The Genetics of Axonal Transport and Axonal Transport Disorders
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[1] M. Nonet,et al. Mutations in Caenorhabditis elegans Cytoplasmic Dynein Components Reveal Specificity of Neuronal Retrograde Cargo , 2004, The Journal of Neuroscience.
[2] L. Goldstein,et al. Kinesin-Dependent Axonal Transport Is Mediated by the Sunday Driver (SYD) Protein , 2000, Cell.
[3] Xiao-Jiang Li,et al. Interaction of Huntingtin-associated Protein-1 with Kinesin Light Chain , 2006, Journal of Biological Chemistry.
[4] N. Hirokawa,et al. Golgi Vesiculation and Lysosome Dispersion in Cells Lacking Cytoplasmic Dynein , 1998, The Journal of cell biology.
[5] L. Goldstein,et al. Microtubule-based transport systems in neurons: the roles of kinesins and dyneins. , 2000, Annual review of neuroscience.
[6] J. Cummings,et al. Alzheimer's disease , 1998, Neurology.
[7] N. Hirokawa,et al. KIF5C, a novel neuronal kinesin enriched in motor neurons. , 2000, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[8] R. Vallee,et al. Retrograde transport by the microtubule-associated protein MAP 1C , 1987, Nature.
[9] L. Goldstein,et al. Do Disorders of Movement Cause Movement Disorders and Dementia? , 2003, Neuron.
[10] T. Schroer,et al. Dynactin increases the processivity of the cytoplasmic dynein motor , 1999, Nature Cell Biology.
[11] S. Heidemann,et al. Polarity orientation of axonal microtubules , 1981, The Journal of cell biology.
[12] D. Borchelt,et al. Axonal Transport of Mutant Superoxide Dismutase 1 and Focal Axonal Abnormalities in the Proximal Axons of Transgenic Mice , 1998, Neurobiology of Disease.
[13] M. Sheetz,et al. Dynactin, a conserved, ubiquitously expressed component of an activator of vesicle motility mediated by cytoplasmic dynein , 1991, The Journal of cell biology.
[14] Fabrice P Cordelières,et al. Huntingtin Controls Neurotrophic Support and Survival of Neurons by Enhancing BDNF Vesicular Transport along Microtubules , 2004, Cell.
[15] T. Reese,et al. Dynein is the motor for retrograde axonal transport of organelles. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[16] R. Vallee,et al. MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties , 1987, The Journal of cell biology.
[17] Ilan Davis,et al. Intracellular mRNA localization: motors move messages. , 2002, Trends in genetics : TIG.
[18] K. Davies,et al. A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes. , 2006, Human molecular genetics.
[19] K. Fischbeck,et al. A motor neuron disease–associated mutation in p150Glued perturbs dynactin function and induces protein aggregation , 2006, The Journal of cell biology.
[20] L. Goldstein,et al. Disruption of Axonal Transport and Neuronal Viability by Amyloid Precursor Protein Mutations in Drosophila , 2001, Neuron.
[21] R. Vallee,et al. Fast transport and retrograde movement of huntingtin and HAP 1 in axons , 1997, Neuroreport.
[22] C. McDermott,et al. Hereditary spastic paraparesis: a review of new developments , 2000, Journal of neurology, neurosurgery, and psychiatry.
[23] N. Hirokawa,et al. Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ , 2001, Cell.
[24] N. Hirokawa,et al. Microtubules provide directional cues for polarized axonal transport through interaction with kinesin motor head , 2003, The Journal of cell biology.
[25] Nobutaka Hirokawa,et al. Kinesin Superfamily Protein 3 (Kif3) Motor Transports Fodrin-Associating Vesicles Important for Neurite Building , 2000, The Journal of cell biology.
[26] E. Mandelkow,et al. Overexpression of Tau Protein Inhibits Kinesin-dependent Trafficking of Vesicles, Mitochondria, and Endoplasmic Reticulum: Implications for Alzheimer's Disease , 1998, The Journal of cell biology.
[27] E. Seeberg,et al. Mutant Huntingtin Impairs Axonal Trafficking in Mammalian Neurons In Vivo and In Vitro , 2004, Molecular and Cellular Biology.
[28] Michael P. Sheetz,et al. Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility , 1985, Cell.
[29] D. Price,et al. Precursor of amyloid protein in Alzheimer disease undergoes fast anterograde axonal transport. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[30] Kunihiro Matsumoto,et al. The Caenorhabditis elegans UNC-14 RUN domain protein binds to the kinesin-1 and UNC-16 complex and regulates synaptic vesicle localization. , 2004, Molecular biology of the cell.
[31] R. Orrell. Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations , 2000, Neuromuscular Disorders.
[32] I. Meinertzhagen,et al. Axonal Transport of Mitochondria to Synapses Depends on Milton, a Novel Drosophila Protein , 2002, Neuron.
[33] Scott T. Brady,et al. Neuropathogenic Forms of Huntingtin and Androgen Receptor Inhibit Fast Axonal Transport , 2003, Neuron.
[34] K. Ray,et al. Kinesin-2 differentially regulates the anterograde axonal transports of acetylcholinesterase and choline acetyltransferase in Drosophila. , 2006, Journal of neurobiology.
[35] L. Goldstein,et al. Identification, partial characterization, and genetic mapping of kinesin-like protein genes in mouse. , 1997, Genomics.
[36] Xinran Liu,et al. Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A , 2003, The Journal of cell biology.
[37] Bin Zhang,et al. Age-Dependent Emergence and Progression of a Tauopathy in Transgenic Mice Overexpressing the Shortest Human Tau Isoform , 1999, Neuron.
[38] K. Fischbeck,et al. Distal spinal and bulbar muscular atrophy caused by dynactin mutation , 2005, Annals of neurology.
[39] R. Kalb,et al. Mutant superoxide dismutase disrupts cytoplasmic dynein in motor neurons , 2005, Neuroreport.
[40] L. Goldstein,et al. Axonal Transport of Amyloid Precursor Protein Is Mediated by Direct Binding to the Kinesin Light Chain Subunit of Kinesin-I , 2000, Neuron.
[41] L. Goldstein,et al. Characterization of KIFC2, a Neuronal Kinesin Superfamily Member in Mouse , 1997, Neuron.
[42] E. Masliah,et al. Axonopathy and Transport Deficits Early in the Pathogenesis of Alzheimer's Disease , 2005, Science.
[43] D. Howland,et al. Disruption of Dynein/Dynactin Inhibits Axonal Transport in Motor Neurons Causing Late-Onset Progressive Degeneration , 2002, Neuron.
[44] Eric F. Wieschaus,et al. Coordination of opposite-polarity microtubule motors , 2002, The Journal of cell biology.
[45] E. Fisher,et al. Genetic Analysis of the Cytoplasmic Dynein Subunit Families , 2006, PLoS genetics.
[46] C. Lively,et al. Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons. , 2006, Molecular biology of the cell.
[47] T. Hays,et al. Cytoplasmic dynein function is essential in Drosophila melanogaster. , 1996, Genetics.
[48] M. Pericak-Vance,et al. A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10). , 2002, American journal of human genetics.
[49] Richard G. Brusch,et al. Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila , 2003, Neuron.
[50] Scott T. Brady,et al. A novel brain ATPase with properties expected for the fast axonal transport motor , 1985, Nature.
[51] D. Perl,et al. Accumulation of Phosphorylated Neurofilaments in Anterior Horn Motoneurons of Amyotrophic Lateral Sclerosis Patients , 1988, Journal of neuropathology and experimental neurology.
[52] Judith Klumperman,et al. Sunday Driver links axonal transport to damage signaling , 2005, The Journal of cell biology.
[53] Kunihiro Matsumoto,et al. UNC-16, a JNK-Signaling Scaffold Protein, Regulates Vesicle Transport in C. elegans , 2001, Neuron.
[54] N. Hirokawa,et al. Targeted Disruption of Mouse Conventional Kinesin Heavy Chain kif5B, Results in Abnormal Perinuclear Clustering of Mitochondria , 1998, Cell.
[55] W. Saxton,et al. Kinesin mutations cause motor neuron disease phenotypes by disrupting fast axonal transport in Drosophila. , 1996, Genetics.
[56] N. Hirokawa,et al. All kinesin superfamily protein, KIF, genes in mouse and human , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[57] E. Mandelkow,et al. Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress , 2002, The Journal of cell biology.
[58] A. Ludolph,et al. A dynein mutation attenuates motor neuron degeneration in SOD1G93A mice , 2006, Experimental Neurology.
[59] L. Goldstein,et al. Principles of cargo attachment to cytoplasmic motor proteins. , 2002, Current opinion in cell biology.
[60] W. Saxton,et al. APLIP1, a Kinesin Binding JIP-1/JNK Scaffold Protein, Influences the Axonal Transport of Both Vesicles and Mitochondria in Drosophila , 2005, Current Biology.
[61] M. Goedert,et al. Tau proteins with FTDP‐17 mutations have a reduced ability to promote microtubule assembly , 1998, FEBS letters.
[62] L. Goldstein,et al. Kinesin-mediated axonal transport of a membrane compartment containing β-secretase and presenilin-1 requires APP , 2001, Nature.
[63] W. Saxton,et al. Cytoplasmic dynein, the dynactin complex, and kinesin are interdependent and essential for fast axonal transport. , 1999, Molecular biology of the cell.
[64] W. Schneider,et al. The Reelin Receptor ApoER2 Recruits JNK-interacting Proteins-1 and -2* , 2000, The Journal of Biological Chemistry.
[65] N. Hirokawa,et al. Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta. , 2001, Cell.
[66] L. Goldstein,et al. Drosophila roadblock and Chlamydomonas Lc7 , 1999, The Journal of cell biology.
[67] S. Gross. Dynactin: Coordinating Motors with Opposite Inclinations , 2003, Current Biology.
[68] H. Geerts,et al. Prominent axonopathy in the brain and spinal cord of transgenic mice overexpressing four-repeat human tau protein. , 1999, The American journal of pathology.
[69] S. Hersch,et al. Interaction of Huntingtin-Associated Protein with Dynactin P150Glued , 1998, The Journal of Neuroscience.
[70] N. Hirokawa,et al. KIF3A/B: a heterodimeric kinesin superfamily protein that works as a microtubule plus end-directed motor for membrane organelle transport , 1995, The Journal of cell biology.
[71] N. Hirokawa,et al. Defect in Synaptic Vesicle Precursor Transport and Neuronal Cell Death in KIF1A Motor Protein–deficient Mice , 1998, The Journal of cell biology.
[72] Lei Wang,et al. Rapid movement of axonal neurofilaments interrupted by prolonged pauses , 2000, Nature Cell Biology.
[73] J. Trojanowski,et al. Neurofilaments and Orthograde Transport Are Reduced in Ventral Root Axons of Transgenic Mice that Express Human SOD1 with a G93A Mutation , 1997, The Journal of cell biology.
[74] E. Mandelkow,et al. Clogging of axons by tau, inhibition of axonal traffic and starvation of synapses , 2003, Neurobiology of Aging.
[75] A. Clark,et al. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis. , 1996, Annals of neurology.
[76] A. Ludolph,et al. Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS , 2004, Neurology.
[77] A. F. Soleng,et al. A thorny question: how does activity maintain dendritic spines? , 1999, Nature Neuroscience.
[78] M. Charlton,et al. The GTPase dMiro Is Required for Axonal Transport of Mitochondria to Drosophila Synapses , 2005, Neuron.
[79] Scott T. Brady,et al. Neurofilaments Are Transported Rapidly But Intermittently in Axons: Implications for Slow Axonal Transport , 2000, The Journal of Neuroscience.
[80] W. Mobley,et al. NGF Signaling in Sensory Neurons Evidence that Early Endosomes Carry NGF Retrograde Signals , 2003, Neuron.
[81] L. Goldstein,et al. Kinesin-II Is Required for Axonal Transport of Choline Acetyltransferase in Drosophila , 1999, The Journal of cell biology.
[82] Bin Zhang,et al. Retarded Axonal Transport of R406W Mutant Tau in Transgenic Mice with a Neurodegenerative Tauopathy , 2004, The Journal of Neuroscience.
[83] J. Richardson,et al. Interactions of the Low Density Lipoprotein Receptor Gene Family with Cytosolic Adaptor and Scaffold Proteins Suggest Diverse Biological Functions in Cellular Communication and Signal Transduction* , 2000, The Journal of Biological Chemistry.
[84] E. Rugarli,et al. Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport. , 2004, The Journal of clinical investigation.
[85] W. Robberecht,et al. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy , 2004, Nature Genetics.
[86] J. Shah,et al. Slow axonal transport: fast motors in the slow lane. , 2002, Current opinion in cell biology.
[87] Shin J. Oh,et al. Mutant dynactin in motor neuron disease , 2003, Nature Genetics.
[88] Jinyun Chen,et al. The kinesin-associated protein UNC-76 is required for axonal transport in the Drosophila nervous system. , 2003, Molecular biology of the cell.
[89] J. Blenis,et al. Cargo of Kinesin Identified as Jip Scaffolding Proteins and Associated Signaling Molecules , 2001, The Journal of cell biology.
[90] P. Worley,et al. Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin. , 1997, Human molecular genetics.
[91] L. Goldstein,et al. Kinesin Light Chains Are Essential for Axonal Transport in Drosophila , 1998, The Journal of cell biology.
[92] I. Vernos,et al. Dynactin is required for bidirectional organelle transport , 2003, The Journal of cell biology.
[93] Mark Ellisman,et al. JNK1 is required for maintenance of neuronal microtubules and controls phosphorylation of microtubule-associated proteins. , 2003, Developmental cell.
[94] M. Fichera,et al. Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia , 2004, Neurology.
[95] E. Raff,et al. Kinesin heavy chain is essential for viability and neuromuscular functions in Drosophila, but mutants show no defects in mitosis , 1991, Cell.
[96] Mark P Mattson,et al. Alzheimer's Presenilin 1 Mutations Impair Kinesin-Based Axonal Transport , 2003, The Journal of Neuroscience.
[97] L. Greensmith,et al. A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice , 2005, The Journal of cell biology.
[98] John X. Morris,et al. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. , 1998, Science.
[99] Guy A. Rouleau,et al. SOD1 mutation is assosiated with accumulation of neurofilaments in amyotrophic lateral scelaries , 1996 .
[100] C. Sung,et al. Cytoplasmic Dynein Regulation by Subunit Heterogeneity and Its Role in Apical Transport , 2001, The Journal of cell biology.
[101] K. Abe,et al. Slow component of axonal transport is impaired in the proximal axon of transgenic mice with a G93A mutant SOD1 gene , 2004, Acta Neuropathologica.
[102] D. Hall,et al. Kinesin-related gene unc-104 is required for axonal transport of synaptic vesicles in C. elegans , 1991, Cell.
[103] N. Hirokawa,et al. The neuron-specific kinesin superfamily protein KIF1A is a uniqye monomeric motor for anterograde axonal transport of synaptic vesicle precursors , 1995, Cell.
[104] I. Meinertzhagen,et al. Mitochondria are redistributed in Drosophila photoreceptors lacking Milton, a kinesin‐associated protein , 2003, The Journal of comparative neurology.
[105] L. Goldstein,et al. Molecular motors: from one motor many tails to one motor many tales. , 2001, Trends in cell biology.
[106] J. Haines,et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis , 1993, Nature.
[107] Yasushi Hiraoka,et al. Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport , 2003, Science.