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Journal of Neurodevelopmental Disorders
|
November 11, 2020
A small-molecule screen reveals novel modulators of MeCP2 and X-chromosome inactivation maintenance
Hyeong-Min Lee, M Bram Kuijer, Nerea Ruiz Blanes, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 1, 2017
Decreased Axon Caliber Underlies Loss of Fiber Tract Integrity, Disproportional Reductions in White Matter Volume, and Microcephaly in Angelman Syndrome Model Mice
Matthew C Judson, Alain C Burette, Courtney L Thaxton, et al.
Epilepsia
|
August 28, 2020
Collaborative Cross mice reveal extreme epilepsy phenotypes and genetic loci for seizure susceptibility
Bin Gu, John R Shorter, Lucy H Williams, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 9, 2015
Maternal Ube3a Loss Disrupts Sleep Homeostasis But Leaves Circadian Rhythmicity Largely Intact
J Christopher Ehlen, Kelly A Jones, Lennisha Pinckney, et al.
JCI Insight
|
October 22, 2021
Dual-isoform hUBE3A gene transfer improves behavioral and seizure outcomes in Angelman syndrome model mice
Matthew C Judson, Charles Shyng, Jeremy M Simon, et al.
Frontiers in Neuroanatomy
|
June 14, 2024
Regional and cellular organization of the autism-associated protein UBE3A/E6AP and its antisense transcript in the brain of the developing rhesus monkey
Chavely Gonzalez Ramirez, Sarah G Salvador, Ridthi Kartik Rekha Patel, et al.
Neuron
|
March 30, 2016
GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility
Matthew C Judson, Michael L Wallace, Michael S Sidorov, et al.
Molecular Autism
|
December 26, 2024
Comparative profiling of white matter development in the human and mouse brain reveals volumetric deficits and delayed myelination in Angelman syndrome
Siddhi S Ozarkar, Ridthi K-R Patel, Tasmai Vulli, et al.
Nature
|
September 3, 2013
Topoisomerases facilitate transcription of long genes linked to autism
Ian F King, Chandri N Yandava, Angela M Mabb, et al.
Human Molecular Genetics
|
November 17, 2023
Heterogeneity in the progression of retinal pathologies in mice harboring patient mimicking Impg2 mutations
Brittany N Williams, Adam Draper, Patrick F Lang, et al.
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of 14
Search research articles
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Showing results (111-120 of 136) with videos related to
Sort By:
Page
of 14
Journal of Neurodevelopmental Disorders
|
November 11, 2020
A small-molecule screen reveals novel modulators of MeCP2 and X-chromosome inactivation maintenance
Hyeong-Min Lee, M Bram Kuijer, Nerea Ruiz Blanes, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 1, 2017
Decreased Axon Caliber Underlies Loss of Fiber Tract Integrity, Disproportional Reductions in White Matter Volume, and Microcephaly in Angelman Syndrome Model Mice
Matthew C Judson, Alain C Burette, Courtney L Thaxton, et al.
Epilepsia
|
August 28, 2020
Collaborative Cross mice reveal extreme epilepsy phenotypes and genetic loci for seizure susceptibility
Bin Gu, John R Shorter, Lucy H Williams, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 9, 2015
Maternal Ube3a Loss Disrupts Sleep Homeostasis But Leaves Circadian Rhythmicity Largely Intact
J Christopher Ehlen, Kelly A Jones, Lennisha Pinckney, et al.
JCI Insight
|
October 22, 2021
Dual-isoform hUBE3A gene transfer improves behavioral and seizure outcomes in Angelman syndrome model mice
Matthew C Judson, Charles Shyng, Jeremy M Simon, et al.
Frontiers in Neuroanatomy
|
June 14, 2024
Regional and cellular organization of the autism-associated protein UBE3A/E6AP and its antisense transcript in the brain of the developing rhesus monkey
Chavely Gonzalez Ramirez, Sarah G Salvador, Ridthi Kartik Rekha Patel, et al.
Neuron
|
March 30, 2016
GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility
Matthew C Judson, Michael L Wallace, Michael S Sidorov, et al.
Molecular Autism
|
December 26, 2024
Comparative profiling of white matter development in the human and mouse brain reveals volumetric deficits and delayed myelination in Angelman syndrome
Siddhi S Ozarkar, Ridthi K-R Patel, Tasmai Vulli, et al.
Nature
|
September 3, 2013
Topoisomerases facilitate transcription of long genes linked to autism
Ian F King, Chandri N Yandava, Angela M Mabb, et al.
Human Molecular Genetics
|
November 17, 2023
Heterogeneity in the progression of retinal pathologies in mice harboring patient mimicking Impg2 mutations
Brittany N Williams, Adam Draper, Patrick F Lang, et al.
Page
of 14