نتائج البحث - Metwally, Mayada

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