Publications by authors named "Julia Lindgren"

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Apoptotic signatures allow early and rapid screening of drug-induced liver injury to accelerate drug discovery.
John Hellgren, Bhavik Chouhan, Aydar Uatay, Ramy Elgendy, Julia Lindgren

Commun Med (Lond)· December 2025

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Barcoded Hybrids of Extracellular Vesicles and Lipid Nanoparticles for Multiplexed Analysis of Tissue Distribution.
Alena Ivanova, Renata Chalupska, Ana Filipa Louro, Mike Firth, Hernán González-King Garibotti, Julia Lindgren

Adv Sci (Weinh)· March 2025

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Mapping spatially resolved transcriptomes in human and mouse pulmonary fibrosis.
Lovisa Franzén, Martina Olsson Lindvall, Michael Hühn, Victoria Ptasinski, Laura Setyo, Julia Lindgren

Nat Genet· August 2024

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Epigenetic modulators link mitochondrial redox homeostasis to cardiac function in a sex-dependent manner.
Zaher ElBeck, Mohammad Bakhtiar Hossain, Humam Siga, Nikolay Oskolkov, Fredrik Karlsson, Julia Lindgren

Nat Commun· March 2024

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(St)aging in place: Information and communication technologies for a health-centered agile dwelling unit.
Nicole Cevallos, Widya A Ramadhani, Julia Lindgren, Bradley Bell, Maria Martinez-Cosio

Front Public Health· February 2023

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Neonicotinoid pesticide and nitrate mixture removal and persistence in floating treatment wetlands.
Julia K Lindgren, Tiffany L Messer, Daniel N Miller, Daniel D Snow, Thomas G Franti

J Environ Qual· November 2022

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Engineered Cas9 extracellular vesicles as a novel gene editing tool.
Xabier Osteikoetxea, Andreia Silva, Elisa Lázaro-Ibáñez, Nikki Salmond, Olga Shatnyeva, Julia Lindgren

J Extracell Vesicles· May 2022

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Modelling human liver fibrosis in the context of non-alcoholic steatohepatitis using a microphysiological system.
Tomasz Kostrzewski, Sophie Snow, Anya Lindström Battle, Samantha Peel, Zahida Ahmad, Julia Lindgren

Commun Biol· September 2021

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β-Mannosidosis caused by a novel homozygous intragenic inverted duplication in .
Maria Blomqvist, Marie Falkenberg Smeland, Julia Lindgren, Per Sikora, Hilde Monica Frostad Riise Stensland

Cold Spring Harb Mol Case Stud· June 2019

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γ-glutamyl transpeptidase deficiency caused by a large homozygous intragenic deletion in GGT1.
Niklas Darin, Karin Leckström, Per Sikora, Julia Lindgren, Gabriella Almén

Eur J Hum Genet· June 2018

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Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case report.
Maria Blomqvist, Karin Ahlberg, Julia Lindgren, Sacha Ferdinandusse, Jorge Asin-Cayuela

J Med Case Rep· August 2017

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