Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment-Reference-Cited by-同舟云学术

Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment

Published:1998-09 Issue:5 Volume:102 Page:1363-1366
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Bozzi F.,Lefranc G.,Badolato R.,Schumacher R. F.,Khalil G.,Loiselet J.,Bresciani S.,O'Shea J. J.,Vezzoni P.,Notarangelo L. D.,Candotti F.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1998.tb08990.x/fullpdf

Reference12 articles.

1. Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants;Buckley;Journal of Pediatrics,1997

2. Stuctural and functional basis for JAK3-deficient severe combined immunodeficiency;Candotti;Blood,1997

3. In vitro correction of JAK3-deficient severe combined immunodeficiency by retroviral-mediated gene transduction;Candotti;Journal of Experimental Medicine,1996

4. European experience of bone-marrow transplantation for severe combined immunodeficiency;Fischer;Lancet,1990

5. Immunologic reconstitution in severe combined immunodeficiency following transplantation with parental bone marrow;Geha;Pediatrics,1974

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