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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Genetic studies of cellular antigens of the chicken and of the antigens of the serum of bison and cattle

Scheinberg, Sam Louis, January 1954 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1954. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 56-61).
2

Cell surface antigens in normal and neoplastic human B lymphocyte differentiation : cellular distribution and functional implications

Howard, Donald Raymond January 1985 (has links)
Differentiation within the lymphoid system produces effector cells which are involved in a variety of immune functions. For T cells these include the provision of help, suppression, cytolytic activity and the regulation of cooperative cellular interactions. The primary function of B lineage cells is the production of specific antibody. Understanding the regulation of normal lymphocyte proliferation and differentiation may lead to a better appreciation of those factors which result in the development of malignancy. The non-Hodgkin's lymphomas are neoplasms of the immune system, the majority of which are B cell in origin. Despite advances in immunology and molecular biology, little is known about the mechanisms involved in B cell activation, proliferation and differentiation or about those events leading to their malignant transformation. The advent of monoclonal antibody technology a decade ago has revolutionized our ability to identify and characterize cell surface antigens. Because the activation and control of proliferation of B cells was already known to involve structures at the cell surface, it was logical to utilize monoclonal antibodies to identify additional cell surface molecules that might be important in the function of normal B lymphocytes and that might allow normal and various types of neoplastic B cells to be distinguished. To achieve this goal, we developed monoclonal antibodies that showed differential reactivity between large actively dividing lymphoma cells and small inactive (quiescent) lymphocytes. These were tested for their ability to inhibit various T and B lymphocyte functions (i.e. responses to anti-µ, lipopolysaccharide, phytohemagglutinin and the mixed lymphocyte response) as well as for their reactivity with cell suspensions from a variety of malignant and nonmalignant hematopoietic tissues. From these studies emerged the following: 1) Cell surface molecules other than Immunoglobulin are involved in regulating the activation of normal B cells. This was shown by the discovery that monoclonal antibodies to both lymphocyte function associated antigen (LFA-1) and certain HLA class II determinants were able to inhibit the activation of peripheral blood mononuclear cells by the B cell mitogens anti-p and LPS. This inhibition was shown to be mediated via effects of these antibodies on T cells and/or monocytes. 2) B lymphoma cells appear to express unique cell surface antigens (defined by monoclonal antibodies LM-26 and LM-155) not detectable on cells of other lineages, and absent from normal resting or activated B lymphocytes. Future investigations will attempt to define the mechanisms by which the indirect involvement of LFA-1 and HLA class II molecules in B cell activation in vitro suggests new regulatory interactions not previously identified. Further studies will be required to define the mechanisms underlying these interactions and their significance in vivo. Similarly, the structure and function of the antigens detected by LM-26 and LM-155 remains to be determined. Nevertheless, the expression of apparently unique molecules on B lymphoma cells holds new promise for the diagnosis, classification and treatment of this group of diseases. / Medicine, Faculty of / Pathology and Laboratory Medicine, Department of / Graduate
3

Genetic studies of the antigens of the erythrocytes in the chicken and their association with physiological characteristics

Briles, Connally Oran, January 1955 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1955. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 54-57).
4

A small scale study evaluating allelic frequencies of human neutrophil antigens in Hong Kong Chinese population

Tam, Wai-kin, 譚偉健 January 2014 (has links)
Background: Human neutrophil antigens (HNA) are involved in a variety of clinical conditions such as transfusion related acute lung injury (TRALI), alloimmune neutropenia (ANN), autoimmune neutropenia (AIN). There are a total of five HNA systems, namely HNA-1, HNA-2, HNA-3, HNA-4 and HNA-5. In this decade, the allelic and genotypic frequencies of HNA were gradually evaluated in Europe, America and East Asia. [1] Despite HNA system being less polymorphic than HLA antigens, genotypic and allelic frequencies differences can still be observed in different geographical locations even of close proximity. For instance, studies in Thailand and China displayed genotypic and allelic frequencies differences. [2] These data highlights the fact that HNA genotypic and allelic frequencies vary among different populations even within the same region, however, the degree of variation remains to be elucidated. However, there is no information on HNA genotypic and allelic frequencies of Hong Kong population. Commercial genotyping kit has been available in the market but given its high reagent cost, it is not very popular in clinical laboratory. For this reason, a comparative affordable and economical in-house PCR-SSP assay was developed in this study. Aim The aim of this study is to evaluate the HNA genotyping and allelic frequencies in Hong Kong Chinese population by the development of an economical in-house PCR-SSP assay. Methods A commercial HNA typing kit was tested with reference samples to ensure this project has a standard and clinical compliance method for HNA genotyping prior to adopting in-house genotyping method. After reference protocol was established, in-house primers were designed and tested in parallel with the commercial method for validation purpose. After in-house method has been validated, 113 local samples were tested to calculate the genotype and allele frequencies in Hong Kong Chinese population using the developed in-house assay. Results A total of 113 Hong Kong Chinese samples were typed for HNA genotyping and results shown that: HNA-1a was 0.664; HNA-1b was 0.336; whereas HNA-1c allele was not detected. HNA-3a was 0.735 and HNA-3b was 0.265. HNA-4a was 0.991 and HNA-4b was 0.009. HNA-5a was 0.845 and HNA-5b was 0.155. Overall, results echoed with an earlier study performed on Han Chinese. [3] The genotyping frequency distribution for HNA-1, 3, 4 and 5 were: HNA-1a/a was 0.451, HNA-1 b/b was 0.124 and HNA-1 a/b was 0.425; HNA-3 a/a was 0.549, HNA-3a/b was 0.372 and HNA-3b/b was 0.08; HNA-4a/a was 0.982, HNA-4a/b was 0.018; HNA-5a/a was 0.708, HNA-5a/b was 0.274 and HNA-5b/b was 0.018. Conclusion This is the first study attempted to define HNA genotype and allelic frequencies by the self-developed in-house PCR-SSP method in Hong Kong Chinese population. The obtained results were comparable to those of gene frequencies in previous Xia’s study in Guangzhou Chinese population but significant difference from earliest reported European frequencies, confirming geographical difference exist. [3-5] However, due to small sample size in this study, further examination in larger sample may allow more representative frequencies for the Hong Kong population. / published_or_final_version / Pathology / Master / Master of Medical Sciences
5

Immunological studies in clonorchiasis, with reference to the life cycle of Clonorchis sinensis in the definitive host

孫捷, Sun, Tsieh. January 1967 (has links)
published_or_final_version / Pathology / Master / Master of Science
6

Regional heterogeneity in the colon and ulcerative colitis

Smithson, John Edmund January 1995 (has links)
No description available.
7

Chicken antibodies: classes of immunoglobulins and enzymatic and reductive dissociation of IgG

Dreesman, Gordon Ronald January 1966 (has links)
Typescript. / Thesis (Ph. D.)--University of Hawaii, 1966. / Bibliography: leaves 172-184. / xiii, 184 l illus. (part mounted), tables
8

Enteric Redmouth Bacterium of salmonids : a biochemical and serological comparison of selected isolates

O'Leary, Patrick John 03 February 1977 (has links)
A comparison of the agglutinating and precipatiating antigens of Enteric Redmouth Bacterium (ERMB) was made. There are two major and one minor agglutinating antigens which describe two serotypes (I and II). Only serotype I metabolizes sorbitol. A bacterin from serotype I cross protected against a challenge of bacteria of serotype II in rainbow trout (Salmo gairdneri), but serotype II could not cross protect from a challenge of serotype I. Two patterns of positive agglutination were observed in a slide agglutination test depending upon the antigenic composition of the bacterium and agglutinating antisera. Incubation temperature altered the motility of ERMB. At 9 C nonfunctional peritrichous flagella were produced. At 18 and 27 C the bacterium was motile. No motility was observed at 37 C due to a complete loss of flagella. The percent quanine plus cytosine for ERMB was found to be 47.95 ± 0.45 (95 percent confidence interval). This work supports the proposal of Yersinia ruckeri as the genus and species designation for ERMB. / Graduation date: 1977
9

Studies on the purification of antibodies ...

Stenbuck, Frederick Augustus, January 1927 (has links)
Thesis (Ph. D.)--Columbia university, New York. / Vita. eContent provider-neutral record in process. Description based on print version record. Bibliography: p. 27.
10

Cellular antigens in duck hybrids

McGibbon, William Henry, January 1942 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1942. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves [i]-ii).

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