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	<title>ADAMTS17 - Revision history</title>
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	<updated>2026-05-11T06:09:03Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=ADAMTS17&amp;diff=6496677&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2025-03-17T03:01:00Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 03:01, 17 March 2025&lt;/td&gt;
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		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=ADAMTS17&amp;diff=6202378&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=ADAMTS17&amp;diff=6202378&amp;oldid=prev"/>
		<updated>2025-02-10T04:53:09Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 04:53, 10 February 2025&lt;/td&gt;
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		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=ADAMTS17&amp;diff=5378130&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=ADAMTS17&amp;diff=5378130&amp;oldid=prev"/>
		<updated>2024-03-09T21:25:35Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;ADAMTS17&amp;#039;&amp;#039;&amp;#039; is a protein that in humans is encoded by the &amp;#039;&amp;#039;&amp;#039;ADAMTS17&amp;#039;&amp;#039;&amp;#039; gene. ADAMTS17 belongs to the [[ADAMTS]] (a disintegrin and metalloproteinase with thrombospondin motifs) family of proteins. These proteins are known to have a wide range of functions, including the breakdown of [[extracellular matrix]], inhibition of [[angiogenesis]], and the control of [[organogenesis]].&lt;br /&gt;
&lt;br /&gt;
== Function ==&lt;br /&gt;
&lt;br /&gt;
ADAMTS17 is a member of the ADAMTS family of proteins. These proteins are secreted [[enzyme|enzymes]] that have a variety of biological functions. They are involved in the processing of [[procollagen]] molecules, the degradation of the extracellular matrix, and the inhibition of angiogenesis. ADAMTS17, like other members of the ADAMTS family, is believed to play a role in organogenesis and developmental processes.&lt;br /&gt;
&lt;br /&gt;
== Clinical significance ==&lt;br /&gt;
&lt;br /&gt;
Mutations in the ADAMTS17 gene have been associated with several medical conditions. These include [[Weill-Marchesani syndrome]], a rare genetic disorder characterized by short stature, brachydactyly, joint stiffness, and eye abnormalities. Mutations in ADAMTS17 have also been linked to primary open-angle [[glaucoma]], one of the leading causes of blindness worldwide.&lt;br /&gt;
&lt;br /&gt;
== See also ==&lt;br /&gt;
&lt;br /&gt;
* [[ADAMTS]]&lt;br /&gt;
* [[Weill-Marchesani syndrome]]&lt;br /&gt;
* [[Glaucoma]]&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
{{Reflist}}&lt;br /&gt;
&lt;br /&gt;
[[Category:ADAMTS]]&lt;br /&gt;
[[Category:Human proteins]]&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Medical genetics]]&lt;br /&gt;
[[Category:Ophthalmology]]&lt;br /&gt;
[[Category:Rheumatology]]&lt;br /&gt;
&lt;br /&gt;
{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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