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This Article:

Jennifer R. Levy, Charlotte J. Sumner, Juliane P. Caviston, Mariko K. Tokito, Srikanth Ranganathan, Lee A. Ligon, Karen E. Wallace, Bernadette H. LaMonte, George G. Harmison, Imke Puls, Kenneth H. Fischbeck, and Erika L.F. Holzbaur
A motor neuron disease–associated mutation in p150Glued perturbs dynactin function and induces protein aggregation
J. Cell Biol. 2006 172: 733-745.

has been cited by the following articles in journals that are participating in CrossRef's forward linking service:

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Lysosomal proliferation and distal degeneration in motor neurons expressing the G59S mutation in the p150Glued subunit of dynactin
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A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice
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Arp11 Affects Dynein–Dynactin Interaction and is Essential for Dynein Function in Aspergillus nidulans
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Gene Expressions Specifically Detected in Motor Neurons (Dynactin 1, Early Growth Response 3, Acetyl-CoA Transporter, Death Receptor 5, and Cyclin C) Differentially Correlate to Pathologic Markers in Sporadic Amyotrophic Lateral Sclerosis
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Huntingtin facilitates dynein/dynactin-mediated vesicle transport
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The Nuclear Factor κB–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset
I MAYSTADT, R REZSOHAZY, M BARKATS, S DUQUE, P VANNUFFEL, S REMACLE, B LAMBERT, M NAJIMI, E SOKAL, and A MUNNICH
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The roles of intracellular protein-degradation pathways in neurodegeneration
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Processive bidirectional motion of dynein–dynactin complexes in vitro
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