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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The Lowe syndrome protein OCRL1 is involved in primary cilia assembly

By Coon Brian G.   Hernandez Victor   Madhivanan Kayalvizhi   Mukherjee Debarati   Hanna Claudia B.   Barinaga-Rementeria Ramirez Irene   Lowe Martin   Beales Philip L.   Aguilar R. Claudio  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1835-1847

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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Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans -Golgi Network

By Dierick Herman A.   Adam Ayla N.   Escara-Wilke June F.   Glover Thomas W.  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 409-416

Oxford University Press

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A C-terminal di-leucine is required for localization of the Menkes protein in the trans -Golgi network

By Petris M.J.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2063-2071

Oxford University Press

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