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)

Manylion Llyfryddiaeth
Prif Awduron:	Renella, R, Roberts, N, Brown, J, De Gobbi, M, Bird, L, Hassanali, T, Sloane-Stanley, J, Sharpe, J, Cordell, J, Ferguson, D, Buckle, V, Higgs, D, Wood, W
Fformat:	Conference item
Cyhoeddwyd:	2010

Eitemau Tebyg

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

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

Congenital dyserythropoietic anemias
gan: Renella, R, et al.
Cyhoeddwyd: (2011)

Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated
gan: Sharon Noy-Lotan, et al.
Cyhoeddwyd: (2009-05-01)

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

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

Recapitulation of erythropoiesis in congenital dyserythropoietic anemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
gan: Caroline Scott, et al.
Cyhoeddwyd: (2020-10-01)

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

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

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

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

Congenital dyserythropoietic anemia masquerading as hereditary spherocytosis
gan: Kaninika Sanyal, et al.
Cyhoeddwyd: (2024-09-01)

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

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

Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anemia type II.
gan: J F Bouhours, et al.
Cyhoeddwyd: (1985-04-01)

CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I: PATIENT WITH ANEMIA AND SKELETAL ANOMALY
gan: Sevde Yazıcı Şahin, et al.
Cyhoeddwyd: (2024-12-01)

CODANIN-1 sequesters ASF1 by using a histone H3 mimic helix to regulate the histone supply
gan: Tae-Kyeong Jeong, et al.
Cyhoeddwyd: (2025-03-01)

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

Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient
gan: Lilian Varricchio, et al.
Cyhoeddwyd: (2019-12-01)

Congenital dyserythropoietic anemia type II and ineffective erythropoiesis: challenges in diagnosis and management
gan: Imo J. Akpan, et al.
Cyhoeddwyd: (2024-07-01)

European <i>EHBP1L1</i> Genotyping Survey of Dyserythropoietic Anemia and Myopathy Syndrome in English Springer Spaniels
gan: Sarah Østergård Jensen, et al.
Cyhoeddwyd: (2024-11-01)

Pyruvate kinase deficiency misdiagnosed as congenital dyserythropoietic anemia type i
gan: A. Koca Yozgat, et al.
Cyhoeddwyd: (2020-10-01)

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

A new type of transfusion-dependent congenital dyserythropoietic anemia
gan: Hermann Heimpel, et al.
Cyhoeddwyd: (2007-10-01)

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

Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III
gan: Gonzalo Hernández, et al.
Cyhoeddwyd: (2022-10-01)

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

The Pleiotropic Effects of GATA1 and KLF1 in Physiological Erythropoiesis and in Dyserythropoietic Disorders
gan: Gloria Barbarani, et al.
Cyhoeddwyd: (2019-02-01)

Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I
gan: Ayça Koca Yozgat, et al.
Cyhoeddwyd: (2022-10-01)

A CASE OF CONGENITAL DYSERYTHROPOIETIC ANEMIA MASKED BY HEMOGLOBIN H DISEASE
gan: Xiaolin Yin
Cyhoeddwyd: (2024-06-01)

Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II
gan: Achille Iolascon, et al.
Cyhoeddwyd: (2009-05-01)

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

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

Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis
gan: Timothy J. Satchwell, et al.
Cyhoeddwyd: (2013-11-01)

Pulmonary Alveolar Proteinosis in Association with Congenital Dyserythropoietic Anemia: A Case Report
gan: Marcus A. Carden, et al.
Cyhoeddwyd: (2012-01-01)

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach
gan: Achille Iolascon, et al.
Cyhoeddwyd: (2012-12-01)

Molecular basis of congenital dyserythropoietic anemia type II and genotype-phenotype relationship
gan: Mario Cazzola, et al.
Cyhoeddwyd: (2010-05-01)

Adrenal extramedullary hematopoiesis in the setting of anti-Diego antibody and congenital dyserythropoietic anemia
gan: Janet Rae Julson, et al.
Cyhoeddwyd: (2022-04-01)

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

Erythroblast Enucleation
gan: Ganesan Keerthivasan, et al.
Cyhoeddwyd: (2011-01-01)