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Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease

BACKGROUND: Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which erythroid precursors in the bone marrow exhibit pathognomonic abnormalities including spongy heterochromatin and chromatin bridges. We have shown previously that the gene...

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Bibliografske podrobnosti
izdano v:BMC Mol Cell Biol
Main Authors: Swickley, Grace, Bloch, Yehoshua, Malka, Lidor, Meiri, Adi, Noy-Lotan, Sharon, Yanai, Amiel, Tamary, Hannah, Motro, Benny
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7092493/
https://ncbi.nlm.nih.gov/pubmed/32293259
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12860-020-00258-1
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