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Gaia Novarino

Showing results (31-40 of 44) with videos related to

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Nature Communications|May 25, 2021
Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain developmentJasmin Morandell, Lena A Schwarz, Bernadette Basilico, et al.
Journal of Medical Genetics|June 20, 2017
A homozygous founder mutation in <i>TRAPPC6B</i> associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic featuresIsaac Marin-Valencia, Gaia Novarino, Anide Johansen, et al.
Cell|March 30, 2023
Large neutral amino acid levels tune perinatal neuronal excitability and survivalLisa S Knaus, Bernadette Basilico, Daniel Malzl, et al.
Cell Reports|April 6, 2022
CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectoriesCarlo Emanuele Villa, Cristina Cheroni, Christoph P Dotter, et al.
Nature Methods|July 10, 2023
Dense 4D nanoscale reconstruction of living brain tissuePhilipp Velicky, Eder Miguel, Julia M Michalska, et al.
Nature|June 17, 2026
Cortical development dynamics across autism spectrum disorder mouse modelsLena A Schwarz, Christoph P Dotter, Sergey Isaev, et al.
Cell|December 3, 2016
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum DisorderDora C Tărlungeanu, Elena Deliu, Christoph P Dotter, et al.
Nature|December 9, 2024
A framework for neural organoids, assembloids and transplantation studiesSergiu P Pașca, Paola Arlotta, Helen S Bateup, et al.
European Journal of Human Genetics : EJHG|August 21, 2014
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndromeAlma Kuechler, Alexander M Zink, Thomas Wieland, et al.
Science (New York, N.Y.)|September 8, 2012
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsyGaia Novarino, Paul El-Fishawy, Hulya Kayserili, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Nature Communications|May 25, 2021
Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain developmentJasmin Morandell, Lena A Schwarz, Bernadette Basilico, et al.
Journal of Medical Genetics|June 20, 2017
A homozygous founder mutation in <i>TRAPPC6B</i> associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic featuresIsaac Marin-Valencia, Gaia Novarino, Anide Johansen, et al.
Cell|March 30, 2023
Large neutral amino acid levels tune perinatal neuronal excitability and survivalLisa S Knaus, Bernadette Basilico, Daniel Malzl, et al.
Cell Reports|April 6, 2022
CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectoriesCarlo Emanuele Villa, Cristina Cheroni, Christoph P Dotter, et al.
Nature Methods|July 10, 2023
Dense 4D nanoscale reconstruction of living brain tissuePhilipp Velicky, Eder Miguel, Julia M Michalska, et al.
Nature|June 17, 2026
Cortical development dynamics across autism spectrum disorder mouse modelsLena A Schwarz, Christoph P Dotter, Sergey Isaev, et al.
Cell|December 3, 2016
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum DisorderDora C Tărlungeanu, Elena Deliu, Christoph P Dotter, et al.
Nature|December 9, 2024
A framework for neural organoids, assembloids and transplantation studiesSergiu P Pașca, Paola Arlotta, Helen S Bateup, et al.
European Journal of Human Genetics : EJHG|August 21, 2014
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndromeAlma Kuechler, Alexander M Zink, Thomas Wieland, et al.
Science (New York, N.Y.)|September 8, 2012
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsyGaia Novarino, Paul El-Fishawy, Hulya Kayserili, et al.
Pageof 5