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Journal of neurochemistry, ISSN 0022-3042, 07/2009, Volume 110, Issue 1, pp. 34 - 44
axonal transport | spastin | hereditary spastic paraplegia | mouse model | axonal spheroid | Hereditary spastic paraplegia | Axonal spheroid | Mouse model | Spastin | Axonal transport | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Cerebrospinal fluid. Meninges. Spinal cord | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Nervous system (semeiology, syndromes) | Spastic Paraplegia, Hereditary - genetics | Axonal Transport - genetics | Spinal Cord - metabolism | Wallerian Degeneration - pathology | Humans | Spastic Paraplegia, Hereditary - metabolism | Mice, Neurologic Mutants | Motor Neurons - pathology | Microtubules - metabolism | Spinal Cord - pathology | Lameness, Animal - metabolism | Amyloid beta-Protein Precursor - metabolism | Spastic Paraplegia, Hereditary - physiopathology | Disease Models, Animal | Wallerian Degeneration - genetics | Genetic Predisposition to Disease - genetics | Wallerian Degeneration - metabolism | Cells, Cultured | Axons - metabolism | Lameness, Animal - pathology | Mitochondria - metabolism | Microtubules - pathology | Mutation - genetics | Down-Regulation - genetics | Motor Neurons - metabolism | Animals | Microtubules - genetics | Axons - pathology | Adenosine Triphosphatases - genetics | Mice | Spinal Cord - physiopathology | Lameness, Animal - genetics | Heat shock proteins | Mitochondrial DNA | Cytoskeletal proteins | Analysis | Paralysis, Spastic | Amyloid beta-protein | Biochemistry | Genetic disorders | Mutation | Paralysis | Index Medicus
Journal Article
Annual review of neuroscience, ISSN 0147-006X, 2008, Volume 31, Issue 1, pp. 151 - 173
Journal Article
by Pilkington, Sarah M and Crowhurst, Ross and Hilario, Elena and Nardozza, Simona and Fraser, Lena and Peng, Yongyan and Gunaseelan, Kularajathevan and Simpson, Robert and Tahir, Jibran and Deroles, Simon C and Templeton, Kerry and Luo, Zhiwei and Davy, Marcus and Cheng, Canhong and McNeilage, Mark and Scaglione, Davide and Liu, Yifei and Zhang, Qiong and Datson, Paul and De Silva, Nihal and Gardiner, Susan E and Bassett, Heather and Chagné, David and McCallum, John and Dzierzon, Helge and Deng, Cecilia and Wang, Yen-Yi and Barron, Lorna and Manako, Kelvina and Bowen, Judith and Foster, Toshi M and Erridge, Zoe A and Tiffin, Heather and Waite, Chethi N and Davies, Kevin M and Grierson, Ella P and Laing, William A and Kirk, Rebecca and Chen, Xiuyin and Wood, Marion and Montefiori, Mirco and Brummell, David A and Schwinn, Kathy E and Catanach, Andrew and Fullerton, Christina and Li, Dawei and Meiyalaghan, Sathiyamoorthy and Nieuwenhuizen, Niels and Read, Nicola and Prakash, Roneel and Hunter, Don and Zhang, Huaibi and McKenzie, Marian and Knäbel, Mareike and Harris, Alastair and Allan, Andrew C and Gleave, Andrew and Chen, Angela and Janssen, Bart J and Plunkett, Blue and Ampomah-Dwamena, Charles and Voogd, Charlotte and Leif, Davin and Lafferty, Declan and Souleyre, Edwige J.F and Varkonyi-Gasic, Erika and Gambi, Francesco and Hanley, Jenny and Yao, Jia-Long and Cheung, Joey and David, Karine M and Warren, Ben and Marsh, Ken and Snowden, Kimberley C and Lin-Wang, Kui and Brian, Lara and Martinez-Sanchez, Marcela and Wang, Mindy and Ileperuma, Nadeesha and Macnee, Nikolai and Campin, Robert and McAtee, Peter and Drummond, Revel S.M and Espley, Richard V and Ireland, Hilary S and Wu, Rongmei and Atkinson, Ross G and Karunairetnam, Sakuntala and Bulley, Sean and Chunkath, Shayhan and Hanley, Zac and Storey, Roy and Thrimawithana, Amali H and Thomson, Susan and David, Charles and Testolin, Raffaele and Huang, Hongwen and Hellens, Roger P and Schaffer, Robert J
BMC genomics, ISSN 1471-2164, 04/2018, Volume 19, Issue 1, pp. 257 - 257
Journal Article