Relevant bibliographies by topics / DNA polymorphic marker

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Academic literature on the topic 'DNA polymorphic marker'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Dissertations / Theses on the topic "DNA polymorphic marker"

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Frölich, Matthias Frank [Verfasser], and Andreas [Akademischer Betreuer] Jung. "The polymorphic DNA marker rs849142 predicts skin toxicity in anti-EGFR treatment of metastatic colorectal cancer / Matthias Frank Frölich ; Betreuer: Andreas Jung." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1170582745/34.

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Taniguchi, Yukio. "Genetic Diversities among Founder Populations of the Endangered Avian Species, the Japanese Crested Ibis and the Oriental Stork in Japan." Kyoto University, 2016. http://hdl.handle.net/2433/204565.

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Kyoto University (京都大学)<br>0048<br>新制・論文博士<br>博士(農学)<br>乙第12986号<br>論農博第2826号<br>新制||農||1038(附属図書館)<br>学位論文||H28||N4961(農学部図書室)<br>32456<br>名古屋大学大学院農学研究科生化学制御専攻<br>(主査)教授 祝前 博明, 教授 今井 裕, 教授 廣岡 博之<br>学位規則第4条第2項該当
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Maufrand, Remy. "Linkage analysis of avirulence in Phytophthora infestans using random applied polymorphic DNA markers." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243431.

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Golembiewski, Robert Craig. "Identification and characterization of creeping bentgrass using randomly amplified polymorphic DNA (RAPD) markers /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487942739809001.

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Allnutt, Theodore Richard. "The study of genetic variation in trees using the random amplified polymorphic DNA (RAPD) technique." Thesis, Liverpool John Moores University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319848.

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Wei, Ling. "Identification of DNA Markers in Triticum aestivum-Aegilops caudata Additions Lines by Randomly Amplified Polymorphic DNA (RAPD) Technology." DigitalCommons@USU, 1995. https://digitalcommons.usu.edu/etd/4543.

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The objective of this study was to identify DNA markers for each of six added C-genome chromosomes in Triticum aestivum L. cv. 'Alceso'-Aegilops caudata L. addition lines using the randomly amplified polymorphic DNA (RAPD) technique. DNA from Ae. caudata, T. aestivum, amphiploid of T. aestivum X Ae. caudata, and six disomic addition lines of wheat having a pair of Ae. caudata chromosomes was used as the template for the amplification of RAPD markers with a total of 58 random 10-mer oligonucleotide primers. Two primers, OPC-08 and OPJ-16, produced one intense band each from the amphiploid of T. aestivum X Ae. caudata and Ae. caudata, which was absent in all six addition lines. Each of these two primers produced a chromosome marker that could be tentatively located to the chromosome CA of Ae. caudata. OPJ-02, OPD-12, OPD-02, OPJ-12, OPD-20, and OPJ-14 produced a marker each for CB, CC, CD, CE, CF, and CG, respectively. OPJ-09 produced C-genome chromosome-specific RAPD markers. Also, OPC-05 and OPJ-19 produced RAPDs from both wheat and Ae. caudata genomes.
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Halldén, Christer. "Characterization and use of a multiplex PCR-based system random amplified polymorphic DNA /." Lund : Lund University, 1998. http://catalog.hathitrust.org/api/volumes/oclc/68945134.html.

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Brown, Richard James. "The development and use of polymorphic DNA markers for use in population studies of Oryzaephilus surinamensis." Thesis, Queen Mary, University of London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362358.

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Kongkiatngam, Prasert. "Genetic studies of red clover (Trifolium pratense L.) using morphological, isozyme and random amplified polymorphic DNA (RAPD) markers." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=29066.

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Genetic variation within and between two cultivars of red clover (Trifolium pratense L.), Essi from Europe and Ottawa from Canada was estimated using morphological, isozyme and random amplified polymorphic DNA (RAPD) markers. A total of 21 enzyme-coding loci with 43 alleles was detected using twelve enzyme systems. The mean number of alleles per locus was 1.81 in Essi and 1.67 in Ottawa. Nine 10-mer primers were used to assay 20 individuals from each cultivar for RAPD markers. Each primer gave from 7 to 20 amplified bands with an average of 14.8 bands per primer. High within-cultivar variation was observed in both cultivars using both isozyme and RAPD markers. The mode of inheritance of seven isozyme loci: Aat-2, Amy-1, Est-4, Est-7, Pgd-1, Pgd-2 and Skd-1, in red clover was verified. The genetic basis of banding patterns for 16 other isozyme loci: Aat-3, Adh-1, Dia-1, Dia-2, Dia-3, Est-1, Est-2, Gpi-2, Idh-1, Mdh-1, Mdh-2, Mdh-3, Mdh-4, Me-1, Me-2 and Pgm-2, was also postulated, based on the segregation patterns observed within cultivars. Two pairs of linked enzyme-coding loci, Est-4/Est-7 and Pgd-2/Skd-1, were found with joint segregation analysis. Estimates of genetic variability of 15 red clover cultivars from three different origins indicated that within-cultivar variation was much higher than between-cultivar variation. Allele frequencies of these isozymes could discriminate the five North American cultivars assayed, but they could not differentiate cultivars from Europe and Japan. The use of RAPD markers obtained from bulked samples was investigated for cultivar identification in red clover. Pooled samples were examined in order to minimize variation within cultivars. Twenty was found to be an appropriate number of red clover individuals per bulk for homogenizing genetic variation within cultivars. Fourteen 10-mer primers were used to amplify genomic DNA from combined leaf samples of 15 red clover cultivars from European, Japanese and North American origin
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Prodöhl, Paulo A. "Multilocus and single locus minisatellite DNA polymorphism in brown trout (Salmo trutta L.) populations." Thesis, Queen's University Belfast, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296801.

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