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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The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B

By Reid Evan  

Human Molecular Genetics, Vol. 14, Iss. 1, 2005-01 ,pp. : 19-38

Oxford University Press

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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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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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Evaluation of loss of function as an explanation for SPG4 -based hereditary spastic paraplegia

By Solowska Joanna M.   Garbern James Y.   Baas Peter W.  

Human Molecular Genetics, Vol. 19, Iss. 14, 2010-07 ,pp. : 2767-2779

Oxford University Press

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