Hurd, D D <br/><br/>
Kinesin mutations cause motor neuron disease phenotypes by disrupting fast axonal transport in Drosophila.  [electronic resource] 

 -  Genetics  Nov 1996 
 - 1075-85 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0016-6731 
<br/><br/><label>Standard No.: </label>10.1093/genetics/144.3.1075  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Animals, Genetically Modified<br/>Axons--metabolism<br/>Biological Transport<br/>Calcium-Binding Proteins<br/>Cell Adhesion Molecules, Neuronal--metabolism<br/>Drosophila--genetics<br/>Female<br/>HSP40 Heat-Shock Proteins<br/>Kinesins--genetics<br/>Male<br/>Membrane Glycoproteins--metabolism<br/>Membrane Proteins--metabolism<br/>Mice<br/>Motor Neuron Disease--metabolism<br/>Mutagenesis<br/>Nerve Tissue Proteins--metabolism<br/>Organelles<br/>Paralysis--etiology<br/>Phenotype<br/>Presynaptic Terminals<br/>Qa-SNARE Proteins<br/>Rabbits<br/>Synaptotagmins