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Joan K. Heath

Researcher at Walter and Eliza Hall Institute of Medical Research

Publications -  119
Citations -  13932

Joan K. Heath is an academic researcher from Walter and Eliza Hall Institute of Medical Research. The author has contributed to research in topics: Zebrafish & Antigen. The author has an hindex of 50, co-authored 119 publications receiving 12979 citations. Previous affiliations of Joan K. Heath include St. Vincent's Institute of Medical Research & St. Vincent's Health System.

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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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Reciprocal regulation of gastrointestinal homeostasis by SHP2 and STAT-mediated trefoil gene activation in gp130 mutant mice

TL;DR: A model whereby mucosal wound healing depends solely on activation of STAT1/3, whereas gastric hyperplasia ensues when the coordinated activation of the STAT1-3 and SHP2-Ras-ERK pathways is disrupted is proposed.

Formation of the digestive system in zebrafish: III

TL;DR: In this article, the morphological events that shape the zebrafish intestinal epithelium were investigated. But the authors focused on the period between 26 and 126 h post-fertilization (hpf) and followed the growth, lumen formation and differentiation of a continuous layer of endoderm into a functional intestinal epithelial with three morphologically distinct segments: the intestinal bulb, mid-intestine and posterior intestine.
Journal ArticleDOI

Estradiol effects on proliferation, messenger ribonucleic acid for collagen and insulin-like growth factor-I, and parathyroid hormone-stimulated adenylate cyclase activity in osteoblastic cells from calvariae and long bones.

TL;DR: For osteoblastic cells in culture, E2 can directly stimulate proliferation as well as collagen and IGF-I mRNA while decreasing PTH responsiveness; these effects could explain the anabolic and anticatabolic effects of E2 on bone.