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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.
31

The cloning of polyhomeotic, a complex Drosophila locus required for segment determination and cuticular differentiation

Freeman, John Douglas January 1987 (has links)
The polyhomeotic (ph) locus of Drosophila melanogaster has been characterized genetically. Early studies showed that ph is a member of the Polycomb (Pc) group. These genes have similar phenotypes and are required for normal segment determination. Recent analyses of amorphic ph mutations show that the ph locus is complex, has a strong maternal effect and plays a role in cuticular development. To test the function of ph at the molecular level, the cloning of the ph locus was undertaken. One strain had been shown to contain a P element insertion near ph. A genomic library was prepared from this strain and a recombinant phage containing this P element insertion was isolated by transposon tagging. The DNA flanking the insertion was used as a starting point for a chromosomal walk. A series of overlapping phage spanning 170 kilobases was isolated. Southern blot analysis was used to determine the locations of important deficiency breakpoints within the region covered by the walk. A distance of approximately 35 kb was shown to separate the two deficiency breakpoints which include ph. This interval was found to contain rearrangements in four of the seven ph alleles which were examined by Southern blot analysis. The interval also contains a repeated sequence. The relationship between the genetic and molecular structure of ph is discussed. / Science, Faculty of / Zoology, Department of / Graduate
32

Molecular cloning and characterization of novel isoforms of calmodulin-dependent protein kinase II

Zhou, Zhihong Lucy January 1995 (has links)
No description available.
33

Cloning, expression and crystallization of black seabream (acanthopagrus schlegeli) antiquitin. / CUHK electronic theses & dissertations collection

January 2005 (has links)
Antiquitin (ATQ) belongs to the superfamily of aldehyde dehydrogenase (ALDH). It is an evolutionarily conserved protein as shown from its high amino acid sequence identity between human and its plant counterparts. Therefore, ATQ is believed to play an important physiological role. Until now, however, studies on ATQ are limited and its cellular function is uncertain. Recently, we have first demonstrated the aldehyde oxidizing ability of ATQ purified from the liver of black seabream (Acanthopagrus schlegeli). To further investigate this protein, different attempts have been made. / Recombinant ATQ has been successfully expressed in E. coli. Kinetics studies showed that it possessed similar characteristics with its native enzyme. The recombinant protein was produced in large amount for protein crystallization. Crystal of ATQ was obtained and its X-ray structure was solved to 2.8 A in complex with NAD+. Tetrameric ATQ was a dimer of dimer. Three domains can be found in the subunit structure of ATQ, the NAD+-binding domain, catalytic domain and oligomerization domain. In each of the NAD+-binding domain, one molecule of NAD + could be found. The overall structure of ATQ was similar to other tetrameric ALDHs, but the coenzyme binding was in a single "hydride transfer" conformation and the density was well-defined which was contrast to most ALDH structures. Structural study of the substrate-binding pocket explained the failure of ATQ in oxidizing several aldehydes which is specific to certain members of ALDH. / The ATQ full-length cDNA of black seabream was obtained. It consisted of 2309 by with a 153 nucleotide long 5' UTR, and a 209 nucleotide long 3' UTR. An ORF of 1533 by which encoded a protein with 511 amino acids was found. This putative protein showed the highest of 87% sequence identity with zebrafish ATQ, and ∼60% with plant ATQs. Tissue distribution was studied by RT-PCR. A high level of mRNA expression was observed in liver and kidney. Subcellular localization study using green fluorescent protein (GFP) fusion protein showed that ATQ was expressed in cytoplasm. However, another in-frame initiation methionine (M1) was found 31 residues before this generally accepted methionine (M2). Both iPSORT analysis and experimental studies using GFP fusion protein indicated that the 31 amino acid peptide contained a mitochondrial-targeting signal. / Tang Wai Kwan. / "July 2005." / Adviser: Fong Wing Ping. / Source: Dissertation Abstracts International, Volume: 67-07, Section: B, page: 3603. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2005. / Includes bibliographical references (p. 130-145). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract in English and Chinese. / School code: 1307.
34

Cloning and characterization of a cDNA clone encoding human p150glued. / CUHK electronic theses & dissertations collection

January 2002 (has links)
Or Man Wai. / "January 2002." / "glued" in title is superscript. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2002. / Includes bibliographical references. / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web.
35

The analysis of cDNA sequences: an algorithm for alignment.

January 1997 (has links)
by Lam Fung Ming. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1997. / Includes bibliographical references (leaves 45-47). / Chapter CHAPTER 1 --- INTRODUCTION --- p.1 / Chapter CHAPTER 2 --- BACKGROUND --- p.4 / Section 2.1 DNA Cloning --- p.5 / Section 2.1.1 Principles of cell-based DNA cloning --- p.5 / Section 2.1.2. Polymerase Chain Reaction --- p.8 / Section 2.2 DNA Libraries --- p.10 / Section 2.3. Expressed Sequence Tags --- p.11 / "Section 2.4 dbEST - Database for ""Expressed Sequence Tag""" --- p.13 / Chapter CHAPTER 3 --- REDUCTION OF PARTIAL SEQUENCE REDUNDANCY AND CDNA ALIGNMENT --- p.15 / Section 3.1 Materials --- p.15 / Section 3.2 Our Algorithm --- p.16 / Section 3.3 Data Storage --- p.24 / Section 3.4 Criterion of Alignment --- p.27 / Section 3.5 Pairwise Alignment --- p.29 / Chapter CHAPTER 4 --- RESULTS AND DISCUSSION --- p.32 / Chapter CHAPTER 5 --- CONCLUSION AND FUTURE DEVELOPMENT --- p.42 / REFERENCES --- p.45 / APPENDIX --- p.i
36

Cloning and characterization of human glutaredoxins /

Lundberg, Mathias, January 2002 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2002. / Härtill 6 uppsatser.
37

Biochemical properties of human glutaredoxins /

Johansson, Catrine, January 2004 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2004. / Härtill 5 uppsatser.
38

The cholecystokinin receptor family : molecular cloning and pharmacological characterization /

Nilsson, Isabelle January 2003 (has links) (PDF)
Diss. (sammanfattning) Linköping : Univ., 2003. / Härtill 4 uppsatser.
39

Random subcloning, pairwise end sequencing, and the molecular evolution of the vertebrate trypsinogens /

Roach, Jared C. January 1998 (has links)
Thesis (Ph. D.)--University of Washington, 1998. / Vita. Includes bibliographical references (leaves [176]-197).
40

Cloning, expression, and characterization of a novel guanylate-binding protein, mGBP3 in the murine erythroid progenitor cells

Han, Byung Hee, January 1997 (has links)
Thesis (Ph. D.)--University of Missouri--Columbia, 1997. / Typescript. Vita. Includes bibliographical references (leaves: 147-162). Also available on the Internet.

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