scholarly article | Q13442814 |
P819 | ADS bibcode | 2014PLoSO...988739H |
P356 | DOI | 10.1371/JOURNAL.PONE.0088739 |
P932 | PMC publication ID | 3919806 |
P698 | PubMed publication ID | 24520420 |
P5875 | ResearchGate publication ID | 260150669 |
P2093 | author name string | Markus A Ruegg | |
Shuo Lin | |||
Filippo Oliveri | |||
Stefan Hettwer | |||
Monika Haubitz | |||
Jan W Vrijbloed | |||
Ruggero G Fariello | |||
Stefan Kucsera | |||
P2860 | cites work | The role of muscle-specific tyrosine kinase (MuSK) and mystery of MuSK myasthenia gravis | Q27008264 |
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The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo | Q28280767 | ||
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Agrin and synaptic laminin are required to maintain adult neuromuscular junctions | Q28511069 | ||
Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction | Q28513062 | ||
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LDL-receptor-related protein 4 is crucial for formation of the neuromuscular junction | Q28592974 | ||
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Muscle-wide secretion of a miniaturized form of neural agrin rescues focal neuromuscular innervation in agrin mutant mice | Q30482979 | ||
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Remodeling of the neuromuscular junction precedes sarcopenia related alterations in myofibers | Q33788155 | ||
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Comparison of muscle ultrastructure in myasthenia gravis with anti-MuSK and anti-AChR antibodies. | Q54631945 | ||
MuSK levels differ between adult skeletal muscles and influence postsynaptic plasticity | Q61855429 | ||
DAB cytochemistry: artifact problems in its current uses | Q71303690 | ||
Activation of muscle-specific receptor tyrosine kinase and binding to dystroglycan are regulated by alternative mRNA splicing of agrin | Q79165764 | ||
Denervation produces different single fiber phenotypes in fast- and slow-twitch hindlimb muscles of the rat | Q83149945 | ||
Elevated levels of a C-terminal agrin fragment identifies a new subset of sarcopenia patients | Q83703672 | ||
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The agrin gene codes for a family of basal lamina proteins that differ in function and distribution | Q34234963 | ||
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A valid mouse model of AGRIN-associated congenital myasthenic syndrome. | Q35532941 | ||
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Acetylcholine receptor-aggregating activity of agrin isoforms and mapping of the active site | Q36382434 | ||
Localization of acetylcholine receptor by 125I-labeled alpha-bungarotoxin binding at mouse motor endplates | Q36517854 | ||
Skeletal Muscle in Motor Neuron Diseases: Therapeutic Target and Delivery Route for Potential Treatments | Q36805205 | ||
The role of MuSK in synapse formation and neuromuscular disease | Q38103527 | ||
Koelle's copper thiocholine method performed with a low-pH phosphate buffer, followed by osmification of the precipitate: revival of two abandoned procedures | Q39239602 | ||
Specific proteolytic cleavage of agrin regulates maturation of the neuromuscular junction | Q39639185 | ||
Increasing MuSK activity delays denervation and improves motor function in ALS mice | Q41877091 | ||
Neuromuscular junction protection for the potential treatment of amyotrophic lateral sclerosis | Q42285046 | ||
Autoantibodies in myasthenia gravis | Q43751539 | ||
Three myosin heavy chain isoforms in type 2 skeletal muscle fibres. | Q44241210 | ||
Expression of mouse agrin in normal, denervated and dystrophic muscle | Q44473154 | ||
The effect of in vitro formation of acetylcholine receptor (AChR) clusters in engineered muscle fibers on subsequent innervation of constructs in vivo | Q46488107 | ||
Purification and enzymological characterization of murine neurotrypsin | Q46520674 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | neuromuscular junction | Q776995 |
P304 | page(s) | e88739 | |
P577 | publication date | 2014-02-10 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Injection of a soluble fragment of neural agrin (NT-1654) considerably improves the muscle pathology caused by the disassembly of the neuromuscular junction | |
P478 | volume | 9 |
Q28080339 | Ageing in relation to skeletal muscle dysfunction: redox homoeostasis to regulation of gene expression |
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Q37602392 | Dietary supplementation with bovine-derived milk fat globule membrane lipids promotes neuromuscular development in growing rats |
Q93055041 | Dissecting the Extracellular Complexity of Neuromuscular Junction Organizers |
Q47570833 | Engineered agrin attenuates the severity of experimental autoimmune myasthenia gravis |
Q33563640 | Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression |
Q49304342 | Increasing Agrin Function Antagonizes Muscle Atrophy and Motor Impairment in Spinal Muscular Atrophy. |
Q52692587 | MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion. |
Q92503428 | Modulation of Agrin and RhoA Pathways Ameliorates Movement Defects and Synapse Morphology in MYO9A-Depleted Zebrafish |
Q64992976 | Motor Endplate-Anatomical, Functional, and Molecular Concepts in the Historical Perspective. |
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Q26766502 | Neuromuscular Junctions as Key Contributors and Therapeutic Targets in Spinal Muscular Atrophy |
Q37097233 | Neuromuscular junction degeneration in muscle wasting |
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