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Isolation of messenger-like RNA from immunochemically precipitated polyribosomes.Delovitch, T. L. January 1971 (has links)
No description available.
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Kinetics of reaction of antibody and its subunits with hapten.Kelly, Kenneth Alexander January 1970 (has links)
No description available.
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Studies on the immunochemical isolation of polyribosomes.Boyd, Susan Lorna. January 1971 (has links)
No description available.
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Isolation and characterization of rabbit ribonucleases by physiochemical and immunochemical methods.Lee, Weng Yek January 1971 (has links)
No description available.
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Regulation of TGFβ-activated-kinase 1 (TAK1) in nuclear factor-κB and tumour necrosis factor/Eiger signalling in Drosophila melanogasterFernando, Merennege Dilan Anush January 2011 (has links)
Drosophila TGFbeta-Activating-Kinase 1 (dTAK1) is an essential component of both the Immune Deficiency (IMD) innate immune and TNF/Eiger apoptotic cascades. The IMD and JNK pathways bifurcate at the level of dTAK1. Hence, elucidating the regulatory mechanism of dTAK1 is pertinent to understanding the regulation of both innate immunity and apoptosis. In this study, Trabid was identified as a novel negative regulator of the Drosophila IMD pathway. Trabid interacted with dTAK1 and decreased K63-linked ubiquitination, thereby reducing immune signalling. Three tandem Npl4 Zinc Fingers (NZF) and C518 were required for Trabid activity. Lysines 142 & 156 were identified as the K63 Ub acceptor sites of dTAK1, required for K63-linked ubiquitination and signalling. Also, results show Lys 156 functioned as the K48 Ub acceptor site. Further, the ZF domain of TAK1-associated Binding Protein 2 (dTAB2) was important in modulating dTAK1 K63-linked ubiquitination and thereby the immune signal. These results indicate an elaborate and multi-tiered mechanism for regulating dTAK1 activity and modulating the immune signal. Further, Ariadne-2 (Ari-2) was identified as a novel component of the Drosophila TNF/Eiger pathway which functioned at the level of dTAK1. Results indicate that Ari-2 is essential for normal development and longevity. It enhances the apoptotic signal when concomitantly over-expressed with Eiger. Further, Ari-2 interacts with dTAK1, dTAB2 and dTRAF2 which are all implicated in TNF/Eiger signalling. Thus, evidence supports the hypothesis that Ari-2 functions as an adaptor, involved in assembling a distinct signalling complex which transduces the apoptotic signal without activating immunity.
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Investigations into a novel osteoclastic antigenRoberts, Ellen January 1996 (has links)
No description available.
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Development of single and double spin-labeling methods and their applications to the study of antibody active sitesHsia, Jen-chang January 1968 (has links)
Typescript. / Thesis (Ph. D.)--University of Hawaii, 1968. / Bibliography: leaves [131]-134. / xi, 134 l illus
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Studies on bacteria resistant and susceptible to humoral immunity in insectsSidén, Inga. January 1983 (has links)
Thesis (Doctoral)--University of Stockholm, 1983. / Reprints of papers included in thesis appended. Includes bibliographical references.
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A Comparative Study of Passive Transfer Mechanisms of Tuberculin and Chemical Contact Delayed Hypersensitivities in the Guiea PigNunez, William Joseph 06 1900 (has links)
This study is concerned with a critical comparison of the passive transfer mechanisms of tuberculin and chemical contact hypersensitivities in the guinea pig by use of a four phase experimental approach.
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A study of the carbohydrate specificity of hyperimmune fowl globulins.Volgenau, Lewis 01 January 1969 (has links)
see pdf
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