C
Christine J. McNamee
Researcher at University of Liverpool
Publications - 17
Citations - 2633
Christine J. McNamee is an academic researcher from University of Liverpool. The author has contributed to research in topics: Neurite & Neurotrimin. The author has an hindex of 9, co-authored 16 publications receiving 1472 citations.
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Journal ArticleDOI
Drug repurposing: progress, challenges and recommendations
Sudeep Pushpakom,Francesco Iorio,Patrick A. Eyers,K. Jane Escott,Shirley Hopper,Andrew D. Wells,Andrew J. Doig,Tim Guilliams,Joanna Latimer,Christine J. McNamee,Alan Norris,Philippe Sanseau,David Cavalla,Munir Pirmohamed +13 more
TL;DR: Approaches used for drug repurposing (also known as drug repositioning) are presented, the challenges faced by the repurpose community are discussed, and innovative ways by which these challenges could be addressed are recommended to help realize the full potential of drugRepurposing.
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Co-localisation, heterophilic interactions and regulated expression of IgLON family proteins in the chick nervous system
TL;DR: It is confirmed that OBCam will bind homophilically and also that LAMP, OBCAM and CEPU-1 will interact heterophilic with each other and proposed that IgLON activity will depend on the complement of IgLons expressed by each neuron.
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Diglons are heterodimeric proteins composed of IgLON subunits, and Diglon-CO inhibits neurite outgrowth from cerebellar granule cells.
TL;DR: It is proposed that IgLONs function predominantly as subunits of heterodimeric proteins (Diglons), and although singly transfected cell lines have little effect on neurite outgrowth, CHO cell lines expressing both CEPU-1 and OBCAM (Diglon-CO) inhibit neuriteOutgrowth from cerebellar granule cells.
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Promotion of neuronal cell adhesion by members of the IgLON family occurs in the absence of either support or modification of neurite outgrowth.
TL;DR: It is suggested that IgLONs may not have a primary role in axon guidance but may be more important for cell–cell adhesion and recognition.
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Identification and Characterization of CEPU-Se—A Secreted Isoform of the IgLON Family Protein, CEPU-1
TL;DR: The characterisation of an alternatively-spliced isoform ofCEPU-1 that is secreted is reported, suggesting that CEPU-Se may act to modulate the ability of CE PU-1, LAMP, and OBCAM to influence neurite outgrowth.