Expression of EBV Encoded viral RNA 1, 2 and anti-inflammatory Cytokine (interleukin-10) in FFPE lymphoma specimens: a preliminary study for diagnostic implication in Pakistan

por Sheikh, Taimoor I, Qadri, Ishtiaq
Publicado 2011

A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient

por Sheikh, Taimoor I, Mittal, Kirti, Willis, Mary J, Vincent, John B
Publicado 2013

Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization

por Sheikh, Taimoor I., Harripaul, Ricardo, Vasli, Nasim, Ghadami, Majid, Santangelo, Susan L., Ayub, Muhammad, Sasanfar, Roksana, Vincent, John B.
Publicado 2021

From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2

por Sheikh, Taimoor I., Ausió, Juan, Faghfoury, Hannah, Silver, Josh, Lane, Jane B., Eubanks, James H., MacLeod, Patrick, Percy, Alan K., Vincent, John B.
Publicado 2016

Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations

por Mok, Rebecca S. F., Zhang, Wenbo, Sheikh, Taimoor I., Pradeepan, Kartik, Fernandes, Isabella R., DeJong, Leah C., Benigno, Gabriel, Hildebrandt, Matthew R., Mufteev, Marat, Rodrigues, Deivid C., Wei, Wei, Piekna, Alina, Liu, Jiajie, Muotri, Alysson R., Vincent, John B., Muller, Lyle, Martinez-Trujillo, Julio, Salter, Michael W., Ellis, James
Publicado 2022

Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability

por Sheikh, Taimoor I., Vasli, Nasim, Pastore, Stephen, Kharizi, Kimia, Harripaul, Ricardo, Fattahi, Zohreh, Pande, Shruti, Naeem, Farooq, Hussain, Abrar, Mir, Asif, Islam, Omar, Girisha, Katta Mohan, Irfan, Muhammad, Ayub, Muhammad, Schwarzer, Christoph, Najmabadi, Hossein, Shukla, Anju, Sladky, Valentina C., Braun, Vincent Zoran, Garcia-Carpio, Irmina, Villunger, Andreas, Vincent, John B.
Publicado 2021

MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2

por Martínez de Paz, Alexia, Khajavi, Leila, Martin, Hélène, Claveria-Gimeno, Rafael, Tom Dieck, Susanne, Cheema, Manjinder S., Sanchez-Mut, Jose V., Moksa, Malgorzata M., Carles, Annaick, Brodie, Nick I., Sheikh, Taimoor I., Freeman, Melissa E., Petrotchenko, Evgeniy V., Borchers, Christoph H., Schuman, Erin M., Zytnicki, Matthias, Velazquez-Campoy, Adrian, Abian, Olga, Hirst, Martin, Esteller, Manel, Vincent, John B., Malnou, Cécile E., Ausió, Juan
Publicado 2019