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Neuromuscular Disorders : NMD|March 27, 1999
Mutual interference of myotonia and muscular dystrophy in the mouse: a study on ADR-MDX double mutantsP Heimann, M Augustin, S Wieneke, et al.
Neuromuscular Disorders : NMD|July 1, 1993
Development of electrical myotonia in the ADR mouse: role of chloride conductance in myotubes and neonatal animalsE Wischmeyer, E Nolte, R Klocke, et al.
Genetical Research|August 1, 1989
cDNA sequence and chromosomal localization of the mouse parvalbumin gene, PvaC Zühlke, F Schöffl, H Jockusch, et al.
Genomics|October 1, 1992
The gene for the cell adhesion molecule M-cadherin maps to mouse chromosome 8 and human chromosome 16q24.1-qter and is near the E-cadherin (uvomorulin) locus in both speciesK Kaupmann, J Becker-Follmann, G Scherer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 26, 2000
Tumor necrosis factor alpha induces a metalloprotease-disintegrin, ADAM8 (CD 156): implications for neuron-glia interactions during neurodegenerationU Schlomann, S Rathke-Hartlieb, S Yamamoto, et al.
FEBS Letters|May 12, 1997
Deletion in the Z-line region of the titin gene in a baby hamster kidney cell line, BHK-21-BiM Jäckel, C Witt, O Antonova, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 8, 1997
The mouse Clc1/myotonia gene: ETn insertion, a variable AATC repeat, and PCR diagnosis of allelesV Schnülle, O Antropova, M Gronemeier, et al.
Genetical Research|October 1, 1995
Chloride channel 2 gene (Clc2) maps to chromosome 16 of the mouse, extending a region of conserved synteny with human chromosome 3qA Lengeling, M Gronemeier, M Ronsiek, et al.
FEBS Letters|July 19, 2000
Conservation of the 3'-untranslated region of the Rab1a gene in amniote vertebrates: exceptional structure in marsupials and possible role for posttranscriptional regulationN Wedemeyer, T Schmitt-John, D Evers, et al.
Genomics|July 15, 1997
Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseasesD Korthaus, N Wedemeyer, A Lengeling, et al.
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