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

Εμφάνιση άλλων εκδόσεων (2)

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	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
Μορφή:	Conference item
Έκδοση:	2010

Παρόμοια τεκμήρια

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.
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Έκδοση: (2011)

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1 alpha localization in erythroblasts
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Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
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Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level
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Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
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Myelolipoma of the posterior mediastinum in a patient with chronic dyserythropoietic anemia
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Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III
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Mutational analysis of the CDAN1 gene in familial and sporadic congenital dyserythropoietic anaemia type 1
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The Pleiotropic Effects of GATA1 and KLF1 in Physiological Erythropoiesis and in Dyserythropoietic Disorders
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Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I
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P1554: INCREASED PREVALENCE OF THROMBOEMBOLIC EVENTS IN PATIENTS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I
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Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I.
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Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis
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Pulmonary Alveolar Proteinosis in Association with Congenital Dyserythropoietic Anemia: A Case Report
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