Showing 1 - 11 results of 11 for search 'Jeffrey L. Noebels', query time: 0.04s Refine Results
  1. 1
    A hyperthermic seizure unleashes a surge of spreading depolarizations in Scn1a-deficient mice

    A hyperthermic seizure unleashes a surge of spreading depolarizations in Scn1a-deficient mice by Isamu Aiba, Yao Ning, Jeffrey L. Noebels

    Published 2023-08-01
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  2. 2
    Arx expansion mutation perturbs cortical development by augmenting apoptosis without activating innate immunity in a mouse model of X-linked infantile spasms syndrome

    Arx expansion mutation perturbs cortical development by augmenting apoptosis without activating innate immunity in a mouse model of X-linked infantile spasms syndrome by Meagan S. Siehr, Cory A. Massey, Jeffrey L. Noebels

    Published 2020-03-01
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  3. 3
    NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure

    NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure by Taesun Eom, Chaolin Zhang, Huidong Wang, Kenneth Lay, John Fak, Jeffrey L Noebels, Robert B Darnell

    Published 2013-01-01
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  4. 4
    Abnormal patterns of sleep and waking behaviors are accompanied by neocortical oscillation disturbances in an Ank3 mouse model of epilepsy-bipolar disorder comorbidity

    Abnormal patterns of sleep and waking behaviors are accompanied by neocortical oscillation disturbances in an Ank3 mouse model of epilepsy-bipolar disorder comorbidity by Juan E. Villacres, Nicholas Riveira, Sohmee Kim, Laura L. Colgin, Jeffrey L. Noebels, Angel Y. Lopez

    Published 2023-12-01
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  5. 5
    Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX)

    Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX) by Karagh E. Loring, Tessa Mattiske, Kristie Lee, Aneta Zysk, Matilda R. Jackson, Jeffrey L. Noebels, Cheryl Shoubridge

    Published 2021-06-01
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  6. 6
    Correction: Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population.

    Correction: Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. by Ciria C Hernandez, Tara L Klassen, Laurel G Jackson, Katharine Gurba, Ningning Hu, Jeffrey L Noebels, Robert L Macdonald

    Published 2016-01-01
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  7. 7
    Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population.

    Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. by Ciria C Hernandez, Tara L Klassen, Laurel G Jackson, Katharine Gurba, Ningning Hu, Jeffrey L Noebels, Robert L Macdonald

    Published 2016-01-01
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  8. 8
    β spectrin-dependent and domain specific mechanisms for Na+ channel clustering

    β spectrin-dependent and domain specific mechanisms for Na+ channel clustering by Cheng-Hsin Liu, Ryan Seo, Tammy Szu-Yu Ho, Michael Stankewich, Peter J Mohler, Thomas J Hund, Jeffrey L Noebels, Matthew N Rasband

    Published 2020-05-01
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  9. 9
    Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects

    Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects by Justine H. Liang, Jonathan Alevy, Viktor Akhanov, Ryan Seo, Cory A. Massey, Danye Jiang, Joy Zhou, Roy V. Sillitoe, Jeffrey L. Noebels, Melanie A. Samuel

    Published 2022-09-01
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  10. 10
    Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein

    Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein by Maoxue Tang, Guangping Gao, Carlos B. Rueda, Hang Yu, David N. Thibodeaux, Tomoyuki Awano, Kristin M. Engelstad, Maria-Jose Sanchez-Quintero, Hong Yang, Fanghua Li, Huapeng Li, Qin Su, Kara E. Shetler, Lynne Jones, Ryan Seo, Jonathan McConathy, Elizabeth M. Hillman, Jeffrey L. Noebels, Darryl C. De Vivo, Umrao R. Monani

    Published 2017-01-01
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  11. 11
    Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy

    Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy by Timothy J Abreo, Emma C Thompson, Anuraag Madabushi, Kristen L Park, Heun Soh, Nissi Varghese, Carlos G Vanoye, Kristen Springer, Jim Johnson, Scotty Sims, Zhigang Ji, Ana G Chavez, Miranda J Jankovic, Bereket Habte, Aamir R Zuberi, Cathleen M Lutz, Zhao Wang, Vaishnav Krishnan, Lisa Dudler, Stephanie Einsele-Scholz, Jeffrey L Noebels, Alfred L George, Atul Maheshwari, Anastasios Tzingounis, Edward C Cooper

    Published 2025-01-01
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