Senescent and Rejuvenated Mtb Subsets on Exit from Latency

Carl Nathan and Gang Lin of Weill Cornell Medical College will test their hypothesis that tuberculosis is able to exit latency by distributing damaged proteins to a senescent cell lineage, while more functional proteins are diverted to a lineage with full replication potential. Regulating this post-latency cell division could be the target of novel drug therapies.

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OPP1024387
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Funding Amount (in original currency)
100000.00
Funding Currency
USD
Funding Amount (in USD)
100000.00
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-
Funding Total (In US dollars)
100000.00
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False