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Journal Abstract Search

186 related items for PubMed ID: 31754242

  • 1. Calcium signalling in mammalian cell lines expressing wild type and mutant human α1-Antitrypsin.
    Malintan NT, Buckingham SD, Lomas DA, Sattelle DB.
    Sci Rep; 2019 Nov 21; 9(1):17293. PubMed ID: 31754242
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  • 3. The serpinopathies studying serpin polymerization in vivo.
    Irving JA, Ekeowa UI, Belorgey D, Haq I, Gooptu B, Miranda E, Pérez J, Roussel BD, Ordóñez A, Dalton LE, Thomas SE, Marciniak SJ, Parfrey H, Chilvers ER, Teckman JH, Alam S, Mahadeva R, Rashid ST, Vallier L, Lomas DA.
    Methods Enzymol; 2011 Nov 21; 501():421-66. PubMed ID: 22078544
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  • 5. Sterol metabolism regulates neuroserpin polymer degradation in the absence of the unfolded protein response in the dementia FENIB.
    Roussel BD, Newton TM, Malzer E, Simecek N, Haq I, Thomas SE, Burr ML, Lehner PJ, Crowther DC, Marciniak SJ, Lomas DA.
    Hum Mol Genet; 2013 Nov 15; 22(22):4616-26. PubMed ID: 23814041
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  • 9. Mineralization of alpha-1-antitrypsin inclusion bodies in Mmalton alpha-1-antitrypsin deficiency.
    Callea F, Giovannoni I, Francalanci P, Boldrini R, Faa G, Medicina D, Nobili V, Desmet VJ, Ishak K, Seyama K, Bellacchio E.
    Orphanet J Rare Dis; 2018 May 16; 13(1):79. PubMed ID: 29769092
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  • 10. A transgenic zebrafish model of hepatocyte function in human Z α1-antitrypsin deficiency.
    Yip E, Giousoh A, Fung C, Wilding B, Prakash MD, Williams C, Verkade H, Bryson-Richardson RJ, Bird PI.
    Biol Chem; 2019 Nov 26; 400(12):1603-1616. PubMed ID: 31091192
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  • 11. Endoplasmic reticulum polymers impair luminal protein mobility and sensitize to cellular stress in alpha1-antitrypsin deficiency.
    Ordóñez A, Snapp EL, Tan L, Miranda E, Marciniak SJ, Lomas DA.
    Hepatology; 2013 May 26; 57(5):2049-60. PubMed ID: 23197448
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  • 12. Aberrant disulphide bonding contributes to the ER retention of alpha1-antitrypsin deficiency variants.
    Ronzoni R, Berardelli R, Medicina D, Sitia R, Gooptu B, Fra AM.
    Hum Mol Genet; 2016 Feb 15; 25(4):642-50. PubMed ID: 26647313
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  • 13. Modulation of calreticulin expression reveals a novel exosome-mediated mechanism of Z variant α1-antitrypsin disposal.
    Khodayari N, Oshins R, Alli AA, Tuna KM, Holliday LS, Krotova K, Brantly M.
    J Biol Chem; 2019 Apr 19; 294(16):6240-6252. PubMed ID: 30833329
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  • 14. Molecular mousetraps, alpha1-antitrypsin deficiency and the serpinopathies.
    Lomas DA.
    Clin Med (Lond); 2005 Apr 19; 5(3):249-57. PubMed ID: 16011217
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  • 15. Characterisation of serpin polymers in vitro and in vivo.
    Belorgey D, Irving JA, Ekeowa UI, Freeke J, Roussel BD, Miranda E, Pérez J, Robinson CV, Marciniak SJ, Crowther DC, Michel CH, Lomas DA.
    Methods; 2011 Mar 19; 53(3):255-66. PubMed ID: 21115126
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  • 16. Polymerogenic neuroserpin causes mitochondrial alterations and activates NFκB but not the UPR in a neuronal model of neurodegeneration FENIB.
    D'Acunto E, Gianfrancesco L, Serangeli I, D'Orsi M, Sabato V, Guadagno NA, Bhosale G, Caristi S, Failla AV, De Jaco A, Cacci E, Duchen MR, Lupo G, Galliciotti G, Miranda E.
    Cell Mol Life Sci; 2022 Jul 21; 79(8):437. PubMed ID: 35864382
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  • 19. Heteropolymerization of α-1-antitrypsin mutants in cell models mimicking heterozygosity.
    Laffranchi M, Berardelli R, Ronzoni R, Lomas DA, Fra A.
    Hum Mol Genet; 2018 May 15; 27(10):1785-1793. PubMed ID: 29538751
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