Item Type | Name |
Concept
|
Demyelinating Diseases
|
Concept
|
Myelin Basic Protein
|
Concept
|
Mice, Inbred Strains
|
Concept
|
Models, Molecular
|
Concept
|
Mice, Transgenic
|
Concept
|
Models, Genetic
|
Concept
|
Mice, Inbred BALB C
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Mice, Nude
|
Concept
|
Schwann Cells
|
Concept
|
Mice, Inbred DBA
|
Concept
|
Neuroglia
|
Concept
|
Myelin Sheath
|
Concept
|
Oligodendroglia
|
Concept
|
Mice, Knockout
|
Concept
|
Hereditary Central Nervous System Demyelinating Diseases
|
Concept
|
Mice
|
Concept
|
Disease Models, Animal
|
Concept
|
Mice, Mutant Strains
|
Concept
|
Mice, SCID
|
Concept
|
Mice, Inbred NOD
|
Academic Article
|
A transgenic mouse model of the slow-channel syndrome.
|
Academic Article
|
The human-severe combined immunodeficiency myasthenic mouse model: a new approach for the study of myasthenia gravis.
|
Academic Article
|
SAG: a Schwann cell membrane glycoprotein.
|
Academic Article
|
Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice.
|
Academic Article
|
A neutralization site of DA strain of Theiler's murine encephalomyelitis virus important for disease phenotype.
|
Academic Article
|
The clinical significance of extracellular matrix in gangliogliomas.
|
Academic Article
|
Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction.
|
Academic Article
|
Theiler's murine encephalomyelitis virus-induced cardiac and skeletal muscle disease.
|
Academic Article
|
Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome.
|
Academic Article
|
Overexpression of gamma-sarcoglycan induces severe muscular dystrophy. Implications for the regulation of Sarcoglycan assembly.
|
Academic Article
|
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol.
|
Academic Article
|
Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome.
|
Academic Article
|
Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome.
|
Academic Article
|
K+ channel blockade impairs remyelination in the cuprizone model.
|
Academic Article
|
Cellular neuropathology of tuberous sclerosis.
|
Academic Article
|
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice.
|
Academic Article
|
Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model.
|
Academic Article
|
Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo.
|
Academic Article
|
Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection.
|
Academic Article
|
Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS.
|
Academic Article
|
The interaction between cytoplasmic prion protein and the hydrophobic lipid core of membrane correlates with neurotoxicity.
|
Academic Article
|
Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction.
|
Academic Article
|
T. gondii RP promoters & knockdown reveal molecular pathways associated with proliferation and cell-cycle arrest.
|
Academic Article
|
Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome.
|
Academic Article
|
The L-coding region of the DA strain of Theiler's murine encephalomyelitis virus causes dysfunction and death of myelin-synthesizing cells.
|
Academic Article
|
A subgenomic segment of Theiler's murine encephalomyelitis virus RNA causes demyelination.
|
Academic Article
|
Properties of mouse leukemia viruses. VI. The core of Friend virus; isolation and constituents.
|
Academic Article
|
Maintenance of isolated oligodendrocytes in long-term culture.
|
Academic Article
|
Distribution of glial fibrillary acidic protein in central nervous system lesions of tuberous sclerosis.
|
Academic Article
|
Fingolimod and related compounds in a spontaneous autoimmune polyneuropathy.
|
Academic Article
|
LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin.
|
Academic Article
|
Neuropathy accompanying IgM lambda monoclonal gammopathy.
|
Academic Article
|
Induction of the morphologic changes of both acute and chronic experimental myasthenia by monoclonal antibody directed against acetylcholine receptor.
|
Academic Article
|
Distribution of S-100 protein outside the central nervous system.
|
Academic Article
|
Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration.
|
Academic Article
|
The hu-SCID myasthenic mouse. A new tool for the investigation of seronegative myasthenia gravis.
|
Academic Article
|
The effect of short-term and chronic immunosuppression on Theiler's virus demyelination.
|
Academic Article
|
Ultrastructural changes accompanying the growth of isolated oligodendrocytes.
|
Academic Article
|
Theiler's murine encephalomyelitis virus neutralization escape mutants have a change in disease phenotype.
|
Academic Article
|
The 1995 Lindberg Award. Nonthermally mediated muscle injury and necrosis in electrical trauma.
|
Academic Article
|
S-100 protein in soft-tissue tumors derived from Schwann cells and melanocytes.
|
Academic Article
|
DA strain of Theiler's murine encephalomyelitis virus induces demyelination in nude mice.
|
Academic Article
|
Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin.
|
Academic Article
|
Cytosolic prion protein toxicity is independent of cellular prion protein expression and prion propagation.
|
Academic Article
|
Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene.
|
Academic Article
|
Acute severe animal model of anti-muscle-specific kinase myasthenia: combined postsynaptic and presynaptic changes.
|
Academic Article
|
Cellular origin of a mouse leukemia viral ribonucleic acid.
|
Academic Article
|
CNS gene delivery by retrograde transport of recombinant replication-defective adenoviruses.
|
Academic Article
|
Virus-induced hemolytic anemia in mice.
|
Academic Article
|
Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currents.
|
Academic Article
|
Synaptic basal lamina-associated congenital myasthenic syndromes.
|