- 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.
Search results
Showing 221 to 230 of 5149 (0.053 seconds)Spelling suggestions: "subject:"geneexpression"" "subject:"genesexpression""
| 221 |
Growth factor production in pregnant equidsLennard, Simon N. January 1994 (has links)
No description available.
|
| 222 |
Studies on the structure and expression of the isocitrate lyase gene of Chlorella fuscaUrwin, Nigel A. R. January 1990 (has links)
No description available.
|
| 223 |
Studies on the expression of bFGF and IGF-I and -II in 3T3 cellsLi, Dajiang January 1997 (has links)
No description available.
|
| 224 |
Analysis of the assembly of a eukaryotic glucose transporter into the Escherichia coli cytoplasmic membraneMehraein-Ghomi, Farideh January 1996 (has links)
No description available.
|
| 225 |
Investigation of the molecular basis for oestrogen's stimulatory action on bone formation in female micePlant, Andrea January 2001 (has links)
No description available.
|
| 226 |
Cloning and expression of the bovine papillomavirus major capsid gene.Driscoll, Barbara. January 1988 (has links)
In order to characterize the protein product of the major capsid protein gene of Bovine Papillomavirus Type 2, 93% of the L1 open reading frame was cloned into two different expression vectors. This coding sequence produced a hybrid product when cloned into the expression vector pKK233-2, which interacted weakly with anti-BPV antisera and proved unable to elicit neutralizing antibodies. When the sequence was cloned into the expression vector pRA10, a more native form of the major capsid protein was produced, which interacted well with anti-BPV sera. Antisera raised against this cloned product was able to neutralize BPV in a tissue culture transformation assay. The 3' end of the L1 open reading frame was cloned into pBA10 in order to characterize the immunogenic potential of the carboxy terminus of the major capsid gene. The carboxy terminus proved to have no greater ability to interact with anti-BPV antisera, showing that the immunogenic epitopes of the protein are probably evenly distributed along the linear sequence.
|
| 227 |
Transcription factors regulating the human beta-globin genesWrighton, N. C. January 1988 (has links)
No description available.
|
| 228 |
Development of methods to analyse growth factor-induced association and loss of proteins from a nucleus-containing fractionBedells, Clare Helen January 1995 (has links)
No description available.
|
| 229 |
Introduction of novel genes into tilapia (Oreochromis niloticus)Rahman, Md Azizur January 1993 (has links)
No description available.
|
| 230 |
The expression of a Xenopus borealis cardiac actin gene in normal and transformed frog embryosWilson, C. January 1986 (has links)
No description available.
|
Page generated in 0.3141 seconds