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Intrathymic progenitor cell transplantation across histocompatibility barriers results in the persistence of early thymic progenitors and T-cell differentiation

Donor hematopoietic stem cells (HSCs) can correct T-cell deficiencies in patients with severe combined immunodeficiency by replacing resident thymus cells. However, as those progenitors that naturally migrate to the thymus are not capable of supporting long-term thymopoiesis, a successful transplant...

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Main Authors: de Barros, Stéphanie C., Vicente, Rita, Chebli, Karim, Jacquet, Chantal, Zimmermann, Valérie S., Taylor, Naomi
格式: Artigo
語言:Inglês
出版: American Society of Hematology 2013
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3596972/
https://ncbi.nlm.nih.gov/pubmed/23305740
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2012-08-447417
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