The Repeated Flurothyl Seizure Model in Mice

Por Ferland, Russell J.
Publicado no Bio Protoc (2017)

Fixation methods can differentially affect ciliary protein immunolabeling

Por Hua, Kiet, Ferland, Russell J.
Publicado no Cilia (2017)

Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl‐induced generalized seizures

Por Kadiyala, Sridhar B., Ferland, Russell J.
Publicado no Epilepsia Open (2016)

Trafficking in and to the primary cilium

Por Hsiao, Yi-Chun, Tuz, Karina, Ferland, Russell J
Publicado em 2012

Dissociation of Seizure Traits in Inbred Strains of Mice using the Flurothyl Kindling Model of Epileptogenesis

Por Papandrea, Dominick, Anderson, Tara M., Herron, Bruce J., Ferland, Russell J.
Publicado em 2008

Segregation of Seizure Traits in C57 Black Mouse Substrains Using the Repeated-Flurothyl Model

Por Kadiyala, Sridhar B., Papandrea, Dominick, Herron, Bruce J., Ferland, Russell J.
Publicado em 2014

Analysis of Flurothyl-induced Myoclonus in Inbred Strains of Mice

Por Papandrea, Dominick, Kukol, Whitney S., Anderson, Tara M., Herron, Bruce J., Ferland, Russell J.
Publicado em 2009

Brefeldin A-inhibited Guanine Exchange Factor 2 Regulates Filamin A Phosphorylation and Neuronal Migration

Por Zhang, Jingping, Neal, Jason, Lian, Gewei, Shi, Bingxing, Ferland, Russell J., Sheen, Volney
Publicado em 2012

Formin 1 and Filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate

Por Hu, Jianjun, Lu, Jie, Lian, Gewei, Ferland, Russell J., Dettenhofer, Markus, Sheen, Volney L.
Publicado em 2014

Filamin A Regulates Neural Progenitor Proliferation and Cortical Size through Wee1-Dependent Cdk1 Phosphorylation

Por Lian, Gewei, Lu, Jie, Hu, Jianjun, Zhang, Jingping, Cross, Sally H., Ferland, Russell J., Sheen, Volney L.
Publicado em 2012

Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: a dissociation of hippocampal Fos from seizure activity

Por Kadiyala, Sridhar B., Papandrea, Dominick, Tuz, Karina, Anderson, Tara M., Jayakumar, Sachidhanand, Herron, Bruce J., Ferland, Russell J.
Publicado no Epilepsy Res (2014)

Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking

Por Hsiao, Yi-Chun, Tong, Zachary J., Westfall, Jennifer E., Ault, Jeffrey G., Page-McCaw, Patrick S., Ferland, Russell J.
Publicado em 2009

Detecting natural selection by empirical comparison to random regions of the genome

Por Yu, Fuli, Keinan, Alon, Chen, Hua, Ferland, Russell J., Hill, Robert S., Mignault, Andre A., Walsh, Christopher A., Reich, David
Publicado em 2009

Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission

Por Kadiyala, Sridhar B., Yannix, Joshua Q., Nalwalk, Julia W., Papandrea, Dominick, Beyer, Barbara S., Herron, Bruce J., Ferland, Russell J.
Publicado no J Neurosci (2016)

Retinal Degeneration and Failure of Photoreceptor Outer Segment Formation in Mice with Targeted Deletion of the Joubert Syndrome Gene, Ahi1

Por Westfall, Jennifer E., Hoyt, Carlton, Liu, Qin, Hsiao, Yi-Chun, Pierce, Eric A., Page-McCaw, Patrick S., Ferland, Russell J.
Publicado em 2010

BranchAnalysis2D/3D Automates Morphometry Analyses of Branching Structures

Por Srinivasan, Aditya, Muñoz-Estrada, Jesús, Bourgeois, Justin R., Nalwalk, Julia W., Pumiglia, Kevin M., Sheen, Volney L., Ferland, Russell J.
Publicado no J Neurosci Methods (2017)

Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus

Por Ferland, Russell J., Smith, Jason, Papandrea, Dominick, Gracias, Jessica, Hains, Leah, Kadiyala, Sridhar B., O’Brien, Brittany, Kang, Eun Yong, Beyer, Barbara S., Herron, Bruce J.
Publicado no G3 (Bethesda) (2017)

The Joubert Syndrome-associated Missense Mutation (V443D) in the Abelson-helper Integration Site 1 (AHI1) Protein Alters Its Localization and Protein-Protein Interactions

Por Tuz, Karina, Hsiao, Yi-Chun, Juárez, Oscar, Shi, Bingxing, Harmon, Erin Y., Phelps, Ian G., Lennartz, Michelle R., Glass, Ian A., Doherty, Dan, Ferland, Russell J.
Publicado em 2013

MS AHI1 genetic risk promotes IFNγ(+) CD4(+) T cells

Por Kaskow, Belinda J., Buttrick, Thomas S., Klein, Hans-Ulrich, White, Charles, Bourgeois, Justin R., Ferland, Russell J., Patsopoulos, Nikolaos, Bradshaw, Elizabeth M., De Jager, Philip L., Elyaman, Wassim
Publicado no Neurol Neuroimmunol Neuroinflamm (2017)

Species differences in the expression of AHI1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies

Por Doering, Jennifer E., Kane, Kelly, Hsiao, Yi-Chun, Yao, Cong, Shi, Bingxing, Slowik, Amber D., Dhagat, Bakul, Scott, Delisha D., Ault, Jeffrey G., Page-McCaw, Patrick S., Ferland, Russell J.
Publicado em 2008