WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus–truncated CXCR4

WHIM(warts, hypogammaglobulinemia, recurrent bacterial infection, and myelokathexis) syndrome is a rare immunodeficiency caused in many cases by autosomal dominant C-terminal truncation mutations in the chemokine receptor CXCR4. A prominent and unexplained feature of WHIM is myelokathexis (hypercell...

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Detalhes bibliográficos
Main Authors: Kawai, Toshinao, Choi, Uimook, Cardwell, Lanise, DeRavin, Suk See, Naumann, Nora, Whiting-Theobald, Narda L., Linton, Gilda F., Moon, Jaehyun, Murphy, Philip M., Malech, Harry L.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2007
Assuntos:
Hematopoiesis
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1785067/
https://ncbi.nlm.nih.gov/pubmed/16946301
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2006-05-025296
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