Issue Archive
Table of Contents
Inside Blood
Blood Work
Plenary Paper
Perspectives
Acute myeloid leukemia in the real world: why population-based registries are needed
Review Article
Clinical Trials and Observations
A phase 1/2 study of chemosensitization with the CXCR4 antagonist plerixafor in relapsed or refractory acute myeloid leukemia
Clinical Trials & Observations
Gene Therapy
CD20-specific adoptive immunotherapy for lymphoma using a chimeric antigen receptor with both CD28 and 4-1BB domains: pilot clinical trial results
Clinical Trials & Observations
Hematopoiesis and Stem Cells
Immunobiology
Anti-CD20 (rituximab) therapy for anti–IFN-γ autoantibody–associated nontuberculous mycobacterial infection
Clinical Trials & Observations
Functional STAT3 deficiency compromises the generation of human T follicular helper cells
Lymphoid Neoplasia
Myeloid Neoplasia
Phagocytes, Granulocytes, and Myelopoiesis
Polycombs and microRNA-223 regulate human granulopoiesis by transcriptional control of target gene expression
Platelets and Thrombopoiesis
Red Cells, Iron, and Erythropoiesis
Stroke With Transfusions Changing to Hydroxyurea (SWiTCH)
Clinical Trials & Observations
Thrombosis and Hemostasis
CD4+ T-cell epitopes associated with antibody responses after intravenously and subcutaneously applied human FVIII in humanized hemophilic E17 HLA-DRB1*1501 mice
Transplantation
Reduced intensity conditioning is superior to nonmyeloablative conditioning for older chronic myelogenous leukemia patients undergoing hematopoietic cell transplant during the tyrosine kinase inhibitor era
Clinical Trials & Observations
Errata
Other Departments
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Cover Image
Cover Image
A schematic representation elucidating the cycling pathway for glucose-6-phosphate (G6P) metabolism in macrophages. G6P participates in 4 major pathways: glycolysis, the hexose monophosphate shunt (HMS), glycogen synthesis, or endoplasmic reticulum (ER) cycling. In cycling, G6P enters the ER via glucose-6-phosphate transporter (G6PT) where it can accumulate until it is hydrolyzed to glucose by G6Pase-β and transported back into the cytoplasm. By limiting the cytoplasmic glucose/G6P availability, cycling regulates the other 3 cytoplasmic pathways for G6P metabolism. Disruption of this cycling in G6Pase-β–deficient macrophages results in impaired energy homeostasis and functionality. See the article by Jun et al on page 4047.
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