Introducing PLoS Genetics

por Frankel, Wayne N
Publicado 2005

PLoS Genetics Turns Three: Looking Back, Looking Ahead

por Frankel, Wayne N., Barsh, Gregory S.
Publicado 2008

Overlaps, gaps, and complexities of mouse models of Developmental and Epileptic Encephalopathy

por Wang, Wanqi, Frankel, Wayne N.
Publicado 2020

PRAS: Predicting functional targets of RNA binding proteins based on CLIP-seq peaks

por Lin, Jianan, Zhang, Yuping, Frankel, Wayne N., Ouyang, Zhengqing
Publicado 2019

Altered Fast Synaptic Transmission in a Mouse Model of DNM1-Associated Developmental Epileptic Encephalopathy

por McCabe, Matthew P., Shore, Amy N., Frankel, Wayne N., Weston, Matthew C.
Publicado 2021

Sensory regulation of absence seizures in a mouse model of Gnb1 encephalopathy

por Teng, Sasa, Zhen, Fenghua, McRae, Briana R., Zhu, Elaine, Frankel, Wayne N., Peng, Yueqing
Publicado 2022

Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice

por Yang, Yan, Mahaffey, Connie L, Bérubé, Nathalie, Maddatu, Terry P, Cox, Gregory A, Frankel, Wayne N
Publicado 2007

Unraveling Genetic Modifiers in the Gria4 Mouse Model of Absence Epilepsy

por Frankel, Wayne N., Mahaffey, Connie L., McGarr, Tracy C., Beyer, Barbara J., Letts, Verity A.
Publicado 2014

A Genetic Interaction Network Model of a Complex Neurological Disease

por Tyler, Anna L., McGarr, Tracy C., Beyer, Barbara J., Frankel, Wayne N., Carter, Gregory W.
Publicado 2014

CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function

por Wagnon, Jacy L., Briese, Michael, Sun, Wenzhi, Mahaffey, Connie L., Curk, Tomaž, Rot, Gregor, Ule, Jernej, Frankel, Wayne N.
Publicado 2012

Heterozygous expression of a Kcnt1 gain-of-function variant has differential effects on SST- and PV-expressing cortical GABAergic neurons

por Shore, Amy N., Qunies, Alshaima’a M., Spitznagel, Brittany D., Weaver, C. David, Emmitte, Kyle A., Frankel, Wayne N., Weston, Matthew C.
Publicado 2023

Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4

por Beyer, Barbara, Deleuze, Charlotte, Letts, Verity A., Mahaffey, Connie L., Boumil, Rebecca M., Lew, Timothy A., Huguenard, John R., Frankel, Wayne N.
Publicado 2008

A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice

por Boumil, Rebecca M., Letts, Verity A., Roberts, Monica C., Lenz, Christine, Mahaffey, Connie L., Zhang, Zhong-wei, Moser, Tobias, Frankel, Wayne N.
Publicado 2010

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy

por Asinof, Samuel K., Sukoff Rizzo, Stacey J., Buckley, Alexandra R., Beyer, Barbara J., Letts, Verity A., Frankel, Wayne N., Boumil, Rebecca M.
Publicado 2015

Epilepsy Benchmarks Area II: Prevent Epilepsy and Its Progression

por Binder, Devin K., Boison, Detlev, Eid, Tore, Frankel, Wayne N., Mingorance, Ana, Smith, Bret N., Dacks, Penny A., Whittemore, Vicky, Poduri, Annapurna
Publicado 2020

The genomic landscape shaped by selection on transposable elements across 18 mouse strains

por Nellåker, Christoffer, Keane, Thomas M, Yalcin, Binnaz, Wong, Kim, Agam, Avigail, Belgard, T Grant, Flint, Jonathan, Adams, David J, Frankel, Wayne N, Ponting, Chris P
Publicado 2012

Synaptic restoration by cAMP/PKA drives activity-dependent neuroprotection to motoneurons in ALS

por Bączyk, Marcin, Alami, Najwa Ouali, Delestrée, Nicolas, Martinot, Clémence, Tang, Linyun, Commisso, Barbara, Bayer, David, Doisne, Nicolas, Frankel, Wayne, Manuel, Marin, Roselli, Francesco, Zytnicki, Daniel
Publicado 2020

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice

por Papale, Ligia A., Beyer, Barbara, Jones, Julie M., Sharkey, Lisa M., Tufik, Sergio, Epstein, Michael, Letts, Verity A., Meisler, Miriam H., Frankel, Wayne N., Escayg, Andrew
Publicado 2009

DBA/2J Genetic Background Exacerbates Spontaneous Lethal Seizures but Lessens Amyloid Deposition in a Mouse Model of Alzheimer’s Disease

por Jackson, Harriet M., Onos, Kristen D., Pepper, Keating W., Graham, Leah C., Akeson, Ellen C., Byers, Candice, Reinholdt, Laura G., Frankel, Wayne N., Howell, Gareth R.
Publicado 2015

Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networks

por McSweeney, K. Melodi, Gussow, Ayal B., Bradrick, Shelton S., Dugger, Sarah A., Gelfman, Sahar, Wang, Quanli, Petrovski, Slavé, Frankel, Wayne N., Boland, Michael J., Goldstein, David B.
Publicado 2016