Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Bardees M. Foda"'
Autor:
Alaaeldin G. Fayez, Ghada Nour Eldeen, Waheba A. Zarouk, Khaled Hamed, Abeer Ramadan, Bardees M. Foda, Maha M. Kobesiy, Mai E. Zekrie, Randa S. Lotfy, Mona F. Sokkar, Hala T. El-Bassyouni
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 20, Iss 1, Pp 1-12 (2022)
Abstract Background The B30.2 variants lead to most relevant severity forms of familial Mediterranean fever (FMF) manifestations. The B30.2 domain plays a key role in protein-protein interaction (PPI) of pyrin with other apoptosis proteins and in reg
Externí odkaz:
https://doaj.org/article/4153f96fa9834f9a9ae5121bbcd39663
Autor:
Sean A. Misek, Bardees M. Foda, Thomas S. Dexheimer, Maisah Akram, Susan E. Conrad, Jens C. Schmidt, Richard R. Neubig, Kathleen A. Gallo
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Single agent and combination therapy with BRAFV600E/K and MEK inhibitors have remarkable efficacy against melanoma tumors with activating BRAF mutations, but in most cases BRAF inhibitor (BRAFi) resistance eventually develops. One resistance mechanis
Externí odkaz:
https://doaj.org/article/13e3b3bcb52f4731ab7a41e5e5dd7d41
Publikováno v:
Journal of Cell Biology. 222
The eukaryotic cytoskeleton plays essential roles in cell signaling and trafficking, broadly associated with immunity and diseases in humans and plants. To date, most studies describing cytoskeleton dynamics and function rely on qualitative/quantitat
Autor:
David V. Serreze, Bardees M. Foda, Aron M. Geurts, Yi-Guang Chen, William M. Ridgway, Ashley E. Ciecko
Publikováno v:
The Journal of Immunology. 204:2887-2899
CD137 modulates type 1 diabetes (T1D) progression in NOD mice. We previously showed that CD137 expression in CD4 T cells inhibits T1D, but its expression in CD8 T cells promotes disease development by intrinsically enhancing the accumulation of β-ce
Autor:
Bardees M. Foda, William R. Drobyski, Moujtaba Y. Kasmani, Galina Petrova, Weiguo Cui, Robert K. Burns, David M. Schauder, Ashley E. Ciecko, Chien-Wei Lin, Yi-Guang Chen
Publikováno v:
J Immunol
In type 1 diabetes (T1D) autoreactive CD8 T cells infiltrate pancreatic islets and destroy insulin-producing β cells. Progression to T1D onset is a chronic process, which suggests that the effector activity of β-cell autoreactive CD8 T cells needs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3a2a6fdca413dd1140960dffa27ea77
https://europepmc.org/articles/PMC8492517/
https://europepmc.org/articles/PMC8492517/
Autor:
Alaaeldin G, Fayez, Ghada Nour, Eldeen, Waheba A, Zarouk, Khaled, Hamed, Abeer, Ramadan, Bardees M, Foda, Maha M, Kobesiy, Mai E, Zekrie, Randa S, Lotfy, Mona F, Sokkar, Hala T, El-Bassyouni
Publikováno v:
Journal, genetic engineeringbiotechnology. 20(1)
The B30.2 variants lead to most relevant severity forms of familial Mediterranean fever (FMF) manifestations. The B30.2 domain plays a key role in protein-protein interaction (PPI) of pyrin with other apoptosis proteins and in regulation the cascade
Autor:
Salwa M. Kassem, Abeer Ramadan, Bardees M. Foda, Nora N. Esmaiel, Wagdy Khalil Bassaly Khalil, Hala T. El-Bassyouni, Khaled H. Hamed, Alaaeldin Fayez, Waheba A. Zarouk, Ghada Nour Eldeen
Publikováno v:
Gene Reports. 14:76-80
Background Assessment of apoptosis by flow cytometry assay and expression of apoptosis-related genes by quantitative Real-Time PCR has been suggested for predicting the patient response to therapeutic regimes of Familial Mediterranean Fever (FMF), as
Publikováno v:
Gene Reports. 14:65-71
Background Alzheimer disease (AD) is one of the leading causes of dementia among elderly. It is a progressive brain disorder associated with unusual behaviors, personality changes, and irreversible decline in thinking ability. Epsilon 4 allele of apo
The eukaryotic cytoskeleton plays essential roles in cell signaling and trafficking, which is broadly associated with immunity and diseases of human and plants. To date, most analyses aiming at defining the temporal and spatial dynamics of the cytosk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3d3adb13a1cdc26f9e08fb33c09e697
https://doi.org/10.1101/2021.05.11.442512
https://doi.org/10.1101/2021.05.11.442512
Publikováno v:
Andrologia. 52
Macrozoospermia is a rare syndrome. The key marker of the disease is a high percentage of spermatozoa with abnormal phenotypes namely enlarged head and multiple tails. The presence of at least 70% of spermatozoa with a large head is usually associate