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Harvard's new kidney engineering technology licensed to San Diego-based Trestle Biotherapeutics

A newly launched startup is building upon innovations developed over several years at the Wyss Institute for Biologically Inspired Engineering at Harvard University, Harvard John A. Paulson School of Engineering & Applied Sciences (SEAS), and Brigham and Womenโ€™s Hospital (Brigham) to engineer functional kidney tissue for renal repair and replacement therapy.
United States Aimee Molineux Joseph Bonventre Jennifer Lewis Ruji Morizane Alice Chen

Harvard University licenses kidney engineering technology to Trestle Biotherapeutics to ...

Wyss Institute for Biologically Inspired Engineering at Harvard University, Feb. 22, 2022 (GLOBE NEWSWIRE) -- (BOSTON/CAMBRIDGE, Mass.) — A newly launched startup is building upon innovations developed over several years
Boston University United States University Of Massachusetts Medical School Massachusetts Institute Of Technology Harvard University Tufts University

Harvard University licenses kidney engineering technology to Trestle Biotherapeutics to ...

Wyss Institute for Biologically Inspired Engineering at Harvard University, Feb. 22, 2022 (GLOBE NEWSWIRE) -- (BOSTON/CAMBRIDGE, Mass.) — A newly launched startup is building upon innovations developed over several years
Boston University United States University Of Massachusetts Medical School Massachusetts Institute Of Technology Harvard University Tufts University

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New DisCo method allows scRNA-seq to efficiently process samples with fewer cells

Single-cell RNA sequencing, or "scRNA-seq" for short, is a technique that allows scientists to study the expression of genes in an individual cell within a mixed population โ€“ which is virtually how all cells exist in the body's tissues.
Bart Deplancke Johannes Bues Joern Pezoldt Ecole Polytechnique Federale Marjan Bio Emily Henderson

Cystic Fibrosis Genetic Modifiers Identified in Novel High-Throughput Screening Platform

A new systematic, high-throughput mapping and characterization of the protein interactomes of normal and mutant CFTR, the gene implicated in cystic fibrosis, could lead to a better understanding of the genetic modifiers of CFTR and the cellular changes associated with the disease. The investigators have used a modified form of a screening technology developed in the lab earlier, to identify proteins interacting with the CFTR membrane channel directly in live mammalian cells.
Tanja Gonska Igor Stagljar Margarida Amaral University Of Toronto Donnelly Centre For Cellular Biomolecular Research

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