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Rachel Lennon

Researcher at Manchester Academic Health Science Centre

Publications -  100
Citations -  3903

Rachel Lennon is an academic researcher from Manchester Academic Health Science Centre. The author has contributed to research in topics: Podocyte & Medicine. The author has an hindex of 28, co-authored 80 publications receiving 2921 citations. Previous affiliations of Rachel Lennon include University of Bristol & National Health Service.

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The human glomerular podocyte is a novel target for insulin action.

TL;DR: Novel conditionally immortalized human podocytes in vitro and human glomeruli ex vivo are reported that the podocyte, the principal cell responsible for prevention of urinary protein loss, is insulin responsive and able to approximately double its glucose uptake within 15 min of insulin stimulation.
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Identification of a Major Epitope Recognized by PLA2R Autoantibodies in Primary Membranous Nephropathy

TL;DR: The location of a major epitope in the N-terminal cysteine-rich ricin domain of PLA2R that is recognized by 90% of human anti-PLA2R autoantibodies is described, which will enable further therapeutic advances for patients with idiopathic membranous nephropathy, including antibody inhibition therapy and immunoadsorption of circulating autoantsibodies.
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3D organoid-derived human glomeruli for personalised podocyte disease modelling and drug screening

TL;DR: 3D human glomeruli sieved from induced pluripotent stem cell-derived kidney organoids retain an improved podocyte identity in vitro facilitating disease modelling and toxicity testing and proving amenable to toxicity screening.
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Global Analysis Reveals the Complexity of the Human Glomerular Extracellular Matrix

TL;DR: The mass spectrometry-based proteomics of enriched ECM extracts is used for a global analysis of human glomerular ECM in vivo and a tissue-specific proteome of 144 structural and regulatory ECM proteins is identified, showing that the composition of glomerul ECM is far more complex than previously appreciated and suggests that many more ECM components may contribute to glomerULAR development and disease processes.