Thematische Bibliographien / Nucleotide sequence

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Auswahl der wissenschaftlichen Literatur zum Thema „Nucleotide sequence“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 25. Juli 2025

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Zeitschriftenartikel zum Thema "Nucleotide sequence"

Fatchiyah, Fatchiyah, Rista Nikmatu Rohmah, Lidwina Faraline Tripisila, et al. "Three-dimension Glyceraldehyde-3-Phosphate Dehydrogenase protein structure of substitution and insertion sequences of GAPDH gene of chicken drumstick meat (Gallus gallus)." Berkala Penelitian Hayati 27, no. 2 (2022): 105–9. http://dx.doi.org/10.23869/bphjbr.27.2.20228.

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The study aimed to observed the 3-D structure of GAPDH protein and identify the GAPDH gene sequences mutation of chicken drumstick meat (Gallus gallus). The sample of chicken meat was randomly taken in four districts in Malang city. In this study, the DNA was isolated from drumstick meat chicken samples, amplified using proper primers, and then sequenced using ABI 3730xl DNA Sequencer. The DNA sequences alignments analyzed by BioEdit software and the control sequence of GAPDH gene was obtained from NCBI GenBank (sequence Gene ID: 374193). Then, the amino acid sequence and 3D structure of GAPDH

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Harasawa, Ryô, and Yasuo Kanamoto. "Differentiation of Two Biovars of Ureaplasma urealyticum Based on the 16S-23S rRNA Intergenic Spacer Region." Journal of Clinical Microbiology 37, no. 12 (1999): 4135–38. http://dx.doi.org/10.1128/jcm.37.12.4135-4138.1999.

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The 16S-23S rRNA intergenic spacer regions of 14 strains representing the 14 serovars of Ureaplasma urealyticum were amplified by PCR and sequenced for genetic differentiation between the two biovars Parvo and T960. Although the spacer region of the Parvo and T960 biovars comprised 302 nucleotides and lacked spacer tRNA genes, 15 nucleotides were different between the two biovars. The four nucleotide sequences of the 16S-23S rRNA intergenic spacer region of serovars 1, 3, 6, and 14 in the Parvo biovar were found to be identical. Similarly, the 10 nucleotide sequences of the 16S-23S rRNA interg

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Kuśmirek, Wiktor. "Estimated Nucleotide Reconstruction Quality Symbols of Basecalling Tools for Oxford Nanopore Sequencing." Sensors 23, no. 15 (2023): 6787. http://dx.doi.org/10.3390/s23156787.

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Currently, one of the fastest-growing DNA sequencing technologies is nanopore sequencing. One of the key stages involved in processing sequencer data is the basecalling process, where the input sequence of currents measured on the nanopores of the sequencer reproduces the DNA sequences, called DNA reads. Many of the applications dedicated to basecalling, together with the DNA sequence, provide the estimated quality of the reconstruction of a given nucleotide (quality symbols are contained on every fourth line of the FASTQ file; each nucleotide in the FASTQ file corresponds to exactly one estim

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Bradford, Patricia A. "Automated Thermal Cycling Is Superior to Traditional Methods for Nucleotide Sequencing ofblaSHV Genes." Antimicrobial Agents and Chemotherapy 43, no. 12 (1999): 2960–63. http://dx.doi.org/10.1128/aac.43.12.2960.

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ABSTRACT Genes encoding SHV-1 and SHV-2 were sequenced by different methods. Nucleotide sequencing of the coding strand by standard dideoxy-chain termination methods resulted in errors in the interpretation of the nucleotide sequence and the derived amino acid sequence in two main regions which corresponded to nucleotide and amino acid changes that had been reported previously. The automated thermal cycling method was clearly superior and consistently resulted in the correct sequences for these genes.

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Lee, Byoungsang, So Yeon Ahn, Charles Park, et al. "Revealing the Presence of a Symbolic Sequence Representing Multiple Nucleotides Based on K-Means Clustering of Oligonucleotides." Molecules 24, no. 2 (2019): 348. http://dx.doi.org/10.3390/molecules24020348.

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In biological systems, a few sequence differences diversify the hybridization profile of nucleotides and enable the quantitative control of cellular metabolism in a cooperative manner. In this respect, the information required for a better understanding may not be in each nucleotide sequence, but representative information contained among them. Existing methodologies for nucleotide sequence design have been optimized to track the function of the genetic molecule and predict interaction with others. However, there has been no attempt to extract new sequence information to represent their inheri

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Fukasawa, Kayoko M., Masako Tanimura, Ikuya Sakai, Farida S. Sharief, Fu-Zon Chung, and Steven S.-L. Li. "Molecular Nature of Spontaneous Mutations in Mouse Lactate Dehydrogenase-A Processed Pseudogenes." Genetics 115, no. 1 (1987): 177–84. http://dx.doi.org/10.1093/genetics/115.1.177.

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ABSTRACT The presence of at least ten mouse LDH-A pseudogenes was demonstrated in the genomic blot analysis, and four different processed pseudogenes have thus far been isolated and characterized. In this report, the nucleotide sequences of two different mouse lactate dehydrogenase-A processed pseudogenes, M11 and M14, were determined and compared with the protein-coding sequences of the mouse and rat LDH-A functional genes. In the pseudogene M11, the sequence of 64 nucleotides from codon no. 257 to 278 was tandemly duplicated. In the pseudogene M14, the sequence of 22 nucleotides from codon n

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Ansell, D. M., A. R. Samuel, W. C. Carpenter, and N. J. Knowles. "Genetic relationships between foot–and–mouth disease type Asia 1 viruses." Epidemiology and Infection 112, no. 1 (1994): 213–24. http://dx.doi.org/10.1017/s0950268800057587.

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SummaryThe sequence of 165 nucleotides at the 3´ end of the 1D (VP1) gene of foot-and-mouth disease (FMD) virus was determined for 44 type Asia 1 strains isolated from throughout Asia between 1954–92. Analysis of the relationships between the virus genomes showed epidemiological links not previously evident. The possible origin of the only outbreak of FMD Asia 1 to have occurred in Europe, in Greece in 1984, was identified because the nucleotide sequence of this virus was closely-related to the sequences of those present in the Middle East between 1983–5.Variation in the region sequenced was n

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Furlong, N. Burr, and Koenraad Marien. "Further Observations on Periodicities of Nucleotide Occurrences in Natural DNA's." Zeitschrift für Naturforschung C 40, no. 11-12 (1985): 854–57. http://dx.doi.org/10.1515/znc-1985-11-1218.

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Abstract There are non-random features in the occurrences of nucleotides in the DNA’s of certain organisms which are detectable by statistical analyses of the entire sequence. Earlier, using the bacteriophage Phi-X 174 DNA sequence, we had reported that the self-information values for one type of dinucleotide association showed a marked periodicity when their autocorrelation coefficients were graphed. A similar, but computationally simpler, analysis has been developed which gives a comparable indication of periodicity. The difference, in average autocorrelation coefficients obtained with this

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Ojkic, Davor, and éva Nagy. "The complete nucleotide sequence of fowl adenovirus type 8." Microbiology 81, no. 7 (2000): 1833–37. http://dx.doi.org/10.1099/0022-1317-81-7-1833.

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The fowl adenovirus type 8 (FAdV-8) genome was sequenced and found to be 45063 nucleotides in length, the longest adenovirus (AdV) genome for which the complete nucleotide sequence has been determined so far. No regions homologous to early regions 1, 3 and 4 (E1, E3 and E4) of mastadenoviruses were recognized. Gene homologues for early region 2 (E2) proteins, intermediate protein IVa2 and late proteins were found by their similarities to protein sequences from other AdVs. However, sequences homologous to intermediate protein IX and late protein V could not be identified. Sequences for virus-as

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Nadel, B., and A. J. Feeney. "Nucleotide deletion and P addition in V(D)J recombination: a determinant role of the coding-end sequence." Molecular and Cellular Biology 17, no. 7 (1997): 3768–78. http://dx.doi.org/10.1128/mcb.17.7.3768.

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During V(D)J recombination, the coding ends to be joined are extensively modified. Those modifications, termed coding-end processing, consist of removal and addition of various numbers of nucleotides. We previously showed in vivo that coding-end processing is specific for each coding end, suggesting that specific motifs in a coding-end sequence influence nucleotide deletion and P-region formation. In this study, we created a panel of recombination substrates containing actual immunoglobulin and T-cell receptor coding-end sequences and dissected the role of each motif by comparing its processin

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Dissertationen zum Thema "Nucleotide sequence"

Wang, Zhenggang. "Improved algorithm for entropic segmentation of DNA sequence /." View abstract or full-text, 2004. http://library.ust.hk/cgi/db/thesis.pl?PHYS%202004%20WANG.

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Thesis (M. Phil.)--Hong Kong University of Science and Technology, 2004.<br>Includes bibliographical references (leaves 56-58). Also available in electronic version. Access restricted to campus users.

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Siu, Kim-Man. "A computational estimation of errors in model genomes using exactly duplicated DNA sequences /." View abstract or full-text, 2005. http://library.ust.hk/cgi/db/thesis.pl?MATH%202005%20SIU.

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Ngwira, Patricia. "Nucleotide sequence diversity in maize and grass-infecting streak geminiviruses: A basis for nucleotide sequence classification and identification /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487945015618607.

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Cai, Zheng. "Repetitive sequence analysis for soybean genome sequences." Diss., Columbia, Mo. : University of Missouri-Columbia, 2005. http://hdl.handle.net/10355/4249.

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Thesis (M.S.)--University of Missouri-Columbia, 2005.<br>"May 2005" The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Includes bibliographical references.

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Mohamed, Maizan. "Sequence analysis of the small (s) RNA segment of viruses in the genus Orthobunyavirus." Thesis, St Andrews, 2007. http://hdl.handle.net/10023/434.

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Huckle, James William. ""Prokaryotic Metallothionein gene isolation, Nucleotide sequence and expression"." Thesis, Durham University, 1993. http://etheses.dur.ac.uk/5662/.

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Metallothioneins (MTs) are low molecular weight, cysteine-rich, metal-binding proteins, which are proposed to have roles in essential trace metal homoeostasis and in the detoxification of metal ions. The genes encoding MTs have been isolated from a wide range of eukaryotes, although MT genes have not previously been isolated from prokaryotes. The polymerase chain reaction (PGR) was initially used to isolate a prokaryotic MT gene fragment from Synechococcus PCC 6301. PGR fragments were amplified using inosine-containing primers designed from the amino acid sequence of a prokaryotic MT. Subseque

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Earle, John Alexander Philip. "The nucleotide sequence of a bovine enterovirus genome." Thesis, Queen's University Belfast, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317112.

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Halsall, John Richard. "Isolation and characterisation of the B42 mating type locus of Coprinus cinereus." Thesis, University of Oxford, 1997. http://ora.ox.ac.uk/objects/uuid:d5340e8b-29d7-4418-be27-f0c06e10ca18.

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C. cinereus, any two of which are sufficient to promote B-regulated development following cell fusion. The isolation of the B42 locus is described along with the DNA sequence analysis that identified nine B mating type genes within a 27kb B42 -specific DNA sequence. Six of the genes, with small transcripts of 800-900nt, encode the mating pheromone precursors and the other three, with 1.9 to 2-5kb transcripts, encode the transmembrane pheromone receptors. The genes are arranged in three groups, designated group 1, 2 and 3, each consisting of one receptor gene and two pheromone genes. B42 and B6

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Musgrave-Brown, Esther. "Development and application of methods for targeted DNA sequencing of pooled samples." Thesis, University of Cambridge, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.648613.

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Cheng, Kai-hong. "Further development of the visual genome explorer a visual genomic comparative tool /." Hong Kong : University of Hong Kong, 2001. http://sunzi.lib.hku.hk/hkuto/record.jsp?B23242437.

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Bücher zum Thema "Nucleotide sequence"

Ray, Gribskov Michael, and Devereux John 1947-, eds. Sequence analysis primer. Oxford University Press, 1994.

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J, Atencio Edwin, GenBank, Europæiske molekylærbiologiske laboratorium, BBN Laboratories, and Los Alamos National Laboratory, eds. Nucleotide sequences 1986/1987: A compilation from the GenBank and EMBL data libraries. Academic Press, 1987.

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John, Smith Bryan, ed. Protein sequencing protocols. 2nd ed. Humana Press, 2002.

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P, Speed T., and Waterman Michael S, eds. Genetic mapping and DNA sequencing. Springer, 1996.

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J, Harwood Adrian, ed. Protocols for gene analysis. Humana Press, 1994.

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1958-, Gribskov Michael, and Devereux John 1947-, eds. Sequence analysis primer. Oxford University Press, 1995.

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Alphey, Luke. DNA sequencing from experimental methods to bioinformatics. Springer, 1997.

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1972-, Mayer Günter, ed. Nucleic acid and peptide aptamers: Methods and protocols. Humana, 2009.

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Riccardo, Cortese, ed. Combinatorial libraries: Synthesis, screening, and application potential. Walter de Gruyter, 1996.

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Roe, Bruce A. DNA isolation and sequencing. John Wiley & Sons, 1996.

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Buchteile zum Thema "Nucleotide sequence"

Kataja, M., and M. Sarvas. "Nucleotide Sequence Analysis System on Minicomputer." In Medical Informatics Europe 85. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-93295-3_68.

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Staden, Rodger. "Staden: Statistical and Structural Analysis of Nucleotide Sequences." In Computer Analysis of Sequence Data. Humana Press, 1994. http://dx.doi.org/10.1385/0-89603-276-0:69.

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Rice, Catherine M., and Graham N. "Submission of Nucleotide Sequence Data to EMBIVGenBank/DDB J." In Computer Analysis of Sequence Data. Humana Press, 1994. http://dx.doi.org/10.1385/0-89603-276-0:413.

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Rosenberg, Aviv A., Alex M. Bronstein, and Ailie Marx. "Recording Silence – Accurate Annotation of the Genetic Sequence Is Required to Better Understand How Synonymous Coding Affects Protein Structure and Disease." In Single Nucleotide Polymorphisms. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_3.

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Wong, Dominic W. S. "Reading the Nucleotide Sequence of a Gene." In The ABCs of Gene Cloning. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77982-9_6.

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Barrell, Bart G., and Paul J. Farrell. "Using Nucleotide Sequence Determination to Understand Viruses." In Concepts in Viral Pathogenesis II. Springer New York, 1986. http://dx.doi.org/10.1007/978-1-4612-4958-0_3.

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Syvänen, A. C., and H. Söderlund. "Nucleotide Sequence Determination As a Diagnostic Tool." In Rapid Methods and Automation in Microbiology and Immunology. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76603-9_4.

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González, Ernesto Álvarez, and Ricardo Balam-Narváez. "Computation of the Observed Spectral Sequence Spectrum for Nucleotide Sequence Alignments." In Communications in Computer and Information Science. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-81698-8_3.

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Sterk, Peter, Tamara Kulikova, Paul Kersey, and Rolf Apweiler. "The EMBL Nucleotide Sequence and Genome Reviews Databases." In Plant Bioinformatics. Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-535-0_1.

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Civardi, L., M. Delledonne, M. Marudelli, and C. Fogher. "Nucleotide sequence of regulatory regions of Azospirillum brasilense." In Nitrogen Fixation. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3486-6_47.

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Konferenzberichte zum Thema "Nucleotide sequence"

Korunova, Nadezhda, Anton Romanov, and Aleksey Filippov. "Phylogeny Reconstruction of an Agricultural Crop Based on Nucleotide Sequence Homology Data Using a Genetic Algorithm." In 2025 International Russian Smart Industry Conference (SmartIndustryCon). IEEE, 2025. https://doi.org/10.1109/smartindustrycon65166.2025.10986228.

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Kim, Sung-soo, Chan-hee Lee, Keon Lee, and Sung-duk Lee. "A New Scheme for Nucleotide Sequence Signature Extraction." In 2006 5th International Conference on Machine Learning and Applications (ICMLA'06). IEEE, 2006. http://dx.doi.org/10.1109/icmla.2006.9.

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Nastac, Iulian, and Rodica Tuduce. "An adaptive intelligent model for nucleotide sequence forecasting." In 2010 4th International Symposium on Communications, Control and Signal Processing (ISCCSP). IEEE, 2010. http://dx.doi.org/10.1109/isccsp.2010.5463295.

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Roozgard, Aminmohammad, Nafise Barzigar, Shuang Wang, Xiaoqian Jiang, Lucila Ohno-Machado, and Samuel Cheng. "Nucleotide sequence alignment using sparse coding and belief propagation." In 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2013. http://dx.doi.org/10.1109/embc.2013.6609568.

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Yang, Sisi. "Complete nucleotide sequence of the RA RagB/SusD gene." In 2017 3rd International Forum on Energy, Environment Science and Materials (IFEESM 2017). Atlantis Press, 2018. http://dx.doi.org/10.2991/ifeesm-17.2018.178.

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Zhu, Li, Ming-zhou Li, Xue-wei Li, et al. "The Nucleotide Sequence Diversity Analysis of the Pig MyoG Gene." In 2008 2nd International Conference on Bioinformatics and Biomedical Engineering (ICBBE '08). IEEE, 2008. http://dx.doi.org/10.1109/icbbe.2008.32.

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Asante, Jessica, Destini McMillan, and Juan Peticco. "Protein association and nucleotide sequence similarities among human alpha-papillomaviruses." In 2016 IEEE Integrated STEM Education Conference (ISEC). IEEE, 2016. http://dx.doi.org/10.1109/isecon.2016.7457565.

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Li, Ying, Sanjie Cao, Yiping Wen, and Xintian Wen. "Complete nucleotide sequence analysis of tolC gene from actinobacillus pleuropneumoniae." In 2014 7th International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2014. http://dx.doi.org/10.1109/bmei.2014.7002882.

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Holden, Todd, S. Dehipawala, E. Cheung, et al. "Diverse nucleotide compositions and sequence fluctuation in Rubisco protein genes." In SPIE Optical Engineering + Applications, edited by Richard B. Hoover, Paul C. W. Davies, Gilbert V. Levin, and Alexei Y. Rozanov. SPIE, 2011. http://dx.doi.org/10.1117/12.893434.

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Prokhorova, E. E., and R. R. Usmanova. "GENETIC POLYMORPHISM OF SNAILS SUCCINEA PUTRIS (GASTROPODA, PULMONATA)." In V International Scientific Conference CONCEPTUAL AND APPLIED ASPECTS OF INVERTEBRATE SCIENTIFIC RESEARCH AND BIOLOGICAL EDUCATION. Tomsk State University Press, 2020. http://dx.doi.org/10.17223/978-5-94621-931-0-2020-33.

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Genotypic diversity of snails Succinea putris L. (Linnaeus, 1758) collected in the north-west of Russia and in the Republic of Belarus was analysed. Homology between the nucleotide sequences of snails from different population made up 100% by the nucleotide sequence of ITS1-5.8S-ITS2 region of rDNA. Genetic variability based on mitochondrial markers was insignificant. Average genetic distances between samples made up 0,009 for СOI gene loci and 0.008 for CytB gene loci. Was found ten haplotypes of the mitochondrial gene CytB and nine haplotypes of the mitochondrial gene СOI. Perhaps the geneti

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Berichte der Organisationen zum Thema "Nucleotide sequence"

Steffenson, B. J., I. Mayrose, Gary J. Muehlbauer, and A. Sharon. ing and comparative sequence analysis of powdery mildew and leaf rust resistance gene complements in wild barley. United States-Israel Binational Agricultural Research and Development Fund, 2021. http://dx.doi.org/10.32747/2021.8134173.bard.

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Our overall, long-term goal is to exploit the genetic diversity present in cereal wild relatives for the development of cultivars with durable disease resistance. Our specific objectives for this proposal were to: 1) Utilize Association Genetics Resistance Gene Enrichment Sequencing (AgRenSeq) to identify and clone powdery mildew and leaf rust resistance gene complements in wild barley and 2) Conduct comparative sequence analyses of the cloned resistance genes to elucidate the basis of their specificity and evolution. The deployment of resistant cultivars is the most effective, economically ef

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Wang, Ying yuan, Zechang Chen, Luxin Zhang, et al. A systematic review and network meta-analysis: Role of SNPs in predicting breast carcinoma risk. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.2.0092.

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Review question / Objective: P: Breast cancer patient; I: Single nucleotide polymorphisms associated with breast cancer risk; C: Healthy person; O: By comparing the proportion of SNP mutations in the tumor group and the control group, the effect of BREAST cancer risk-related SNP was investigated; S: Case-control study. Condition being studied: Breast cancer (BC) is one of the most common cancers among women, and its morbidity and mortality have continued to increase worldwide in recent years, reflecting the strong invasiveness and metastasis characteristics of this cancer. BC is a complex dise

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Sherman, Amir, Rebecca Grumet, Ron Ophir, Nurit Katzir, and Yiqun Weng. Whole genome approach for genetic analysis in cucumber: Fruit size as a test case. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7594399.bard.

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The Cucurbitaceae family includes a broad array of economically and nutritionally important crop species that are consumed as vegetables, staple starches and desserts. Fruit of these species, and types within species, exhibit extensive diversity as evidenced by variation in size, shape, color, flavor, and others. Fruit size and shape are critical quality determinants that delineate uses and market classes and are key traits under selection in breeding programs. However, the underlying genetic bases for variation in fruit size remain to be determined. A few species the Cucurbitaceae family were

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Patarakul, Kanitha, and Yong Poovoravan. Study of homology of mce and invA genes among different serovars of Leptospira interrogans and their in vivo expression. Faculty of Medicine, Chulalongkorn University, 2010. https://doi.org/10.58837/chula.res.2010.13.

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Leptospirosis is a worldwide zoonotic disease. Pathogenesis of leptospirosis is not well understood. Identification of virulence factors of pathogenic Leptospira and their roles in pathogenesis is crucial. Based on available whole-genome sequences of Leptospira, two presumptive virulence genes which are homologous to the invasionA (invA) gene of Rickettsia prowazekii and the mammalian cell entry (mce) gene of Mycobacterium tuberculosis, have been identified. The function of these genes may involve in the attachment and invasion of eukaryotic cells. We proposed that these gene homologues should

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Joel, Daniel M., Steven J. Knapp, and Yaakov Tadmor. Genomic Approaches for Understanding Virulence and Resistance in the Sunflower-Orobanche Host-Parasite Interaction. United States Department of Agriculture, 2011. http://dx.doi.org/10.32747/2011.7592655.bard.

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Oroginal Objectives: (i) identify DNA markers linked to the avirulence (Avr) locus and locate the Avr locus through genetic mapping with an inter-race Orobanche cumana population; (ii) develop high-throughput fingerprint DNA markers for genotypingO. cumana races; (iii) identify nucleotide binding domain leucine rich repeat (NB-LRR) genes encoding R proteins conferring resistance to O. cumana in sunflower; (iv) increase the resolution of the chromosomal segment harboring Or₅ and related R genes through genetic and physical mapping in previously and newly developed mapping populations of sunflow

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Bennett, Alan B., Arthur A. Schaffer, Ilan Levin, Marina Petreikov, and Adi Doron-Faigenboim. Manipulating fruit chloroplasts as a strategy to improve fruit quality. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7598148.bard.

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The Original Objectives were modified and two were eliminated to reflect the experimental results: Objective 1 - Identify additional genetic variability in SlGLK2 and IPin wild, traditional and heirloom tomato varieties Objective 2 - Determine carbon balance and horticultural characteristics of isogenic lines expressing functional and non-functional alleles of GLKsand IP Background: The goal of the research was to understand the unique aspects of chloroplasts and photosynthesis in green fruit and the consequences of increasing the chloroplast capacity of green fruit for ripe fruit sugars, yiel

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Wongpiyabovorn, Jongkonnee, Nattiya Hirankarn, Yingyos Avihingsanon, Tewin Tencomnao, Yong Poovorawan, and Kriangsak Ruchusatsawat. The association between immunogenetics and genetic susceptibility of psoriasis in Thai population. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.27.

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Psoriasis is T-cell-mediated skin autoimmunity, required environmental triggers and genetic susceptibility factors to become manifested. Psoriasis is a chronic skin disease characterized by the abnormal hyperproliferation and differentiation of the epidermis, elongated and prominent blood vessels and a thick perivascular lymphocytic infiltrate. Vascular endothelial growth factor (VEGF) gene play important role in pathogenesis of various diseases with angiogenic basis such as breast cancer and autoimmune disease including psoriasis. Many studies analyzed the association of VEGF gene polymorphis

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Breiman, Adina, Jan Dvorak, Abraham Korol, and Eduard Akhunov. Population Genomics and Association Mapping of Disease Resistance Genes in Israeli Populations of Wild Relatives of Wheat, Triticum dicoccoides and Aegilops speltoides. United States Department of Agriculture, 2011. http://dx.doi.org/10.32747/2011.7697121.bard.

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Wheat is the most widely grown crop on earth, together with rice it is second to maize in total global tonnage. One of the emerging threats to wheat is stripe (yellow) rust, especially in North Africa, West and Central Asia and North America. The most efficient way to control plant diseases is to introduce disease resistant genes. However, the pathogens can overcome rapidly the effectiveness of these genes when they are wildly used. Therefore, there is a constant need to find new resistance genes to replace the non-effective genes. The resistance gene pool in the cultivated wheat is depleted a

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Levisohn, Sharon, Maricarmen Garcia, David Yogev, and Stanley Kleven. Targeted Molecular Typing of Pathogenic Avian Mycoplasmas. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7695853.bard.

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Intraspecies identification (DNA "fingerprinting") of pathogenic avian mycoplasmas is a powerful tool for epidemiological studies and monitoring strain identity. However the only widely method available for Mycoplasma gallisepticum (MG) and M. synoviae (MS)wasrandom amplified polymorphic DNA (RAPD). This project aimed to develop alternative and supplementary typing methods that will overcome the major constraints of RAPD, such as the need for isolation of the organism in pure culture and the lack of reproducibility intrinsic in the method. Our strategy focussed on recognition of molecular mark

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Funkenstein, Bruria, and Cunming Duan. GH-IGF Axis in Sparus aurata: Possible Applications to Genetic Selection. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7580665.bard.

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Many factors affect growth rate in fish: environmental, nutritional, genetics and endogenous (physiological) factors. Endogenous control of growth is very complex and many hormone systems are involved. Nevertheless, it is well accepted that growth hormone (GH) plays a major role in stimulating somatic growth. Although it is now clear that most, if not all, components of the GH-IGF axis exist in fish, we are still far from understanding how fish grow. In our project we used as the experimental system a marine fish, the gilthead sea bream (Sparus aurata), which inhabits lagoons along the Mediter

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