Hasil Pencarian - Mohammed Uddin

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  1. 1
    169 Using network analysis to follow meningococcal septic shock pathogenesis in infants

    169 Using network analysis to follow meningococcal septic shock pathogenesis in infants oleh Mohammed Uddin, Asrar Rashid, Javed Ismail, Govind Benakatti

    Diterbitkan 2021-04-01
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  2. 2
    Fibromuscular Dysplasia: Renal Artery Dissection and Infarction in a Young Male

    Fibromuscular Dysplasia: Renal Artery Dissection and Infarction in a Young Male oleh Mustafa Bdiwi, John Dayco, Mohammed Uddin, Luis Afonso

    Diterbitkan 2024-05-01
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  3. 3
    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES

    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES oleh Mohammed Uddin Rasheed, Nooruddin Thajuddin, Parveez Ahamed, Zelalem Teklemariam, Kaiser Jamil

    Diterbitkan 2014-07-01
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  4. 4
    Genome-wide signatures of 'rearrangement hotspots' within segmental duplications in humans.

    Genome-wide signatures of 'rearrangement hotspots' within segmental duplications in humans. oleh Mohammed Uddin, Mitch Sturge, Lynette Peddle, Darren D O'Rielly, Proton Rahman

    Diterbitkan 2011-01-01
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  5. 5
    Computational Analysis of Short Linear Motifs in the Spike Protein of SARS-CoV-2 Variants Provides Possible Clues into the Immune Hijack and Evasion Mechanisms of Omicron Variant

    Computational Analysis of Short Linear Motifs in the Spike Protein of SARS-CoV-2 Variants Provides Possible Clues into the Immune Hijack and Evasion Mechanisms of Omicron Variant oleh Anjana Soorajkumar, Ebrahim Alakraf, Mohammed Uddin, Stefan S. Du Plessis, Alawi Alsheikh-Ali, Richard K. Kandasamy

    Diterbitkan 2022-08-01
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  6. 6
    NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system

    NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system oleh Kyle W. Davis, Colleen G. Bilancia, Megan Martin, Rena Vanzo, Megan Rimmasch, Yolanda Hom, Mohammed Uddin, Moises A. Serrano

    Diterbitkan 2022-03-01
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  7. 7
    Human leukocyte antigen B polymorphism and association between HLA‐B27 and endoplasmic reticulum aminopeptidase 1 rs30187 SNP in patients with ankylosing spondylitis in Bangladesh

    Human leukocyte antigen B polymorphism and association between HLA‐B27 and endoplasmic reticulum aminopeptidase 1 rs30187 SNP in patients with ankylosing spondylitis in Bangladesh... oleh Md Kamrul H. Sajib, Shamim Ahmed, Syed A. Haq, Minhaj R. Choudhury, Mohammed Uddin, Furkan Uddin, Muhammad S. A. Khan, Mohammad M. Zaman

    Diterbitkan 2022-03-01
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  8. 8
    Host transcriptomic profiling of COVID-19 patients with mild, moderate, and severe clinical outcomes

    Host transcriptomic profiling of COVID-19 patients with mild, moderate, and severe clinical outcomes oleh Ruchi Jain, Sathishkumar Ramaswamy, Divinlal Harilal, Mohammed Uddin, Tom Loney, Norbert Nowotny, Hanan Alsuwaidi, Rupa Varghese, Zulfa Deesi, Abdulmajeed Alkhajeh, Hamda Khansaheb, Alawi Alsheikh-Ali, Ahmad Abou Tayoun

    Diterbitkan 2021-01-01
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  9. 9
    Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes

    Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes oleh Marc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, Ryan K. C. Yuen, Susan Walker, Jennifer Howe, Mohammed Uddin, Ny Hoang, Janet A. Buchanan, Christina Chrysler, Ann Thompson, Peter Szatmari, Stephen W. Scherer

    Diterbitkan 2017-05-01
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  10. 10
    Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1Research in context

    Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1Research in context oleh Syed S. Islam, Mohammed Uddin, Abu Shadat M. Noman, Hosneara Akter, Nusrat J. Dity, Mohammad Basiruzzman, Furkan Uddin, Jahanara Ahsan, Sunera Annoor, Ayodele A. Alaiya, Monther Al-Alwan, Herman Yeger, Walid A. Farhat

    Diterbitkan 2019-05-01
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  11. 11
    Utility of clinical exome sequencing in a complex Emirati pediatric cohort

    Utility of clinical exome sequencing in a complex Emirati pediatric cohort oleh Nour Abu Mahfouz, Praseetha Kizhakkedath, Alia Ibrahim, Maha El Naofal, Sathishkumar Ramaswamy, Divinlal Harilal, Yasmeen Qutub, Mohammed Uddin, Alan Taylor, Zeinab Alloub, Ammar AlBanna, Walid Abuhammour, Basil Fathalla, Ahmad Abou Tayoun

    Diterbitkan 2020-01-01
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  12. 12
    The clinical presentation of avoidant restrictive food intake disorder in children and adolescents is largely independent of sex, autism spectrum disorder and anxiety traitsResearch in context

    The clinical presentation of avoidant restrictive food intake disorder in children and adolescents is largely independent of sex, autism spectrum disorder and anxiety traitsResearc... oleh Rosie Watts, Tanith Archibald, Pippa Hembry, Maxine Howard, Cate Kelly, Rachel Loomes, Laura Markham, Harry Moss, Alfonce Munuve, Anca Oros, Amy Siddall, Charlotte Rhind, Mohammed Uddin, Zain Ahmad, Rachel Bryant-Waugh, Christopher Hübel

    Diterbitkan 2023-09-01
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  13. 13
    Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

    Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly oleh Marc Woodbury-Smith, Eric Deneault, Ryan K. C. Yuen, Susan Walker, Mehdi Zarrei, Giovanna Pellecchia, Jennifer L. Howe, Ny Hoang, Mohammed Uddin, Christian R. Marshall, Christina Chrysler, Ann Thompson, Peter Szatmari, Stephen W. Scherer

    Diterbitkan 2017-11-01
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  14. 14
    Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome

    Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome oleh Ghausia Begum, Ammar Albanna, Asma Bankapur, Nasna Nassir, Richa Tambi, Bakhrom K. Berdiev, Hosneara Akter, Noushad Karuvantevida, Barbara Kellam, Deena Alhashmi, Wilson W. L. Sung, Bhooma Thiruvahindrapuram, Alawi Alsheikh-Ali, Stephen W. Scherer, Mohammed Uddin

    Diterbitkan 2021-02-01
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  15. 15
    SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions

    SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions oleh Mohammed Uddin, Farah Mustafa, Tahir A. Rizvi, Tom Loney, Hanan Al Suwaidi, Ahmed H. Hassan Al-Marzouqi, Afaf Kamal Eldin, Nabeel Alsabeeha, Thomas E. Adrian, Cesare Stefanini, Norbert Nowotny, Alawi Alsheikh-Ali, Abiola C. Senok

    Diterbitkan 2020-05-01
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  16. 16
    Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells

    Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells oleh Nasna Nassir, Asma Bankapur, Bisan Samara, Abdulrahman Ali, Awab Ahmed, Ibrahim M. Inuwa, Mehdi Zarrei, Seyed Ali Safizadeh Shabestari, Ammar AlBanna, Jennifer L. Howe, Bakhrom K. Berdiev, Stephen W. Scherer, Marc Woodbury-Smith, Mohammed Uddin

    Diterbitkan 2021-11-01
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  17. 17
    Curcumin improves D-galactose and normal-aging associated memory impairment in mice: In vivo and in silico-based studies.

    Curcumin improves D-galactose and normal-aging associated memory impairment in mice: In vivo and in silico-based studies. oleh Md Ashrafur Rahman, Arif Anzum Shuvo, Asim Kumar Bepari, Mehedi Hasan Apu, Manik Chandra Shill, Murad Hossain, Mohammed Uddin, Md Rabiul Islam, Monjurul Kader Bakshi, Javed Hasan, Atiqur Rahman, Ghazi Mohammad Sayedur Rahman, Hasan Mahmud Reza

    Diterbitkan 2022-01-01
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  18. 18
    Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region

    Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region oleh Rabeya Akter Mim, Anjana Soorajkumar, Noor Kosaji, Muhammad Mizanur Rahman, Shaoli Sarker, Noushad Karuvantevida, Tamannyat Binte Eshaque, Md Atikur Rahaman, Amirul Islam, Mohammod Shah Jahan Chowdhury, Nusrat Shams, K. M. Furkan Uddin, Hosneara Akter, Mohammed Uddin

    Diterbitkan 2024-04-01
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  19. 19
    Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes

    Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes oleh Muhammad M. Rahman, KM Furkan Uddin, Nesreen K. Al Jezawi, Noushad Karuvantevida, Hosneara Akter, Nushrat J. Dity, Md. Ashiquir Rahaman, Maksuda Begum, Md. Atikur Rahaman, Md. Abdul Baqui, Zeena Salwa, Serajul Islam, Marc Woodbury‐Smith, Mohammed Basiruzzaman, Mohammed Uddin

    Diterbitkan 2019-10-01
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  20. 20
    Application of a gene modular approach for clinical phenotype genotype association and sepsis prediction using machine learning in meningococcal sepsis

    Application of a gene modular approach for clinical phenotype genotype association and sepsis prediction using machine learning in meningococcal sepsis oleh Asrar Rashid, Arif R. Anwary, Feras Al-Obeidat, Joe Brierley, Mohammed Uddin, Hoda Alkhzaimi, Amrita Sarpal, Mohammed Toufiq, Zainab A. Malik, Raziya Kadwa, Praveen Khilnani, M Guftar Shaikh, Govind Benakatti, Javed Sharief, Syed Ahmed Zaki, Abdulrahman Zeyada, Ahmed Al-Dubai, Wael Hafez, Amir Hussain

    Diterbitkan 2023-01-01
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