M
Melissa H. Little
Researcher at University of Melbourne
Publications - 273
Citations - 15990
Melissa H. Little is an academic researcher from University of Melbourne. The author has contributed to research in topics: Induced pluripotent stem cell & Kidney. The author has an hindex of 65, co-authored 259 publications receiving 13673 citations. Previous affiliations of Melissa H. Little include Washington University in St. Louis & Royal Children's Hospital.
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Journal ArticleDOI
Kidney organoids from human iPS cells contain multiple lineages and model human nephrogenesis
Minoru Takasato,Minoru Takasato,Pei Xuan Er,Han Sheng Chiu,Barbara Maier,Gregory J. Baillie,Charles Ferguson,Robert G. Parton,Ernst J. Wolvetang,Matthias S Roost,Susana M. Chuva de Sousa Lopes,Melissa H. Little,Melissa H. Little,Melissa H. Little +13 more
TL;DR: The developmental mechanism regulating the preferential induction of collecting duct versus kidney mesenchyme progenitors is identified and kidney organoids that contain nephrons associated with a collecting duct network surrounded by renal interstitium and endothelial cells are generated.
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Directing human embryonic stem cell differentiation towards a renal lineage generates a self-organizing kidney
Minoru Takasato,Pei Xuan Er,M. Becroft,Jessica M. Vanslambrouck,Edouard G. Stanley,Andrew G. Elefanty,Melissa H. Little +6 more
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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A side order of stem cells: the SP phenotype.
TL;DR: The SP phenotype may prove invaluable for the initial isolation of resident tissue stem cells in the absence of definitive cell‐surface markers and may have broad‐ranging applications in stem cell biology, from the purification of novel stem cell populations to the development of autologous stem cell therapies.
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Mammalian Kidney Development: Principles, Progress, and Projections
TL;DR: Recent insights into central regulatory processes governing organ assembly and renal disease are focused on, and future directions for the field are predicted.
Journal ArticleDOI
Mice Lacking the Vascular Endothelial Growth Factor-B Gene (Vegfb) Have Smaller Hearts, Dysfunctional Coronary Vasculature, and Impaired Recovery From Cardiac Ischemia
Daniela Bellomo,John P. Headrick,Ginters Silins,Carol Paterson,Penny S. Thomas,Michael Gartside,Arne W. Mould,Marian M. Cahill,Ian D. Tonks,Sean M. Grimmond,Steve Townson,Christine A. Wells,Melissa H. Little,Margaret C. Cummings,Nicholas K. Hayward,Graham F. Kay +15 more
TL;DR: A role for VEGF-B in the development or function of coronary vasculature is revealed and potential clinical use in therapeutic angiogenesis is suggested.