A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition

By Tarrade Anne   Fassier Coralie   Charvin Delphine   Vitte Jérémie   Peris Leticia   Thorel Alain   Mouisel Etienne   Fonknechten Nuria   Roblot Natacha   Seilhean Danielle   Diérich Andrée   Hauw Jean Jacques   Melki Judith  

Human Molecular Genetics, Vol. 15, Iss. 24, 2006-12 ,pp. : 3544-3558

Oxford University Press

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Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon

By Errico Alessia   Claudiani Pamela   D'Addio Marilena   Rugarli Elena I.  

Human Molecular Genetics, Vol. 13, Iss. 18, 2004-09 ,pp. : 2121-2132

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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Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth

By Lee Syann  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 627-637

Oxford University Press

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DISC1–NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1

By Kamiya Atsushi   Tomoda Toshifumi   Chang Jennifer   Takaki Manabu   Zhan Caixin   Morita Masahiko   Cascio Matthew B.   Elashvili Sarah   Koizumi Hiroyuki   Takanezawa Yasukazu   Dickerson Faith   Yolken Robert   Arai Hiroyuki   Sawa Akira  

Human Molecular Genetics, Vol. 15, Iss. 22, 2006-11 ,pp. : 3313-3323

Oxford University Press

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