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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.Cell Stem Cell|October 7, 2022
Pervasive donor DNA integration defies precision gene editing of hematopoietic stem cellsDaniel E BauerNature Reviews. Drug Discovery|July 14, 2025
CRISPR-based therapeutic genome editing for inherited blood disordersSébastien Levesque, Daniel E BauerHematology/Oncology Clinics of North America|March 12, 2023
Molecular Basis and Genetic Modifiers of ThalassemiaNicolò Tesio, Daniel E BauerLancet (London, England)|June 30, 2016
Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategiesGuillaume Lettre, Daniel E BauerCell Stem Cell|December 12, 2018
Getting Past HSC Security: Cyclosporine H Gives Lentiviruses an Entry PassDaniel E Bauer, Sung-Yun PaiPageof 13