Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
2005
Total Cost
Indirect Cost
Name
Pirc, Inc.
Department
Type
DUNS #
City
State
Country
Zip Code
Dvorak, C C; Patel, K; Puck, J M et al. (2017) Unconditioned unrelated donor bone marrow transplantation for IL7R?- and Artemis-deficient SCID. Bone Marrow Transplant 52:1036-1038
Beaumel, Sylvain; Picciocchi, Antoine; Debeurme, Franck et al. (2017) Down-regulation of NOX2 activity in phagocytes mediated by ATM-kinase dependent phosphorylation. Free Radic Biol Med 113:1-15
Kwan, Antonia; Hu, Diana; Song, Miran et al. (2015) Successful newborn screening for SCID in the Navajo Nation. Clin Immunol 158:29-34
O'Neill, Sharon; Brault, Julie; Stasia, Marie-Jose et al. (2015) Genetic disorders coupled to ROS deficiency. Redox Biol 6:135-56
Hsu, Amy P; Pittaluga, Stefania; Martinez, Bianca et al. (2015) IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotype. J Clin Immunol 35:449-53
Brigida, Immacolata; Sauer, Aisha V; Ferrua, Francesca et al. (2014) B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients. J Allergy Clin Immunol 133:799-806.e10
Shearer, William T; Dunn, Elizabeth; Notarangelo, Luigi D et al. (2014) Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience. J Allergy Clin Immunol 133:1092-8
Kwan, Antonia; Church, Joseph A; Cowan, Morton J et al. (2013) Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years. J Allergy Clin Immunol 132:140-50
Reese, Vanessa C; Oropeza, Claudia E; McLachlan, Alan (2013) Independent activation of hepatitis B virus biosynthesis by retinoids, peroxisome proliferators, and bile acids. J Virol 87:991-7
Martel, Cécile; Mollin, Michelle; Beaumel, Sylvain et al. (2012) Clinical, functional and genetic analysis of twenty-four patients with chronic granulomatous disease - identification of eight novel mutations in CYBB and NCF2 genes. J Clin Immunol 32:942-58

Showing the most recent 10 out of 42 publications