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Publisher: Wiley-Blackwell

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Volume 203, Number 1, February 2005

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Molecular basis of immunodeficiency
pp. 5-9(5)
Author: Conley, Mary Ellen

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Inherited disorders of human Toll-like receptor signaling: immunological implications
pp. 10-20(11)
Authors: Ku, Cheng-Lung; Yang, Kun; Bustamante, Jacinta; Puel, Anne; von Bernuth, Horst; Santos, Orchidée Filipe; Lawrence, Tatiana; Chang, Huey-Hsuan; Al-Mousa, Hamoud; Picard, Capucine; Casanova, Jean-Laurent

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Human disease resulting from gene mutations that interfere with appropriate nuclear factor-κB activation
pp. 21-37(17)
Authors: Orange, Jordan S.; Levy, Ofer; Geha, Raif S.

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Defects in the interferon-γ and interleukin-12 pathways
pp. 38-47(10)
Authors: Rosenzweig, Sergio D.; Holland, Steven M.

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Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features
pp. 48-66(19)
Authors: Lougaris, Vassilios; Badolato, Raffaele; Ferrari, Simona; Plebani, Alessandro

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Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects
pp. 67-79(13)
Authors: Durandy, Anne; Revy, Patrick; Imai, Kohsuke; Fischer, Alain

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DNA deamination in immunity
pp. 80-97(18)
Author: Petersen-Mahrt, Svend

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Severe combined immunodeficiency. A model disease for molecular immunology and therapy
pp. 98-109(12)
Authors: Fischer, Alain; Le Deist, Françoise; Hacein-Bey-Abina, Salima; André-Schmutz, Isabelle; de Saint Basile, Geneviève; de Villartay, Jean-Pierre; Cavazzana-Calvo, Marina

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Interleukin-7 receptor α (IL-7Rα) deficiency: cellular and molecular bases. Analysis of clinical, immunological, and molecular features in 16 novel patients
pp. 110-126(17)
Authors: Giliani, Silvia; Mori, Luigi; de Saint Basile, Geneviève; Le Deist, Francoise; Rodriguez-Perez, Carmen; Forino, Concetta; Mazzolari, Evelina; Dupuis, Sophie; Elhasid, Ronit; Kessel, Aharon; Galambrun, Claire; Gil, Juana; Fischer, Alain; Etzioni, Amos; Notarangelo, Luigi D.

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Jak3, severe combined immunodeficiency, and a new class of immunosuppressive drugs
pp. 127-142(16)
Authors: Pesu, Marko; Candotti, Fabio; Husa, Matthew; Hofmann, Sigrun R.; Notarangelo, Luigi D.; O'Shea, John J.

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FOXP3 acts as a rheostat of the immune response
pp. 156-164(9)
Authors: Ochs, Hans D.; Ziegler, Steven F.; Torgerson, Troy R.

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Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis
pp. 165-179(15)
Authors: Ménasché, Gael; Feldmann, Jérôme; Fischer, Alain; de Saint Basile, Geneviève

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Molecular and cellular pathogenesis of X-linked lymphoproliferative disease
pp. 180-199(20)
Authors: Nichols, Kim E.; Ma, Cindy S.; Cannons, Jennifer L.; Schwartzberg, Pamela L.; Tangye, Stuart G.

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Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling
pp. 200-215(16)
Authors: Lindvall, Jessica M.; Blomberg, K. Emelie M.; Väliaho, Jouni; Vargas, Leonardo; Heinonen, Juhana E.; Berglöf, Anna; Mohamed, Abdalla J.; Nore, Beston F.; Vihinen, Mauno; Smith, C. I. Edvard

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Genetic analysis of patients with defects in early B-cell development
pp. 216-234(19)
Authors: Conley, Mary Ellen; Broides, Arnon; Hernandez-Trujillo, Vivian; Howard, Vanessa; Kanegane, Hirokazu; Miyawaki, Toshio; Shurtleff, Sheila A.

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CXCR4 mutations in WHIM syndrome: a misguided immune system?
pp. 235-243(9)
Author: Diaz, George A.

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Hyper-IgE syndromes
pp. 244-250(7)
Authors: Grimbacher, Bodo; Holland, Steven M.; Puck, Jennifer M.

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