<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Edigene on Bioecon</title><link>https://en.bioecon.ru/companies/edigene/</link><description>Recent content in Edigene on Bioecon</description><generator>Hugo</generator><language>en-US</language><lastBuildDate>Sat, 11 Jul 2026 14:19:14 +0700</lastBuildDate><atom:link href="https://en.bioecon.ru/companies/edigene/index.xml" rel="self" type="application/rss+xml"/><item><title>Prime editing</title><link>https://en.bioecon.ru/technology/prime-editing/</link><pubDate>Fri, 26 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/prime-editing/</guid><description>Search-and-replace genome editing with a Cas9 nickase fused to a reverse transcriptase and an extended pegRNA — writing all 12 base substitutions and small indels without a double-strand break.</description></item><item><title>Genome editing</title><link>https://en.bioecon.ru/technology/genome-editing/</link><pubDate>Wed, 24 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/genome-editing/</guid><description>Programmable genome editors — CRISPR-Cas9, base editors and prime editors — delivered ex vivo or in vivo via lipid nanoparticles to treat genetic disease, from the first approved CRISPR therapy Casgevy to in-vivo redosable CRISPR and single-dose cardiovascular base editing.</description></item><item><title>Base editing</title><link>https://en.bioecon.ru/technology/base-editing/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/base-editing/</guid><description>Base editors (CBE/ABE) make single-nucleotide changes C·G→T·A and A·T→G·C without double-strand breaks — treating monogenic disease (sickle cell, beta-thalassemia) at up to 90% efficiency with no indels.</description></item><item><title>Personalized &amp; regenerative medicine</title><link>https://en.bioecon.ru/technology/personalized-regenerative-medicine/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/personalized-regenerative-medicine/</guid><description>Gene and cell therapy platforms for rare monogenic and oncological diseases: AAV vectors, lentiviral HSC editing, ex vivo CRISPR (Casgevy) and in vivo CRISPR (LNP delivery) now deliver durable one-time treatments approved by FDA and EMA.</description></item></channel></rss>