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Christopher A Walsh

Showing results (251-260 of 319) with videos related to

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Neuron|February 26, 2020
Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5Andrew Kodani, Connor Kenny, Abbe Lai, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2021
Early role for a Na<sup>+</sup>,K<sup>+</sup>-ATPase (<i>ATP1A3</i>) in brain developmentRichard S Smith, Marta Florio, Shyam K Akula, et al.
Nature|April 21, 2022
Somatic genomic changes in single Alzheimer's disease neuronsMichael B Miller, August Yue Huang, Junho Kim, et al.
American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.
Neuron|December 19, 2014
Katanin p80 regulates human cortical development by limiting centriole and cilia numberWen F Hu, Oz Pomp, Tawfeg Ben-Omran, et al.
Science (New York, N.Y.)|July 28, 2022
Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutabilityTaejeong Bae, Liana Fasching, Yifan Wang, et al.
American Journal of Human Genetics|March 5, 2013
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanElizabeth Stevens, Keren J Carss, Sebahattin Cirak, et al.
Nature Genetics|October 2, 2012
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar developmentGaneshwaran H Mochida, Vijay S Ganesh, Maria I de Michelena, et al.
Epilepsia|June 16, 2022
The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commissionImad Najm, Dennis Lal, Mario Alonso Vanegas, et al.
American Journal of Human Genetics|March 25, 2014
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizuresXiaochang Zhang, Jiqiang Ling, Giulia Barcia, et al.
Pageof 32

Showing results (251-260 of 319) with videos related to

Sort By:
Pageof 32
Neuron|February 26, 2020
Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5Andrew Kodani, Connor Kenny, Abbe Lai, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2021
Early role for a Na<sup>+</sup>,K<sup>+</sup>-ATPase (<i>ATP1A3</i>) in brain developmentRichard S Smith, Marta Florio, Shyam K Akula, et al.
Nature|April 21, 2022
Somatic genomic changes in single Alzheimer's disease neuronsMichael B Miller, August Yue Huang, Junho Kim, et al.
American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.
Neuron|December 19, 2014
Katanin p80 regulates human cortical development by limiting centriole and cilia numberWen F Hu, Oz Pomp, Tawfeg Ben-Omran, et al.
Science (New York, N.Y.)|July 28, 2022
Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutabilityTaejeong Bae, Liana Fasching, Yifan Wang, et al.
American Journal of Human Genetics|March 5, 2013
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanElizabeth Stevens, Keren J Carss, Sebahattin Cirak, et al.
Nature Genetics|October 2, 2012
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar developmentGaneshwaran H Mochida, Vijay S Ganesh, Maria I de Michelena, et al.
Epilepsia|June 16, 2022
The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commissionImad Najm, Dennis Lal, Mario Alonso Vanegas, et al.
American Journal of Human Genetics|March 25, 2014
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizuresXiaochang Zhang, Jiqiang Ling, Giulia Barcia, et al.
Pageof 32