<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian journal of Pediatric Hematology and Oncology</title>
<title_fa>Iranian journal of Pediatric Hematology and Oncology</title_fa>
<short_title>Iran J Ped Hematol Oncol</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ijpho.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>2008-8892</journal_id_issn>
<journal_id_issn_online>2228-6993</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>7</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1398</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>10</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>Evaluation expression of HOXB1 gene in myeloid leukemia using Real Time PCR assay</title_fa>
	<title>The Relationship between Mutation in HOXB1 Gene and Acute Myeloid Leukemia</title>
	<subject_fa>قلب</subject_fa>
	<subject>Heart</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div&gt;&lt;strong&gt;Background: &lt;/strong&gt;HOX genes are an exceedingly preserved family of homeodomain-involving transcription factors. They are related to a number of malignancies, comprising acute myeloid leukemia (AML). This study aimed to evaluate the effect of &lt;em&gt;HOXB1&lt;/em&gt; 7bp deletion mutation on &lt;em&gt;HOXB1&lt;/em&gt;gene expression in 36 individuals.&lt;br&gt;
&lt;strong&gt;Materials and Methods: &lt;/strong&gt;The present cross-sectional study was done on a large Iranian family. In this experimental study, 5 homozygous 7bp deletion individuals along with their unaffected siblings and their parents were investigated. The candidate gene, &lt;em&gt;HOXB1&lt;/em&gt; was screened and analyzed in blood samples of these participants. After RNA extraction, cDNA was synthesized according to manufacturer&amp;rsquo;s protocol. &lt;em&gt;HOXB1 &lt;/em&gt;expression level was analyzed by 2&amp;Delta;&amp;Delta;CT method. All laboratory procedures used in this experimental study were carried out in genetic laboratory of Shahid Sadoughi University of Medical Sciences.&lt;br&gt;
&lt;strong&gt;Results: &lt;/strong&gt;Sequence analysis of &lt;em&gt;HOXB1&lt;/em&gt; gene by ABI Prism 3130 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA) revealed a family with 5 homozygous (22&amp;plusmn;17 years) and 22 healthy heterozygous carriers (42&amp;plusmn;19 years) for 7bp deletion in &lt;em&gt;HOXB1&lt;/em&gt; gene along with 9&amp;nbsp; healthy wild type (55&amp;plusmn;41 years). Gene expression analysis by RT-qPCR demonstrated that expression level of &lt;em&gt;HOXB1&lt;/em&gt; gene in wild type and heterozygous carriers specimens had similar levels (p=0.05).&lt;br&gt;
&lt;strong&gt;Conclusion: &lt;/strong&gt;Although &lt;em&gt;HOXB1&lt;/em&gt; mutations has been reported in AML, but association between &lt;em&gt;HOXB1&lt;/em&gt; mutation and AML was not found in our study. Additionally, &lt;em&gt;HOXB1&lt;/em&gt; expression levels showed no significant difference between wild type and heterozygous carriers. So, &lt;em&gt;HOXB1&lt;/em&gt; gene expression cannot provide a powerful tool to differentiate wild type from heterozygous carries.&lt;/div&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Acute Myeloid Leukemia, Gene expression, HOXB1 </keyword>
	<start_page>229</start_page>
	<end_page>235</end_page>
	<web_url>http://ijpho.ssu.ac.ir/browse.php?a_code=A-10-675-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Mohammad yahya</first_name>
	<middle_name></middle_name>
	<last_name>Vahidi mehrjardi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mmvahidi@gmail.com</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Genetic, ShahidSadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seyed Mohsen </first_name>
	<middle_name></middle_name>
	<last_name>Aghaei Zarch </last_name>
	<suffix></suffix>
	<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></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Genetic, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammadreza</first_name>
	<middle_name></middle_name>
	<last_name>Dehghani</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>dehghani.dr@gmail.com</email>
	<code></code>
	<orcid>0000-0001-5134-9438</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Medical Genetics Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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