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Menna R. Clatworthy

Researcher at Wellcome Trust Sanger Institute

Publications -  174
Citations -  10024

Menna R. Clatworthy is an academic researcher from Wellcome Trust Sanger Institute. The author has contributed to research in topics: Immune system & Transplantation. The author has an hindex of 39, co-authored 136 publications receiving 7028 citations. Previous affiliations of Menna R. Clatworthy include Cambridge University Hospitals NHS Foundation Trust & Laboratory of Molecular Biology.

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The Human Cell Atlas

Aviv Regev, +81 more
- 05 Dec 2017 - 
TL;DR: An open comprehensive reference map of the molecular state of cells in healthy human tissues would propel the systematic study of physiological states, developmental trajectories, regulatory circuitry and interactions of cells, and also provide a framework for understanding cellular dysregulation in human disease.
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The adaptor MAVS promotes NLRP3 mitochondrial localization and inflammasome activation.

TL;DR: It is shown that the mitochondria-associated adaptor molecule, MAVS, is required for optimal NLRP3 inflammasome activity, and this work reveals unexpected polygamous involvement of PYD/CARD-domain-containing adapters in innate immune signaling events.
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Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage

TL;DR: Activated PI3K-δ syndrome (APDS), a PID associated with a dominant gain-of-function mutation in which lysine replaced glutamic acid at residue 1021 (E1021K) in the p110δ protein, the catalytic subunit of phosphoinositide 3-kinase δ (PI3Kδ), encoded by the PIK3CD gene is described.
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Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors

TL;DR: It is determined that Wilms tumor, a pediatric kidney cancer, originates from aberrant fetal cells, whereas adult kidney cancers are likely derived from a specific subtype of proximal convoluted tubular cell.
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FcγRIIB in autoimmunity and infection: evolutionary and therapeutic implications

TL;DR: Increased understanding of the function of FcγRIIB has potentially far-reaching therapeutic implications, being involved in the mechanism of action of intravenous immunoglobulin, controlling the efficacy of monoclonal antibody therapy and providing a direct therapeutic target.