Robert Wollmann to Mice
This is a "connection" page, showing publications Robert Wollmann has written about Mice.
Connection Strength
0.272
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Synaptic basal lamina-associated congenital myasthenic syndromes. Ann N Y Acad Sci. 2012 Dec; 1275:36-48.
Score: 0.042
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Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction. Hum Mol Genet. 2010 Jun 15; 19(12):2370-9.
Score: 0.035
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Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction. J Neurosci. 1997 Jun 01; 17(11):4170-9.
Score: 0.014
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The L-coding region of the DA strain of Theiler's murine encephalomyelitis virus causes dysfunction and death of myelin-synthesizing cells. J Virol. 2011 Sep; 85(18):9377-84.
Score: 0.009
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T. gondii RP promoters & knockdown reveal molecular pathways associated with proliferation and cell-cycle arrest. PLoS One. 2010 Nov 22; 5(11):e14057.
Score: 0.009
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Theiler's murine encephalomyelitis virus neutralization escape mutants have a change in disease phenotype. J Virol. 1989 Oct; 63(10):4469-73.
Score: 0.008
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Fingolimod and related compounds in a spontaneous autoimmune polyneuropathy. J Neuroimmunol. 2009 Sep 29; 214(1-2):93-100.
Score: 0.008
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Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS. J Neurosci. 2008 Nov 05; 28(45):11537-49.
Score: 0.008
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Cellular origin of a mouse leukemia viral ribonucleic acid. J Virol. 1968 Nov; 2(11):1241-8.
Score: 0.008
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Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection. J Neuroinflammation. 2008 Oct 23; 5:48.
Score: 0.008
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A subgenomic segment of Theiler's murine encephalomyelitis virus RNA causes demyelination. J Virol. 2008 Jun; 82(12):5879-86.
Score: 0.008
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Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene. J Neurosci. 2007 Dec 26; 27(52):14515-24.
Score: 0.007
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Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo. J Neurosci. 2007 Nov 21; 27(47):13022-7.
Score: 0.007
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Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome. J Clin Invest. 2007 Oct; 117(10):2903-12.
Score: 0.007
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Cytosolic prion protein toxicity is independent of cellular prion protein expression and prion propagation. J Virol. 2007 Mar; 81(6):2831-7.
Score: 0.007
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Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model. Neurobiol Dis. 2006 Aug; 23(2):462-70.
Score: 0.007
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The interaction between cytoplasmic prion protein and the hydrophobic lipid core of membrane correlates with neurotoxicity. J Biol Chem. 2006 May 12; 281(19):13559-13565.
Score: 0.007
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Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice. Nat Genet. 2006 Feb; 38(2):245-50.
Score: 0.006
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K+ channel blockade impairs remyelination in the cuprizone model. Glia. 2004 Nov 01; 48(2):156-65.
Score: 0.006
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DA strain of Theiler's murine encephalomyelitis virus induces demyelination in nude mice. Ann Neurol. 1984 May; 15(5):494-9.
Score: 0.006
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Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol. Science. 2002 Nov 29; 298(5599):1781-5.
Score: 0.005
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Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome. J Neurosci. 2002 Aug 01; 22(15):6447-57.
Score: 0.005
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Overexpression of gamma-sarcoglycan induces severe muscular dystrophy. Implications for the regulation of Sarcoglycan assembly. J Biol Chem. 2001 Jun 15; 276(24):21785-90.
Score: 0.005
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Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. J Cell Biol. 1998 Sep 07; 142(5):1279-87.
Score: 0.004
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Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome. Ann N Y Acad Sci. 1998 May 13; 841:167-80.
Score: 0.004
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Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currents. Synapse. 1997 Dec; 27(4):367-77.
Score: 0.004
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Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice. Dev Biol. 1997 Jul 15; 187(2):131-42.
Score: 0.004
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A neutralization site of DA strain of Theiler's murine encephalomyelitis virus important for disease phenotype. Virology. 1996 Dec 15; 226(2):327-37.
Score: 0.003
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Theiler's murine encephalomyelitis virus-induced cardiac and skeletal muscle disease. J Virol. 1996 Dec; 70(12):8926-33.
Score: 0.003
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A transgenic mouse model of the slow-channel syndrome. Muscle Nerve. 1996 Jan; 19(1):79-87.
Score: 0.003
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Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration. Cell. 1995 Apr 21; 81(2):233-43.
Score: 0.003
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CNS gene delivery by retrograde transport of recombinant replication-defective adenoviruses. Gene Ther. 1995 Mar; 2(2):132-7.
Score: 0.003
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The human-severe combined immunodeficiency myasthenic mouse model: a new approach for the study of myasthenia gravis. Ann Neurol. 1993 Jul; 34(1):48-56.
Score: 0.003
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The hu-SCID myasthenic mouse. A new tool for the investigation of seronegative myasthenia gravis. Ann N Y Acad Sci. 1993 Jun 21; 681:303-5.
Score: 0.003
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Virus-induced hemolytic anemia in mice. Cancer Res. 1970 Apr; 30(4):1003-10.
Score: 0.002
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The effect of short-term and chronic immunosuppression on Theiler's virus demyelination. J Neuroimmunol. 1982 Jun; 2(3-4):223-34.
Score: 0.001