<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Journal of Clinical and Basic Research</title>
<title_fa>Journal of Clinical and Basic Research</title_fa>
<short_title>jcbr</short_title>
<subject>Medical Sciences</subject>
<web_url>http://jcbr.goums.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>2538-3736</journal_id_issn>
<journal_id_issn_online>2538-3736</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61186/jcbr</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>1405</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2026</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<volume>10</volume>
<number>1</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>Molecular insights into skin pigmentation: Unraveling the role of key genes and Mirnas in melanogenesis</title>
	<subject_fa></subject_fa>
	<subject>Genetics</subject>
	<content_type_fa>مروری</content_type_fa>
	<content_type>Review</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;span style=&quot;font-size:12px;&quot;&gt;&lt;span style=&quot;font-family:Times New Roman;&quot;&gt;&lt;b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;Background:&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt; Human skin pigmentation is a complex phenotype governed by an interplay of genetic, biochemical, and physiological factors. Melanogenesis involves tightly regulated enzymatic pathways that control the balance between eumelanin and pheomelanin synthesis, ultimately determining individual skin color and influencing susceptibility to pigmentation disorders and UV-related health outcomes.&lt;/span&gt;&lt;br&gt;
&lt;b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;Methods:&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt; An extensive literature review was conducted to construct a comprehensive molecular framework of skin pigmentation. Key genes involved in melanogenesis, including TYR, along with regulatory microRNAs (miRNAs), were systematically analyzed. Relevant studies addressing environmental influences&lt;/span&gt;&lt;span style=&quot;background:red&quot;&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;particularly ultraviolet (UV) exposure&lt;/span&gt;&lt;span style=&quot;background:red&quot;&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;and pigmentation disorders were also evaluated.&lt;/span&gt;&lt;br&gt;
&lt;b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;Results:&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt; This review elucidates the central roles of melanogenic genes and miRNAs in regulating pigment production and melanocyte function. Multiple miRNAs were identified as critical modulators of melanogenesis-related pathways. Furthermore, the molecular mechanisms underlying pigmentation disorders, including oculocutaneous albinism, were characterized. Environmental factors, especially UV radiation, were shown to exert significant effects on melanogenic signaling and skin color variation.&lt;/span&gt;&lt;br&gt;
&lt;b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;Conclusion&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;background-color:#ffffff;&quot;&gt;: Skin pigmentation is regulated through a multifaceted network of genetic, epigenetic, and environmental factors. By integrating current molecular insights, this review advances understanding of melanogenesis and associated disorders, providing a robust foundation for future research and potential therapeutic strategies targeting pigmentation-related conditions.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Pigmentation, Skin Color (Skin Pigmentation), Eumelanin (eumelanin [Supplementary Concept]), Melanogenesis, Molecular Pathway</keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://jcbr.goums.ac.ir/browse.php?a_code=A-10-127-12&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Fatemeh</first_name>
	<middle_name></middle_name>
	<last_name> Vaghefi </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>fatemeh_vqf@yahoo.com</email>
	<code>10031947532846006792</code>
	<orcid>0009-0000-1444-0953</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran; Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Farzaneh </first_name>
	<middle_name></middle_name>
	<last_name>Motallebi </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>farzanehh.motallebii@gmail.com</email>
	<code>10031947532846006791</code>
	<orcid>0009-0006-7228-8826</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran; Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Teymoor </first_name>
	<middle_name></middle_name>
	<last_name>Khosravi </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>tkhosravi1375@gmail.com</email>
	<code>10031947532846006793</code>
	<orcid>10031947532846006793</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran; Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Zainab </first_name>
	<middle_name></middle_name>
	<last_name>M. Al Sudani </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>zainabmohamedzm0@gmail.com</email>
	<code>10031947532846006794</code>
	<orcid>0009-0006-7947-4111</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran; Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohaddeseh </first_name>
	<middle_name></middle_name>
	<last_name>Mohsenipour </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>mhds.mohsenipour@gmail.com</email>
	<code>10031947532846006795</code>
	<orcid>0009-0004-5079-3288</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran; Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Arian </first_name>
	<middle_name></middle_name>
	<last_name>Rahimzadeh </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>arianrahimzadeh1380@gmail.com</email>
	<code>10031947532846006796</code>
	<orcid>0009-0001-3732-4012</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran; Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Morteza </first_name>
	<middle_name></middle_name>
	<last_name>Oladnabi </last_name>
	<suffix></suffix>
	<first_name_fa>مرتضی</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>اولادنبی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>oladnabidozin@yahoo.com</email>
	<code>10031947532846006797</code>
	<orcid>10031947532846006797</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Gorgan Congenital Malformations Research Center, Jorjani Clinical sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran; IranIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran; Department of Medical Genetics, School of Advanced Technologies in Medicine, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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