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Summary Anatomy Item Literature (441) Expression Attributions Wiki
XB-ANAT-320

Papers associated with spleen (and ighx)

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Immune defenses against Batrachochytrium dendrobatidis, a fungus linked to global amphibian declines, in the South African clawed frog, Xenopus laevis., Ramsey JP., Infect Immun. September 1, 2010; 78 (9): 3981-92.


Identification of IgF, a hinge-region-containing Ig class, and IgD in Xenopus tropicalis., Zhao Y., Proc Natl Acad Sci U S A. August 8, 2006; 103 (32): 12087-92.                                  


IgD, like IgM, is a primordial immunoglobulin class perpetuated in most jawed vertebrates., Ohta Y., Proc Natl Acad Sci U S A. July 11, 2006; 103 (28): 10723-8.              


Cloning and expression of the turtle (Trachemys scripta) immunoglobulin joining (J)-chain cDNA., Iwata A., Immunogenetics. October 1, 2002; 54 (7): 513-9.


Development of the early B cell population in Xenopus., Mussmann R., Eur J Immunol. September 1, 1998; 28 (9): 2947-59.


Sequence and expression pattern of J chain in the amphibian, Xenopus laevis., Hohman VS., Mol Immunol. October 1, 1997; 34 (14): 995-1002.


Is Xenopus IgX an analog of IgA?, Mussmann R., Eur J Immunol. December 1, 1996; 26 (12): 2823-30.


NK-like activity against allogeneic tumour cells demonstrated in the spleen of control and thymectomized Xenopus., Horton TL., Immunol Cell Biol. August 1, 1996; 74 (4): 365-73.


Ontogeny and thymus-dependence of T cell surface antigens in Xenopus: flow cytometric studies on monoclonal antibody-stained thymus and spleen., Gravenor I., Dev Comp Immunol. January 1, 1995; 19 (6): 507-23.


Evolution of vertebrate IgM: complete amino acid sequence of the constant region of Ambystoma mexicanum mu chain deduced from cDNA sequence., Fellah JS., Eur J Immunol. October 1, 1992; 22 (10): 2595-601.


Immune system activation associated with a naturally occurring infection in Xenopus laevis., Haynes L., Dev Comp Immunol. January 1, 1992; 16 (6): 453-62.


Sequence of C region of L chains from Xenopus laevis Ig., Zezza DJ., J Immunol. June 1, 1991; 146 (11): 4041-7.


B-lymphocyte populations in Xenopus laevis., Hadji-Azimi I., Dev Comp Immunol. January 1, 1990; 14 (1): 69-84.


Immunoglobulin Fc receptor molecules on Xenopus laevis splenocytes., Coosemans V., Immunology. December 1, 1988; 65 (4): 641-5.


Monoclonal autoantibodies recognizing histone variants., van Hemert FJ., Immunol Invest. May 1, 1988; 17 (3): 195-215.


The characterization of the toad splenocytes which bind mouse anti-human IL-2 receptor antibody., Langeberg L., Immunol Lett. October 1, 1987; 16 (1): 43-8.


A third immunoglobulin class in amphibians., Hsu E., J Immunol. September 1, 1985; 135 (3): 1998-2004.


A cell surface marker of thymus-dependent lymphocytes in Xenopus laevis is identifiable by mouse monoclonal antibody., Nagata S., Eur J Immunol. August 1, 1985; 15 (8): 837-41.


Anti-immunoglobulin M induces both B-lymphocyte proliferation and differentiation in Xenopus laevis., Schwager J., Differentiation. January 1, 1985; 30 (1): 29-34.


Studies on Xenopus immunoglobulins using monoclonal antibodies., Hsu E., Mol Immunol. April 1, 1984; 21 (4): 257-70.


Mitogen-induced B-cell differentiation in Xenopus laevis., Schwager J., Differentiation. January 1, 1984; 27 (3): 182-8.


Ontogeny and characterization of mitogen-reactive lymphocytes in the thymus and spleen of the amphibian, Xenopus laevis., Williams NH., Immunology. June 1, 1983; 49 (2): 301-9.


Effector and regulator functions of splenic and thymic lymphocytes in the clawed toad Xenopus., Hsu E., Ann Immunol (Paris). January 1, 1983; 134D (3): 277-92.


Monoclonal anti-IgM can separate T cell from B cell proliferative responses in the frog, Xenopus laevis., Bleicher PA., J Immunol. October 1, 1981; 127 (4): 1549-55.


The identification of messenger RNA coding for immunoglobulin heavy and light chains of Xenopus laevis., Cochran MD., Biochim Biophys Acta. May 30, 1980; 607 (3): 470-9.


Immunoglobulin heavy chain mRNA in mitogen-stimulated B cells., Stevens RH., Eur J Immunol. January 1, 1975; 5 (1): 47-53.

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