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  1. 1.   Myosin-Va mediates RNA distribution in primary fibroblasts from multiple organs
  2. Salerno, V. P.; Calliari, A.; Provance, D. W.; Sotelo-Silveira, J. R.; Sotelo, J. R.; Mercer, J. A.
  3. Cell Motility and the Cytoskeleton. 2008 65(5): 422-433.
  1. 2.   A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat
  2. Ishida, Y.; David, V. A.; Eizirik, E.; Schaffer, A. A.; Neelam, B. A.; Roelke, M. E.; Hannah, S. S.; O'Brien, S. J.; Menotti-Raymond, M.
  3. Genomics. 2006, Dec; 88(6): 698-705.
  1. 3.   Mouse coat color mutations: From fancy mice to functional genomics
  2. Steingrimsson, E.; Copeland, N. G.; Jenkins, N. A.
  3. Developmental Dynamics. 2006, Sep; 235(9): 2401-2411.
  1. 4.   dsu functions in a MYO5A-independent pathway to suppress the coat color of dilute mice
  2. O'Sullivan, T. N.; Wu, X. F. S.; Rachel, R. A.; Huang, J. D.; Swing, D. A.; Matesic, L. E.; Hammer, J. A.; Copeland, N. G.; Jenkins, N. A.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2004, NOV 30; 101(48): 16831-16836.
  1. 5.   Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6
  2. Zhang, Q.; Zhao, B. H.; Li, W.; Oiso, N.; Novak, E. K.; Rusiniak, M. E.; Gautam, R.; Chintala, S.; O'Brien, E. P.; Zhang, Y.; Roe, B. A.; Elliott, R. W.; Eicher, E. M.; Liang, P.; Kratz, C.; Legius, E.; Spritz, R. A.; O'Sullivan, T. N.; Copeland, N. G.; Jenkins, N. A.; Swank, R. T.
  3. Nature Genetics. 2003 33(2): 145-153.
  1. 6.   A mutation in Rab27a causes the vesicle transport defects observed in ashen mice
  2. Wilson, S. M.; Yip, R.; Swing, D. A.; O'Sullivan, T. N.; Zhang, Y.; Novak, E. K.; Swank, R. T.; Russell, L. B.; Copeland, N. G.; Jenkins, N. A.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2000 97(14): 7933-7938.
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