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U. S. Melo et al.
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AMERICAN JOURNAL OF HUMAN GENETICS (2016)
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CELL REPORTS (2016)
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EXPERIMENTAL NEUROLOGY (2014)
Distinct Roles for μ-Calpain and m-Calpain in Synaptic NMDAR-Mediated Neuroprotection and Extrasynaptic NMDAR-Mediated Neurodegeneration
Yubin Wang et al.
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Mandana Amini et al.
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Cellular Pathways of Hereditary Spastic Paraplegia
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Calpains - An elaborate proteolytic system
Yasuko Ono et al.
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Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
Josef Finsterer et al.
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Brain-Derived Neurotrophic Factor and Epidermal Growth Factor Activate Neuronal m-Calpain via Mitogen-Activated Protein Kinase-Dependent Phosphorylation
Sohila Zadran et al.
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Hua-Ling Chen et al.
PLOS ONE (2010)
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Cyclin-dependent kinase 5 governs learning and synaptic plasticity via control of NMDAR degradation
Ammar H. Hawasli et al.
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Proteolysis of glutamate receptor-interacting protein by calpain in rat brain: implications for synaptic plasticity
XY Lu et al.
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