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Andrew G. Elefanty

Researcher at University of Melbourne

Publications -  186
Citations -  14197

Andrew G. Elefanty is an academic researcher from University of Melbourne. The author has contributed to research in topics: Embryonic stem cell & Induced pluripotent stem cell. The author has an hindex of 56, co-authored 169 publications receiving 12623 citations. Previous affiliations of Andrew G. Elefanty include Princess Margaret Hospital for Children & Royal Children's Hospital.

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Differentiation of Human Embryonic Stem Cells and Induced Pluripotent Stem Cells to Cardiomyocytes: A Methods Overview

TL;DR: A review of the basic biology underlying the differentiation of human pluripotent cells to cardiac lineages can be found in this paper, where the authors describe current state-of-the-art protocols, as well as ongoing refinements.
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Directing human embryonic stem cell differentiation towards a renal lineage generates a self-organizing kidney

TL;DR: This study has successfully directed the differentiation of human embryonic stem cells (hESCs) through posterior primitive streak and IM under fully chemically defined monolayer culture conditions using growth factors used during normal embryogenesis, resulting in the synchronous induction of UB and MM that forms a self-organizing structure, including nephron formation, in vitro.
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SIRPA is a specific cell-surface marker for isolating cardiomyocytes derived from human pluripotent stem cells

TL;DR: This screen identified the signal-regulatory protein alpha (SIRPA) as a marker expressed specifically on cardiomyocytes derived from hESCs and human induced pluripotent stem cells (hiPSCs), and PECAM, THY1, PDGFRB and ITGA1 as markers of the nonmyocyte population.
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Functional Maturation of hPSC-Derived Forebrain Interneurons Requires an Extended Timeline and Mimics Human Neural Development

TL;DR: It is found that early-stage progenitors progress via a radial glial-like stem cell enriched in the human fetal brain, and MGE-derived cortical interneuron deficiencies are implicated in a broad range of neurodevelopmental and degenerative disorders, highlighting the importance of these results for modeling human neural development and disease.