Sedehizade F, Klocke R, Jockusch H. Expression of nerve-regulated genes in muscles of mouse mutants affected by spinal muscular atrophies and muscular dystrophies. Muscle & Nerve. 1997;20(2):186-194.The expression of the genes for the alpha-subunit of AChR (AChR alpha), for the myogenic factors myogenin and MyoD, for the calcium-binding protein parvalbumin (PV), and for the muscular chloride channel CIC-1 was studied in the three mouse spinal muscular atrophies (SMAs). These were the mutants ''wobbler'' (WR), ''muscle deficient'' (MDF) and ''progressive motor neuronopathy'' (PMN). Murine myopathies ''muscular dystrophy with myositis'' (MDM) and ''X-linked muscular dystrophy'' (MDX) were used as controls. AChR alpha and myogenin mRNA lev...
Heimann P, Augustin M, Wieneke S, Heising S, Jockusch H. Mutual interference of myotonia and muscula...
Jockusch H, KAUPMANN K, GRONEMEIER M, SCHLEEF M, KLOCKE R. EXPLORING THE MAMMALIAN NEUROMUSCULAR SYS...
The RNA-mediated pathogenesis model for the myotonic dystrophies DM1 and DM2 proposes that mutant tr...
AbstractThe mouse mutants ADR ("arrested development of righting") and the allelic CRP ("cramp") are...
AbstractThe mouse mutants ADR ("arrested development of righting") and the allelic CRP ("cramp") are...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
Mutations in the survival motor neuron (SMN1) gene lead to the neuromuscular disease spinal muscular...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
AbstractA mouse model of the devastating human disease “spinal muscular atrophy” (SMA) was used to i...
<p>(A) mRNA levels of AChRγ subunit, a marker for blocked neuromuscular transmission and denervation...
Audrey J. Caudron1, Agnieszka M. Lichanska2, Helen M. Cooper3 and Peter G. Noakes1. 1School of Biome...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
International audienceDisease processes and trauma affecting nerve-evoked muscle activity, motor neu...
Spinal bulbar muscular atrophy (SBMA) is a slowly progressive, androgen-dependent neuromuscular dise...
The disruption of the survival motor neuron (SMN1) gene leads to the children’s genetic disease spin...
Heimann P, Augustin M, Wieneke S, Heising S, Jockusch H. Mutual interference of myotonia and muscula...
Jockusch H, KAUPMANN K, GRONEMEIER M, SCHLEEF M, KLOCKE R. EXPLORING THE MAMMALIAN NEUROMUSCULAR SYS...
The RNA-mediated pathogenesis model for the myotonic dystrophies DM1 and DM2 proposes that mutant tr...
AbstractThe mouse mutants ADR ("arrested development of righting") and the allelic CRP ("cramp") are...
AbstractThe mouse mutants ADR ("arrested development of righting") and the allelic CRP ("cramp") are...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
Mutations in the survival motor neuron (SMN1) gene lead to the neuromuscular disease spinal muscular...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
AbstractA mouse model of the devastating human disease “spinal muscular atrophy” (SMA) was used to i...
<p>(A) mRNA levels of AChRγ subunit, a marker for blocked neuromuscular transmission and denervation...
Audrey J. Caudron1, Agnieszka M. Lichanska2, Helen M. Cooper3 and Peter G. Noakes1. 1School of Biome...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
International audienceDisease processes and trauma affecting nerve-evoked muscle activity, motor neu...
Spinal bulbar muscular atrophy (SBMA) is a slowly progressive, androgen-dependent neuromuscular dise...
The disruption of the survival motor neuron (SMN1) gene leads to the children’s genetic disease spin...
Heimann P, Augustin M, Wieneke S, Heising S, Jockusch H. Mutual interference of myotonia and muscula...
Jockusch H, KAUPMANN K, GRONEMEIER M, SCHLEEF M, KLOCKE R. EXPLORING THE MAMMALIAN NEUROMUSCULAR SYS...
The RNA-mediated pathogenesis model for the myotonic dystrophies DM1 and DM2 proposes that mutant tr...