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Daniel H Geschwind

Showing results (211-220 of 474) with videos related to

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Science (New York, N.Y.)|February 27, 2025
4D marmoset brain map reveals MRI and molecular signatures for onset of multiple sclerosis-like lesionsJing-Ping Lin, Alexis Brake, Maxime Donadieu, et al.
Experimental Neurology|April 1, 2023
Na<sub>v</sub>1.7 gain-of-function mutation I228M triggers age-dependent nociceptive insensitivity and C-LTMR dysregulationNivanthika K Wimalasena, Daniel G Taub, Jaehoon Shim, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2022
A neural stem cell paradigm of pediatric hydrocephalusPhan Q Duy, Pasko Rakic, Seth L Alper, et al.
Cancer Research Communications|October 10, 2022
Pathway-based approach reveals differential sensitivity to E2F1 inhibition in glioblastomaAlvaro G Alvarado, Kaleab Tessema, Sree Deepthi Muthukrishnan, et al.
American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
Nature Communications|June 26, 2021
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disordersBenxia Hu, Hyejung Won, Won Mah, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autismChrista Lese Martin, Jacqueline A Duvall, Yesim Ilkin, et al.
Neuron|December 12, 2023
Genome-wide study reveals novel roles for formin-2 in axon regeneration as a microtubule dynamics regulator and therapeutic target for nerve repairNgan Pan Bennett Au, Tan Wu, Xinyu Chen, et al.
JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.
Pageof 48

Showing results (211-220 of 474) with videos related to

Sort By:
Pageof 48
Science (New York, N.Y.)|February 27, 2025
4D marmoset brain map reveals MRI and molecular signatures for onset of multiple sclerosis-like lesionsJing-Ping Lin, Alexis Brake, Maxime Donadieu, et al.
Experimental Neurology|April 1, 2023
Na<sub>v</sub>1.7 gain-of-function mutation I228M triggers age-dependent nociceptive insensitivity and C-LTMR dysregulationNivanthika K Wimalasena, Daniel G Taub, Jaehoon Shim, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2022
A neural stem cell paradigm of pediatric hydrocephalusPhan Q Duy, Pasko Rakic, Seth L Alper, et al.
Cancer Research Communications|October 10, 2022
Pathway-based approach reveals differential sensitivity to E2F1 inhibition in glioblastomaAlvaro G Alvarado, Kaleab Tessema, Sree Deepthi Muthukrishnan, et al.
American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
Nature Communications|June 26, 2021
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disordersBenxia Hu, Hyejung Won, Won Mah, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autismChrista Lese Martin, Jacqueline A Duvall, Yesim Ilkin, et al.
Neuron|December 12, 2023
Genome-wide study reveals novel roles for formin-2 in axon regeneration as a microtubule dynamics regulator and therapeutic target for nerve repairNgan Pan Bennett Au, Tan Wu, Xinyu Chen, et al.
JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.
Pageof 48