检索结果 - Metwally, Mayada

IFNL3 genotype is associated with pulmonary fibrosis in patients with systemic sclerosis 由 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

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Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease 由 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

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Copy number variation and expression of exportin-4 associates with severity of fibrosis in metabolic associated fatty liver disease 由 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

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Mistranslation Drives Alterations in Protein Levels and the Effects of a Synonymous Variant at the Fibroblast Growth Factor 21 Locus 由 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

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

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