Zobrazeno 1 - 10
of 220
pro vyhledávání: '"Sameer, C."'
Autor:
Sameer C. Dhamne, Meera E. Modi, Audrey Gray, Simone Bonazzi, Lucas Craig, Elizabeth Bainbridge, Lahin Lalani, Chloe E. Super, Samantha Schaeffer, Ketthsy Capre, Danuta Lubicka, Guiqing Liang, Doug Burdette, Stephanie M. McTighe, Sarika Gurnani, Sheryl Anne D. Vermudez, Daniel Curtis, Christopher J. Wilson, Mustafa Q. Hameed, Angelica D'Amore, Alexander Rotenberg, Mustafa Sahin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 10, Pp 1790-1801 (2023)
Abstract Objective Tuberous sclerosis complex (TSC) is a neurodevelopmental disorder caused by autosomal‐dominant pathogenic variants in either the TSC1 or TSC2 gene, and it is characterized by hamartomas in multiple organs, such as skin, kidney, l
Externí odkaz:
https://doaj.org/article/5e6e60c1d4644ed1b4ab20f434f5f54a
Autor:
Dhamne, Sameer C.1 (AUTHOR), Modi, Meera E.1 (AUTHOR), Gray, Audrey2 (AUTHOR), Bonazzi, Simone2 (AUTHOR), Craig, Lucas2 (AUTHOR), Bainbridge, Elizabeth1 (AUTHOR), Lalani, Lahin1 (AUTHOR), Super, Chloe E.1 (AUTHOR), Schaeffer, Samantha1 (AUTHOR), Capre, Ketthsy2 (AUTHOR), Lubicka, Danuta2 (AUTHOR), Liang, Guiqing2 (AUTHOR), Burdette, Doug2 (AUTHOR), McTighe, Stephanie M.2 (AUTHOR), Gurnani, Sarika1 (AUTHOR), Vermudez, Sheryl Anne D.1 (AUTHOR), Curtis, Daniel2 (AUTHOR), Wilson, Christopher J.2 (AUTHOR), Hameed, Mustafa Q.1 (AUTHOR), D'Amore, Angelica1 (AUTHOR)
Publikováno v:
Annals of Clinical & Translational Neurology. Oct2023, Vol. 10 Issue 10, p1790-1801. 12p.
Autor:
Christopher J. Yuskaitis, Leigh‐Ana Rossitto, Karenna J. Groff, Sameer C. Dhamne, Bo Zhang, Lahin K. Lalani, Achint K. Singh, Alexander Rotenberg, Mustafa Sahin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 7, Pp 1388-1397 (2021)
Abstract Objective To confirm the critical factors affecting seizure susceptibility in acute pentylenetetrazole (PTZ) mouse epilepsy models and evaluate the prior literature for these factors. Methods Serial cohorts of wild‐type mice administered i
Externí odkaz:
https://doaj.org/article/017d06ddc55843abbeaf81a9da71de13
Autor:
Patel, Archana A., Jannati, Ali, Dhamne, Sameer C., Sapuwa, Monica, Kalanga, Elizabeth, Mazumdar, Maitreyi, Birbeck, Gretchen L., Rotenberg, Alexander
Publikováno v:
In Epilepsy & Behavior December 2020 113
Autor:
Balakrishnan, D., Mariappan, Umasree, Revuru, Sai Thanooj Kumar, Sameer, C., Yalla, Satya Praveen Kumar Reddy, Bayya, Pranav Naadh
Publikováno v:
AIP Conference Proceedings; 2024, Vol. 3180 Issue 1, p1-9, 9p
Autor:
Roman Gersner, Carmen Paredes, Mustafa Q. Hameed, Sameer C. Dhamne, Alvaro Pascual‐Leone, Alexander Rotenberg
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 3, Pp 384-389 (2020)
Abstract Automated anesthesia systems that continuously monitor cortical excitability (CE) changes to govern drug infusion rates, are desirable. Paired‐pulse transcranial magnetic stimulation (ppTMS), with electromyography (EMG), provides noninvasi
Externí odkaz:
https://doaj.org/article/a323175ca9f64ce9a1baf0e1da5b78b3
Autor:
Purtell, Hannah, Dhamne, Sameer C., Gurnani, Sarika, Bainbridge, Elizabeth, Modi, Meera E., Lammers, Stephen H.T., Super, Chloe E., Hameed, Mustafa Q., Johnson, Ervin L., III, Sahin, Mustafa, Rotenberg, Alexander
Publikováno v:
In Epilepsy & Behavior December 2018 89:94-98
Autor:
Yuskaitis, Christopher J., Jones, Brandon M., Wolfson, Rachel L., Super, Chloe E., Dhamne, Sameer C., Rotenberg, Alexander, Sabatini, David M., Sahin, Mustafa, Poduri, Annapurna
Publikováno v:
In Neurobiology of Disease March 2018 111:91-101
Autor:
Christopher J. Yuskaitis, Brandon M. Jones, Rachel L. Wolfson, Chloe E. Super, Sameer C. Dhamne, Alexander Rotenberg, David M. Sabatini, Mustafa Sahin, Annapurna Poduri
Publikováno v:
Neurobiology of Disease, Vol 111, Iss , Pp 91-101 (2018)
DEPDC5 is a newly identified epilepsy-related gene implicated in focal epilepsy, brain malformations, and Sudden Unexplained Death in Epilepsy (SUDEP). In vitro, DEPDC5 negatively regulates amino acid sensing by the mTOR complex 1 (mTORC1) pathway, b
Externí odkaz:
https://doaj.org/article/8d170fb56a97490b916b45841e461d6c
Autor:
Sameer C. Dhamne, Jill L. Silverman, Chloe E. Super, Stephen H. T. Lammers, Mustafa Q. Hameed, Meera E. Modi, Nycole A. Copping, Michael C. Pride, Daniel G. Smith, Alexander Rotenberg, Jacqueline N. Crawley, Mustafa Sahin
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-19 (2017)
Abstract Background Autism spectrum disorder (ASD) is a clinically and biologically heterogeneous condition characterized by social, repetitive, and sensory behavioral abnormalities. No treatments are approved for the core diagnostic symptoms of ASD.
Externí odkaz:
https://doaj.org/article/cbfc325951d148b3b709fe4711ef7df7