Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

934 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations.
Nissenkorn A, Almog Y, Adler I, Safrin M, Brusel M, Marom M, Bercovich S, Yakubovich D, Tzadok M, Ben-Zeev B, Rubinstein M. Nissenkorn A, et al. Among authors: rubinstein m. PLoS One. 2019 Feb 8;14(2):e0211901. doi: 10.1371/journal.pone.0211901. eCollection 2019. PLoS One. 2019. PMID: 30735520 Free PMC article.
Mitochondrial Regulation of the Hippocampal Firing Rate Set Point and Seizure Susceptibility.
Styr B, Gonen N, Zarhin D, Ruggiero A, Atsmon R, Gazit N, Braun G, Frere S, Vertkin I, Shapira I, Harel M, Heim LR, Katsenelson M, Rechnitz O, Fadila S, Derdikman D, Rubinstein M, Geiger T, Ruppin E, Slutsky I. Styr B, et al. Among authors: rubinstein m. Neuron. 2019 Jun 5;102(5):1009-1024.e8. doi: 10.1016/j.neuron.2019.03.045. Epub 2019 Apr 29. Neuron. 2019. PMID: 31047779 Free PMC article.
Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations.
Mora-Jimenez L, Valencia M, Sanchez-Carpintero R, Tønnesen J, Fadila S, Rubinstein M, Gonzalez-Aparicio M, Bunuales M, Fernandez-Pierola E, Nicolas MJ, Puerta E, Miguelez C, Minguez PG, Lumbreras S, Gonzalez-Aseguinolaza G, Ricobaraza A, Hernandez-Alcoceba R. Mora-Jimenez L, et al. Among authors: rubinstein m. Mol Ther Nucleic Acids. 2021 Aug 19;25:585-602. doi: 10.1016/j.omtn.2021.08.003. eCollection 2021 Sep 3. Mol Ther Nucleic Acids. 2021. PMID: 34589280 Free PMC article.
Dissecting the phenotypes of Dravet syndrome by gene deletion.
Rubinstein M, Han S, Tai C, Westenbroek RE, Hunker A, Scheuer T, Catterall WA. Rubinstein M, et al. Brain. 2015 Aug;138(Pt 8):2219-33. doi: 10.1093/brain/awv142. Epub 2015 May 27. Brain. 2015. PMID: 26017580 Free PMC article.
Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A).
Rabinski T, Sagiv ST, Hausman-Kedem M, Fattal-Valevski A, Rubinstein M, Avraham KB, Vatine GD. Rabinski T, et al. Among authors: rubinstein m. Stem Cell Res. 2021 Mar;51:102178. doi: 10.1016/j.scr.2021.102178. Epub 2021 Jan 15. Stem Cell Res. 2021. PMID: 33482465 Free article.
934 results