Search Results - "Lindgren, Julia"

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  1. 1

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

    Published in Journal of environmental quality (01-11-2022)
    “…Mesocosm and microcosm experiments were conducted to explore the applicability of floating treatment wetlands (FTWs), an ecologically based management…”
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    Journal Article
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    Engineered Cas9 extracellular vesicles as a novel gene editing tool by Osteikoetxea, Xabier, Silva, Andreia, Lázaro‐Ibáñez, Elisa, Salmond, Nikki, Shatnyeva, Olga, Stein, Josia, Schick, Jan, Wren, Stephen, Lindgren, Julia, Firth, Mike, Madsen, Alexandra, Mayr, Lorenz M., Overman, Ross, Davies, Rick, Dekker, Niek

    Published in Journal of extracellular vesicles (01-05-2022)
    “…Extracellular vesicles (EVs) have shown promise as biological delivery vehicles, but therapeutic applications require efficient cargo loading. Here, we…”
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    (St)aging in place: Information and communication technologies for a health-centered agile dwelling unit by Cevallos, Nicole, Ramadhani, Widya A, Lindgren, Julia, Bell, Bradley, Martinez-Cosio, Maria, Harvey, Thomas E, Nanda, Upali, Mustata Wilson, Gabriela

    Published in Frontiers in public health (27-01-2023)
    “…As the number of older adults is growing rapidly in the U.S., the need for personalized, innovative, and sustainable Information and Communication Technologies…”
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  6. 6

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

    Published in Journal of medical case reports (08-08-2017)
    “…The peroxisome biogenesis disorders, which are caused by mutations in any of 13 different PEX genes, include the Zellweger spectrum disorders. Severe defects…”
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    γ-glutamyl transpeptidase deficiency caused by a large homozygous intragenic deletion in GGT1 by Darin, Niklas, Leckström, Karin, Sikora, Per, Lindgren, Julia, Almén, Gabriella, Asin-Cayuela, Jorge

    Published in European journal of human genetics : EJHG (01-06-2018)
    “…γ-Glutamyl transpeptidase deficiency (glutathionuria, OMIM 231950) is a rare disease, with only six patients reported in the literature, although this…”
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    β-Mannosidosis caused by a novel homozygous intragenic inverted duplication in MANBA by Blomqvist, Maria, Smeland, Marie Falkenberg, Lindgren, Julia, Sikora, Per, Riise Stensland, Hilde Monica Frostad, Asin-Cayuela, Jorge

    Published in Cold Spring Harbor molecular case studies (01-06-2019)
    “…β-Mannosidosis is a lysosomal storage disorder characterized by accumulation of disaccharides due to deficiency of the lysosomal enzyme β-mannosidase. The…”
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    Mental ill health among asylum seekers and other immigrants in Sweden by Lindgren, Julia, Ekblad, Solvig, Asplund, Maria, Irestig, Robert, Burström, Bo

    “…Purpose - The aim of this paper is to explore mental ill health among newly arrived immigrants to Sweden, in relation to their legal status and previous…”
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