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The human endogenous retrovirus K(HML-2) has a broad envelope-mediated cellular tropism and is prone to inhibition at a post-entry, pre-integration step
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We show that HERV-K(HML-2) has a broad cell and tissue tropism.

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We demonstrate that HERV-K(HML-2) has a broad species tropism.

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HERV-K(HML-2) does not use the receptors of MMTV and JSRV for entry.

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We identify a post-entry, pre-integration inhibition of HERV-K(HML-2).

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We identify early RT products in cells infected with HERV-K(HML-2).

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