Результаты поиска - Nassir, Nasna
- Отображение 1 - 8 результаты of 8
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SARS‐CoV‐2 May Hijack GPCR Signaling Pathways to Compromise Lung Ion and Fluid Transport по Abdel Hameid, Reem, Tambi, Richa, Nassir, Nasna, Begum, Ghausia, Zehra, Binte, Akter, Hosneara, Cormet‐Boyaka, Estelle, Kuebler, Wolfgang, Uddin, Mohammed, Berdiev, Bakhrom
Опубликовано 2021Текст -
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Mutational Landscape of Autism Spectrum Disorder Brain Tissue по Woodbury-Smith, Marc, Lamoureux, Sylvia, Begum, Ghausia, Nassir, Nasna, Akter, Hosneara, O’Rielly, Darren D., Rahman, Proton, Wintle, Richard F., Scherer, Stephen W., Uddin, Mohammed
Опубликовано 2022Текст -
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Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome по Begum, Ghausia, Albanna, Ammar, Bankapur, Asma, Nassir, Nasna, Tambi, Richa, Berdiev, Bakhrom K., Akter, Hosneara, Karuvantevida, Noushad, Kellam, Barbara, Alhashmi, Deena, Sung, Wilson W. L., Thiruvahindrapuram, Bhooma, Alsheikh-Ali, Alawi, Scherer, Stephen W., Uddin, Mohammed
Опубликовано 2021Текст -
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Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells по Nassir, Nasna, Bankapur, Asma, Samara, Bisan, Ali, Abdulrahman, Ahmed, Awab, Inuwa, Ibrahim M., Zarrei, Mehdi, Safizadeh Shabestari, Seyed Ali, AlBanna, Ammar, Howe, Jennifer L., Berdiev, Bakhrom K., Scherer, Stephen W., Woodbury-Smith, Marc, Uddin, Mohammed
Опубликовано 2021Текст -
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Analyzing single cell transcriptome data from severe COVID-19 patients по Nassir, Nasna, Tambi, Richa, Bankapur, Asma, Karuvantevida, Noushad, Khansaheb, Hamdah Hassan, Zehra, Binte, Begum, Ghausia, Hameid, Reem Abdel, Ahmed, Awab, Deesi, Zulfa, Alkhajeh, Abdulmajeed, Uddin, K.M.Furkan, Akter, Hosneara, Safizadeh Shabestari, Seyed Ali, Gaudet, Mellissa, Hachim, Mahmood Yaseen, Alsheikh-Ali, Alawi, Berdiev, Bakhrom K., Al Heialy, Saba, Uddin, Mohammed
Опубликовано 2022Текст -
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Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh по Akter, Hosneara, Hossain, Mohammad Shahnoor, Dity, Nushrat Jahan, Rahaman, Md. Atikur, Furkan Uddin, K. M., Nassir, Nasna, Begum, Ghausia, Hameid, Reem Abdel, Islam, Muhammad Sougatul, Tusty, Tahrima Arman, Basiruzzaman, Mohammad, Sarkar, Shaoli, Islam, Mazharul, Jahan, Sharmin, Lim, Elaine T., Woodbury-Smith, Marc, Stavropoulos, Dimitri James, O’Rielly, Darren D., Berdeiv, Bakhrom K., Nurun Nabi, A. H. M., Ahsan, Mohammed Nazmul, Scherer, Stephen W., Uddin, Mohammed
Опубликовано 2021Текст -
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Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19 по Nassir, Nasna, Tambi, Richa, Bankapur, Asma, Al Heialy, Saba, Karuvantevida, Noushad, Khansaheb, Hamda Hassan, Zehra, Binte, Begum, Ghausia, Hameid, Reem Abdel, Ahmed, Awab, Deesi, Zulfa, Alkhajeh, Abdulmajeed, Uddin, K.M. Furkan, Akter, Hosneara, Safizadeh Shabestari, Seyed Ali, Almidani, Omar, Islam, Amirul, Gaudet, Mellissa, Kandasamy, Richard Kumaran, Loney, Tom, Tayoun, Ahmad Abou, Nowotny, Norbert, Woodbury-Smith, Marc, Rahman, Proton, Kuebler, Wolfgang M., Yaseen Hachim, Mahmood, Casanova, Jean-Laurent, Berdiev, Bakhrom K., Alsheikh-Ali, Alawi, Uddin, Mohammed
Опубликовано 2021Текст