Search Results - "Sinai, Laleh"

Activating Endogenous Neural Precursor Cells Using Metformin Leads to Neural Repair and Functional Recovery in a Model of Childhood Brain Injury by Dadwal, Parvati, Mahmud, Neemat, Sinai, Laleh, Azimi, Ashkan, Fatt, Michael, Wondisford, Fredric E., Miller, Freda D., Morshead, Cindi M.

“…The development of cell replacement strategies to repair the injured brain has gained considerable attention, with a particular interest in mobilizing…”
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SRC Inhibition Reduces NR2B Surface Expression and Synaptic Plasticity in the Amygdala by Sinai, Laleh, Duffy, Steven, Roder, John C

“…The Src protein tyrosine kinase plays a central role in the regulation of N-methyl-d-aspartate receptor (NMDAR) activity by regulating NMDAR subunit 2B (NR2B)…”
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Mutation I810N in the α3 isoform of Na⁺,K⁺-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS by Clapcote, Steven J, Duffy, Steven, Xie, Gang, Kirshenbaum, Greer, Bechard, Allison R, Rodacker Schack, Vivien, Petersen, Janne, Sinai, Laleh, Saab, Bechara J, Lerch, Jason P, Minassian, Berge A, Ackerley, Cameron A, Sled, John G, Cortez, Miguel A, Henderson, Jeffrey T, Vilsen, Bente, Roder, John C

“…In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly…”
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Organization of rat vibrissa motor cortex and adjacent areas according to cytoarchitectonics, microstimulation, and intracellular stimulation of identified cells by Brecht, Michael, Krauss, Andreas, Muhammad, Sajjad, Sinai-Esfahani, Laleh, Bellanca, Sebastiano, Margrie, Troy W.

“…The relationship between motor maps and cytoarchitectonic subdivisions in rat frontal cortex is not well understood. We use cytoarchitectonic analysis of…”
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Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I1,2 by Sinai, Laleh, Ivakine, Evgueni A., Lam, Emily, Deurloo, Marielle, Dida, Joana, Zirngibl, Ralph A.

“…Src tyrosine kinase phosphorylates the general transcription factor protein TFII-I, which is deleted in the neurodevelopmental disorder Williams-Beuren…”
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Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I by Sinai, Laleh, Ivakine, Evgueni A, Lam, Emily, Deurloo, Marielle, Dida, Joana, Zirngibl, Ralph A, Jung, Cynthia, Aubin, Jane E, Feng, Zhong-Ping, Yeomans, John, McInnes, Roderick R, Osborne, Lucy R, Roder, John C

“…Src is a nonreceptor protein tyrosine kinase that is expressed widely throughout the central nervous system and is involved in diverse biological functions…”
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Mutation I810N in the [alpha]3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS by Clapcote, Steven J, Duffy, Steven, Xie, Gang, Kirshenbaum, Greer, Bechard, Allison R, Schack, Vivien Rodacker, Petersen, Janne, Sinai, Laleh, Saab, Bechara J, Lerch, Jason P, Minassian, Berge A, Ackerley, Cameron A, Sled, John G, Cortez, Miguel A, Henderson, Jeffrey T, Vilsen, Bente, Roder, John C

“…In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly…”
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Mutation 1810N in the α3 Isoform of Na⁺, K⁺-ATPase Causes Impairments in the Sodium Pump and Hyperexcitability in the CNS by Clapcote, Steven J., Duffy, Steven, Xie, Gang, Kirshenbaum, Greer, Bechard, Allison R., Schack, Vivien Rodacker, Petersen, Janne, Sinai, Laleh, Saab, Bechara J., Lerch, Jason P., Minassian, Berge A., Ackerley, Cameron A., Sled, John G., Cortez, Miguel A., Henderson, Jeffrey T., Vilsen, Bente, Roder, John C., Wright, Ernest Marshal

“…In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly…”
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Mutation I810N in the a3 isoform of Na super(+),K super(+)-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS by Clapcote, Steven J, Duffy, Steven, Xie, Gang, Kirshenbaum, Greer, Bechard, Allison R, Rodacker Schack, Vivien, Petersen, Janne, Sinai, Laleh, Saab, Bechara J, Lerch, Jason P, Minassian, Berge A, Ackerley, Cameron A, Sled, John G, Cortez, Miguel A, Henderson, Jeffrey T, Vilsen, Bente, Roder, John C

“…In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly…”
Get full text

Mutation I810N in the α3 isoform of Na⁺,K⁺-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS by Clapcote, Steven J, Duffy, Steven, Xie, Gang, Kirshenbaum, Greer, Bechard, Allison R, Rodacker Schack, Vivien, Petersen, Janne, Sinai, Laleh, Saab, Bechara J, Lerch, Jason P, Minassian, Berge A, Ackerley, Cameron A, Sled, John G, Cortez, Miguel A, Henderson, Jeffrey T, Vilsen, Bente, Roder, John C

“…In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly…”
Get full text

Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS by Clapcote, Steven J, Duffy, Steven, Xie, Gang, Kirshenbaum, Greer, Bechard, Allison R, Rodacker Schack, Vivien, Petersen, Janne, Sinai, Laleh, Saab, Bechara J, Lerch, Jason P, Minassian, Berge A, Ackerley, Cameron A, Sled, John G, Cortez, Miguel A, Henderson, Jeffrey T, Vilsen, Bente, Roder, John C

“…In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly…”
Get full text

The Role of Src Tyrosine Kinase in Synaptic Plasticity and Neurological Disorders by Sinai-Esfahani, Mirjam-Laleh

“…The non-receptor protein tyrosine kinase Src is expressed throughout the central nervous system and is involved in diverse biological functions like cell…”
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