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A microsatellite-based consensus linkage map for species of Eucalyptus and a novel set of 230 microsatellite markers for the genus 总被引:1,自引:0,他引:1
Rosana PV Brondani Emlyn R Williams Claudio Brondani Dario Grattapaglia 《BMC plant biology》2006,6(1):20-16
Background
Eucalypts are the most widely planted hardwood trees in the world occupying globally more than 18 million hectares as an important source of carbon neutral renewable energy and raw material for pulp, paper and solid wood. Quantitative Trait Loci (QTLs) in Eucalyptus have been localized on pedigree-specific RAPD or AFLP maps seriously limiting the value of such QTL mapping efforts for molecular breeding. The availability of a genus-wide genetic map with transferable microsatellite markers has become a must for the effective advancement of genomic undertakings. This report describes the development of a novel set of 230 EMBRA microsatellites, the construction of the first comprehensive microsatellite-based consensus linkage map for Eucalyptus and the consolidation of existing linkage information for other microsatellites and candidate genes mapped in other species of the genus. 相似文献4.
Sherry C. Wen Sharon J. Tollefson Monika Johnson Pavlo Gilchuk Kelli L. Boyd Bryan Shepherd Sebastian Joyce John V. Williams 《Journal of virology》2014,88(18):10963-10969
Human metapneumovirus (HMPV) is a major cause of respiratory disease. The role of NK cells in protection against HMPV is unclear. We show that while HMPV-infected C57BL/6 mice had higher numbers of functional lung NK cells than mock-treated mice, comparing NK cell-depleted and control mice did not reveal differences in lung viral titers, histopathology, cytokine levels, or T cell numbers or function. These data indicate that NK cells are not required for host control of HMPV. 相似文献
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Yu. S. Nikolaiev P. V. Gilchuk O. B. Gorbatiuk A. I. Flyak A. J. Labyntsev D. M. Irodov D. V. Kolibo V. A. Kordium 《Cytology and Genetics》2011,45(3):133-142
A highly efficient and inexpensive laboratory method of production and purification of polyclonal antibodies against the human
cell surface CD34 marker was developed. It was demonstrated that unglycosy-lated recombinant protein cloned in E. coli cells and containing the extracellular fragment of the human CD34 antigen maintained the necessary antigenic determinants
during isolation from bacteria and during immunization, induced the production of specific polyclonal antibodies, which could
recognize the native antigen on the cell surface. The obtained antibodies can be used for CD34+ cell phenotyping by the immunocytochemistry and flow cytometry methods. 相似文献
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JB Parentes-Vieira PV Lopes-Costa CG Pires AR dos Santos JD Pereira-Filho BB da Silva 《International Seminars in Surgical Oncology : ISSO》2007,4(1):22
Background
The objective of this study was to evaluate angiogenesis according to CD34 antigen expression in estrogen receptor (ER)-positive and negative breast carcinomas.Methods
This study comprised 64 cases of infiltrating ductal carcinoma in postmenopausal women divided into two groups: Group A: ER-positive, n = 35; and Group B: ER-negative, n = 29. The anti-CD34 monoclonal antibody was used as a marker for endothelial cells. Microvessel count was carried out in 10 fields per slide using a 40× objective lens (magnification 400×). Statistical analysis of the data was performed using Student's t-test (p < 0.05).Results
The mean number of vessels stained with the anti-CD34 antibody in the estrogen receptor-positive and negative tumors was 23.51 ± 1.15 and 40.24 ± 0.42, respectively. The number of microvessels was significantly greater in the estrogen receptor-negative tumors (p < 0.001).Conclusion
ER-negative tumors have significantly greater CD34 antigen expression compared to ER-positive tumors.7.
In silico analysis of the DNA encoding single-chain Fv antibodies (ScFv) specific to the human recombinant interferon β1b
and α2b (rhIFN-β1b, rhIFN-α2b) has been carried out. The V-, D- and J-gene segments, the complementarity-determining (CDR) and framework (FR) regions, n-nucleotides as well as mutation rates which take place during the affinity maturation of the examined sequences have been
determined. For the panel of ScFv against rhIFN-β1b isolated from an immune combinatorial cDNA library uniqueness of the CDRH3
loop by the length and amino acid composition has been shown. Multiple alignments with the nearest homologies from the NCBI
databases have revealed that the sequences of ScFv obtained are new.
The article is published in the original. 相似文献
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Comparative analysis of the zeta-crystallin/quinone reductase gene in guinea pig and mouse 总被引:1,自引:0,他引:1
Gonzalez P; Hernandez-Calzadilla C; Rao PV; Rodriguez IR; Zigler JS Jr; Borras T 《Molecular biology and evolution》1994,11(2):305-315
zeta-Crystallin is a novel nicotinamide adenine dinucleotide
phosphate:quinone reductase, present at enzymatic levels in various tissues
of different species, which is highly expressed in the lens of some
hystricomorph rodents and camelids. We report here the complementary DNA
(cDNA) cloning of zeta-crystallin from liver libraries in guinea pig (Cavia
porcellus), where zeta-crystallin is highly expressed in the lens, and in
the laboratory mouse (Mus musculus), where expression in the lens occurs
only at enzymatic levels. A 5' untranslated sequence different from the one
previously reported for the guinea pig lens cDNA was found in these clones.
We also report the isolation of genomic clones including the complete
guinea pig zeta-crystallin gene and the 5' region of this gene in mouse.
These results show the presence of two promoters in the guinea pig
zeta-crystallin gene, one responsible for expression at enzymatic levels
and the other responsible for the high expression in the lens. The guinea
pig lens promoter is not present in the mouse gene. This is the first
example in which the recruitment of an enzyme as a lens crystallin can be
explained by the acquisition of an alternative lens- specific promoter.
相似文献
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IB Masters MM Eastburn PW Francis R Wootton PV Zimmerman RS Ware AB Chang 《Respiratory research》2005,6(1):16