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P. Hande Özdinler

Researcher at Northwestern University

Publications -  49
Citations -  7357

P. Hande Özdinler is an academic researcher from Northwestern University. The author has contributed to research in topics: Amyotrophic lateral sclerosis & Motor neuron. The author has an hindex of 22, co-authored 46 publications receiving 6597 citations. Previous affiliations of P. Hande Özdinler include Harvard University & LSU Health Sciences Center New Orleans.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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IGF-I Specifically Enhances Axon Outgrowth of Corticospinal Motor Neurons

TL;DR: It is reported that insulin-like growth factor-1 (IGF-I) specifically enhances the extent and rate of murine CSMN axon outgrowth, mediated via the IGF-I receptor and downstream signaling pathways; this is distinct from IGF- I support of neuronal survival.
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Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis

TL;DR: In vivo and in vitro studies find that PrP(c) is expressed in multipotent neural precursors and mature neurons but is not detectable in glia, and loss- and gain-of-function experiments demonstrate thatPrP( c) levels correlate with differentiation of multipotent Neural precursor into mature neurons in vitro and that PrPs positively influence neuronal differentiation in a dose-dependent manner.
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Corticospinal Motor Neurons and Related Subcerebral Projection Neurons Undergo Early and Specific Neurodegeneration in hSOD1G93A Transgenic ALS Mice

TL;DR: Previously unknown neuron type-specific vulnerability of CSMN/sensory and association SCPN is indicated, and it is identified that characteristic dual CSMN and SMN degeneration is conserved in hSOD1G93A mice.
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Pathophysiological and diagnostic implications of cortical dysfunction in ALS

TL;DR: Changes in cortical function that develop in ALS could prove useful as diagnostic biomarkers, potentially enhancing the diagnosis of ALS at an early stage of the disease process and providing potential for more-effective management of patients with ALS.