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Crispin R. Dass

Researcher at Curtin University

Publications -  243
Citations -  17596

Crispin R. Dass is an academic researcher from Curtin University. The author has contributed to research in topics: PEDF & Cancer. The author has an hindex of 54, co-authored 230 publications receiving 15472 citations. Previous affiliations of Crispin R. Dass include Peter MacCallum Cancer Centre & Johnson & Johnson.

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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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Doxorubicin: an update on anticancer molecular action, toxicity and novel drug delivery systems

TL;DR: The frontline drug doxorubicin has been used for treating cancer for over 30 years but causes toxicity to most major organs, especially life‐threatening cardiotoxicity, which forces the treatment to become dose‐limiting.
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Recent developments in liposomes, microparticles and nanoparticles for protein and peptide drug delivery.

TL;DR: This review discusses the recent developments in the fields of liposome, microparticle and nanoparticle pertinent to protein and peptide delivery covering those systems tested and/or validated in vivo.
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Current research on pharmacologic and regenerative therapies for osteoarthritis.

TL;DR: Current research focuses on the development of new OA drugs (such as sprifermin/recombinant human fibroblast growth factor-18, tanezumab/monoclonal antibody against β-nerve growth factor), which aims for more effectiveness and less incidence of adverse effects than the traditional ones.
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Transcription factor Egr-1 supports FGF-dependent angiogenesis during neovascularization and tumor growth

TL;DR: It is shown that RNA-cleaving phosphodiester-linked DNA-based enzymes (DNAzymes), targeting a specific motif in the 5′ untranslated region of early growth response (Egr-1) mRNA, inhibit EGr-1 protein expression, microvascular endothelial cell replication and migration, and microtubule network formation on basement membrane matrices.