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      <title>Huntington&#39;s Disease  by BIO100</title>
      <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6</link>
      <description></description>
      <language>en-us</language>
      <pubDate>2023-09-30 19:09:16 UTC</pubDate>
      <lastBuildDate>2023-10-12 15:56:26 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Mutation of DNA sequencing </title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727095483</link>
         <description><![CDATA[<div>Huntington disease is caused by a mutation in the gene for a protein called huntingtin. This defect causes the DNA amino acids cytosine, adenine, an guanine to abnormally repeat, causing an expanded hHtt protein. Most people have fewer than 27 CAG repeats in their HD gene, so they are not at risk for the disease (NIH).</div>]]></description>
         <enclosure url="https://www.fcneurology.net/wp-content/uploads/2022/07/huntingtons-disease-diagram.jpg" />
         <pubDate>2023-09-30 19:23:43 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727095483</guid>
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      <item>
         <title>Autosomal dominance</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727098256</link>
         <description><![CDATA[<div>HD is an autosomal dominant disorder, which means one you need one copy of the non typical gene to be inherited. Each child has a 50% chance of inheriting a copy of chromosome 4 that carries the HD mutation (Mayo).</div>]]></description>
         <enclosure url="https://www.mayoclinic.org/-/media/kcms/gbs/patient-consumer/images/2013/11/15/17/37/r7_autosomaldominantthu_jpg.jpg" />
         <pubDate>2023-09-30 19:29:57 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727098256</guid>
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      <item>
         <title>Source</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727102075</link>
         <description><![CDATA[<div><br><br></div>]]></description>
         <enclosure url="https://www.ninds.nih.gov/health-information/disorders/huntingtons-disease" />
         <pubDate>2023-09-30 19:39:18 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727102075</guid>
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      <item>
         <title>Source</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727102302</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.mayoclinic.org/diseases-conditions/huntingtons-disease/symptoms-causes/syc-20356117" />
         <pubDate>2023-09-30 19:39:50 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727102302</guid>
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      <item>
         <title>Frequency</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727104203</link>
         <description><![CDATA[<div>Huntington disease affects an estimated <strong>3 to 7 per 100,000 people of European ancestry</strong>. The disorder appears to be less common in some other populations, including people of Japanese, Chinese, and African descent (MedlinePlus). </div>]]></description>
         <enclosure url="https://huntingtonstudygroup.org/wp-content/uploads/2015/08/hd-prevalence-map.png" />
         <pubDate>2023-09-30 19:44:28 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727104203</guid>
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      <item>
         <title>Source</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727104580</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://medlineplus.gov/genetics/condition/huntington-disease/" />
         <pubDate>2023-09-30 19:45:31 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727104580</guid>
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      <item>
         <title>Temporary Treatment</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727108985</link>
         <description><![CDATA[<div>There is currently no cure for Huntington's Disease. However, there are treatments to alleviate symptoms such as:</div><ul><li>Medications to lessen the mental and physical effects of the disease like anti psychotics to control hallucinations, delusions, and violent outbursts.</li><li>Therapy for depression and anxiety.</li><li>Physical therapies to help movement problems.</li></ul><div><br></div><div><br></div>]]></description>
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         <pubDate>2023-09-30 19:56:07 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2727108985</guid>
      </item>
      <item>
         <title>Method of Testing</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734483316</link>
         <description><![CDATA[<div>The most effective and accurate method of testing for Huntington disease—called the <strong>direct genetic test</strong>—counts the number of CAG repeats in the Huntington gene, using DNA taken from a blood sample. The presence of 36 or more repeats supports a diagnosis of Huntington disease . A test result of 26 or fewer repeats rules out Huntington's Disease (NIH) .&nbsp;<br>&nbsp; &nbsp; &nbsp; Testing for Huntington disease informs the family if they are at risk of developing it later on in life. However, many choose to not know until symptoms appear.&nbsp;</div>]]></description>
         <enclosure url="https://web.stanford.edu/group/hopes/cgi-bin/hopes_test/sites/hopes/files/f_s03repeats.jpg" />
         <pubDate>2023-10-05 19:11:36 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734483316</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734485652</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://huntingtonstudygroup.org/hd-insights/how-many-people-have-huntington-disease/" />
         <pubDate>2023-10-05 19:13:39 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734485652</guid>
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      <item>
         <title>Mechanism of Pathogenesis and Recent Developments in Its Therapeutic Strategies</title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734498837</link>
         <description><![CDATA[<div>It was first hypothesized that Huntington disease is caused by a misfolded huntingtin protein interrupting the neurological functioning of the brain due to a amplification of adenosine-guanine chain in the huntingtin's amino terminal end. However. studies have recently shown that opposed to this first believed hypothesis, that change in the mRNA of the protein gives rise to misfolded protein and the fragments accumulate, by making interaction with the other elements in cells resulting in the problems associated with HD. This experiment highlights the possible cause, pathogenesis, and therapy treatments that can reduce and down-regulate the expression of huntingtin, lowering the aggregation of the huntingtin protein.</div>]]></description>
         <enclosure url="https://www.researchgate.net/profile/Ozoemena-Eje/publication/370902657_29_Journal_of_Chemical_Reviews_Article_info_Journal_of_Chemical_Reviews/links/6469dde8c9802f2f72ee9e4d/29-Journal-of-Chemical-Reviews-Article-info-Journal-of-Chemical-Reviews.pdf" />
         <pubDate>2023-10-05 19:26:26 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734498837</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734500542</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://youtu.be/X89AjFBpmu0?si=LTDm62onmDL1Ncj5" />
         <pubDate>2023-10-05 19:28:10 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734500542</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734504149</link>
         <description><![CDATA[<div>RNA-targeting CRISPR–Cas13d system has shown to improve motor coordination, attenuated striatal atrophy, and reduction of mutant HTT protein aggregates in patients with no adverse effects and minimal off-target transcriptomic effects.  Demonstrating a therapeutic approach for HD, and a strategy with implications for the treatment of other dominantly inherited disorders.&nbsp;</div>]]></description>
         <enclosure url="https://www.nature.com/articles/s41593-022-01207-1" />
         <pubDate>2023-10-05 19:31:54 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734504149</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734505268</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.alz.org/alzheimers-dementia/what-is-dementia/types-of-dementia/huntington-s-disease" />
         <pubDate>2023-10-05 19:33:05 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734505268</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734505645</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://youtu.be/ej7-OhSb4H0?si=k8jBtc5cWKx6_aUZ" />
         <pubDate>2023-10-05 19:33:29 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2734505645</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2743875437</link>
         <description><![CDATA[<div>Huntington's disease is a condition that damages nerve cells in the brain causing them to stop proper functioning. This incapacitates patients by affecting their ability to move, think, and behave normally. </div>]]></description>
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         <pubDate>2023-10-12 15:52:35 UTC</pubDate>
         <guid>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2743875437</guid>
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      <item>
         <title></title>
         <author>BIO100NS</author>
         <link>https://padlet.com/BIO100NS/tgdarm3rc3kt4ru6/wish/2743880852</link>
         <description><![CDATA[<div>Due to lack of community knowledge on Huntington's disease, suffers of the disease may experience discrimination, ignorance, and social isolation. Leading to depression, anxiety, and an overall degradation of life. </div>]]></description>
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         <pubDate>2023-10-12 15:56:13 UTC</pubDate>
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