Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

By Errico A.   Ballabio A.   Rugarli E.I.  

Human Molecular Genetics, Vol. 11, Iss. 2, 2002-01 ,pp. : 153-163

Oxford University Press

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The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling

By Tsang Hilda T.H.   Edwards Thomas L.   Wang Xinnan   Connell James W.   Davies Rachel J.   Durrington Hannah J.   O'Kane Cahir J.   Luzio J. Paul   Reid Evan  

Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3805-3821

Oxford University Press

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Functional conservation of human Spastin in a Drosophila model of autosomal dominant-hereditary spastic paraplegia

By Du Fang   Ozdowski Emily F.   Kotowski Ingrid K.   Marchuk Douglas A.   Sherwood Nina Tang  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1883-1896

Oxford University Press

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Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

By Sanderson Christopher M.   Connell James W.   Bright Nicholas A.   Duley Simon   Thompson Amanda   Luzio J. Paul   Reid Evan  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 307-318

Oxford University Press

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CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

By van der Zee Julie   Urwin Hazel   Engelborghs Sebastiaan   Bruyland Marc   Vandenberghe Rik   Dermaut Bart   De Pooter Tim   Peeters Karin   Santens Patrick   De Deyn Peter P.   Fisher Elizabeth M.   Collinge John   Isaacs Adrian M.   Van Broeckhoven Christine  

Human Molecular Genetics, Vol. 17, Iss. 2, 2008-01 ,pp. : 313-322

Oxford University Press

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