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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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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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

By Fonknechten Nùria  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 637-644

Oxford University Press

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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

By Fonknechten Nùria   Mavel Delphine   Byrne Paula   Davoine Claire-Sophie   Cruaud Corinne   Bönsch Dominikus   Samson Delphine   Coutinho Paula   Hutchinson Michael   McMonagle Paul   Burgunder Jean-Marc   Tartaglione Antonio   Heinzlef Olivier   Feki Imed   Deufel Thomas   Parfrey Nollaig   Brice Alexis   Fontaine Bertrand   Prud'homme Jean-François   Weissenbach Jean   Dürr Alexandra   Hazan Jamilé  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 461-461

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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