Codanin-1 Mutations in Congenital Dyserythropoietic Anemia Type 1 Affect HP1 Localization in Erythroblasts

Blood - United States
doi 10.1182/blood-2010-09-308478
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Society of Hematology

Related search

Characterization of the Interactions Between Codanin-1 and C15Orf41, Two Proteins Implicated in Congenital Dyserythropoietic Anemia Type I Disease

BMC Molecular and Cell Biology
Cell BiologyMolecular Biology
2020English

Codanin-1, the Protein Encoded by the Gene Mutated in Congenital Dyserythropoietic Anemia Type I (CDAN1), Is Cell Cycle Regulated

Blood
BiochemistryImmunologyCell BiologyHematology
2008English

Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene

American Journal of Hematology
Hematology
2018English

Congenital Dyserythropoietic Anemia Type III

2020English

Thrombocytopenia With Congenital Dyserythropoietic Anemia

2020English

Congenital Dyserythropoietic Anemia Type 1: Report of One Patient and Analysis of Previously Reported Patients Treated With Interferon Alpha

Indian Journal of Hematology and Blood Transfusion
Hematology
2015English

Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene

Turkish Journal of Haematology
Hematology
2015English

Glycophorin a in Two Patients With Congenital Dyserythropoietic Anemia Type I and Type II Is Partly Unglycosylated.

Acta Biochimica Polonica
BiochemistryGeneticsMolecular Biology
2000English

A Case of Congenital Dyserythropoietic Anemia Type 1 in a Japanese Adult With a CDAN1 Gene Mutation and an Inappropriately Low Serum Hepcidin-25 Level

Internal Medicine
Internal MedicineMedicine
2012English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy