<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Projects | Ayesha Aiman</title><link>https://ayeshaaiman.netlify.app/project/</link><atom:link href="https://ayeshaaiman.netlify.app/project/index.xml" rel="self" type="application/rss+xml"/><description>Projects</description><generator>Wowchemy (https://wowchemy.com)</generator><language>en-us</language><lastBuildDate>Sun, 28 Aug 2022 00:00:00 +0000</lastBuildDate><image><url>https://ayeshaaiman.netlify.app/media/icon_hu526bd703046e832ca61acfebb737825a_5312_512x512_fill_lanczos_center_3.png</url><title>Projects</title><link>https://ayeshaaiman.netlify.app/project/</link></image><item><title>Research Interest</title><link>https://ayeshaaiman.netlify.app/project/1.research_interests/</link><pubDate>Sat, 27 Aug 2022 00:00:00 +0000</pubDate><guid>https://ayeshaaiman.netlify.app/project/1.research_interests/</guid><description>&lt;!--
Multiple sclerosis (MS) is a metabolically dependent neurodegenerative disorder caused by persistent axonal loss of the brain and spinal cord. It is the most prevalent cause of non-traumatic neurological disability among young adults, especially females, in Western countries. DMTs and cost-effective pharmacotherapies can help patients address their condition by lowering their risk of relapse, postponing disability, and/or having fewer Magnetic resonance imaging (MRI) lesion loads. Interferon is one of the first-line therapies to treat MS patients in India. This project addresses the desire for developing novel therapeutic regimens and their essential role in improving patients’ health. --></description></item><item><title>Characterization of recombinant IFN β-1b and elucidation of its role as a therapy/regimen against Multiple Sclerosis</title><link>https://ayeshaaiman.netlify.app/project/2.phd_research/</link><pubDate>Sun, 28 Aug 2022 00:00:00 +0000</pubDate><guid>https://ayeshaaiman.netlify.app/project/2.phd_research/</guid><description>&lt;p>Multiple sclerosis (MS) is a metabolically dependent neurodegenerative disorder caused by persistent axonal loss of the brain and spinal cord. It is the most prevalent cause of non-traumatic neurological disability among young adults, especially females, in Western countries. DMTs and cost-effective pharmacotherapies can help patients address their condition by lowering their risk of relapse, postponing disability, and/or having fewer brain lesion loads. Interferon is one of the first-line therapies to treat MS patients in India. This project addresses the desire for developing novel therapeutic regimens and their essential role in improving patients’ health.&lt;/p></description></item></channel></rss>