<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2020</year>
	    <month>>October-December</month>
	    <day></day>
    </pubdate>
    <volume>12</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_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>33014315</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Screening PAX9, MSX1 and WNT10A Mutations in 4 Iranian Families with Non-Syndromic Tooth Agenesis</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Background: Tooth agenesis is one of the most common developmental anomalies in human and the main reasons for its occurrence are still unknown. Mutations of several genes such as &lt;em&gt;PAX9&lt;/em&gt;, &lt;em&gt;MSX1&lt;/em&gt;, &lt;em&gt;AXIN2&lt;/em&gt;, &lt;em&gt;KDF1&lt;/em&gt; and &lt;em&gt;WNT10A&lt;/em&gt; have been reported which are associated with non-syndromic tooth agenesis. However, &lt;em&gt;PAX9&lt;/em&gt;, &lt;em&gt;MSX1&lt;/em&gt; and &lt;em&gt;WNT10A&lt;/em&gt; are commonly reported in the literature. Hence, the aim of this study was to investigate the mutations of these genes in 4 Iranian families with non-syndromic tooth agenesis.&lt;/p&gt;

&lt;p&gt;Methods: DNA extractions from peripheral blood cells of patients with non-syndromic tooth agenesis from 4 unrelated Iranian families were performed by salting out method, and the candidate genes were amplified then followed by Sanger sequencing method.&lt;/p&gt;

&lt;p&gt;Results: One missense variant (rs4904210) and 4 Single Nucleotide Polymorphisms (SNPs) (rs2236007, rs12883298, rs12882923 and rs12883049) were found in &lt;em&gt;PAX9&lt;/em&gt; gene. Five variants (rs149370601, rs8670, rs186861426 and rs774949973) including a missense variant (rs36059701) were detected in &lt;em&gt;MSX1&lt;/em&gt; gene and no variants were found in &lt;em&gt;WNT10A&lt;/em&gt; gene.&lt;/p&gt;

&lt;p&gt;Conclusion: All variants were analyzed based on bioinformatics websites and Iranian gene databases, and as a result, it was revealed that variants of &lt;em&gt;PAX9&lt;/em&gt;, &lt;em&gt;MSX1&lt;/em&gt; and &lt;em&gt;WNT10A&lt;/em&gt; may not play a role in non-syndromic tooth agenesis among Iranian cases.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Iran, MSX1, Mutation, PAX9, Tooth agenesis, WNT10A</keyword>
	<start_page>236</start_page>
	<end_page>240</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=30435</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/30435.pdf</pdf_url>
	<author_list><author><first_name>Shiva</first_name><middle_name></middle_name><last_name>Safari</last_name><suffix></suffix><affiliation>, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>51633</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Asghar</first_name><middle_name></middle_name><last_name>Ebadifar</last_name><suffix></suffix><affiliation>Department of Orthodontic,     Faculty of Dentistry, Shahid Behehsti University of Medical Sciences, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>891</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hossien</first_name><middle_name></middle_name><last_name>Najmabadi</last_name><suffix></suffix><affiliation>Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>51634</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Koorosh</first_name><middle_name></middle_name><last_name>Kamali</last_name><suffix></suffix><affiliation>Department of Public Health, Faculty of Public Health, Zanjan University of Medical Sciences, Zanjan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>89</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Seyedeh Sedigheh</first_name><middle_name></middle_name><last_name>Abedini</last_name><suffix></suffix><affiliation>Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>51635</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

