Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Reem Jada"'
Autor:
Reem Jada, Liron Zag, Veronika Borisov, Nina S. Levy, Shai Netser, Renad Jabarin, Shlomo Wagner, Kinneret Schragenheim-Rozales, Reut Shalgi, Andrew P. Levy
Publikováno v:
International Journal of Hyperthermia, Vol 38, Iss 1, Pp 1495-1501 (2021)
Objectives Mutations in the human IQSEC2 gene are associated with drug-resistant epilepsy and severe behavioral dysfunction. We have focused on understanding one human IQSEC2 missense mutation (A350V) for which we have created a corresponding A350V I
Externí odkaz:
https://doaj.org/article/84ce4ee8e3184e6091fc234735250169
Autor:
Eli J. Rogers, Reem Jada, Kinneret Schragenheim-Rozales, Megha Sah, Marisol Cortes, Matthew Florence, Nina S. Levy, Rachel Moss, Randall S. Walikonis, Raz Palty, Reut Shalgi, Daniela Lichtman, Alexandra Kavushansky, Nashaat Z. Gerges, Itamar Kahn, George K. E. Umanah, Andrew P. Levy
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 12 (2019)
We have recently described an A350V mutation in IQSEC2 associated with intellectual disability, autism and epilepsy. We sought to understand the molecular pathophysiology of this mutation with the goal of developing targets for drug intervention. We
Externí odkaz:
https://doaj.org/article/14ef286995ec4aa7b07fafd45f233f65
Autor:
Kinneret Schragenheim-Rozales, Nina S. Levy, Shai Netser, Reut Shalgi, Renad Jabarin, Reem Jada, Veronika Borisov, Liron Zag, Shlomo Wagner, Andrew P. Levy
Publikováno v:
International Journal of Hyperthermia, Vol 38, Iss 1, Pp 1495-1501 (2021)
Objectives Mutations in the human IQSEC2 gene are associated with drug-resistant epilepsy and severe behavioral dysfunction. We have focused on understanding one human IQSEC2 missense mutation (A350V) for which we have created a corresponding A350V I
Autor:
Owen Kane, Almedia McCoy, Reem Jada, Veronika Borisov, Liron Zag, Amir Zag, Kinneret Schragenheim-Rozales, Reut Shalgi, Nina S. Levy, Andrew P. Levy, Eric D. Marsh
Publikováno v:
Epilepsy research. 182
IQSEC2 is an X-linked gene localized to the post synaptic density encoding a GTP exchange factor that regulates NMDA mediated changes in synaptic function. Mutations in the IQSEC2 gene are associated with drug resistant epilepsy, intellectual disabil
Autor:
Liron Mizrahi, Ayat Asleh, Boris Brant, Andrew P. Levy, Reem Jada, George K.E. Umanah, Tchelet Stern, Nina S. Levy, Shani Stern, Idan Rosh, Huda Adwan Shekhidem, Yam Stern, Polina Ofer
Publikováno v:
Molecular psychiatry. 26(12)
Mutations in the IQSEC2 gene are associated with drug-resistant, multifocal infantile and childhood epilepsy; autism; and severe intellectual disability (ID). We used induced pluripotent stem cell (iPSC) technology to obtain hippocampal neurons to in
Publikováno v:
Neurobiology of Learning and Memory. 154:5-11
Metaplasticity is the dynamic regulation of the ability to induce activity-dependent synaptic plasticity and is governed by the prior history of the synapses. Previous reports by others and us have shown that behavioral stress induces a form of emoti
Autor:
Nashaat Z. Gerges, Reem Jada, Reut Shalgi, Megha Sah, Eli Rogers, Daniela Lichtman, Rachel E. Moss, Matthew A. Florence, George K.E. Umanah, Marisol Cortes, Nina S. Levy, Itamar Kahn, Alexandra Kavushansky, Randall S. Walikonis, Raz Palty, Kinneret Schragenheim-Rozales, Andrew P. Levy
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 12 (2019)
Frontiers in Molecular Neuroscience
Frontiers in Molecular Neuroscience
We have recently described an A350V mutation in IQSEC2 associated with intellectual disability, autism and epilepsy. We sought to understand the molecular pathophysiology of this mutation with the goal of developing targets for drug intervention. We
Publikováno v:
Neurobiology of learning and memory. 154
Metaplasticity is the dynamic regulation of the ability to induce activity-dependent synaptic plasticity and is governed by the prior history of the synapses. Previous reports by others and us have shown that behavioral stress induces a form of emoti
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 20, Iss 12, p 3038 (2019)
International Journal of Molecular Sciences, Vol 20, Iss 12, p 3038 (2019)
Mutations in IQSEC2 cause intellectual disability (ID), which is often accompanied by seizures and autism. A number of studies have shown that IQSEC2 is an abundant protein in excitatory synapses and plays an important role in neuronal development as