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Publications by Jacqueline A. Sharpe
Codanin-1 Mutations in Congenital Dyserythropoietic Anemia Type 1 Affect HP1 Localization in Erythroblasts
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Related publications
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 Biology
Molecular Biology
Codanin-1, the Protein Encoded by the Gene Mutated in Congenital Dyserythropoietic Anemia Type I (CDAN1), Is Cell Cycle Regulated
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene
American Journal of Hematology
Hematology
Congenital Dyserythropoietic Anemia Type III
Thrombocytopenia With Congenital Dyserythropoietic Anemia
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
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
Turkish Journal of Haematology
Hematology
Glycophorin a in Two Patients With Congenital Dyserythropoietic Anemia Type I and Type II Is Partly Unglycosylated.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
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 Medicine
Medicine
