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Albert J Becker

Showing results (151-160 of 166) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|March 10, 2020
DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical InterneuronsDaniel Pensold, Julia Reichard, Karen M J Van Loo, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2021
A CRISPR-Cas9-engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctionsMiguel Rodríguez de Los Santos, Marion Rivalan, Friederike S David, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Journal of Neurology|August 14, 2024
Rasmussen's encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activityTobias Bauer, Randi D von Wrede, Suresh Pujar, et al.
Acta Neuropathologica|May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibilityKatri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.
Annals of Clinical and Translational Neurology|November 22, 2017
NMDAR encephalitis: passive transfer from man to mouse by a recombinant antibodyManish Malviya, Sumanta Barman, Kristin S Golombeck, et al.
Epilepsia|February 6, 2019
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsyHerbert Schulz, Ann-Kathrin Ruppert, Federico Zara, et al.
Science Advances|June 9, 2023
Translational imaging of TSPO reveals pronounced innate inflammation in human and murine CD8 T cell-mediated limbic encephalitisMarco Gallus, Wolfgang Roll, Andre Dik, et al.
Nature Neuroscience|December 23, 2015
Systems genetics identifies a convergent gene network for cognition and neurodevelopmental diseaseMichael R Johnson, Kirill Shkura, Sarah R Langley, et al.
Human Molecular Genetics|June 19, 2014
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsyEva M Reinthaler, Dennis Lal, Sebastien Lebon, et al.
Pageof 17

Showing results (151-160 of 166) with videos related to

Sort By:
Pageof 17
Cerebral Cortex (New York, N.Y. : 1991)|March 10, 2020
DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical InterneuronsDaniel Pensold, Julia Reichard, Karen M J Van Loo, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2021
A CRISPR-Cas9-engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctionsMiguel Rodríguez de Los Santos, Marion Rivalan, Friederike S David, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Journal of Neurology|August 14, 2024
Rasmussen's encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activityTobias Bauer, Randi D von Wrede, Suresh Pujar, et al.
Acta Neuropathologica|May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibilityKatri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.
Annals of Clinical and Translational Neurology|November 22, 2017
NMDAR encephalitis: passive transfer from man to mouse by a recombinant antibodyManish Malviya, Sumanta Barman, Kristin S Golombeck, et al.
Epilepsia|February 6, 2019
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsyHerbert Schulz, Ann-Kathrin Ruppert, Federico Zara, et al.
Science Advances|June 9, 2023
Translational imaging of TSPO reveals pronounced innate inflammation in human and murine CD8 T cell-mediated limbic encephalitisMarco Gallus, Wolfgang Roll, Andre Dik, et al.
Nature Neuroscience|December 23, 2015
Systems genetics identifies a convergent gene network for cognition and neurodevelopmental diseaseMichael R Johnson, Kirill Shkura, Sarah R Langley, et al.
Human Molecular Genetics|June 19, 2014
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsyEva M Reinthaler, Dennis Lal, Sebastien Lebon, et al.
Pageof 17