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<Article>
<Journal>
				<PublisherName>Shiraz University Press</PublisherName>
				<JournalTitle>Molecular Biology Research Communications</JournalTitle>
				<Issn>2322-181X</Issn>
				<Volume>4</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>The binding assessment with human serum albumin of novel six-coordinate Pt(IV) complexes, containing bidentate nitrogen donor/methyl ligands</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>167</FirstPage>
			<LastPage>179</LastPage>
			<ELocationID EIdType="pii">3165</ELocationID>
			
<ELocationID EIdType="doi">10.22099/mbrc.2015.3165</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Reza</FirstName>
					<LastName>Yousefi</LastName>
<Affiliation>Protein Chemistry Laboratory (PCL), Department of Biology, Shiraz University, Shiraz, Iran.

Institute of Biotechnology, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Asghar</FirstName>
					<LastName>Taheri-Kafrani</LastName>
<Affiliation>Department of Biotechnology, Faculty of Advanced Sciences and Technologies, University of Isfahan, Isfahan, 81746-73441, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sayed Masoud</FirstName>
					<LastName>Nabavizadeh</LastName>
<Affiliation>Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Zahra</FirstName>
					<LastName>Pouryasin</LastName>
<Affiliation>Protein Chemistry Laboratory (PCL), Department of Biology, College of Sciences, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Bagher</FirstName>
					<LastName>Shahsavani</LastName>
<Affiliation>Protein Chemistry Laboratory (PCL), Department of Biology, College of Sciences, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Kazem</FirstName>
					<LastName>Khoshaman</LastName>
<Affiliation>Protein Chemistry Laboratory (PCL), Department of Biology, College of Sciences, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mehdi</FirstName>
					<LastName>Rashidi</LastName>
<Affiliation>Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>05</Month>
					<Day>25</Day>
				</PubDate>
			</History>
		<Abstract>The interactions between platinum complexes and human serum albumin (HSA) play crucial roles in the distribution, metabolism, and activity of platinum-based anticancer drugs. Octahedral platinum (IV) complexes represent a significant class of anticancer agents that display molecular pharmacological properties different from cisplatin. In this study, the interaction between two Pt(IV) complexes with the general formula [Pt(X)2Me2 (tbu2bpy)], where tbu2bpy = 4,4′-ditert-butyl-2,2′-bipyridine, with two leaving groups of X = Cl (Com1) or Br (Com2), and HSA were investigated, using Ultraviolet-Visible (UV-Vis) spectroscopy, fluorescence spectroscopy, circular dichroism (CD) and molecular docking simulation. The spectroscopic and thermodynamic data revealed that the HSA/Pt(IV) complexes interactions were spontaneous process and Com2 demonstrated stronger interaction and binding constant in comparison with Com1. Also, the results suggest approximately similar structural alteration of HSA in the presence of these Pt complexes. Molecular docking revealed that both Pt(IV) complexes bind with HSA in subdomain IB, literally the same as each other. This study suggests that variation in the leaving group, displaying differing departure rate, has no significant contribution in denaturing prosperities of the Pt(IV) complexes against HSA. </Abstract>
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			<Param Name="value">Platinum (IV) complexes</Param>
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			<Object Type="keyword">
			<Param Name="value">Spectroscopic studies</Param>
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			<Object Type="keyword">
			<Param Name="value">Molecular docking simulation</Param>
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<ArchiveCopySource DocType="pdf">https://mbrc.shirazu.ac.ir/article_3165_ecc2d55b361bb567ec45b604cd1fd6ba.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Shiraz University Press</PublisherName>
				<JournalTitle>Molecular Biology Research Communications</JournalTitle>
				<Issn>2322-181X</Issn>
				<Volume>4</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Expression of growth hormone gene during early development of Siberian sturgeon (Acipenser baerii)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>181</FirstPage>
			<LastPage>188</LastPage>
			<ELocationID EIdType="pii">3166</ELocationID>
			
<ELocationID EIdType="doi">10.22099/mbrc.2015.3166</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Zeinab</FirstName>
					<LastName>Abdolahnejad</LastName>
<Affiliation>Fisheries Department, Faculty of Natural Resources, University of Guilan, Sowmeh Sara-Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Pourkazemi</LastName>
<Affiliation>Iran Fishery Research Organization (IFRO), Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Majid Reza</FirstName>
					<LastName>Khoshkholgh</LastName>
<Affiliation>Fisheries Department, Faculty of Natural Resources, University of Guilan, Sowmeh Sara-Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Mahtab</FirstName>
					<LastName>Yarmohammadi</LastName>
<Affiliation>International Sturgeon Research Institute, Rasht-Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>05</Month>
					<Day>27</Day>
				</PubDate>
			</History>
		<Abstract>The mRNA expression of growth hormone (&lt;em&gt;GH&lt;/em&gt;) gene in early development stages of Siberian sturgeon was investigated using RT-PCR method. Samples were collected from unfertilized eggs up to 50 days post hatched (dph) larvae in 11 different times. Ribosomal protein L6 (RPL6) transcripts were used as the internal standard during quantification of &lt;em&gt;GH &lt;/em&gt;mRNA expression. The results showed that the &lt;em&gt;GH&lt;/em&gt; mRNA could be observed in the eyed eggs and even at unfertilized eggs of Siberian sturgeon. The highest amounts of &lt;em&gt;GH &lt;/em&gt;mRNA were found at 25 and 50 dph larvae, while the lowest levels were detected at 1 and 3 dph larvae stage. These findings suggest that, the &lt;em&gt;GH&lt;/em&gt; mRNA play a key role during developmental stages of Siberian sturgeon. </Abstract>
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			<Object Type="keyword">
			<Param Name="value">Growth hormone</Param>
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			<Object Type="keyword">
			<Param Name="value">mRNA expression</Param>
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			<Object Type="keyword">
			<Param Name="value">RT-PCR</Param>
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<ArchiveCopySource DocType="pdf">https://mbrc.shirazu.ac.ir/article_3166_004ad7f4d0e422dda0d9ed4b9d3af5a1.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Shiraz University Press</PublisherName>
				<JournalTitle>Molecular Biology Research Communications</JournalTitle>
				<Issn>2322-181X</Issn>
				<Volume>4</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Molecular systematics and distribution review of the endemic cyprinid species, Persian chub, Acanthobrama persidis (Coad, 1981) in Southern Iran (Teleostei: Cyprinidae)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>189</FirstPage>
			<LastPage>206</LastPage>
			<ELocationID EIdType="pii">3173</ELocationID>
			
<ELocationID EIdType="doi">10.22099/mbrc.2015.3173</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Azad</FirstName>
					<LastName>Teimori</LastName>
<Affiliation>Kerman University</Affiliation>

</Author>
<Author>
					<FirstName>Hamid Reza</FirstName>
					<LastName>Esmaeili</LastName>
<Affiliation>Department of Biology,
College of Sciences, 
Shiraz  University</Affiliation>

</Author>
<Author>
					<FirstName>Golnaz</FirstName>
					<LastName>Sayyadzadeh</LastName>
<Affiliation>Shiraz University</Affiliation>

</Author>
<Author>
					<FirstName>Neda</FirstName>
					<LastName>Zarei</LastName>
<Affiliation>Shiraz University</Affiliation>

</Author>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Gholamhosseini</LastName>
<Affiliation>Shiraz University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>05</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>The Iranian Persian chub is an endemic species of the family Cyprinidae known only from few localities in drainages of Southern Iran. It was originally described in the genus &lt;em&gt;Pseudophoxinus&lt;/em&gt; as (&lt;em&gt;Pseudophoxinus persidis&lt;/em&gt;) and then &lt;em&gt;Petroleuciscus&lt;/em&gt; (as &lt;em&gt;Petroleuciscus persidis&lt;/em&gt;). In this study, we examined phylogenetic relationships of the Iranian Persian chubwith other relatives in the family Cyprinidae based on the mitochondrial cytochrome b gene to estimate the phylogenetic (and taxonomic) position of the species. Our molecular phylogenies show that new fish sequences from the drainages in southern Iran are clustered with sequences of the genus &lt;em&gt;Acanthobrama&lt;/em&gt; from GenBank while the sequences from two other genera (&lt;em&gt;Pseudophoxinus&lt;/em&gt; and &lt;em&gt;Petroleuciscus&lt;/em&gt;) are in distinct clade. Therefore, we conclude that the populations of Persian Chub in drainages of southern Iran (i.e., Kol, Kor, Maharlu and Persis) belong to the genus &lt;em&gt;Acanthobrama &lt;/em&gt;andspecies&lt;em&gt; Acanthobrama persidis. &lt;/em&gt;The predicted geographic distributions for the species showed a large area of suitable climate for &lt;em&gt;A. persidis&lt;/em&gt; across south and west of Iran especially in the Kor River basin. Some other parts in the Persis and Tigris are also might have been suitable habitats for this cyprinid species showing possible dispersal route of &lt;em&gt;Acanthobrama&lt;/em&gt; from Tigris to the Persis, Kor and Kol basins.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Pseudophoxinus</Param>
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			<Param Name="value">Petroleuciscus</Param>
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			<Object Type="keyword">
			<Param Name="value">Iranian drainages</Param>
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<ArchiveCopySource DocType="pdf">https://mbrc.shirazu.ac.ir/article_3173_0a41e187c5794418cbd45cd917a5fb43.pdf</ArchiveCopySource>
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<Article>
<Journal>
				<PublisherName>Shiraz University Press</PublisherName>
				<JournalTitle>Molecular Biology Research Communications</JournalTitle>
				<Issn>2322-181X</Issn>
				<Volume>4</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Description of a myxozoan parasite Myxobolus sp.n PKB2014 from an edible fish, with emphasis on its molecular characterization</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>207</FirstPage>
			<LastPage>216</LastPage>
			<ELocationID EIdType="pii">3179</ELocationID>
			
<ELocationID EIdType="doi">10.22099/mbrc.2015.3179</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Somerita</FirstName>
					<LastName>Panda</LastName>
<Affiliation>University of Kalyani</Affiliation>

</Author>
<Author>
					<FirstName>Subarna</FirstName>
					<LastName>Ghosh</LastName>
<Affiliation>University of Kalyani</Affiliation>

</Author>
<Author>
					<FirstName>Probir Kumar</FirstName>
					<LastName>Bandyopadhyay</LastName>
<Affiliation>UNIVERSITY OF KALYANI</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>02</Month>
					<Day>18</Day>
				</PubDate>
			</History>
		<Abstract>In India, more than 104 species of &lt;em&gt;Myxobolus&lt;/em&gt; have so far been reported infecting freshwater as well as marine fishes. The study focuses on the description of a new myxosporean species, &lt;em&gt;Myxobolus&lt;/em&gt; sp.n PKB 2014 from the gill lamellae of an Indian major carp &lt;em&gt;Labeo rohita.&lt;/em&gt; The species have been described on the basis of morphological characterization of the spores, tissue architecture and 18S rDNA sequence data. The plasmodia of &lt;em&gt;Myxobolus&lt;/em&gt; sp.n PKB 2014 were round in shape measuring, 50 to 70 μm in diameter and spores were ellipsoidal in frontal view measures 14.7 ± 0.51 μm. The 18S rRNA nucleotide sequence with 806 bp of &lt;em&gt;Myxobolus&lt;/em&gt; sp.n PKB 2014 (Accession number   KJ652226) clustered phylogenitically with other &lt;em&gt;Myxobolus&lt;/em&gt; spp. infecting cyprinid gills with 90-99% similarity. According to the phylogenetic study we concluded that &lt;em&gt;M. wulli&lt;/em&gt; was the closest relative having 99% similarity with the species under description but the sequence was distinct in each species which additionally exhibited different morphological features. The infection rate was low to moderate. After through comparison it can be concluded that the species being described here is new to science which is designated as &lt;em&gt;Myxobolus&lt;/em&gt; sp.n.PKB 2014. </Abstract>
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			<Param Name="value">Myxobolus sp.n PKB2014</Param>
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			<Object Type="keyword">
			<Param Name="value">West Bengal</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Labeo rohita</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">18S rRNA</Param>
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			<Object Type="keyword">
			<Param Name="value">Phylogenetic relationship</Param>
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<ArchiveCopySource DocType="pdf">https://mbrc.shirazu.ac.ir/article_3179_028448edd3b98239227dfaa8daaa6332.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Shiraz University Press</PublisherName>
				<JournalTitle>Molecular Biology Research Communications</JournalTitle>
				<Issn>2322-181X</Issn>
				<Volume>4</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Promoter hypermethylation of KLOTHO; an anti-senescence related gene in colorectal cancer patients of Kashmir valley</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>217</FirstPage>
			<LastPage>224</LastPage>
			<ELocationID EIdType="pii">3231</ELocationID>
			
<ELocationID EIdType="doi">10.22099/mbrc.2015.3231</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Perveez</FirstName>
					<LastName>Malik</LastName>
<Affiliation>Department of General and Minimal Access Surgery, SKIMS Srinagar, India</Affiliation>

</Author>
<Author>
					<FirstName>Ajaz</FirstName>
					<LastName>Malik</LastName>
<Affiliation>Department of General and Minimal Access Surgery, SKIMS Srinagar, India</Affiliation>

</Author>
<Author>
					<FirstName>Dil</FirstName>
					<LastName>Afroze</LastName>
<Affiliation>Department of Immunology and Molecular Medicine, SKIMS Srinagar, India</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>07</Month>
					<Day>30</Day>
				</PubDate>
			</History>
		<Abstract>Hypermethylation of CpG islands located in the promoter regions of genes is a major event in the development of the majority of cancer types, due to the subsequent aberrant silencing of important tumor suppressor genes. &lt;em&gt;KLOTHO&lt;/em&gt;; a novel gene associated primarily with suppressing senescence has been shown to contribute to tumorigenesis as a result of its impaired function. Recently the relevance of &lt;em&gt;KLOTHO &lt;/em&gt;promoter hypermethylation in colorectal carcinoma in humans has been reported. We analyzed the promoter hypermethylation of &lt;em&gt;KLOTHO&lt;/em&gt; gene in 50 histopathologically confirmed tumor and adjacent normal tissues of colorectal cancer patients. Methylation was assessed by bisulfite conversion of DNA followed by methylation specific-polymerase chain reaction. Methylation status was compared with gender, smoking status and histopathological parameters of patients. Promoter hypermethylation in &lt;em&gt;KLOTHO&lt;/em&gt; gene was detected in 86% (43/50) of tumor tissues and 14% (7/50) of adjacent normal tissues. The methylation pattern differed significantly between tumor and adjacent normal tissues (&lt;em&gt;P&lt;/em&gt;&lt;0.0001). However, no association was found between promoter hypermethylation status and gender (&lt;em&gt;P&lt;/em&gt;=0.68), smoking status (&lt;em&gt;P&lt;/em&gt;=0.64) or other histopathological parameters (&lt;em&gt;P&gt;&lt;/em&gt;0.05) of colorectal cancer patients. We conclude that this novel tumor suppressor gene is epigenetically inactivated in colorectal cancer in our population paving way towards the potential of &lt;em&gt;KLOTHO&lt;/em&gt; promoter hypermethylation as a predictor of the prognosis in colorectal cancer patients.</Abstract>
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			<Param Name="value">KLOTHO</Param>
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			<Object Type="keyword">
			<Param Name="value">Promoter hypermethylation</Param>
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			<Object Type="keyword">
			<Param Name="value">Colorectal cancer</Param>
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			<Object Type="keyword">
			<Param Name="value">Tumor suppressor</Param>
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<ArchiveCopySource DocType="pdf">https://mbrc.shirazu.ac.ir/article_3231_a7a392e08e513e577af96cfd9b8706b6.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Shiraz University Press</PublisherName>
				<JournalTitle>Molecular Biology Research Communications</JournalTitle>
				<Issn>2322-181X</Issn>
				<Volume>4</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Genetic variation in the narrow-clawed crayfish (Astacus leptodactylus) populations as assessed by PCR-RFLP of mitochondrial COI gene</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>225</FirstPage>
			<LastPage>237</LastPage>
			<ELocationID EIdType="pii">3265</ELocationID>
			
<ELocationID EIdType="doi">10.22099/mbrc.2015.3265</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Majidreza</FirstName>
					<LastName>Khoshkholgh</LastName>
<Affiliation>Department of Fisheries, Faculty of Natural Resources, University of Guilan, Sowmehsara, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sajad</FirstName>
					<LastName>Nazari</LastName>
<Affiliation>Genetic and Breeding Research Center for Coldwater Fishes, Yasouj, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>04</Month>
					<Day>27</Day>
				</PubDate>
			</History>
		<Abstract>The genetic variation and population structure of narrow-clawed crayfish (&lt;em&gt;Astacus leptodactylus&lt;/em&gt;) was examined by means of polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP) analysis of the cytochrome oxidase subunit I (&lt;em&gt;COI&lt;/em&gt;) of mitochondrial DNA. A total of 194 adult specimens were collected from seven sample sites including, two in the south Caspian Sea and one each in Anzali wetland and Aras reservoir and three rivers Chafrood, Masule Rudkhan and Siah Darvishan. The PCR products were digested with 19 restriction enzymes and five enzymes revealed polymorphism patterns (&lt;em&gt;Dde&lt;/em&gt;І, &lt;em&gt;Mbo&lt;/em&gt;І, &lt;em&gt;Taq&lt;/em&gt;I, &lt;em&gt;Rsa&lt;/em&gt;І and &lt;em&gt;Hinf&lt;/em&gt;І). Twenty eight composite haplotypes were showed with the number of haplotypes in each population sample ranging from 8 to 13. Private haplotypes were found at very low frequencies. Two regional (Siah Darvishan River and Astara) groups were clearly recognized by cluster and molecular variance model (AMOVA) analyses (&lt;em&gt;P&lt;/em&gt;&lt;0.0001). Each of these groups revealed dominant haplotypes while these haplotypes play less important rule in population structures of the other geographic areas. Intrapopulation haplotype (&lt;em&gt;h&lt;/em&gt;) and nucleotide (&lt;em&gt;π&lt;/em&gt;) diversities were high for each locality, ranging &lt;em&gt;h&lt;/em&gt;=0.7560±0.030 and &lt;em&gt;π=&lt;/em&gt; 0.00334±0.00301, respectively. Results of this study discerned two genetically divergent populations of narrow-clawed crayfish including Siah Darvishan River and Astara. Thus, the population structure of the narrow-clawed crayfish, as inferred from mtDNA analysis, is constituted by genetically separate groups that nearly reflect their geographic distribution.</Abstract>
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			<Param Name="value">Astacus leptodactylus</Param>
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			<Param Name="value">Mitochondrial DNA</Param>
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			<Param Name="value">PCR-RFLP</Param>
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			<Param Name="value">Genetic diversity</Param>
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<ArchiveCopySource DocType="pdf">https://mbrc.shirazu.ac.ir/article_3265_a1ac3058a017448170346f7a3395ffb2.pdf</ArchiveCopySource>
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