Search Results - Metwally, Mayada

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  1. 1
    IFNL3 genotype is associated with pulmonary fibrosis in patients with systemic sclerosis

    IFNL3 genotype is associated with pulmonary fibrosis in patients with systemic sclerosis by Metwally, Mayada, Thabet, Khaled, Bayoumi, Ali, Nikpour, Mandana, Stevens, Wendy, Sahhar, Joanne, Zochling, Jane, Roddy, Janet, Tymms, Kathleen, Strickland, Gemma, Lester, Susan, Rischmueller, Maureen, Ngian, Gene-Siew, Walker, Jennifer, Hissaria, Pravin, Shaker, Olfat, Liddle, Christopher, Manolios, Nicholas, Beretta, Lorenzo, Proudman, Susanna, George, Jacob, Eslam, Mohammed

    Published 2019
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  2. 2
    Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease

    Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease by Bayoumi, Ali, Jalil, Ismail, Metwally, Mayada, Adams, Leon A., Aller, Rocio, García-Monzón, Carmelo, Arias-Loste, María Teresa, Miele, Luca, Petta, Salvatore, Craxì, Antonio, Gallego-Durán, Rocio, Fischer, Janett, Berg, Thomas, Qiao, Liang, Liddle, Christopher, Bugianesi, Elisabetta, Romero-Gomez, Manuel, George, Jacob, Eslam, Mohammed

    Published 2020
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  3. 3
    Copy number variation and expression of exportin-4 associates with severity of fibrosis in metabolic associated fatty liver disease

    Copy number variation and expression of exportin-4 associates with severity of fibrosis in metabolic associated fatty liver disease by Metwally, Mayada, Bayoumi, Ali, Khan, Anis, Adams, Leon A., Aller, Rocio, García-Monzón, Carmelo, Arias-Loste, María Teresa, Bugianesi, Elisabetta, Miele, Luca, Anna, Alisi, Latchoumanin, Olivier, Han, Shuanglin, Alenizi, Shafi, Sharkawy, Rasha EL, Elattar, Afaf, Gallego-Durán, Rocio, Fischer, Janett, Berg, Thomas, Liddle, Christopher, Romero-Gomez, Manuel, George, Jacob, Eslam, Mohammed

    Published 2021
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  4. 4
    Mistranslation Drives Alterations in Protein Levels and the Effects of a Synonymous Variant at the Fibroblast Growth Factor 21 Locus

    Mistranslation Drives Alterations in Protein Levels and the Effects of a Synonymous Variant at the Fibroblast Growth Factor 21 Locus by Bayoumi, Ali, Elsayed, Asmaa, Han, Shuanglin, Petta, Salvatore, Adams, Leon A., Aller, Rocio, Khan, Anis, García‐Monzón, Carmelo, Arias‐Loste, María Teresa, Miele, Luca, Latchoumanin, Olivier, Alenizi, Shafi, Gallego‐Durán, Rocio, Fischer, Janett, Berg, Thomas, Craxì, Antonio, Metwally, Mayada, Qiao, Liang, Liddle, Christopher, Yki‐Järvinen, Hannele, Bugianesi, Elisabetta, Romero‐Gomez, Manuel, George, Jacob, Eslam, Mohammed

    Published 2021
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  5. 5
    A variant in the MICA gene is associated with liver fibrosis progression in chronic hepatitis C through TGF-β1 dependent mechanisms

    A variant in the MICA gene is associated with liver fibrosis progression in chronic hepatitis C through TGF-β1 dependent mechanisms by Sharkawy, Rasha El, Bayoumi, Ali, Metwally, Mayada, Mangia, Alessandra, Berg, Thomas, Romero-Gomez, Manuel, Abate, Maria Lorena, Irving, William L., Sheridan, David, Dore, Gregory J., Spengler, Ulrich, Lampertico, Pietro, Bugianesi, Elisabetta, Weltman, Martin, Mollison, Lindsay, Cheng, Wendy, Riordan, Stephen, Santoro, Rosanna, Gallego-Durán, Rocío, Fischer, Janett, Nattermann, Jacob, D’Ambrosio, Roberta, McLeod, Duncan, Powell, Elizabeth, latchoumanin, Olivier, Thabet, Khaled, Najim, Mustafa A. M., Douglas, Mark W., Liddle, Christopher, Qiao, Liang, George, Jacob, Eslam, Mohammed

    Published 2019
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