Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Recapitulation of erythropoiesis in congenital dyserythropoietic anemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities

29 Oct 2020

Abstract excerpt

The investigation of inherited disorders of erythropoiesis has elucidated many of the principles underlying the production of normal red blood cells and how this is perturbed in human disease. Congenital Dyserythropoietic Anaemia type 1 (CDA-I) is a rare form of anaemia caused by mutations in two genes of unknown function: CDAN1 and CDIN1 (previously called C15orf41), whilst in some cases, the underlying genetic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood groups and transfusion
Share to Erythrocyte Function and Pathophysiology
Share to Single-cell and spatial transcriptomics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33121234
DOI: 10.3324/haematol.2020.260158

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recapitulation of erythropoiesis in congenital dyserythropoietic anemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalitiesPMID 33121234Read ↗

Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I)Semantic proximity Read ↗

Molecular and cellular characterization of congenital dyserythropoietic anaemia type 1Semantic proximity Read ↗

The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type ISemantic proximity Read ↗

Congenital dyserythropoietic anemiasSemantic proximity Read ↗

Codanin-1 mutations engineered in human erythroid cells demonstrate role of CDAN1 in terminal erythroid maturation.Semantic proximity Read ↗

Genetic and functional insights into CDA-I prevalence and pathogenesis.Semantic proximity Read ↗

Anemia-associated mutations disrupt the CDIN1-Codanin1 complex in inherited congenital dyserythropoietic anemia I (CDA-I) disease.Semantic proximity Read ↗

A novel human cellular model of CDA IV enables comprehensive analysis revealing the molecular basis of the disease phenotype.Semantic proximity Read ↗

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.Semantic proximity Read ↗

A complex comprising C15ORF41 and Codanin-1: the products of two genes mutated in congenital dyserythropoietic anaemia type I (CDA-I).Semantic proximity Read ↗

Inherited CDA-I disease: anemia-associated mutations disrupt CDIN1-Codanin1 complexSemantic proximity Read ↗

The congenital dyserythropoieitic anemias: genetics and pathophysiology.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.