Hasil Pencarian - Mohammed Aldrees

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  1. 1
    Elucidating the Reprograming of Colorectal Cancer Metabolism Using Genome-Scale Metabolic Modeling

    Elucidating the Reprograming of Colorectal Cancer Metabolism Using Genome-Scale Metabolic Modeling oleh Cheng Zhang, Mohammed Aldrees, Mohammed Aldrees, Mohammed Aldrees, Muhammad Arif, Xiangyu Li, Adil Mardinoglu, Adil Mardinoglu, Adil Mardinoglu, Mohammad Azhar Aziz, Mohammad Azhar Aziz, Mohammad Azhar Aziz

    Diterbitkan 2019-07-01
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  2. 2
    Physician well-being: prevalence of burnout and associated risk factors in a tertiary hospital, Riyadh, Saudi Arabia

    Physician well-being: prevalence of burnout and associated risk factors in a tertiary hospital, Riyadh, Saudi Arabia oleh Turki Mohammed Aldrees, Sami Aleissa, Mohammed Zamakhshary, Motasim Badri, Mir Sadat-Ali

    Diterbitkan 2013-09-01
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  3. 3
    What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients

    What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients oleh Nora Alhazmi, Ali Alaqla, Bader Almuzzaini, Mohammed Aldrees, Ghaida Alnaqa, Farah Almasoud, Omar Aldibasi, Hala Alshamlan

    Diterbitkan 2024-08-01
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  4. 4
    Clonal diversity and genetic profiling of antibiotic resistance among multidrug/carbapenem-resistant Klebsiella pneumoniae isolates from a tertiary care hospital in Saudi Arabia

    Clonal diversity and genetic profiling of antibiotic resistance among multidrug/carbapenem-resistant Klebsiella pneumoniae isolates from a tertiary care hospital in Saudi Arabia oleh Taher uz Zaman, Maha Alrodayyan, Maha Albladi, Mohammed Aldrees, Mohammed Ismail Siddique, Sameera Aljohani, Hanan H. Balkhy

    Diterbitkan 2018-05-01
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  5. 5
    Multi-drug carbapenem-resistant Klebsiella pneumoniae infection carrying the OXA-48 gene and showing variations in outer membrane protein 36 causing an outbreak in a tertiary care hospital in Riyadh, Saudi Arabia

    Multi-drug carbapenem-resistant Klebsiella pneumoniae infection carrying the OXA-48 gene and showing variations in outer membrane protein 36 causing an outbreak in a tertiary care... oleh Taher uz Zaman, Mohammed Aldrees, Sameera M. Al Johani, Maha Alrodayyan, Faizah A. Aldughashem, Hanan H. Balkhy

    Diterbitkan 2014-11-01
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  6. 6
    Mutated neuron navigator 3 as a candidate gene for a rare neurodevelopmental disorder

    Mutated neuron navigator 3 as a candidate gene for a rare neurodevelopmental disorder oleh Muhammad Umair, Meshael Alharbi, Essra Aloyouni, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Muhammad Bilal, Majid Alfadhel

    Diterbitkan 2024-07-01
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  7. 7
    Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay

    Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay oleh Abeer Al Tuwaijri, Yusra Alyafee, Mashael Alharbi, Maryam Ballow, Mohammed Aldrees, Qamre Alam, Rola A. Sleiman, Muhammad Umair, Majid Alfadhel

    Diterbitkan 2022-08-01
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  8. 8
    Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features

    Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features oleh Fuad Al Mutairi, Faisal Joueidi, Maha Alshalan, Essra Aloyouni, Mariam Ballow, Mohammed Aldrees, Abdulkareem Al Abdulrahman, Abeer Al Tuwaijri, Safdar Abbas, Muhammad Umair, Majid Alfadhel

    Diterbitkan 2024-08-01
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  9. 9
    Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype

    Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype oleh Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Hamad AlEidi, Mariam Ballow, Mohammed Aldrees, Qamre Alam, Abdulkareem Al Abdulrahman, Muhammad Talal Alrifai, Majid Alfadhel

    Diterbitkan 2023-04-01
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  10. 10
    Evolving sequence mutations in the Middle East Respiratory Syndrome Coronavirus (MERS-CoV)

    Evolving sequence mutations in the Middle East Respiratory Syndrome Coronavirus (MERS-CoV) oleh Mohammed Ali AlBalwi, Anis Khan, Mohammed AlDrees, Udayaraja GK, Balavenkatesh Manie, Yaseen Arabi, Ibrahim Alabdulkareem, Sameera AlJohani, Majed Alghoribi, Ahmed AlAskar, Abdulaziz AlAjlan, Ali Hajeer

    Diterbitkan 2020-10-01
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  11. 11
    Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish

    Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish oleh Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, Marwan Nashabat, Kheloud M. Alhamoudi, Kheloud M. Alhamoudi, Muhammad Bilal, Yusra Alyafee, Abeer Al Tuwaijri, Manar Aldarwish, Ahmed Al-Rumayyan, Hamad Alkhalaf, Mohammad A. M. Wadaan, Majid Alfadhel, Majid Alfadhel

    Diterbitkan 2021-10-01
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