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The American Journal of Pathology|August 7, 2002
Impaired hair follicle morphogenesis and cycling with abnormal epidermal differentiation in nackt mice, a cathepsin L-deficient mutationFernando Benavides, Matthew F Starost, Mónica Flores, et al.
Genomics|May 7, 2002
Unique genetic variation revealed by a microsatellite polymorphism survey in ten wild-derived inbred strainsSusana Campino, Catja Behrschmidt, Sébastien Bagot, et al.
Virology Journal|November 20, 2004
The Israeli strain IS-98-ST1 of West Nile virus as viral model for West Nile encephalitis in the Old WorldMarianne Lucas, Marie-Pascale Frenkiel, Tomoji Mashimo, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 19, 2007
Progressive motor neuronopathy: a critical role of the tubulin chaperone TBCE in axonal tubulin routing from the Golgi apparatusMichael K E Schaefer, Henning Schmalbruch, Emmanuelle Buhler, et al.
Plos One|June 23, 2012
Alopecia in a viable phospholipase C delta 1 and phospholipase C delta 3 double mutantFabian Runkel, Maik Hintze, Sebastian Griesing, et al.
Genomics|October 16, 2003
Structural and functional genomics and evolutionary relationships in the cluster of genes encoding murine 2',5'-oligoadenylate synthetasesTomoji Mashimo, Philippe Glaser, Marianne Lucas, et al.
Infection and Immunity|June 18, 2002
Deletion of T cells bearing the V beta8.1 T-cell receptor following mouse mammary tumor virus 7 integration confers resistance to murine cerebral malariaOlivier Gorgette, Alexandre Existe, Mariama Idrissa Boubou, et al.
Plos Genetics|January 22, 2011
A mutation in the gene encoding mitochondrial Mg²+ channel MRS2 results in demyelination in the ratTakashi Kuramoto, Mitsuru Kuwamura, Satoko Tokuda, et al.
Genomics|March 7, 2006
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouseDominique Simon-Chazottes, Sylvie Tutois, Michael Kuehn, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain geneSylvie Besse, Valérie Allamand, Jean-Thomas Vilquin, et al.
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