Relevant bibliographies by topics / Internal transcribed spacer 1

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Academic literature on the topic 'Internal transcribed spacer 1'

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

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Journal articles on the topic "Internal transcribed spacer 1"

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van der Heijden, Harold M. J. F., Wil J. M. Landman, Sophie Greve, and Ron Peek. "Genotyping ofHistomonas meleagridisisolates based on Internal Transcribed Spacer-1 sequences." Avian Pathology 35, no. 4 (2006): 330–34. http://dx.doi.org/10.1080/03079450600815499.

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Booy, G., J. Van der Schoot, and B. Vosman. "Heterogeneity of the internal transcribed spacer 1 (ITS1) inTulipa (Liliaceae)." Plant Systematics and Evolution 225, no. 1-4 (2000): 29–41. http://dx.doi.org/10.1007/bf00985457.

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Carbone, Ignazio, and Linda M. Kohn. "Ribosomal DNA Sequence Divergence within Internal Transcribed Spacer 1 of the Sclerotiniaceae." Mycologia 85, no. 3 (1993): 415. http://dx.doi.org/10.2307/3760703.

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Lebuhn, Michael, Stephan Bathe, Wafa Achouak, Anton Hartmann, Thierry Heulin, and Michael Schloter. "Comparative sequence analysis of the internal transcribed spacer 1 of Ochrobactrum species." Systematic and Applied Microbiology 29, no. 4 (2006): 265–75. http://dx.doi.org/10.1016/j.syapm.2005.11.003.

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Henry, Travis, Peter C. Iwen, and Steven H. Hinrichs. "Identification of Aspergillus Species Using Internal Transcribed Spacer Regions 1 and 2." Journal of Clinical Microbiology 38, no. 4 (2000): 1510–15. http://dx.doi.org/10.1128/jcm.38.4.1510-1515.2000.

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Aspergillus species are the most frequent cause of invasive mold infections in immunocompromised patients. Although over 180 species are found within the genus, 3 species, Aspergillus flavus, A. fumigatus, and A. terreus, account for most cases of invasive aspergillosis (IA), with A. nidulans, A. niger, and A. ustus being rare causes of IA. The ability to distinguish between the various clinically relevant Aspergillus species may have diagnostic value, as certain species are associated with higher mortality and increased virulence and vary in their resistance to antifungal therapy. A method to
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Chen, Y. C., J. D. Eisner, M. M. Kattar, et al. "Polymorphic Internal Transcribed Spacer Region 1 DNA Sequences Identify Medically Important Yeasts." Journal of Clinical Microbiology 39, no. 11 (2001): 4042–51. http://dx.doi.org/10.1128/jcm.39.11.4042-4051.2001.

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Carbone, Ignazio, and Linda M. Kohn. "Ribosomal DNA Sequence Divergence within Internal Transcribed Spacer 1 of the Sclerotiniaceae." Mycologia 85, no. 3 (1993): 415–27. http://dx.doi.org/10.1080/00275514.1993.12026293.

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Schmiderer, Corinna, Brigitte Lukas, Joana Ruzicka, and Johannes Novak. "What Else Is in Salviae officinalis folium? Comprehensive Species Identification of Plant Raw Material by DNA Metabarcoding." Planta Medica 84, no. 06/07 (2017): 428–33. http://dx.doi.org/10.1055/s-0043-121470.

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AbstractQuality control of drugs consists of identifying the raw material to avoid unwanted admixtures or exchange of material as well as looking for abiotic and biotic contaminations. So far, identity and microbial contamination are analyzed by separate processes and separate methods. Species identification by their DNA (“DNA barcoding”) has the potential to supplement existing methods of identification. The introduction of next-generation sequencing methods offers completely new approaches like the identification of whole communities in one analysis, termed “DNA metabarcoding”. Here we prese
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Fan, Congzhao, Xiaojin Li, Jun Zhu, Jingyuan Song, and Hui Yao. "Endangered Uyghur Medicinal PlantFerulaIdentification through the Second Internal Transcribed Spacer." Evidence-Based Complementary and Alternative Medicine 2015 (2015): 1–6. http://dx.doi.org/10.1155/2015/479879.

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The medicinal plantFerulahas been widely used in Asian medicine, especially in Uyghur medicine in Xinjiang, China. Given that various substitutes and closely related species have similar morphological characteristics,Ferulais difficult to distinguish based on morphology alone, thereby causing confusion and threatening the safe use ofFerula. In this study, internal transcribed spacer 2 (ITS2) sequences were analyzed and assessed for the accurate identification of two salableFerulaspecies (Ferula sinkiangensisandFerula fukangensis) and eight substitutes or closely related species. Results showed
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Kim, Jae-Seok, Yong-Kyun Kim, Ji Young Park, et al. "Analysis of Internal Transcribed Spacer 1 Sequences of Pneumocystis jiroveci from Clinical Specimens." Chonnam Medical Journal 44, no. 2 (2008): 82. http://dx.doi.org/10.4068/cmj.2008.44.2.82.

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Dissertations / Theses on the topic "Internal transcribed spacer 1"

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Müller, Juceli. "Qualidade fisiológica e associação de Fusarium spp. a sementes de sorgo sacarino." Universidade Federal de Santa Maria, 2017. http://repositorio.ufsm.br/handle/1/11796.

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The present work aims to determine the physiological and sanitary quality of Sweet sorghum (Sorghum bicolor (L.) Moench) seeds, as well as to identify pathogens associated with seed, their transmission to seedlings and the subsequent pathogenicity of isolates obtained, In addition, molecularly identify the fungal species pathogenic to this crop. The experiments were carried out in the Teaching and Seed Research Laboratory (TSRL), of the Plant Engineering Department; In the Elocy Minussi Phytopathology Laboratory, Department of Plant Protection, and at the Biological Institute of São Paulo. Swe
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Cheung, Mei, and 張微. "Internal transcribed spacer as the DNA barcode for pathogenic fungi." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/206495.

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Identification of pathogenic fungi isolated from clinical specimens in clinical microbiology laboratories is primarily based on observing fungal phenotypic structures under the microscope and performing biochemical tests for fungal cultures. This conventional method is very time-consuming and labor-dependent. It usually requires several weeks for the fungi to grow sufficiently on culture media, and the identification processes on fungal phenotypic structure rely very much on experienced staff. Therefore, a more accurate and rapid method for pathogenic fungal identification is necessary for cli
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Bodo, Slotta Tracey A. "Phylogenetic Analysis of Iliamna (Malvaceae) Using the Internal Transcribed Spacer Region." Thesis, Virginia Tech, 2000. http://hdl.handle.net/10919/33211.

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The genus Iliamna Greene has a taxonomically complex history. Since its desciption in 1906, the genus was not recognized for some time, several species were initially placed into other genera, and the species status of a few was questioned. Today, eight species of Iliamna are recognized. Six species are located in western North America and two are found isolated to the east. Species in Iliamna are very similar morphologically with only a few characters distinguishing several as separate entities. The need for systematic study became apparent since all but one species are considered rare or end
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Menezes, Josiane Pacheco. "Caracterização populacional e molecular, e seleção de trichoderma spp. para biocontrole de fusarium sp. em crisãntemo." Universidade Federal de Santa Maria, 2007. http://repositorio.ufsm.br/handle/1/3245.

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Trichoderma spp. is one of the most researched fungi as biocontrole agent of diseases, being antagonistic to several phytopathogens in different crops. The soilborne pathogen Fusarium oxysporum causes wilt in several crops, including chrysanthemum, is of difficult control, due mainly to its survival capacity in the soil for long periods, even without the presence of the host. Studies about the population dynamics of Trichoderma spp. and Fusarium spp. and of the associated native microbiota they necessary, especially, to observe the impact of the biocontrols addition in the soil. Ornamental pla
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Hao, Gang, and 郝剛. "Molecular phylogeny of the illiciales based on internal transcribed spacer sequences of ribosomal DNA." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31238567.

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Hao, Gang. "Molecular phylogeny of the illiciales based on internal transcribed spacer sequences of ribosomal DNA /." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21029027.

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Ragozine, Vincent. "Analyses of ribosomal DNA internal transcribed spacer sequences from : Juglans nigra and leaf-associated fungi in Zoar Valley, NY /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1211685563.

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Ragozine, Vincent Kyle. "Analyses of ribosomal DNA internal transcribed spacer sequences from Juglans nigra and leaf-associated fungi in Zoar Valley, NY." Youngstown State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1211685563.

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Heidemann, Stefan [Verfasser]. "DNA-Polymorphismen der internal transcribed spacer-Region zur Differenzierung anthropophiler und zoophiler Spezies von Trichophyton mentagrophytes sensu lato / Stefan Heidemann." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2010. http://d-nb.info/1024334767/34.

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Förster, Frank [Verfasser], and Thomas [Akademischer Betreuer] Dandekar. "Making the most of phylogeny: Unique adaptations in tardigrades and 216374 internal transcribed spacer 2 structures / Frank Förster. Betreuer: Thomas Dandekar." Würzburg : Universitätsbibliothek der Universität Würzburg, 2012. http://d-nb.info/1022061232/34.

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Books on the topic "Internal transcribed spacer 1"

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Grubisha, Lisa C. Systematics of the genus Rhizopogon inferred from nuclear ribosomal DNA large subunit and internal transcribed spacer sequences. 1998.

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Abdennadher, Mourad. Molecular fingerprinting, rDNA internal transcribed spacer sequence, and karyotype analysis of Ustilago hordei and related smut fungi. 1995.

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Moynihan, Jeremy. Molecular phylogeny of the Caribbean endemic Neolaugeria (Rubiaceae), based on the internal transcribed spacer regions of nuclear ribosomal DNA. 1999.

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Book chapters on the topic "Internal transcribed spacer 1"

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Fujita, Shin-ichi. "Internal Transcribed Spacer (ITS)-PCR Identification of MRSA." In Methods in Molecular Biology. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-664-1_5.

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Fujita, Shin-ichi. "Internal Transcribed Spacer (ITS)-PCR Identification of MRSA." In Methods in Molecular Biology. Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-468-1_4.

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Therese, K. Lily, R. Bagyalakshmi, and H. N. Madhavan. "Application of Polymerase Chain Reaction and PCR-Based Methods Targeting Internal Transcribed Spacer Region for Detection and Species-Level Identification of Fungi." In Laboratory Protocols in Fungal Biology. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-2356-0_27.

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Baayen, R. P., C. Waalwijk, and W. Gams. "Fusarium Sections Elegans and Liseola: Taxonomy, rDNA Internal Transcribed Spacer Sequences and Diagnostics." In Developments in Plant Pathology. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-0043-1_61.

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"Internal Transcribed Spacers." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_8630.

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"Plant DNA Barcoding." In Advances in Environmental Engineering and Green Technologies. IGI Global, 2021. http://dx.doi.org/10.4018/978-1-7998-4312-2.ch006.

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DNA barcoding has evolved as an effective species identification tool in diverse areas such as phylogeny, ecology, population genetics, and biodiversity. In this approach, a short DNA sequence from a standardized locus is employed for species identification. The technique is simple, time and cost effective, and accurate. Selection of correct DNA marker is the main criterion for success in DNA barcoding. Compared to animals, DNA barcoding is more difficult in plants, as there are multiple consensuses about selection of barcoding markers for plants DNA barcoding. Some common plant barcoding markers are chloroplast genes such as matK, rbcL, ropC1, ropB, and trnL; chloroplast intergenic specers trnH-psbA, atpF-atpH, and pdbK-psbI; and the nuclear ribosomal internal transcribed spacer (ITS). These markers can be used alone or in combinations with other markers or spacers. In this chapter, the basic requirements, selection of markers, databases, advantages, and limitations of DNA barcoding have been discussed.
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"Transcribed spacer." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_17186.

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Lau, David Tai-Wai, Pang-Chui Shaw, and Paul Pui-Hay But. "Authentication of Medicinal Dendrobium Species by the Internal Transcribed Spacer of Ribosomal DNA." In Authentication of Chinese Medicinal Materials by DNA Technology. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812706591_0009.

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"Genes." In Examining the Causal Relationship Between Genes, Epigenetics, and Human Health. IGI Global, 2019. http://dx.doi.org/10.4018/978-1-5225-8066-9.ch009.

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Gene expression patterns are dependent on their internal cell environment of their DNA, their immediate internal cell environment, and the integrity of their DNA. It also depends on the cell's external environment comprised of signals from other parts of the body including chemicals, nutrients, and/or mechanical stress. Gene regulation is achieved by a wide range of mechanisms that cells use to control whether genes are transcribed, when they are transcribed, and to regulate the quantity of certain proteins based on the cellular and/or environmental feedback. Proper regulation of gene expression is required by organisms to respond to continually changing environmental conditions. Some bacterial genes are transcribed as a unit under a regulatory system called an operon which contains functionally related genes. Three well studied operons include the lactose operon, histidine operon, and tryptophan operon. Gene regulation in higher organisms can occur at various stages from DNA level to protein assembly. This chapter explores this aspect of genes.
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Conference papers on the topic "Internal transcribed spacer 1"

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M., Nor-Zuhailah, Fatihah N.H.N., Nashriyah M, Ali A.M., and Choong Chee Yen. "MOLECULAR SYSTEMATICS of Ficus deltoidea Jack (Moraceae) BASED ON INTERNAL TRANSCRIBED SPACER." In Annual International Conference on BioInformatics and Computational Biology & Annual International Conference on Advances in Biotechnology. Global Science and Technology Forum, 2011. http://dx.doi.org/10.5176/978-981-08-8119-1_biotech19.

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Rosa, Marcos P., Jose V. C. Vargas, Vanessa M. Kava, et al. "Hydrogen and Compounds With Biological Activity From Microalgae." In ASME 2019 13th International Conference on Energy Sustainability collocated with the ASME 2019 Heat Transfer Summer Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/es2019-3965.

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Abstract Microalgae have a high biotechnological potential as a source of biofuels (biodiesel, biohydrogen) and other high-added value products (e.g., pharmaceuticals, proteins, pigments). However, for microalgae cultivation to be economically competitive with other fuel sources, it is necessary to apply the concept of biorefinery. This seems to be the most ambitious strategy to achieve viability. Therefore, the objectives of this study were to isolate and identify the main microalgae line used to produce biofuels at Federal University of Parana, Brazil, using the rDNA sequence and micromorpho
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Hidayat, Topik, Didik Priyandoko, Dina Karina Islami, and Putri Yunitha Wardiny. "Molecular phylogenetic analysis of Indonesia Solanaceae based on DNA sequences of internal transcribed spacer region." In PROCEEDINGS OF INTERNATIONAL SEMINAR ON MATHEMATICS, SCIENCE, AND COMPUTER SCIENCE EDUCATION (MSCEIS 2015). AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4941148.

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"Intragenomic polymorphism of internal transcribed spacer ITS1 in the locus 35S rRNA of polyploid Avena species." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-148.

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da Silva, M. L. R. B., V. A. L. B. Cavalcanti, A. C. E. S. Mergulhão, and M. C. C. P. de Lyra. "Sequencing of the region of ribosomal internal transcribed spacer (ITS) of Metarhizium anisopliae in Pernambuco state." In Proceedings of the III International Conference on Environmental, Industrial and Applied Microbiology (BioMicroWorld2009). WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789814322119_0028.

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Amrullah, Muhammad Haidar, Annisa Sholikhah, Farida Aryani Dian, et al. "Phylogenetic study of Cantigi Ungu (Vaccinium varingifolium) based on universal internal transcribed spacer (ITSu) DNA barcoding." In THE 6TH INTERNATIONAL CONFERENCE ON BIOLOGICAL SCIENCE ICBS 2019: “Biodiversity as a Cornerstone for Embracing Future Humanity”. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0015822.

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Chen, Ren-Fang, Li Xu, Mao-De Yu, Xiu-Qun Liu, and Long-Qing Chen. "Determination of the Origin and Evolution of Morus (Moraceae) by Analyzing the Internal Transcribed Spacer (ITS) Sequences." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5518058.

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Mkumbe, Baraka Stewart, Sajidan, Artini Pangastuti, and Ari Susilowati. "Phylogenetic analysis based on internal transcribed spacer region (ITS1-5.8S-ITS2) of Aspergillus niger producing phytase from Indonesia." In Proceedings of the 17th International Conference on Ion Sources. Author(s), 2018. http://dx.doi.org/10.1063/1.5054419.

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Peck, Kayla, Robert Stedtfeld, Jordan RoseFigura, et al. "Abstract 1484: Microbial sequencing using a single-pool target enrichment of multiple variable regions of the 16S rRNA gene, the nuclear ribosomal internal transcribed spacer (ITS) region, and antimicrobial resistance genes." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-1484.

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Peck, Kayla, Robert Stedtfeld, Jordan RoseFigura, et al. "Abstract 1484: Microbial sequencing using a single-pool target enrichment of multiple variable regions of the 16S rRNA gene, the nuclear ribosomal internal transcribed spacer (ITS) region, and antimicrobial resistance genes." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-1484.

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