weitere Publikationen der AG Naim

Chaudet, M. M., Amiri, M., Marth, N., Naim, H. Y., & Rose, D. R. (2019). Phylogenetic analysis reveals key residues in substrate hydrolysis in the isomaltase domain of sucrase-isomaltase and its role in starch digestion. Biochimica et Biophysica Acta / General Subjects, 1863(9), 1410–1416. https://doi.org/10.1016/j.bbagen.2019.06.011
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Ghanem, P., Zouein, A., Mohamad, M., Hodroj, M. H., Haykal, T., Abou Najem, S., Naim, H. Y., & Rizk, S. (2019). The vitamin E derivative gamma tocotrienol promotes anti-tumor effects in acute myeloid leukemia cell lines. Nutrients, 11(11: 2808). https://doi.org/10.3390/nu11112808
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Hoter, A., & Naim, H. Y. (2019). Heat shock proteins and ovarian cancer: important roles and therapeutic opportunities. Cancers, 11(9: 1389). https://doi.org/10.3390/cancers11091389
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Hoter, A., & Naim, H. Y. (2019). The functions and therapeutic potential of heat shock proteins in inflammatory bowel disease: an update. International Journal of Molecular Sciences, 20(21: 5331). https://doi.org/10.3390/ijms20215331
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Hoter, A., Rizk, S., & Naim, H. Y. (2019). The multiple roles and therapeutic potential of molecular chaperones in prostate cancer. Cancers, 11(8: 1194). https://doi.org/10.3390/cancers11081194
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Hoter, A., Rizk, S., & Naim, H. Y. (2019). Cellular and molecular adaptation of arabian camel to heat stress. Frontiers in Genetics, 10: 588. https://doi.org/10.3389/fgene.2019.00588
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Husein, D. M., & Naim, H. Y. (2019). Impaired cell surface expression and digestive function of sucrase-isomaltase gene variants are associated with reduced efficacy of low FODMAPs diet in patients with IBS-D. Gut, 69(8). https://doi.org/10.1136/gutjnl-2019-319411
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Husein, D. M., Wanes, D., Marten, L. M., Zimmer, K.-P., & Naim, H. Y. (2019). Heterozygotes are a potential new entity among homozygotes and compound heterozygotes in congenital sucrase-isomaltase deficiency. Nutrients, 11(10: 2290). https://doi.org/10.3390/nu11102290
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Shammas, H., Kuech, E.-M., Rizk, S., Das, A. M., & Naim, H. Y. (2019). Different Niemann-Pick C1 genotypes generate protein phenotypes that vary in their intracellular processing, trafficking and localization. Scientific Reports, 9(1: 5292). https://doi.org/10.1038/s41598-019-41707-y
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Wanes, D., Husein, D. M., & Naim, H. Y. (2019). Congenital lactase deficiency: mutations, functional and biochemical implications, and future perspectives. Nutrients, 11(2: 461). https://doi.org/10.3390/nu11020461
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