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Seminars in Hematology|July 1, 2018
Genetic therapies for sickle cell diseaseErica B Esrick, Daniel E BauerHematology. American Society of Hematology. Education Program|December 10, 2021
β-Thalassemia: evolving treatment options beyond transfusion and iron chelationArielle L Langer, Erica B EsrickAmerican Journal of Hematology|March 27, 2015
Inactivation of HDAC1 or HDAC2 induces gamma globin expression without altering cell cycle or proliferationErica B Esrick, Marie McConkey, Katherine Lin, et al.Blood|December 9, 2024
β-Thalassemia minor is associated with high rates of worsening anemia in pregnancyArielle L Langer, Brynn B Goggins, Erica B Esrick, et al.Pediatric Blood & Cancer|July 20, 2023
Bidirectional processes linking social determinants of health and pediatric sickle cell anemia management: A qualitative studyKristin A Long, Ariel O Blakey, Christina M Amaro, et al.Science (New York, N.Y.)|October 15, 2011
Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencingJian Xu, Cong Peng, Vijay G Sankaran, et al.Blood Advances|October 5, 2018
Successful hematopoietic stem cell mobilization and apheresis collection using plerixafor alone in sickle cell patientsErica B Esrick, John P Manis, Heather Daley, et al.Nature Communications|September 20, 2023
Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sicklingDaniel C De Souza, Nicolas Hebert, Erica B Esrick, et al.Nature Medicine|November 17, 2023
Clonal selection of hematopoietic stem cells after gene therapy for sickle cell diseaseMichael Spencer Chapman, Alyssa H Cull, Marioara F Ciuculescu, et al.The New England Journal of Medicine|December 7, 2020
Post-Transcriptional Genetic Silencing of BCL11A to Treat Sickle Cell DiseaseErica B Esrick, Leslie E Lehmann, Alessandra Biffi, et al.Pageof 2