 2020-03-11

1 reference

congenital dyserythropoietic anemia type I

inferred from title

1 reference

1

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24 January 2020

Nigel A Roberts

2

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24 January 2020

Marco De Gobbi

4

1 reference

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24 January 2020

Louise E Bird

5

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24 January 2020

Tasneem Hassanali

6

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24 January 2020

David Ferguson

9

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24 January 2020

Douglas Higgs

12

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24 January 2020

author name string

Jill M Brown

3

1 reference

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24 January 2020

Jacqueline A Sharpe

7

1 reference

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24 January 2020

Jacqueline Sloane-Stanley

8

1 reference

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24 January 2020

Jacqueline Cordell

10

1 reference

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24 January 2020

Veronica J Buckle

11

1 reference

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24 January 2020

William G Wood

13

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24 January 2020

language of work or name

English

0 references

publication date

1 March 2011

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24 January 2020

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24 January 2020

volume

117

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24 January 2020

issue

25

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24 January 2020

page(s)

6928-6938

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Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis

24 January 2020

cites work

1 reference

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7 January 2021

The congenital dyserythropoietic anemias

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7 January 2021

Coordination of COPII vesicle trafficking by Sec23.

1 reference

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7 January 2021

Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data

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7 January 2021

The HP1 protein family: getting a grip on chromatin

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7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

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7 January 2021

Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

1 reference

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7 January 2021

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

1 reference

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7 January 2021

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

1 reference

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7 January 2021

HP1 and the dynamics of heterochromatin maintenance

1 reference

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7 January 2021

INCENP centromere and spindle targeting: identification of essential conserved motifs and involvement of heterochromatin protein HP1

1 reference

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7 January 2021

Coregulated human globin genes are frequently in spatial proximity when active

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Cloning and functional characterization of mammalian homologues of the COPII component Sec23

1 reference

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7 January 2021

Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25

1 reference

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7 January 2021

A versatile ligation-independent cloning method suitable for high-throughput expression screening applications

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7 January 2021

The UCSC Genome Browser Database: 2008 update

1 reference

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7 January 2021

ER stress controls iron metabolism through induction of hepcidin

1 reference

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7 January 2021

Production of homozygous mutant ES cells with a single targeting construct

1 reference

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7 January 2021

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.

1 reference

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7 January 2021

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I

1 reference

https://api.crossref.org/works/10.1182%2FBLOOD-2010-09-308478

7 January 2021

Diamond-Blackfan anemia: erythropoiesis lost in translation

1 reference

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7 January 2021

Tissue-specific histone modification and transcription factor binding in alpha globin gene expression.

1 reference

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7 January 2021

Runx1-mediated hematopoietic stem-cell emergence is controlled by a Gata/Ets/SCL-regulated enhancer

1 reference

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7 January 2021

Biologic properties and enucleation of red blood cells from human embryonic stem cells

1 reference

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7 January 2021

Diamond-Blackfan anemia: a ribosomal puzzle

1 reference

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7 January 2021

Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated.

1 reference

https://api.crossref.org/works/10.1182%2FBLOOD-2010-09-308478

7 January 2021

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

1 reference

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7 January 2021

10.1182/BLOOD-2010-09-308478

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21364188%20AND%20SRC:MED&resulttype=core&format=json

release_sbuxkwci3fg73fwfyfrihjuesy

24 January 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/sbuxkwci3fg73fwfyfrihjuesy

24 November 2022

mapped directly with Wikidata item

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