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Depletion of BBSome Subunits Alters Receptor Endocytosis and Promotes EMT via TGF-β Signalling
Abstract Background: Ciliopathies are genetic disorders caused by defects in the structure or function of the cilia and their related structures. Bardet-Biedl syndrome (BBS) is a complex ciliopathy with varied symptoms, probably due to altered membrane receptor sig
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