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Ann M. Turnley

Researcher at University of Melbourne

Publications -  101
Citations -  5483

Ann M. Turnley is an academic researcher from University of Melbourne. The author has contributed to research in topics: Neural stem cell & Neurogenesis. The author has an hindex of 41, co-authored 101 publications receiving 5185 citations. Previous affiliations of Ann M. Turnley include Royal Adelaide Hospital & Royal Melbourne Hospital.

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Axonal Regeneration and Lack of Astrocytic Gliosis in EphA4-Deficient Mice

TL;DR: It is demonstrated that adult mice lacking EphA4 (-/-), a molecule essential for correct guidance of spinal cord axons during development, exhibit axonal regeneration and functional recovery after spinal cord hemisection.
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Cellular distribution and developmental expression of AMP-activated protein kinase isoforms in mouse central nervous system.

TL;DR: Preference nuclear localization of the α2, β1, and γ1 subunits suggests new functions of the AMP‐activated protein kinase, and the different expression patterns and cellular localization between the two catalytic subunits α1 and α2 point to different physiological roles.
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LIF receptor signaling limits immune-mediated demyelination by enhancing oligodendrocyte survival

TL;DR: This study shows that the neurotrophic cytokine leukemia inhibitory factor (LIF) directly prevents oligodendrocyte death in animal models of MS and demonstrates that this therapeutic effect complements endogenous LIF receptor signaling, which already serves to limit oligodendedrocytes loss during immune attack.
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Neural precursor differentiation into astrocytes requires signaling through the leukemia inhibitory factor receptor

TL;DR: It is shown that neural precursors isolated from the developing forebrain of mice that are deficient in the gene for the low-affinity leukemia inhibitory factor receptor (LIFR-/-) fail to generate astrocytes expressing glial fibrillary acidic protein (GFAP) when cultured in vitro, and indeed the LIF-deficient animals show a significant reduction in the number of GFAP cells in the hippocampus.