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Relevant bibliographies by topics / Species Diagnostic

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Journal articles

Academic literature on the topic 'Species Diagnostic'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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Journal articles on the topic "Species Diagnostic"

1

Steffen, Pascal, Marcel Kwiatkowski, Wesley D. Robertson, et al. "Protein species as diagnostic markers." Journal of Proteomics 134 (February 2016): 5–18. http://dx.doi.org/10.1016/j.jprot.2015.12.015.

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2

Fladerer, Petra. "Diagnostic Methods of Mycobacterial Species." Wiener Medizinische Wochenschrift 153, no. 15-16 (2003): 332–35. http://dx.doi.org/10.1007/s10354-003-0004-5.

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3

Wiens, John J., and Maria R. Servedio. "Species delimitation in systematics: inferring diagnostic differences between species." Proceedings of the Royal Society of London. Series B: Biological Sciences 267, no. 1444 (2000): 631–36. http://dx.doi.org/10.1098/rspb.2000.1049.

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4

Fotedar, R., D. Stark, N. Beebe, D. Marriott, J. Ellis, and J. Harkness. "Laboratory Diagnostic Techniques for Entamoeba Species." Clinical Microbiology Reviews 20, no. 3 (2007): 511–32. http://dx.doi.org/10.1128/cmr.00004-07.

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SUMMARY The genus Entamoeba contains many species, six of which (Entamoeba histolytica, Entamoeba dispar, Entamoeba moshkovskii, Entamoeba polecki, Entamoeba coli, and Entamoeba hartmanni) reside in the human intestinal lumen. Entamoeba histolytica is the causative agent of amebiasis and is considered a leading parasitic cause of death worldwide in humans. Although recent studies highlight the recovery of E. dispar and E. moshkovskii from patients with gastrointestinal symptoms, there is still no convincing evidence of a causal link between the presence of these two species and the symptoms of the host. New approaches to the identification of E. histolytica are based on detection of E. histolytica-specific antigen and DNA in stool and other clinical samples. Several molecular diagnostic tests, including conventional and real-time PCR, have been developed for the detection and differentiation of E. histolytica, E. dispar, and E. moshkovskii in clinical samples. The purpose of this review is to discuss different methods that exist for the identification of E. histolytica, E. dispar, and E. moshkovskii which are available to the clinical diagnostic laboratory. To address the need for a specific diagnostic test for amebiasis, a substantial amount of work has been carried out over the last decade in different parts of the world. The molecular diagnostic tests are increasingly being used for both clinical and research purposes. In order to minimize undue treatment of individuals infected with other species of Entamoeba such as E. dispar and E. moshkovskii, efforts have been made for specific diagnosis of E. histolytica infection and not to treat based simply on the microscopic examination of Entamoeba species in the stool. The incorporation of many new technologies into the diagnostic laboratory will lead to a better understanding of the public health problem and measures to control the disease.

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5

Balasaravanan, T., P. Chezhian, R. Kamalakannan, et al. "Identification of Species-Diagnostic ISSR Markers for Six Eucalyptus Species." Silvae Genetica 55, no. 1-6 (2006): 119–22. http://dx.doi.org/10.1515/sg-2006-0017.

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Abstract Eucalyptus is planted worldwide for raw material in paper and rayon industry. It is a potential out-crosser and the natural populations are highly heterogeneous displaying strong inbreeding depression. Eucalyptus hybrids have been intensively utilized for their vigor, higher wood quality and resistance to diseases. Identification of species for hybridization is predominantly based on morphological characters and is not always reliable. Hence, DNA marker based species identification and hybrid validation is an important and efficient tool in breeding programs. In the present study, attempts were made to identify species - diagnostic markers for six eucalypt species (E. camaldulensis Dehnh, E. citriodora Hook, E. grandis W. Hill ex Maiden, E. pellita F. Muell, E. tereticornis Sm and E. urophylla S.T. Blake) using ISSR-PCR fingerprints. PCR amplification using seven ISSR primers resulted in significant polymorphism among the population from different species. E. citriodora and E. tereticornis showed monomorphic frequency of maximum 37.5% and minimum 14.3% respectively. Twenty species-diagnostic markers were identified for E. camaldulensis, E. citriodora, E. grandis and E. urophylla while no marker was detected for E. pellita and E. tereticornis. A maximum of eleven and a minimum of one species-diagnostic marker were recorded for E. citriodora and E. camaldulensis respectively. Among the twenty markers, nine were present in all the individuals of a particular species.

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6

Ujházyová, Mariana, and Karol Ujházy. "Comparing diagnostic species combinations of Carpathian calcicolous beech forests using different approaches." Phytocoenologia 42, no. 3-4 (2012): 231–48. http://dx.doi.org/10.1127/0340-269x/2012/0042-0531.

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7

Román, B., C. I. González Verdejo, Z. Satovic, M. D. Madrid, J. I. Cubero, and S. Nadal. "DetectingOrobanche species by using cpDNA diagnostic markers." Phytoparasitica 35, no. 2 (2007): 129–35. http://dx.doi.org/10.1007/bf02981106.

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8

García, Raymond O., Jim P. Kerns, and Lindsey Thiessen. "Ralstonia solanacearum Species Complex: A Quick Diagnostic Guide." Plant Health Progress 20, no. 1 (2019): 7–13. http://dx.doi.org/10.1094/php-04-18-0015-dg.

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Ralstonia solanacearum (Smith 1896) Yabuuchi et al. 1996 is ranked second among the top 10 most economically important plant pathogenic bacteria. The soil-borne bacterium affects over 200 plant species worldwide, including economically and nutritionally important crops, such as potato (Solanum tuberosum), tomato (Solanum lycopersicum), and bananas (Musa spp.). R. solanacearum is a species complex, meaning that the species is composed of strains with differential characteristics, including different metabolic requirements, centers of origin, host range, and ideal environmental conditions for infection. Its nature and the fact that it is a species complex can make R. solanacearum a difficult bacterium to work with, especially when lacking experience. Inappropriate isolation or storage of the pathogen can lead to inaccurate diagnostics or misleading conclusions. Thus, the objectives of this diagnostic guide are to provide adequate methods for isolation, storage, and identification and to discuss other relevant aspects related to this important plant pathogenic bacterium.

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9

Chytrý, Milan, Lubomír Tichý, Jason Holt, and Zoltán Botta‐Dukát. "Determination of diagnostic species with statistical fidelity measures." Journal of Vegetation Science 13, no. 1 (2002): 79–90. http://dx.doi.org/10.1111/j.1654-1103.2002.tb02025.x.

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10

Fitsailo, T. V. "Ecology of diagnostic species of Rhamno-Prunetea class." Ukrainian Botanical Journal 74, no. 3 (2017): 263–75. http://dx.doi.org/10.15407/ukrbotj74.03.263.

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