101. Red Cells and Erythropoiesis, Excluding Iron: Poster I

A Single Mutation in the SENP1 Region Regulates the Excessive Erythropoiesis in the Andes

BMI-1 Transduced Human Erythroid Cells: A Representative System for Modeling Transcriptional Programs during Terminal Erythroid Differentiation

Dexamethasone Targets E2F4 to Induce Erythroid Progenitor Renewal

Establishing a Patient-Derived Immortalized Erythroid Progenitor Cell Model to Investigate Disease Mechanisms and Lentiviral Gene Therapy Vector in Congenital Dyserythropoietic Anemia Type II

Evaluating the Clinical Impact of Hemoglobinopathy and Hereditary Red Blood Cell Disorder Co-Inheritance in a Cohort of 315 Patients

High Incidence of Thalassemia Traits Among Myelodysplastic Syndrome Patients May Mask Macrocytic Anemia but Not the Enhanced Proteasome Proteolytic Activity

Inducible, Erythroid-Specific Knockout of Codanin-1 in Adult Mice Replicates Congenital Dyserythropoietic Anemia Type-Ia

Loss of ATG5 in Humans Causes Syndromic Congenital Dyserythropoietic Anemia with Impaired Mitophagy in Late Stages of Terminal Erythropoiesis

Poster Test

Single-Cell Sequencing Reveals Differential Erythroid Lineage Differentiation in Patients with PNH

The G6PD a- Variant Does Not Modulate Pulmonary Hypertension Phenotypes in Mice

Toward the Creation of Diagnostic Algorithms for Congenital Hemolytic Anemia Using Advanced Parameters from Modern Hematology Analyzers