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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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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Impaired neural development in a zebrafish model for Lowe syndrome

By Ramirez Irene Barinaga-Rementeria   Pietka Grzegorz   Jones David R.   Divecha Nullin   Alia A.   Baraban Scott C.   Hurlstone Adam F. L.   Lowe Martin  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1744-1759

Oxford University Press

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“Lowe syndrome: A particularly severe phenotype without clinical kidney involvement”

By  

American Journal Of Medical Genetics Part A, Vol. 176, Iss. 2, 2018-02 ,pp. : 460-464

John Wiley & Sons Inc

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