<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>International Journal of Medical Laboratory</title>
<title_fa>مجله بین المللی علوم آزمایشگاهی</title_fa>
<short_title>IJML</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ijml.ssu.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2423-3706</journal_id_issn>
<journal_id_issn_online>2423-3714</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi></journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1401</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2022</year>
	<month>11</month>
	<day>1</day>
</pubdate>
<volume>9</volume>
<number>4</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Mutational Screening in Exon 6 of the PSEN2 Gene in Iranian Patients with Late-Onset Alzheimer&#039;s Disease</title>
	<subject_fa>ژنتیک/ بیوتکنولوژی</subject_fa>
	<subject>Genetics/ Biotechnology</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;Background and Aims: &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;One of the most important genes involved in Alzheimer&amp;#39;s disease (AD) is the presenilin2 (&lt;i&gt;PSEN2&lt;/i&gt;) gene, which is one of the main constituents of the gamma-secretase complex. Mutations in this gene promote the formation of amyloid plaques resulting in AD. The study aimed to evaluate the mutation variant in exon 6 of the &lt;i&gt;PSEN2&lt;/i&gt; gene in patients with Late-Onset AD (LOAD). Due to the important role of the &lt;i&gt;PSEN2&lt;/i&gt; gene in the formation of beta-amyloid aggregates and the investigation involves an association between &lt;i&gt;PSEN2&lt;/i&gt; mutations and their pathogenicity in LOAD progression&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;, we presented this exon as a more efficient alternative.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;Materials and Methods:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt; The thirty patients with LOAD and 16 healthy subjects as a control group were involved in this experimental study. DNA was extracted from blood samples and purified. The desired gene fragment was propagated using polymerase chain reaction and the products were electrophoresed and the results were analyzed.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;Result:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt; A novel mutation was found in PSEN2 IVS6 + 30 G &amp;rarr; C at the intron region of exon 6 in 20 cases of patients suffering from LOAD and 12 subjects in control cohort. In this mutation a guanine base was substituted by cytosine base&lt;b&gt; &lt;/b&gt;which this position was 30 nucleotides separated from coding region.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt;Conclusions:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;letter-spacing:-.2pt&quot;&gt; The novel mutation was identified in both studied groups. These findings reveal no relationship between &lt;i&gt;PSEN2&lt;/i&gt; mutation and pathogenicity of LOAD disease. However, further studies are required to find the role of &lt;i&gt;PSEN2&lt;/i&gt; mutation in LOAD progression.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Alzheimer's disease, Exon6, Presenilin2 gene</keyword>
	<start_page>304</start_page>
	<end_page>310</end_page>
	<web_url>http://ijml.ssu.ac.ir/browse.php?a_code=A-10-392-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Seyed Ali</first_name>
	<middle_name></middle_name>
	<last_name>Salari</last_name>
	<suffix></suffix>
	<first_name_fa>سید علی</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>سالاری</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>salari2006@yahoo.com</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biology, Science and Arts University, Yazd, Iran</affiliation>
	<affiliation_fa>Department of Biology, Science and Arts University, Yazd, Iran</affiliation_fa>
	 </author>


	<author>
	<first_name>Seyed Mohsen</first_name>
	<middle_name></middle_name>
	<last_name>Miresmaeili</last_name>
	<suffix></suffix>
	<first_name_fa>سید محسن</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>میر اسماعیلی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>salari2006@yahoo.com</email>
	<code></code>
	<orcid>0000-0001-8623-2889</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Biology, Science and Arts University, Yazd, Iran</affiliation>
	<affiliation_fa>Department of Biology, Sciences and Arts University, Yazd, Iran</affiliation_fa>
	 </author>


	<author>
	<first_name>Mahta</first_name>
	<middle_name></middle_name>
	<last_name>Mazaheri Naeini </last_name>
	<suffix></suffix>
	<first_name_fa>مهتا</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>مظاهری</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>salari2006@yahoo.com</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Medical Genetics, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa>Department of Medical Genetics, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
