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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.
51

HSP70 RNA expression in rainbow trout (Oncorhynchus mykiss) clonal lines

Heredia-Middleton, Pilar, January 2005 (has links) (PDF)
Thesis (M.S. in environmental science)--Washington State University, December 2005. / Includes bibliographical references (p. 45-49).
52

Heat shock protein localization after exercise based on muscle fiber type in mouse biceps brachii

Rothenheber, Nicole Christine. January 2010 (has links)
Honors Project--Smith College, Northampton, Mass., 2010. / Includes bibliographical references (p. 52-65).
53

Functional study of ClpB95 and ClpB80, the alternative translation products of the E. coli clpB transcript /

Chow, I-Ting, January 2005 (has links)
Thesis (Ph. D.)--University of Washington, 2005. / Vita. Includes bibliographical references (leaves 106-117).
54

Structure and function studies of Hsp47 : a collagen-specific molecular chaperone /

Thomson, Christy A. Ananthanarayanan, Vettai S. January 1900 (has links)
Thesis (Ph.D.)--McMaster University, 2003. / Advisor: V.S. Ananthanarayanan. Includes bibliographical references. Also available via World Wide Web.
55

A role for the major inducible 70 KDA heat shock protein (HSP72) in experimental measles encephalitis

Carsillo, Thomas John, January 2006 (has links)
Thesis (Ph. D.)--Ohio State University, 2006. / Title from first page of PDF file. Includes bibliographical references (p. 117-135).
56

Expression and function of the small heat shock protein Hsp27 during embryogenesis of zebrafish Danio rerio

Ustyugov, Alexey, January 2007 (has links) (PDF)
Thesis (M.S. in biochemistry)--Washington State University, December 2007. / Includes bibliographical references (p. 36-47).
57

The role of osmolyte transporters and heat shock proteins in adaptation of Atlantic salmon to selected stressors /

Zarate, Jacques. January 2006 (has links)
Thesis (Ph. D.)--University of Rhode Island, 2006. / Includes bibliographical references (leaves 138-154).
58

Mechanism of client protein binding by heat shock protein 90 /

Fang, Lin, January 2006 (has links)
Thesis (Ph. D.)--University of Oregon, 2006. / Typescript. Includes vita and abstract. Includes bibliographical references (leaves 115-121). Also available for download via the World Wide Web; free to University of Oregon users.
59

Physiological and molecular adaptations during diapause development and overwintering in a heteropteran bug, Pyrrhocoris apterus / Physiological and molecular adaptations during diapause development and overwintering in a heteropteran bug, Pyrrhocoris apterus

BOROVANSKÁ, Michaela January 2009 (has links)
In this thesis I present complex experimental data on the physiological and molecular adaptations during diapause development and overwintering in a linden bug, Pyrrhocoris apterus (Heteroptera, Pyrrhocoridae). I focus on adjustments of the enzymatic complement, which is involved in the biosynthesis of cryoprotectants, and heat shock proteins, which are expressed in response to temperature stress.
60

Heat shock protein 70 (hsp70) gene polymorphism: implications for tuberculosis susceptibility in the Cape Coloured population from South Africa

Boshoff, Tuschka 10 November 2011 (has links)
Ph.D. / Heat shock proteins (HSP) (in particular hsp70) are increasingly synthesised during and following exposure to stressful insults, playing an important role in protection and adaptation. Protective effects of HSP concerning infection and immunity include self/non-self discrimination, enhancement of the immune response, immune protection, thermotolerance and cytoprotection from inflammatory mediators (reactive oxygen species and cytokines). Considering the general protective role of hsp70 and its specific immunological functions, including antigen processing and presentation, variation in hsp 70 genes may contribute towards differential coping with stress and disease susceptibility. In humans, three members of the hsp70 gene family, hspl0-1, hsp70-2 and hsp70-hom, were mapped to the MHC class Ill region approximately 280 kbp centromeric to the TNFa gene and 92 kbp telomeric to the C2 gene. Polymorphisms in MHC-Iocalized hsp70 genes have been implicated in susceptibility to a number of diseases, independently or in combination with class II polymorphisms due to linkage disequilibrium (LD). MHC alleles are most often associated with immunosuppressive diseases. Tuberculosis (TB) has a strong immunological basis, involving cell-mediated immunity with human leukocyte antigen (HLA) variants implicated in its susceptibility/resistance. In the light of the above, the role of hsp70 polymorphism in TB susceptibility, alone or in combination with MHC class II alleles, was investigated through the following objectives: 1) Typing of hsp70 gene polymorphism (hsp70-1, hsp70-2 and hsp70-hom) in controls and TB cases from the Cape Coloured population of South Africa 2) Comparison between Cape Coloureds and Caucasoid populations with regard to hsp70 allele and genotype distribution 3) Studying linkage disequilibrium between members of MHC class II (HLADRB1) and Ill (hsp70) alleles in the Cape Coloureds 4) Simulation of MHC class II and Ill haplotypes in this particular population Hsp70 polymorphism was studied in controls (n=106) and TB cases (n=107) from the complex hybrid Cape Coloured population inhabiting the Western Cape region of South Africa - a population showing increased susceptibility to TB. PCR-RFLP and PAGE analysis were used to determine the hsp70 allele frequencies and genotype distribution of the individuals studied, while linkage disequilibrium between MHC class II and Ill, and within class Ill alleles, was investigated using the software "Graphical Overview of Linkage Disequilibruim" (GOLD). Haplotypes comprising MHC class II and Ill alleles were simulated using the software PHASE.

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