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Ian F. Musgrave

Researcher at University of Adelaide

Publications -  112
Citations -  2706

Ian F. Musgrave is an academic researcher from University of Adelaide. The author has contributed to research in topics: Imidazoline receptor & Protein kinase C. The author has an hindex of 27, co-authored 105 publications receiving 2398 citations. Previous affiliations of Ian F. Musgrave include Australian National University & University of Queensland.

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Host-defence peptides from the glandular secretions of amphibians: structure and activity

TL;DR: This review covers the literature on the subject of biologically active peptide from the glands of amphibians, which include neuropeptides, antimicrobial and anticancer active peptides, antiviral agents, fungicides and peptides which complex with Ca2+ calmodulin.
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(−)-Epigallocatechin-3-Gallate (EGCG) Maintains κ-Casein in Its Pre-Fibrillar State without Redirecting Its Aggregation Pathway

TL;DR: It is proposed that EGCG is directed to the amyloidogenic sheet-turn-sheet motif of monomeric RCMkappa-CN with high affinity by strong non-specific hydrophobic associations, and additional non-covalent pi-pi stacking interactions between the polyphenolic and aromatic residues common to theAmyloidsogenic sequence are also implicated.
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Alzheimer disease: amyloidogenesis, the presenilins and animal models.

TL;DR: There is an emphasis on the importance of animal models in elucidating the molecular mechanisms behind the development of Alzheimer's disease and how the zebrafish, Danio rerio, can be used as a model organism for analysis of presenilin function and Alzheimer's Disease pathogenesis.
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Gallic acid is the major component of grape seed extract that inhibits amyloid fibril formation.

TL;DR: It is shown, using in vitro thioflavin T assays and transmission electron microscopy, that grape seed extract inhibits fibril formation of kappa-casein (κ-CN), a milk protein which forms amyloid fibrils spontaneously under physiological conditions and it is concluded that the gallate moiety has the fibrIL-inhibitory activity.