Hannah Itell
@HannahItell
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Postdoc in the @IG_Lab at the Vanderbilt Vaccine Center // previously @davidsoncollege @mcbseattle @fredhutch
Nashville, TN
Joined October 2018
Extremely excited to share this new paper from my graduate work in the Overbaugh lab! @NatureMicrobiol @FredHutch @MCBSeattle
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@hirenj @NatureMicrobiol @fredhutch @MCBSeattle -- Since heparan sulfate hinders X4 binding, determining the exact stage that X4s are blocked (binding vs fusion since we narrowed it to entry here) could help inform this
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@MollyOhainle @NatureMicrobiol @fredhutch @MCBSeattle Thanks Molly!! Another exciting finding from HIV-CRISPR screens 😍
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@Gowda_24 @NatureMicrobiol @fredhutch @MCBSeattle -- so it isn't surprising that, as genetic diversity accumulates over the course of infection, X4 viruses emerge
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@Ella_Maru @NatureMicrobiol @fredhutch @MCBSeattle It is possible though that the glycosylation profile on target cells in different anatomical sites is different than that in the blood and initial infection sites – so as the virus spreads to different areas, the effect of host glycosylation on R5 vs X4 infection may vary
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RT @fredhutch: 40 years after the discovery of #HIV, a vaccine still eludes researchers because of the virus' complex biology. Researcher…
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RT @science_seattle: 🦠 @fredhutch researchers led by Dr. @HannahItell discover why some HIV-1 variants are more transmissible than others,…
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RT @NatureMicrobiol: Hot off the press 🔥 Host cell glycosylation selects for infection with CCR5- versus CXCR4-tropic HIV-1 Spearheaded b…
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