Search Results - "Lukacs, L"

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  1. 1

    Food Allergy Among Children in the United States by Branum, Amy M, Lukacs, Susan L

    Published in Pediatrics (Evanston) (01-12-2009)
    “…The goals were to estimate the prevalence of food allergy and to describe trends in food allergy prevalence and health care use among US children. A…”
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    Mechanism of parkin activation by phosphorylation by Sauvé, Véronique, Sung, George, Soya, Naoto, Kozlov, Guennadi, Blaimschein, Nina, Miotto, Lis Schwartz, Trempe, Jean-François, Lukacs, Gergely L., Gehring, Kalle

    Published in Nature structural & molecular biology (01-07-2018)
    “…Mutations in the ubiquitin ligase parkin are responsible for a familial form of Parkinson’s disease. Parkin and the PINK1 kinase regulate a quality-control…”
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  3. 3

    PINK1 autophosphorylation is required for ubiquitin recognition by Rasool, Shafqat, Soya, Naoto, Truong, Luc, Croteau, Nathalie, Lukacs, Gergely L, Trempe, Jean‐François

    Published in EMBO reports (01-04-2018)
    “…Mutations in PINK1 cause autosomal recessive Parkinson's disease (PD), a neurodegenerative movement disorder. PINK1 is a kinase that acts as a sensor of…”
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    SARS-CoV-2 Seroprevalence among Healthcare, First Response, and Public Safety Personnel, Detroit Metropolitan Area, Michigan, USA, May-June 2020 by Akinbami, Lara J, Vuong, Nga, Petersen, Lyle R, Sami, Samira, Patel, Anita, Lukacs, Susan L, Mackey, Lisa, Grohskopf, Lisa A, Shehu, Amy, Atas, Jenny

    Published in Emerging infectious diseases (01-12-2020)
    “…To estimate seroprevalence of severe acute respiratory syndrome 2 (SARS-CoV-2) among healthcare, first response, and public safety personnel, antibody testing…”
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  6. 6

    Ubiquitin-dependent sorting in endocytosis by Piper, Robert C, Dikic, Ivan, Lukacs, Gergely L

    Published in Cold Spring Harbor perspectives in biology (01-01-2014)
    “…When ubiquitin (Ub) is attached to membrane proteins on the plasma membrane, it directs them through a series of sorting steps that culminate in their delivery…”
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  7. 7

    Cooperative assembly and misfolding of CFTR domains in vivo by Du, Kai, Lukacs, Gergely L

    Published in Molecular biology of the cell (01-04-2009)
    “…The cystic fibrosis transmembrane conductance regulator (CFTR) architecture consists of two membrane spanning domains (MSD1 and -2), two nucleotide binding…”
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  8. 8

    Allosteric folding correction of F508del and rare CFTR mutants by elexacaftor-tezacaftor-ivacaftor (Trikafta) combination by Veit, Guido, Roldan, Ariel, Hancock, Mark A, Da Fonte, Dillon F, Xu, Haijin, Hussein, Maytham, Frenkiel, Saul, Matouk, Elias, Velkov, Tony, Lukacs, Gergely L

    Published in JCI insight (17-09-2020)
    “…Based on its clinical benefits, Trikafta - the combination of folding correctors VX-661 (tezacaftor), VX-445 (elexacaftor), and the gating potentiator VX-770…”
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  9. 9

    Peripheral Protein Quality Control Removes Unfolded CFTR from the Plasma Membrane by Okiyoneda, Tsukasa, Barrière, Hervé, Bagdány, Miklós, Rabeh, Wael M, Du, Kai, Höhfeld, Jörg, Young, Jason C, Lukacs, Gergely L

    “…Therapeutic efforts to restore biosynthetic processing of the cystic fibrosis transmembrane conductance regulator lacking the F508 residue (ΔF508CFTR) are…”
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  10. 10

    Correction of Both NBD1 Energetics and Domain Interface Is Required to Restore ΔF508 CFTR Folding and Function by Rabeh, Wael M., Bossard, Florian, Xu, Haijin, Okiyoneda, Tsukasa, Bagdany, Miklos, Mulvihill, Cory M., Du, Kai, di Bernardo, Salvatore, Liu, Yuhong, Konermann, Lars, Roldan, Ariel, Lukacs, Gergely L.

    Published in Cell (20-01-2012)
    “…The folding and misfolding mechanism of multidomain proteins remains poorly understood. Although thermodynamic instability of the first nucleotide-binding…”
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    Selective Binding of HSC70 and its Co-Chaperones to Structural Hotspots on CFTR by Baaklini, Imad, Gonçalves, Conrado de Campos, Lukacs, Gergely L., Young, Jason C.

    Published in Scientific reports (06-03-2020)
    “…Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) channel cause cystic fibrosis. Chaperones, including HSC70, DNAJA1 and DNAJA2, play…”
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  14. 14

    Fixing cystic fibrosis by correcting CFTR domain assembly by Okiyoneda, Tsukasa, Lukacs, Gergely L

    Published in The Journal of cell biology (15-10-2012)
    “…For cystic fibrosis (CF) patients most therapies focus on alleviating the disease symptoms. Yet the cellular basis of the disease has been well studied;…”
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  15. 15

    Folding correctors can restore CFTR posttranslational folding landscape by allosteric domain–domain coupling by Soya, Naoto, Xu, Haijin, Roldan, Ariel, Yang, Zhengrong, Ye, Haoxin, Jiang, Fan, Premchandar, Aiswarya, Veit, Guido, Cole, Susan P. C., Kappes, John, Hegedüs, Tamás, Lukacs, Gergely L.

    Published in Nature communications (27-10-2023)
    “…The folding/misfolding and pharmacological rescue of multidomain ATP-binding cassette (ABC) C-subfamily transporters, essential for organismal health, remain…”
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  16. 16

    Curcumin, a Major Constituent of Turmeric, Corrects Cystic Fibrosis Defects by Egan, Marie E., Pearson, Marilyn, Weiner, Scott A., Rajendran, Vanathy, Rubin, Daniel, Glöckner-Pagel, Judith, Canny, Susan, Du, Kai, Lukacs, Gergely L., Caplan, Michael J.

    “…Cystic fibrosis is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR). The most common mutation, ΔF508,…”
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  17. 17

    Mutation-specific downregulation of CFTR2 variants by gating potentiators by Avramescu, Radu G, Kai, Yukari, Xu, Haijin, Bidaud-Meynard, Aurélien, Schnúr, Andrea, Frenkiel, Saul, Matouk, Elias, Veit, Guido, Lukacs, Gergely L

    Published in Human molecular genetics (15-12-2017)
    “…Approximately 50% of cystic fibrosis (CF) patients are heterozygous with a rare mutation on at least one allele. Several mutants exhibit functional defects,…”
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  18. 18

    Synergy-based small-molecule screen using a human lung epithelial cell line yields ΔF508-CFTR correctors that augment VX-809 maximal efficacy by Phuan, Puay-Wah, Veit, Guido, Tan, Joseph, Roldan, Ariel, Finkbeiner, Walter E, Lukacs, Gergely L, Verkman, A S

    Published in Molecular pharmacology (01-07-2014)
    “…The most prevalent cystic fibrosis transmembrane conductance regulator (CFTR) mutation causing cystic fibrosis, ΔF508, impairs folding of nucleotide binding…”
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  19. 19

    Protein homeostasis at the plasma membrane by Apaja, Pirjo M, Lukacs, Gergely L

    Published in Physiology (Bethesda, Md.) (01-07-2014)
    “…The plasma membrane (PM) and endocytic protein quality control (QC) in conjunction with the endosomal sorting machinery either repairs or targets…”
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    Intracellular routing of plasmid DNA during non-viral gene transfer by Lechardeur, Delphine, Verkman, A.S., Lukacs, Gergely L.

    Published in Advanced drug delivery reviews (05-04-2005)
    “…Gene transfer using non-viral vectors is a promising approach for the safe delivery of therapeutic DNA in genetic and acquired human diseases. Whereas the lack…”
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