Resultados de procura - Walid El‐Sayed

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  1. 1
    Hypoxia-driven intratumor heterogeneity and immune evasion

    Hypoxia-driven intratumor heterogeneity and immune evasion por Stéphane Terry, Agnete S. T. Engelsen, Stéphanie Buart, Walid El‐Sayed, Goutham Hassan Venkatesh, Salem Chouaı̈b

    Publicado 2020
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  2. 2
    Measurement of student engagement in health professions education: a review of literature

    Measurement of student engagement in health professions education: a review of literature por Salah Kassab, Mohamed M. Al‐Eraky, Walid El‐Sayed, Hossam Hamdy, Henk G. Schmidt

    Publicado 2023
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  3. 3
    Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

    Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta por James A. Poulter, Walid El‐Sayed, Richard F. Shore, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell

    Publicado 2013
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  4. 4
    Role of Hypoxic Stress in Regulating Tumor Immunogenicity, Resistance and Plasticity

    Role of Hypoxic Stress in Regulating Tumor Immunogenicity, Resistance and Plasticity por Stéphane Terry, Rania Faouzi Zaarour, Goutham Hassan Venkatesh, Amirtharaj Francis, Walid El‐Sayed, Stéphanie Buart, Pamela Eguiguren Bravo, Jérôme Thiery, Salem Chouaı̈b

    Publicado 2018
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  5. 5
    ChatGPT usage and attitudes are driven by perceptions of usefulness, ease of use, risks, and psycho-social impact: a study among university students in the UAE

    ChatGPT usage and attitudes are driven by perceptions of usefulness, ease of use, risks, and psycho-social impact: a study among university students in the UAE por Malik Sallam, Walid El‐Sayed, Muhammad Y. Al‐Shorbagy, Muna Barakat, Sami El Khatib, Wissam Ghach, Nisreen Alwan, Souheil Hallit, Diana Malaeb

    Publicado 2024
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  6. 6
    Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

    Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta por Walid El‐Sayed, David Parry, Richard F. Shore, Mushtaq Ahmed, Hussain Jafri, Yasmin Abdul Rashid, Suhaila Al‐Bahlani, Sharifa Al-Harasi, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell

    Publicado 2009
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  7. 7
    A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency

    A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency por David Parry, Tim D. Holmes, Nikita Gamper, Walid El‐Sayed, Nishani T. Hettiarachchi, Mushtaq Ahmed, Graham P. Cook, Clare V. Logan, Colin A. Johnson, Shelagh Joss, Chris Peers, Katrina Prescott, Sinisa Savic, Chris F. Inglehearn, Alan J. Mighell

    Publicado 2015
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  8. 8
    Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

    Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta por David Parry, Alan J. Mighell, Walid El‐Sayed, Richard F. Shore, I K Jalili, Hélène Dollfus, Agnès Bloch‐Zupan, Román Carlos, Ian Carr, Louise Downey, Katharine M. Blain, David Mansfield, Mehdi Shahrabi, Mansour Heidari, Parissa Aref, Mohsen Abbasi, Michel Michaelides, Anthony T. Moore, Jennifer Kirkham, Chris F. Inglehearn

    Publicado 2009
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  9. 9
    Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta

    Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta por David Parry, Claire E. L. Smith, Walid El‐Sayed, James A. Poulter, Richard F. Shore, Clare V. Logan, Chihiro Mogi, Kōichi Sato, Fumikazu Okajima, Akihiro Harada, Hong Zhang, Mine Koruyucu, Figen Seymen, Jan C.‐C. Hu, James P. Simmer, Mushtaq Ahmed, Hussain Jafri, Colin A. Johnson, Chris F. Inglehearn, Alan J. Mighell

    Publicado 2016
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  10. 10
    Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

    Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta por David Parry, Steven J. Brookes, Clare V. Logan, James A. Poulter, Walid El‐Sayed, Suhaila Al‐Bahlani, Sharifa Al-Harasi, Jihad Sayed, El Mostafa Raïf, Richard F. Shore, Mayssoon Dashash, Martin Barron, Joanne Morgan, Ian Carr, Graham R. Taylor, Colin A. Johnson, Michael J. Aldred, Michael J. Dixon, J. Tim Wright, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell

    Publicado 2012
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