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Lin Mei

Researcher at Case Western Reserve University

Publications -  266
Citations -  18002

Lin Mei is an academic researcher from Case Western Reserve University. The author has contributed to research in topics: Neuromuscular junction & Agrin. The author has an hindex of 69, co-authored 245 publications receiving 15903 citations. Previous affiliations of Lin Mei include University of Arizona & Chinese Academy of Sciences.

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Essential Roles of c-JUN and c-JUN N-Terminal Kinase (JNK) in Neuregulin-Increased Expression of the Acetylcholine Receptor e-Subunit

TL;DR: It is suggested that neuregulin activates multiple signaling cascades that converge to regulate AChR ε-subunit gene expression, indicating an essential role of c-JUN in neurgulin signaling.
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Human homologue of Drosophila CNK interacts with Ras effector proteins Raf and Rlf

TL;DR: The ability ofCNK2 to interact with both Ras effector proteins Raf and Rlf suggests that CNK2 may integrate signals between MAPK and Ral pathways through a complex interplay of components.
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Swedish mutant APP suppresses osteoblast differentiation and causes osteoporotic deficit, which are ameliorated by N‐acetyl‐L‐cysteine

TL;DR: A role for APPswe in suppressing OB differentiation and bone formation is demonstrated, a detrimental factor for AD‐associated osteoporotic deficit is implicate, and a potential clinical value of NAC is revealed in the treatment of osteopOrotic deficits.
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Dynamic ErbB4 Activity in Hippocampal-Prefrontal Synchrony and Top-Down Attention in Rodents

TL;DR: A role of ErbB4-dependent GABA activity in the hippocampus is identified in synchronizing the hippocampal-prefrontal pathway and it is demonstrated that acute, dynamic Erb B4 signaling is required to command top-down attention.
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The cloned murine M1 muscarinic receptor is associated with the hydrolysis of phosphatidylinositols in transfected murine B82 cells.

TL;DR: Data suggest that the M1 muscarinic receptor encoded by the gene is coupled to the hydrolysis of phosphatidylinositols after transfecting this gene into the B82 cells.