Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1 alpha localization in erythroblasts

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1 alpha localization in erythroblasts

Show other versions (2)

Congenital dyserythropoietic anemia type 1 (CDA-1), a rare inborn anemia characterized by abnormal chromatin ultrastructure in erythroblasts, is caused by abnormalities in codanin-1, a highly conserved protein of unknown function. We have produced 3 monoclonal antibodies to codanin-1 that demonstrat...

Full description

Bibliographic Details
Main Authors:	Renella, R, Roberts, N, Brown, J, De Gobbi, M, Bird, L, Hassanali, T, Sharpe, J, Sloane-Stanley, J, Ferguson, D, Cordell, J, Buckle, V, Higgs, D, Wood, W
Format:	Journal article
Language:	English
Published:	2011

Similar Items

Codanin-1 Mutations In Congenital Dyserythropoietic Anemia Type 1 Affect HP1 alpha Localization In Erythroblasts
by: Renella, R, et al.
Published: (2010)

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.
by: Renella, R, et al.
Published: (2011)

Congenital dyserythropoietic anemias
by: Renella, R, et al.
Published: (2011)

Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease
by: Grace Swickley, et al.
Published: (2020-03-01)

A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I
by: Renella, R, et al.
Published: (2008)

Modelling the erythroblastic island niche of dyserythropoietic anaemia type IV patients using induced pluripotent stem cells
by: Alisha May, et al.
Published: (2023-04-01)

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
by: Ahmed, MR, et al.
Published: (2006)

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.
by: Babbs, C, et al.
Published: (2013)

Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level
by: Scott, C, et al.
Published: (2022)

Rare congenital Dyserythropoietic anemia of childhood: A case report
by: Hamzeh F. Al Hussien, et al.
Published: (2023-02-01)

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
by: Scott, C, et al.
Published: (2020)

Atypical congenital dyserythropoietic anaemia: a novel mutation in LPIN2 causes Majeed syndrome with incomplete penetrance
by: Roy, N, et al.
Published: (2013)

Congenital dyserythropoietic anemia in children: Case series with review of literature
by: Jasmita Dass, et al.
Published: (2024-06-01)

Myelolipoma of the posterior mediastinum in a patient with chronic dyserythropoietic anemia
by: Cristiano Claudino Oliveira, et al.
Published: (2016-09-01)

An <i>EHPB1L1</i> Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever Littermates
by: G. Diane Shelton, et al.
Published: (2022-08-01)

Mutational analysis of the CDAN1 gene in familial and sporadic congenital dyserythropoietic anaemia type 1
by: Ahmed, MR, et al.
Published: (2003)

P1554: INCREASED PREVALENCE OF THROMBOEMBOLIC EVENTS IN PATIENTS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I
by: M. Asleh, et al.
Published: (2022-06-01)

Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I.
by: Ahmed, MR, et al.
Published: (2006)

<i>EHBP1L1</i> Frameshift Deletion in English Springer Spaniel Dogs with Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) or Neonatal Losses
by: Sarah Østergård Jensen, et al.
Published: (2022-08-01)

Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts
by: Steven Heshusius, et al.
Published: (2022-01-01)

The impact of erythroblast enucleation efficiency on the severity of anemia in patients with myelodysplastic syndrome
by: Chao An, et al.
Published: (2023-11-01)

CIRCULATING HEMATOPOIETIC STEM AND PROGENITOR CELLS AND ERYTHROBLASTS COUNTING IS INCREASED IN PATIENTS WITH SICKLE CELL ANEMIA
by: J Milhomens, et al.
Published: (2023-10-01)

HP1B is a euchromatic Drosophila HP1 homolog with links to metabolism.
by: Benjamin B Mills, et al.
Published: (2018-01-01)

Garland of Erythroblasts around a Macrophage: Erythroblastic Island
by: Chandan Kumar, et al.
Published: (2020-05-01)

Congenital dyserythropoietic anemia type IV with kruppel-like factor 1 E325K mutation in a preterm neonate: Case and literature review
by: Reema Garegrat, et al.
Published: (2022-01-01)

P1470: IDENTIFICATION OF THE PRO20THR NOVEL VARIANT IN CDIN1 GENE ALLOWED EXPLORING THE BIOLOGICAL PROCESSES IMPAIRED IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I
by: Roberta Marra, et al.
Published: (2023-08-01)

Scalable in vitro production of defined mouse erythroblasts
by: Helena S. Francis, et al.
Published: (2022-01-01)

Scalable in vitro production of defined mouse erythroblasts.
by: Helena S Francis, et al.
Published: (2022-01-01)

Acute liver failure in a pediatric patient with congenital dyserythropoietic anemia type I treated with deferasirox
by: Galina Ling, et al.
Published: (2015-09-01)

Inside Out Integrin Activation Mediated by PIEZO1 Signaling in Erythroblasts
by: Francesca Aglialoro, et al.
Published: (2020-07-01)

Scalable in vitro production of defined mouse erythroblasts
by: Francis, HS, et al.
Published: (2022)

Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
by: Fatih Demircioğlu, et al.
Published: (2015-07-01)

Successful Treatment of Iron Overload with Phlebotomies in Two Siblings with Congenital Dyserythropoietic Anemia – Type II (CDA-II)
by: Ladislav Chrobák
Published: (2006-01-01)

Stimulation of erythroblast maturation in vitro by sphingolipids
by: R.B. Clayton, et al.
Published: (1974-11-01)

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia
by: Akie Kobayashi, et al.
Published: (2022-02-01)

Is there a role for CTCF binding sites in regulating the structure or function of the a globin gene cluster?
by: Anguita, E, et al.
Published: (2005)

Involutions fixing HP1(2m)∪HP2(2m)∪HP(2n+1) of the fixed point set
by: Suqian ZHAO
Published: (2015-12-01)

DOT1L Mediated Gene Repression in Extensively Self-Renewing Erythroblasts
by: Shaon Borosha, et al.
Published: (2022-03-01)

New Cases and Mutations in <i>SEC23B</i> Gene Causing Congenital Dyserythropoietic Anemia Type II
by: Melina Mara Musri, et al.
Published: (2023-06-01)

Ultrastructural characteristics of erythroid cells in congenital dyserythropoietic anemia type II, with a focus on peripheral cisternae and double membranes
by: Yong-Xin Ru, et al.
Published: (2023-03-01)