SEVERE COMBINED IMMUNODEFICIENCY CAUSED BY DEFECTS IN COMMON CYTOKINE RECEPTOR γc SIGNALING PATHWAYS
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[1] S. Müller,et al. Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation: a retrospective European survey from the European group for bone marrow transplantation and the european society for immunodeficiency. , 1999, The Journal of pediatrics.
[2] J. Church,et al. Severe Combined Immunodeficiency: Otolaryngological Presentation and Management , 1999, The Annals of otology, rhinology, and laryngology.
[3] P. Appasamy. Biological and clinical implications of interleukin-7 and lymphopoiesis. , 1999, Cytokines, cellular & molecular therapy.
[4] A. Fischer. Thirty years of bone marrow transplantation for severe combined immunodeficiency. , 1999, The New England journal of medicine.
[5] J. Roberts,et al. Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency. , 1999, The New England journal of medicine.
[6] H. Ochs,et al. A novel mutant γc chain from a patient with typical phenotype of X‐linked severe combined immunodeficiency (SCID) has partial signalling function for mediating IL‐2 and IL‐4 receptor action , 1999, Clinical and experimental immunology.
[7] J Wagner,et al. B cell lymphoproliferative disorders following hematopoietic stem cell transplantation: risk factors, treatment and outcome , 1999, Bone Marrow Transplantation.
[8] K. Sugamura,et al. Functional role of interleukin-4 (IL-4) and IL-7 in the development of X-linked severe combined immunodeficiency. , 1999, Blood.
[9] K. Schwarz,et al. Mutations in the gene for the common gamma chain (γc) in X-linked severe combined immunodeficiency , 1998, Human Genetics.
[10] Steven F. Ziegler,et al. Defective IL7R expression in T-B+NK + severe combined immunodeficiency , 1998, Nature Genetics.
[11] T. Dassopoulos,et al. IL-15 receptor maintains lymphoid homeostasis by supporting lymphocyte homing and proliferation. , 1998, Immunity.
[12] Sandro Santagata,et al. Partial V(D)J Recombination Activity Leads to Omenn Syndrome , 1998, Cell.
[13] J. Tschopp,et al. Biochemical mechanisms of IL-2-regulated Fas-mediated T cell apoptosis. , 1998, Immunity.
[14] A. Fischer,et al. Natural and engineered disorders of lymphocyte development. , 1998, Science.
[15] J. D. Di Santo,et al. In vivo roles of receptor tyrosine kinases and cytokine receptors in early thymocyte development. , 1998, Current opinion in immunology.
[16] Hirohisa Imai. Cost analysis of treatments for severe combined immunodeficiency patients caused by adenosine deaminase deficiency: comparison of gene therapy and bone marrow transplantation. , 1998, [Hokkaido igaku zasshi] The Hokkaido journal of medical science.
[17] C. Roifman,et al. An interleukin-2 receptor gamma chain mutation with normal thymus morphology. , 1997, The Journal of clinical investigation.
[18] A. Villa,et al. Structural and functional basis for JAK3-deficient severe combined immunodeficiency. , 1997, Blood.
[19] Werner Müller,et al. On the role of the common cytokine receptor γ chain in B-cell vs. T-cell development , 1997, Research in Immunology.
[20] J. Disanto,et al. Cytokines: Shared receptors, distinct functions , 1997, Current Biology.
[21] P. Clark,et al. B-cell-negative severe combined immunodeficiency associated with a common γ chain mutation , 1997, Human Genetics.
[22] H. Dadi,et al. Human immune disorder arising from mutation of the α chain of the interleukin-2 receptor , 1997 .
[23] A. Fischer,et al. Deregulated TCRαβ T cell population provokes extramedullary hematopoiesis in mice deficient in the common γ chain , 1997 .
[24] J. Puck,et al. Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency. , 1997, Blood.
[25] J. Johnston,et al. Interleukin-4 Signaling in B Lymphocytes from Patients with X-linked Severe Combined Immunodeficiency* , 1997, The Journal of Biological Chemistry.
[26] M. Ogawa,et al. Pro-thymocyte expansion by c-kit and the common cytokine receptor gamma chain is essential for repertoire formation. , 1997, Immunity.
[27] J. Puck,et al. Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants. , 1997, The Journal of pediatrics.
[28] Rosen Fs. Severe combined immunodeficiency: a pediatric emergency. , 1997, The Journal of pediatrics.
[29] C. Croce,et al. A potential role for interleukin-15 in the regulation of human natural killer cell survival. , 1997, The Journal of clinical investigation.
[30] W. Leonard,et al. The Common Cytokine Receptor γ Chain Plays an Essential Role in Regulating Lymphoid Homeostasis , 1997, The Journal of experimental medicine.
[31] J. Puck,et al. Treatment of X-linked severe combined immunodeficiency by in utero transplantation of paternal bone marrow. , 1996, The New England journal of medicine.
[32] U. Dirksen,et al. Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells. , 1996, The New England journal of medicine.
[33] I. Puzanov,et al. IL-15 can substitute for the marrow microenvironment in the differentiation of natural killer cells. , 1996, Journal of immunology.
[34] U. Pannicke,et al. RAG Mutations in Human B Cell-Negative SCID , 1996, Science.
[35] A. Fischer,et al. T-lymphocyte differentiation and proliferation in the absence of the cytoplasmic tail of the common cytokine receptor gamma c chain in a severe combined immune deficiency X1 patient , 1996 .
[36] J. Miyazaki,et al. Interleukin 7 receptor-deficient mice lack gammadelta T cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[37] K. Sugamura,et al. gamma-c gene transfer into SCID X1 patients' B-cell lines restores normal high-affinity interleukin-2 receptor expression and function. , 1996, Blood.
[38] J. Johnston,et al. Retroviral-mediated gene correction for X-linked severe combined immunodeficiency. , 1996, Blood.
[39] N. Taylor,et al. Correction of interleukin-2 receptor function in X-SCID lymphoblastoid cells by retrovirally mediated transfer of the gamma-c gene. , 1996, Blood.
[40] M. Caligiuri,et al. Role of interleukin-15 in the development of human CD56+ natural killer cells from CD34+ hematopoietic progenitor cells. , 1996, Blood.
[41] M. Bogue,et al. Mechanism of V(D)J recombination. , 1996, Cancer surveys.
[42] K. Izuhara,et al. Signal Transduction Pathway of Interleukin-4 and Interleukin-13 in Human B Cells Derived from X-linked Severe Combined Immunodeficiency Patients (*) , 1996, The Journal of Biological Chemistry.
[43] J. D. Di Santo,et al. Common cytokine receptor gamma chain (gamma c)-dependent cytokines: understanding in vivo functions by gene targeting. , 1995, Immunological reviews.
[44] W. Leonard,et al. Mutation of Jak3 in a Patient with SCID: Essential Role of Jak3 in Lymphoid Development , 1995, Science.
[45] J. Ihle. Cytokine receptor signalling , 1995, Nature.
[46] F. Alt,et al. Interleukin-2 receptor alpha chain regulates the size and content of the peripheral lymphoid compartment. , 1995, Immunity.
[47] J. Puck,et al. Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency. , 1995, American journal of human genetics.
[48] T. Taniguchi. Cytokine signaling through nonreceptor protein tyrosine kinases. , 1995, Science.
[49] S. Burdach,et al. Lymphopenia in interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredundant cytokine , 1995, The Journal of experimental medicine.
[50] E. Brooks,et al. Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency. , 1995, The Journal of clinical investigation.
[51] A. Fischer,et al. Lymphoid development in mice with a targeted deletion of the interleukin 2 receptor gamma chain. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[52] C. Ware,et al. Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice , 1994, The Journal of experimental medicine.
[53] F. Rieux-Laucat,et al. Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[54] W. Leonard,et al. The defective gene in X-linked severe combined immunodeficiency encodes a shared interleukin receptor subunit: implications for cytokine pleiotropy and redundancy. , 1994, Current opinion in immunology.
[55] J. Sleasman,et al. Arrested rearrangement of TCR V beta genes in thymocytes from children with X-linked severe combined immunodeficiency disease. , 1994, Journal of immunology.
[56] V. Fung,et al. Cloning of a T cell growth factor that interacts with the beta chain of the interleukin-2 receptor. , 1994, Science.
[57] W. Leonard,et al. The Molecular Basis of X‐Linked Severe Combined Immunodeficiency: The Role of the Interleukin‐2 Receptor γ Chain as a Common γ Chain, γc , 1994, Immunological reviews.
[58] A. Fischer,et al. Interleukin‐2 (IL‐2) receptor γ chain mutations in X‐linked severe combined immunodeficiency disease result in the loss of high‐affinity IL‐2 receptor binding , 1994, European journal of immunology.
[59] A. Fischer,et al. Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients. , 1993, The Journal of pediatrics.
[60] A. Fischer. Primary T-cell immunodeficiencies. , 1993, Current opinion in immunology.
[61] R. Sorensen,et al. Disseminated bacillus Calmette-Guérin infections in patients with primary immunodeficiencies. , 1993, American journal of clinical pathology.
[62] A. Monaco,et al. Fine mapping of the human SCIDX1 locus at Xq12-13.1. , 1993, Human molecular genetics.
[63] W. Leonard,et al. Interleukin-2 receptor γ chain mutation results in X-linked severe combined immunodeficiency in humans , 1993, Cell.
[64] Martin Bachmann,et al. Disruption of the murine IL-4 gene blocks Th2 cytokine responses , 1993, Nature.
[65] O. Parolini,et al. Nonrandom X chromosome inactivation in natural killer cells from obligate carriers of X-linked severe combined immunodeficiency. , 1993, Journal of immunology.
[66] N. Tanaka,et al. Cloning of the gamma chain of the human IL-2 receptor. , 1992, Science.
[67] A. Fischer,et al. Genetic study of a new X-linked recessive immunodeficiency syndrome. , 1992, The Journal of clinical investigation.
[68] K. Rajewsky,et al. Generation and analysis of interleukin-4 deficient mice. , 1991, Science.
[69] A. Weiner,et al. Genetic evidence for base pairing between U2 and U6 snRNA in mammalian mRNA splicing , 1991, Nature.
[70] I. Horak,et al. Development and function of T cells in mice rendered interleukin-2 deficient by gene targeting , 1991, Nature.
[71] E. Brooks,et al. A novel X-linked combined immunodeficiency disease. , 1990, The Journal of clinical investigation.
[72] C. Griscelli,et al. Human severe combined immunodeficiency disease: phenotypic and functional characteristics of peripheral B lymphocytes. , 1990, Journal of immunology.
[73] N. Flomenberg,et al. Absence of interleukin 2 production in a severe combined immunodeficiency disease syndrome with T cells , 1990, The Journal of experimental medicine.
[74] Kendall A. Smith,et al. Interleukin-2: inception, impact, and implications. , 1988, Science.
[75] J. Puck,et al. Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[76] A. Fischer,et al. Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[77] E. Lotzová,et al. Immunoregulation in an Isolated 12-year-old Boy with Congenital Severe Combined Immunodeficiency , 1984, Pediatric Research.
[78] C. Griscelli,et al. Severe combined immunodeficiency disease: a pathological analysis of 26 cases. , 1983, Clinical immunology and immunopathology.
[79] R. Siegel,et al. Mature T lymphocyte apoptosis--immune regulation in a dynamic and unpredictable antigenic environment. , 1999, Annual review of immunology.
[80] J. Renauld,et al. Interleukin 9 and its receptor: an overview of structure and function. , 1998, International reviews of immunology.
[81] W. Leonard,et al. Jaks and STATs: biological implications. , 1998, Annual review of immunology.
[82] J. Banchereau,et al. Interleukin-4 and interleukin-13: their similarities and discrepancies. , 1998, International reviews of immunology.
[83] A. Flake,et al. In utero hematopoietic stem cell transplantation. A status report. , 1997, JAMA.
[84] J. Puck,et al. Mutation Analysis of IL 2 RG in Human X-Linked Severe Combined Immunodeficiency , 1997 .
[85] C. Martínez-A,et al. Lessons from immunological, biochemical, and molecular pathways of the activation mediated by IL-2 and IL-4. , 1996, Advances in immunology.
[86] A. Fischer,et al. T-lymphocyte differentiation and proliferation in the absence of the cytoplasmic tail of the common cytokine receptor gamma c chain in a severe combined immune deficiency X1 patient. , 1996, Blood.
[87] N. Tanaka,et al. The Common γ-Chain for Multiple Cytokine Receptors , 1995 .
[88] F. Rosen,et al. The primary immunodeficiencies. , 1995, The New England journal of medicine.
[89] P. Gell,et al. Clinical aspects of immunology , 1968 .