Výsledky vyhledávání - Mohammed Uddin
- Zobrazuji výsledky 1 - 20 z 37
- Přejít na další stránku
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
Tissue engineering the retinal ganglion cell nerve fiber layer Autor Karl E. Kador, Ramon B. Montero, Praseeda Venugopalan, Jonathan Hertz, Allison N. Zindell, Daniel A. Valenzuela, Mohammed Uddin, Erin Lavik, Kenneth J. Muller, Fotios M. Andreopoulos, Jeffrey L. Goldberg
Vydáno 2013Artigo -
10
Host transcriptomic profiling of COVID-19 patients with mild, moderate, and severe clinical outcomes Autor Ruchi Jain, Sathishkumar Ramaswamy, Divinlal Harilal, Mohammed Uddin, Tom Loney, Norbert Nowotny, Hanan Al Suwaidi, Rupa Varghese, Zulfa Deesi, Abdulmajeed Alkhajeh, Hamda Khansaheb, Alawi Alsheikh‐Ali, Ahmad Abou Tayoun
Vydáno 2020Artigo -
11
Cell-specific MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy Autor Shelley L. Forrest, Seojin Lee, Nasna Nassir, Iván Martínez-Valbuena, Valerie Sackmann, Jun Li, Awab Ahmed, Maria Carmela Tartaglia, Lars M. Ittner, Anthony E. Lang, Mohammed Uddin, Gábor G. Kovács
Vydáno 2023Artigo -
12
Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes Autor 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
Vydáno 2017Artigo -
13
Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants Autor Ada J. S. Chan, Cheryl Cytrynbaum, Ny Hoang, Patricia Ambrozewicz, Rosanna Weksberg, Irene Drmic, Anne M. Ritzema, Russell Schachar, Susan Walker, Mohammed Uddin, Mehdi Zarrei, Ryan K. C. Yuen, Stephen W. Scherer
Vydáno 2019Artigo -
14
Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly Autor Marc Woodbury‐Smith, Éric Deneault, Ryan K. C. Yuen, Susan Walker, Mehdi Zarrei, Giovanna Pellecchia, Jennifer Howe, Ny Hoang, Mohammed Uddin, Christian R. Marshall, Christina Chrysler, Ann Thompson, Péter Szatmári, Stephen W. Scherer
Vydáno 2017Artigo -
15
The clinical presentation of avoidant restrictive food intake disorder in children and adolescents is largely independent of sex, autism spectrum disorder and anxiety traits Autor 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
Vydáno 2023Artigo -
16
SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions Autor Mohammed Uddin, Farah Mustafa, Tahir A. Rizvi, Tom Loney, Hanan Al Suwaidi, Ahmad Al Marzouqi, Afaf Kamal Eldin, Nabeel H. M. Alsabeeha, Thomas E. Adrian, Cesare Stefanini, Norbert Nowotny, Alawi Alsheikh‐Ali, Abiola Senok
Vydáno 2020Pré-impressão -
17
Copy number variation in Han Chinese individuals with autism spectrum disorder Autor Matthew J. Gazzellone, Xue Zhou, Anath C. Lionel, Mohammed Uddin, Bhooma Thiruvahindrapuram, Shuang Liang, Caihong Sun, Jia Wang, Mingyang Zou, Kristiina Tammimies, Susan Walker, Thanuja Selvanayagam, John Wei, Zhuozhi Wang, Lijie Wu, Stephen W. Scherer
Vydáno 2014Artigo -
18
SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions Autor Mohammed Uddin, Farah Mustafa, Tahir A. Rizvi, Tom Loney, Hanan Al Suwaidi, Ahmed H. Hassan Al-Marzouqi, Afaf Kamal Eldin, Nabeel H. M. Alsabeeha, Thomas E. Adrian, Cesare Stefanini, Norbert Nowotny, Alawi Alsheikh‐Ali, Abiola Senok
Vydáno 2020Revisão -
19
Overexpression of sonic hedgehog in the triple negative breast cancer: clinicopathological characteristics of high burden breast cancer patients from Bangladesh Autor Abu Shadat Mohammod Noman, Mohammed Uddin, Md. Zillur Rahman, Mohammad Nayeem, Sharmin Alam, Zehedina Khatun, Md Wahiduzzaman, Afrin Sultana, Md Lutfur Rahman, M. Y. Ali, Dipta Barua, Imtiaz Ahmed, M. S. Islam, Abdelilah Aboussekhra, Herman Yeger, Walid A. Farhat, Syed S. Islam
Vydáno 2016Artigo -
20
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases Autor Shruti Sinha, Fatma Rabea, Sathishkumar Ramaswamy, Ikram Chekroun, Maha El Naofal, Ruchi Jain, Roudha Alfalasi, Nour Halabi, Sawsan Yaslam, Massomeh Sheikh Hassani, Shruti Shenbagam, Alan Taylor, Mohammed Uddin, Mohamed A. Almarri, Stefan S. du Plessis, Alawi Alsheikh‐Ali, Ahmad Abou Tayoun
Vydáno 2025Artigo
Vyhledávací nástroje:
Související témata
Biology
Medicine
Genetics
Gene
Genome
Psychiatry
Autism
Autism spectrum disorder
Copy-number variation
Disease
Internal medicine
Pathology
Phenotype
Computational biology
Mutation
Psychology
Intellectual disability
Neuroscience
Coronavirus disease 2019 (COVID-19)
Gene expression
Infectious disease (medical specialty)
Proband
Virology
Biochemistry
Bioinformatics
Cell biology
Cognition
Developmental psychology
Environmental health
Exome sequencing