Lowe syndrome protein Ocrl1 is translocated to membrane ruffles upon Rac GTPase activation: a new perspective on Lowe syndrome pathophysiology

By Faucherre Adèle  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1441-1448

Oxford University Press

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Lowe syndrome protein OCRL1 interacts with Rac GTPase in the trans-Golgi network

By Faucherre A.  

Human Molecular Genetics, Vol. 12, Iss. 19, 2003-10 ,pp. : 2449-2456

Oxford University Press

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Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase

By Coon Brian G.   Mukherjee Debarati   Hanna Claudia B.   Riese David J.   Lowe Martin   Aguilar R. Claudio  

Human Molecular Genetics, Vol. 18, Iss. 23, 2009-12 ,pp. : 4478-4491

Oxford University Press

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Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia

By Ward Christopher J.  

Human Molecular Genetics, Vol. 12, Iss. 20, 2003-10 ,pp. : 2703-2710

Oxford University Press

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The Meckel syndrome protein meckelin ( TMEM67 ) is a key regulator of cilia function but is not required for tissue planar polarity

By Leightner Amanda C.   Hommerding Cynthia J.   Peng Ying   Salisbury Jeffrey L.   Gainullin Vladimir G.   Czarnecki Peter G.   Sussman Caroline R.   Harris Peter C.  

Human Molecular Genetics, Vol. 22, Iss. 10, 2013-05 ,pp. : 2024-2040

Oxford University Press

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