Relevant bibliographies by topics / Development molecular markers

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Development molecular markers'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Development molecular markers"

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Varshney, R. K., M. Prasad, R. Kota, R. Sigmund, Valkoun Börner A, J, U. Scholz, N. Stein, and A. Graner. "Functional molecular markers in barley: Development and applications." Czech Journal of Genetics and Plant Breeding 41, Special Issue (July 31, 2012): 128–33. http://dx.doi.org/10.17221/6152-cjgpb.

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Teneva, A., and M. P. Petrovic. "Application of molecular markers in livestock improvement." Biotehnologija u stocarstvu 26, no. 3-4 (2010): 135–54. http://dx.doi.org/10.2298/bah1004135t.

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With recent developments in DNA technologies, a large number of genetic polymorphisms at DNA sequence level has been introduced over the last decades as named DNA-based markers. The discovery of new class of DNA profiling markers has facilitated the development of marker-based gene tags, mapbased cloning of livestock important genes, variability studies, phylogenetic analysis, synteny mapping, marker-assisted selection of favourable genotypes, etc. The most commonly used DNA-based markers have advantages over the traditional phenotypic and biochemical markers since they provide data that can be analyzed objectively. In this article the main applications of molecular markers in present-day breeding strategies for livestock improvement - parentage determination, genetic distance estimation, genetic diversity, gene mapping and marker-assisted selection have been reviewed.
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Guthrie, Sarah C. "Molecular markers in sea urchin development." Trends in Neurosciences 8 (January 1985): 185–87. http://dx.doi.org/10.1016/0166-2236(85)90074-8.

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Chinnappareddy, L. R. D., K. Khandagale, A. Chennareddy, and V. G. Ramappa. "Molecular markers in the improvement of Allium crops." Czech Journal of Genetics and Plant Breeding 49, No. 4 (November 26, 2013): 131–39. http://dx.doi.org/10.17221/111/2013-cjgpb.

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The genus Allium (Family: Alliaceae) is the most important among the bulbous vegetable crops. characterization of Alliums based on phenotypic traits is influenced by the environment and leads to biased diversity estimates. Recognizing the potential of DNA markers in plant breeding, researchers have adopted the molecular markers for marker-assisted selection (MAS), quantitative trait loci (QTL) mapping and characterization of different quality traits in Alliums. This review presents details about the use of DNA markers in Alliums for cultivar identification, diversity studies, SSR development, colour improvement, total soluble solids (TSS), cytoplasmic male sterility (CMS) and efforts of DNA sequencing. As there are no such reports to describe the above work under a single heading, we decided to mine literature for those who are working in onion, garlic, chives and leek improvement to generate new insights in the subject.
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Nam, Vu Tuan, Pham Le Bich Hang, Nguyen Nhat Linh, Luu Han Ly, Huynh Thi Thu Hue, Nguyen Hai Ha, Ha Hong Hanh, and Le Thi Thu Hien. "Molecular markers for analysis of plant genetic diversity." Vietnam Journal of Biotechnology 18, no. 4 (May 24, 2021): 589–608. http://dx.doi.org/10.15625/1811-4989/18/4/15326.

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Genetic diversity plays an important role in diversity conservation at multiple levels and supports to monitor and assess genetic variation. In plants, genetic diversity provides the ability to adapt and respond to environmental conditions that helps plants to survive through changing environments. Genetic diversity analyses based on molecular genetic markers are effective tools for conservation and reintroduction of rare and endangered species. In recent years, the development of various chemical and molecular techniques for studying genetic diversity has received great attention. While biochemical markers are primarily used in the diagnosis of pathogens, DNA markers have been developed and widely applied for identification of species and population based on the genotype of an organism that is more stable and not easily affected by the environmental factors. PCR-based molecular marker tools, such as restriction fragment length polymorphisms (RFLPs), random amplified polymorphic DNA (RAPD), simple sequence repeats (SSRs) are used for analysing the difference in the targeted DNA sequences. With the rapid and robust development of genomic sequencing technology it is now possible to obtain and analyse DNA sequences of the whole genome of studied organisms. However, each type of DNA markers has different principles, as well as the pros and cons of specificity. In this article, we review methods and point out DNA markers, which are considered as reliable and widely used tools for the detection of genetic variation. In addition, we present the application of DNA marker in analysing genetic diversity of wild, domestic and medicinal plants, as well as some perspectives on the future of DNA marker’s application in the analysis of genetic diversity.
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Hormi-Carver, Kathy, and Rhonda F. Souza. "Molecular Markers and Genetics in Cancer Development." Surgical Oncology Clinics of North America 18, no. 3 (July 2009): 453–67. http://dx.doi.org/10.1016/j.soc.2009.03.002.

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Ipek, M., A. Ipek, and P. W. Simon. "Molecular markers development and application in garlic." Acta Horticulturae, no. 1297 (November 2020): 653–58. http://dx.doi.org/10.17660/actahortic.2020.1297.86.

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Gitler, Aaron D., Min Min Lu, Yue Qin Jiang, Jonathan A. Epstein, and Peter J. Gruber. "Molecular markers of cardiac endocardial cushion development." Developmental Dynamics 228, no. 4 (November 24, 2003): 643–50. http://dx.doi.org/10.1002/dvdy.10418.

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Soriano, Jose Miguel. "Molecular Marker Technology for Crop Improvement." Agronomy 10, no. 10 (September 24, 2020): 1462. http://dx.doi.org/10.3390/agronomy10101462.

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Since the 1980s, agriculture and plant breeding have changed with the development of molecular marker technology. In recent decades, different types of molecular markers have been used for different purposes: mapping, marker-assisted selection, characterization of genetic resources, etc. These have produced effective genotyping, but the results have been costly and time-consuming, due to the small number of markers that could be tested simultaneously. Recent advances in molecular marker technologies such as the development of high-throughput genotyping platforms, genotyping by sequencing, and the release of the genome sequences of major crop plants open new possibilities for advancing crop improvement. This Special Issue collects sixteen research studies, including the application of molecular markers in eleven crop species, from the generation of linkage maps and diversity studies to the application of marker-assisted selection and genomic prediction.
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Szczechura, Wojciech, Mirosława Staniaszek, and Hanna Habdas. "Tomato Molecular Markers." Vegetable Crops Research Bulletin 74, no. 1 (January 1, 2011): 5–23. http://dx.doi.org/10.2478/v10032-011-0001-y.

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Tomato Molecular MarkersTomato (Solanum lycopersicumL.) is one of the most popular vegetable grown in many regions of the world. Due to its high taste quality and nutritional value increase interest in the cultivation of this species and its consumption. Using the latest achievements in fields of genetics, molecular biology and biotechnology, breeders can create new varieties with improved useful traits. Introduction of DNA markers, especially those based on the polymerase chain reaction (PCR) has led to breakthrough in the plants genetic research, including tomato. They are successfully used for plant genomes mapping, phylogenetics studies, selection of parental forms in plant breeding, and above all to identify the genes of important traits. For tomato have been identified and mapped 9309 molecular markers. High-density genetic maps development gives an opportunity to use them in genetic research and breeding programs. Identification of DNA markers closely linked to studied gene can significantly facilitate the identification of desirable traits in material breeding, or accelerate the plants selection for elimination of genotypes with undesirable genes. Material breeding selection using molecular markers, defined as MAS (marker-assisted-selection) is increasingly being used in tomato breeding programs, contributing to facilitated identification of genes or QTL and their transfer into the cultivated species from wild form.
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Dissertations / Theses on the topic "Development molecular markers"

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Valdman, Alexander. "Molecular genetic markers of prostate cancer development /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-618-9/.

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Hoerder, Anna. "Mouse cortical subplate neurones : molecular markers, connectivity and development." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442449.

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Tar'an, Bunyamin. "Development and application of molecular markers in common bean breeding." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0015/NQ47413.pdf.

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Song, Youqiang. "Development of polymorphic molecular markers for bovine gene mapping and selection." Thesis, University of Reading, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.262235.

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Liu, Shaolin 1968. "Oligonucleotides applied in genomics, bioinformatics and development of molecular markers for rice and barley." Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=85569.

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A genome sequence can be conceptualized as a 'book' written with four nucleotide 'letters' in oligonucleotide (oligo) 'words'. These words can be used in genomics, bioinformatics and the development of molecular markers. The whole-genome sequence for rice (Oryza sativa L.) is almost finished and has been assembled into pseudomolecules. For barley ( Hordeum vulgare L.) expressed sequence tags (ESTs) have been assembled into 21,981 tentative consensus sequences (TCs). The availability of such sequence information provides opportunities to investigate oligo usage within and between genomes. For the first of three studies reported in this thesis, a C++ program was written to automatically design oligos that are conserved between two sets of sequence information. In silico mapping between rice coding sequences (CDS) and barley TCs indicated that oligos between 18 and 24 bp provide good specificity and sensitivity (83% and 86%, respectively, for 20mers). Conserved oligos used as PCR primers had a high (91%) success rate on barley lines. Sequencing of PCR products revealed conservation in exon sequence, size and order between barley and rice. Introns were not conserved in sequence but were relatively stable in size. Map locations of eight new markers in barley revealed both genome colinearity and rearrangements between barley and rice. The second study reported in this thesis examined word frequency within the rice genome. A non-random landscape composed of high-frequency and low-frequency zones was observed. Interestingly, high-frequency words seemed to be rice specific while single-copy words were gene specific and conserved across species. As in the first study, oligos of 12 bp or less were not specific, and 18 bp seemed to be a critical length for the specificity of oligos. The third study reported in this thesis involved the development of molecular markers for known genes using public sequence information. Six new polymorphic markers were d
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Fazaeli, Asghar. "Development of molecular markers for the typing and genetic analysis of Toxoplasma gondii." Thesis, University of Aberdeen, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367484.

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To develop robust and reproducible methods for molecular typing of Toxoplasma strains, the DNA regions of 5S rDNA, 28S-18S rDNA IGS SAG2, and GRA6 loci were examined. The 5S sequences were identical among 24 different strains; sequencing of the IGS region showed a few polymorphisms (0.66%) distinguishing virulence types. The IGS PCR-RFLP methods were developed and used to examine 29 strains of different virulence types. Sequence analysis of the IGS 5'-end showed great diversity between Neospora caninum and T. gondii. The IGS-RFLPs also clearly distinguished between those two closely related species. Nucleotide sequencing of the SAG2 locus (a surface antigen coding gene) showed 1.37% polymorphisms among 24 strains. Apart from a single nucleotide change at the 5'-flanking region, the type III and type I strains were identical. However, three new alleles of this locus were identified in minor variants of the strains. Analysis of the coding region of the GRA6 locus (a dense granule antigen coding gene) revealed a great degree of polymorphisms (3.24%) among 33 strains. Nine different alleles, representing the three current types and the minor variants of strains were characterised at this locus. A PCR-RFLP based on GRA6 polymorphisms was developed which could distinguish the three major types of T. gondii. This marker proved to be a suitable tool for a population study of the Toxoplasma parasite. The predominance of non-synonymous nucleotide substitutions in SAG2 and GRA6 genes confirmed positive selection in these loci, suggesting they play an important role in the parasite virulence. Phylogenetic analysis based on the multi-locus sequence alignment showed the existence of more than three lineages in Toxoplasma populations.
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Bickley, Jane. "Development of molecular markers for studying the ecology and epidemiology of Helicobacter pylori." Thesis, Open University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386793.

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Pharmawati, Made. "DNA-based approaches for development of markers to assist Grevillea and Leucadendron breeding." University of Western Australia. School of Plant Biology, 2006. http://theses.library.uwa.edu.au/adt-WU2006.0110.

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[Truncated abstract] Grevillea and Leucadendron belong to Proteaceae and both have economic importance to the floriculture industry. Grevillea is a highly diverse genus endemic to Australia and very attractive for landscaping. Leucadendron is a South African Proteaceae but is cultivated in Australia and is well known as a cut flower. This thesis focuses on the application of DNA-based molecular markers to these genera. Several groupings within Grevillea were suggested by previous researchers based on morphological characteristics. In this thesis the monophyly of the groupings among 12 Grevillea species from New South Wales was tested using random amplified polymorphic DNA (RAPD) and inter simple sequence repeat (ISSR) analyses. To test the robustness of the data, UPGMA using Jaccard similarity, Neighbor Joining using total character difference and Wagner parsimony analyses were undertaken. The relationship trees generated supported monophyly of the groupings. Chloroplast DNA (cpDNA) was used to develop phylogenetic relationships among Leucadendron species. Inheritance and variation of cpDNA were evaluated using PCR-RFLP. The study demonstrated that cpDNA was inherited maternally and a phylogenetic tree of Leucadendron species using parsimony analysis was constructed. ... A fingerprinting study conducted using ISSR, produced a dendrogram showing the relationships among 30 cultivars. From the results, i a fingerprinting key was developed. Three examples of synonymous cultivar pairs were identified. In Leucadendron the male and female flowers develop on separate plants, and sex identification is only possible at time of flowering. ISSR, suppression subtractive hybridisation (SSH), and SSH combined with mirror orientation selection (MOS) were used in attempts of identifying sex-dependent DNA fragments at earlier stages of plant development. Neither of these techniques was able to identify sex-specific markers in Leucadendron. Nevertheless, the results did indicate that cpDNA copy number may differentiate male and female plants. Also, it was demonstrated that the genomes of male and female plants are quite homologous, which increases the difficulty in identifying sex-specific sequences. This thesis highlights the potential of DNA-based markers to determine species relationships in Grevillea and Leucadendron, as well as to identify Leucadendron cultivars. The information produced during the research for this thesis provides a basis for Grevillea and Leucadendron variety development and may be used to assist the design of interspecific crosses, to identify cultivars and the parents of hybrids. In addition, the results offer insights into the likelihood, problems and strategies of finding sex-specific markers for genes controlling sex in Leucadendron. ii
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Rosales, Rivera Luis Carlos. "Development of an electrochemical sensor for coeliac disease serological markers." Doctoral thesis, Universitat Rovira i Virgili, 2012. http://hdl.handle.net/10803/96661.

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La celiaquía, intolerancia al gluten, es una enfermedad autoinmune que afecta principalmente a la parte próxima del intestino delgado y que está presente en el 1% de la población mundial. La ingestión de gluten (proteína presente en el trigo, la cebada, el centeno) desencadena la producción de anticuerpos anti-gliadina (AGA) y anti-transglutaminasa tisular (anti-tTG) que pueden provocar inflamación y daños en el intestino delgado. La detección de estos anticuerpos mediante el uso de pruebas serológicas representa una alternativa rápida, confiable y no invasiva. El objetivo principal de esta Tesis es el desarrollo de inmunosensores usando monocapas de tioles autoensambladas en superficies de oro que sean rápidos, sensibles y de bajo coste, pero eficientes para su uso en muestras reales. Dos estrategias para inmovilizar los antígenos fueron exploradas: i) Usando monocapas autoensambladas de un alcanotiol bípedo, que posee grupos carboxílicos, ii) Introduciendo grupos disulfuro a través de los distintos grupos presentes en los antígenos: carboxílicos, aminos e hidroxilos. Ambas estrategias para construir los inmunosensores fueron optimizadas y usadas para la detección amperométrica de los marcadores serológicos de la celiaquía en muestras humanas de suero.
Coeliac disease (CD), a gluten-sensitive enteropathy, is an autoimmune disorder of the upper small intestine triggered from the gluten ingestion (cereal protein found in wheat, rye and barley) and affects 1% of the population around the globe. The ingestion of gluten, triggers the production of a series of autoantibodies against gliadin (AGA) and tissue transglutaminase (anti-tTG) which can provoke inflammation and damage some parts of the intestine. The detection of those antibodies through serological testing represent a non-invasive, fast and reliable approach. The main objective of this Thesis is the development of a sensitive, rapid and cost-efficient real-sample-oriented immunosensor using thiol-self assembled monolayers on gold surfaces. Two strategies for the antigen immobilisation have been investigated: i) The use of monolayers of a carboxylic acid-ended bipodal alkanethiol, ii) The introduction of disulfide groups through three different moieties of the antigens: amine, carboxylic and hydroxyl. Both immunosensor approaches were optimized and used for the amperometric detection of CD serological markers from human serum samples.
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Chadwick, Martin. "Development of molecular markers linked to quantitative and qualitative assessment of bitterness in lettuce." Thesis, University of Reading, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.628530.

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Taste is an important factor in foods, particularly minimally processed foods such as salad. The sensory profile of lettuce was assessed using members of an F9 recombinant inbred line (RIL) mapping population derived from the iceberg cultivar Lactuca sativa cv. Salinas and Lactuca serrio/a UC96US23, its wild progenitor. Customers were able to discern differences in bitterness in samples as the result of bitter sesquiterpene lactones (SLs), and sweetness from sugars, with high correlation between scores for these taste parameters and concentration of the metabolites. Customers preferred sweeter varieties over more bitter varieties. Subsequent analysis of 104 RILs and the parents of the mapping population by 'H NMR for a range of metabolites identified 285 NMR peaks representing 39 known compounds. NMR analysis was done in three environments, representing controlled environment, a restricted nitrogen field environment, and a high nitrogen field environment. The change in metabolome was assessed for each of the parents, showing variation in a range of compounds such as sugars, phenolics, fatty acids and amino acids. This was compared to other analysis methods to confirm that NMR was robust enough to quantify traits for quantitative trait loci (QTL) analysis
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Books on the topic "Development molecular markers"

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Krul, Kenneth G. The promise of small-molecule mimetic drugs. Waltham, Mass: Decision Resources, 1997.

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(Editor), Giampietro Gasparini, and Daniel F. Hayes (Editor), eds. Biomarkers in Breast Cancer (Cancer Drug Discovery and Development). Humana Press, 2005.

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M, Hampton Garret, and Sikora Karol, eds. Genomics in cancer drug discovery and development. Amsterdam: Elsevier/AP, 2007.

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Helentjaris, Timothy. Development and Application of Molecular Markers to Problems in Plant Genetics (Current Communications in Cell and Molecular Biology). Cold Spring Harbor Laboratory Press, 1989.

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(Editor), Garret Hampton, Karol Sikora (Editor), George F. Vande Woude (Series Editor), and George Klein (Series Editor), eds. Genomics in Cancer Drug Discovery and Development, Volume 96 (Advances in Cancer Research). Academic Press, 2006.

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(Editor), Garret Hampton, Karol Sikora (Editor), George F. Vande Woude (Series Editor), and George Klein (Series Editor), eds. Genomics in Cancer Drug Discovery and Development, Volume 96 (Advances in Cancer Research). Academic Press, 2006.

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Hongtrakul, Vipa. The development and analysis of sequence-based DNA markers in sunflower for DNA fingerprinting and candidate gene analysis. 1997.

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Walsh, Scott R. A. Development of molecular markers for the detection and differentiation of Entomophaga strains pathogenic for insects. 1996.

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Singh, Shree Ram, and Pranela Rameshwar. MicroRNA in Development and in the Progression of Cancer. Springer, 2016.

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Singh, Shree Ram, and Pranela Rameshwar. MicroRNA in Development and in the Progression of Cancer. Springer, 2014.

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Book chapters on the topic "Development molecular markers"

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Livneh, O., and E. Vardi. "Molecular Genetic Markers." In Hybrid Cultivar Development, 201–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-07822-8_8.

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Dumitrescu, Ramona G. "Epigenetic Markers of Early Tumor Development." In Methods in Molecular Biology, 3–14. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-612-8_1.

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Storer, Mekayla, and William M. Keyes. "Detection of Senescence Markers During Mammalian Embryonic Development." In Methods in Molecular Biology, 199–210. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6670-7_19.

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Vignes, Hélène, and Ronan Rivallan. "Development of Microsatellite Markers Using Next-Generation Sequencing." In Methods in Molecular Biology, 179–86. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0997-2_11.

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Schubert, R., and G. Müller-Starck. "Development and Application of Molecular Markers in Conifers." In Molecular Techniques in Crop Improvement, 139–60. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-017-2356-5_5.

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Pootakham, Wirulda, Jeremy R. Shearman, and Sithichoke Tangphatsornruang. "Development of Molecular Markers in Hevea brasiliensis for Marker-Assisted Breeding." In The Rubber Tree Genome, 67–79. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-42258-5_5.

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Singh, Sanjay, Kanchan Kumari, Shweta Chaturvedi, Nutan Pandey, and Ashley Varghese. "Molecular Characterization of Anogeissus acuminata Genotypes Employing RAPD Markers." In Applications of Biotechnology for Sustainable Development, 7–14. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-5538-6_2.

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Nakagawa, H., and M. Ebina. "Development of Molecular Markers for the Analysis of Apomixis." In Developments in Plant Breeding, 161–73. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-9700-5_9.

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Chamberlin, Mark A., and Shai J. Lawit. "Development and Observation of Mature Megagametophyte Cell-Specific Fluorescent Markers." In Methods in Molecular Biology, 55–65. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7286-9_5.

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Atia, Mohamed A. M., Mahmoud M. Sakr, Morad M. Mokhtar, and Sami S. Adawy. "Development of Sex-Specific PCR-Based Markers in Date Palm." In Methods in Molecular Biology, 227–44. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7159-6_19.

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Conference papers on the topic "Development molecular markers"

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STAPULIONYTĖ, Asta, Skaistė BONDZINSKAITĖ, Monika STRAVINSKAITĖ, Raimondas ŠIUKŠTA, Ričardas TARAŠKEVIČIUS, and Tatjana ČĖSNIENĖ. "SOIL GENOTOXICITY BIOMONITORING IN RECULTIVATED FACTORY AREA USING THE CYTOGENETIC AND MOLECULAR ASSAYS IN TWO PLANT TEST-SYSTEMS." In RURAL DEVELOPMENT. Aleksandras Stulginskis University, 2018. http://dx.doi.org/10.15544/rd.2017.025.

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Soil pollution with industrial leftovers is of real danger to living organisms since harmful effects can arise after exposure to the contaminants in the soil. In our study, we applied a plant bioassay battery to monitor soil genotoxicity after short-term exposure to the soil. The soil was collected in 3 rounds: at the central part of the brownfield before (S-I) and after (S-III) topsoil removal, and at the brownfield periphery (S-II). The permissible value of the total contamination index is <16 and the corresponding values were 780 in S-I, 69 in S-II and 133 in S-III soil showing that whole brownfield territory is extremely polluted with heavy metals. Cytogenetic markers were recorded in Allium and Tradescantia test-systems and two types of molecular markers, RAPD and ISSR, were analysed in Allium. Our results revealed that the most polluted soil sample has induced an alarming increase of apoptotic cells in onion roots. Chromosome aberration and micronuclei frequency in Allium decreased inconsistently along with the pollution reduction in the soil. Increased frequencies of all cytogenetic markers were revealed in Tradescantia cuttings after exposure to the S-I soil extracts. Cluster analysis of Allium RAPD and ISSR markers showed that the most polluted soil samples induced genetic changes in onions different from those induced by the least polluted soil. Both plant test-systems in this study confirm that soil from the brownfield is harmful to plants and is potentially hazardous to humans.
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Glukhova, Olga E., and Dmitriy S. Shmygin. "Perspectives of graphene-nucleotide complexes for the development of new bioelectronics devices." In Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications X, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2018. http://dx.doi.org/10.1117/12.2291427.

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Davoyan, E. R., L. A. Bespalova, R. O. Davoyan, E. V. Agaeva, D. S. Mikov, D. M. Boldakov, Yu S. Zubanova, and Zh N. Khudokormova. "Breeding of common wheat for leaf rust resistance using DNA markers." In CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE. Federal State Budget Scientific Institution “Research Institute of Agriculture of Crimea”, 2020. http://dx.doi.org/10.33952/2542-0720-2020-5-9-10-57.

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The article presents the results of the characterization of 277 lines of common wheat developed in the National Center of Grain named after P.P. Lukyanenko by the presence of molecular markers linked to leaf rust resistance genes Lr9, Lr19, Lr24, Lr37, Lr26. Lines with Lr9 and Lr19 were not identified. We detected 52 lines carrying Lr24; 80 lines with Lr26; 141 lines with Lr37. Lines carrying a combination of leaf rust resistance genes were selected using molecular markers. The presence of a combination of Lr37 + Lr26 was established in 31 lines. The combination of Lr24 + Lr26 was detected in 12 lines. Line 125-15 Ms 2 carries a combination of Lr37 + Lr24. A pyramid of three genes was found in the line 144-15 Ms 2. Currently, the selected lines are widely involved in the breeding process.
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Huang, Honghu, Jia Zhou, Yiping Huang, and Minhang Bao. "Development of a multi-channel immunosensor for determnination of serum hepatic fibrosis markers." In 2006 1st IEEE International Conference on Nano/Micro Engineered and Molecular Systems. IEEE, 2006. http://dx.doi.org/10.1109/nems.2006.334575.

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Takahashi, Yoko, Frederico O. Gleber-Netto, Diana Bell, Dianna Roberts, Tong-Xin Xie, Ahmed S. Abdelmeguid, Curtis Pickering, Jeffrey N. Myers, and Ehab Y. Hanna. "Development of Clinically Applicable Molecular Markers Distinguishing Sinonasal Undifferentiated Carcinoma from Sinonasal Squamous Cell Carcinoma." In 30th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1702337.

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Salimova, D. R., A. S. Orina, Ph B. Gannibal, and A. O. Berstetskiy. "Differentiation of Alternaria japonica and Alternaria tenuissima, isolated from cruciferous cultures by morphological, molecular and biochemical markers." In CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE. Federal State Budget Scientific Institution “Research Institute of Agriculture of Crimea”, 2019. http://dx.doi.org/10.33952/09.09.2019.114.

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Ceceris, Kyra D., Paul R. Ervin, and Theresa R. Cassino. "Comparison of signal transduction drug response markers in immortalized cell lines and primary patient specimens." In AACR International Conference: Molecular Diagnostics in Cancer Therapeutic Development– Sep 27-30, 2010; Denver, CO. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/diag-10-a31.

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El-Hawary, Ibrahim. "Development of some molecular and biochemical markers associated with tolerance to insect attacks in sugar beet,Beta vulgaris." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.113714.

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"Development of molecular markers for the identification of prolamins genes and their correlation with baking qualities of grain." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Novosibirsk ICG SB RAS 2021, 2021. http://dx.doi.org/10.18699/plantgen2021-157.

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Yakhnenko, Alena, Nikita Yushin, Ivan Nebesnykh, Igor Khanaev, Inga Zinicovscaia, and Elena Kravchenko. "Molecular markers development for studying of the heavy metal response gene expression levels in endemic sponges of Lake Baikal." In PROCEEDINGS OF THE 24TH INTERNATIONAL SCIENTIFIC CONFERENCE OF YOUNG SCIENTISTS AND SPECIALISTS (AYSS-2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0063872.

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Reports on the topic "Development molecular markers"

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Lokshin, Anna. Integrated Development of Serum Molecular Markers for Early Diagnosis of Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, September 2006. http://dx.doi.org/10.21236/ada462774.

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Gunter, L. E. Towards the Development of a Molecular Map in Switchgrass: I. Microsatellite Marker Development. Office of Scientific and Technical Information (OSTI), August 2001. http://dx.doi.org/10.2172/788504.

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