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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Mycology Research</JournalTitle>
				<Issn>2383-3181</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Rolling Circle Amplification (RCA): an approach for quick detection and identification of fungal species</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>55</FirstPage>
			<LastPage>62</LastPage>
			<ELocationID EIdType="pii">51633</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Sahar</FirstName>
					<LastName>Javaheri Tehrani</LastName>
<Affiliation>1Department of Biology, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mansour</FirstName>
					<LastName>Aliabadian</LastName>
<Affiliation>Department of Biology, Ferdowsi University of Mashhad, Mashhad, Iran; Research Department of Zoological Innovations, Institute of Applied Zoology, Faculty of Sciences, Ferdowsi
University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abdolmajid</FirstName>
					<LastName>Fata</LastName>
<Affiliation>3Department of Parasitology and Mycology, Research Center for Cutaneous Leishmaniasis, School of Medicine,
Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Javad</FirstName>
					<LastName>Najafzadeh</LastName>
<Affiliation>Department of Parasitology and Mycology and Cancer Molecular Pathology Research Center, Ghaem Hospital, School
of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>07</Month>
					<Day>20</Day>
				</PubDate>
			</History>
		<Abstract>Conventional methods for fungal identification in the clinical laboratory rely on morphological and&lt;br /&gt;physiological tests. These tests often need several days or weeks to complete and are frequently&lt;br /&gt;unspecific. Molecular identification mostly implies sequencing, which is relatively expensive and&lt;br /&gt;time-consuming, as well as impractical for large numbers of isolates. The Rolling Circle&lt;br /&gt;Amplification approach, known as RCA, is a quick, critical and economic method for fungal species&#039;&lt;br /&gt;identification. Despite its high speed, this method is highly sensitive, and it has been widely used for&lt;br /&gt;the detection of pathogenic fungi. The specific probes are designed based on the differences in the&lt;br /&gt;nucleotide regions of the target gene for the target species. The amplification product can be&lt;br /&gt;visualized by agarose gel electrophoresis, but can also be visualized in gel-free systems using&lt;br /&gt;fluorescence staining of the amplified product by SYBR Green in combination with a UV&lt;br /&gt;transilluminator. Thus, the simplicity, sensitivity, robustness and low costs make RCA an attractive&lt;br /&gt;technique for the reliable identification of sibling species and other closely related fungi.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Padlock probes</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Rolling Circle Amplification (RCA)</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Single nucleotide polymorphisms</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://jmr.ut.ac.ir/article_51633_79ef0527e818b60dec21d143a1aeaee2.pdf</ArchiveCopySource>
</Article>
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