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Bonnie Nijhof

Showing results (1-10 of 14) with videos related to

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Neuroscience and Biobehavioral Reviews|March 26, 2014
Drosophila models of early onset cognitive disorders and their clinical applicationsMonique van der Voet, Bonnie Nijhof, Merel A W Oortveld, et al.
Frontiers in Neuroscience|December 25, 2014
Age-related decreased inhibitory vs. excitatory gene expression in the adult autistic brainLouie N van de Lagemaat, Bonnie Nijhof, Daniëlle G M Bosch, et al.
Plos Computational Biology|March 22, 2016
A New Fiji-Based Algorithm That Systematically Quantifies Nine Synaptic Parameters Provides Insights into Drosophila NMJ MorphometryBonnie Nijhof, Anna Castells-Nobau, Louis Wolf, et al.
Journal of Visualized Experiments : Jove|May 19, 2017
Two Algorithms for High-throughput and Multi-parametric Quantification of Drosophila Neuromuscular Junction MorphologyAnna Castells-Nobau, Bonnie Nijhof, Ilse Eidhof, et al.
American Journal of Human Genetics|January 11, 2016
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent ModulesKorinna Kochinke, Christiane Zweier, Bonnie Nijhof, et al.
Plos One|December 5, 2013
Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disabilityJoke Vandewalle, Marion Langen, Marlen Zschätzsch, et al.
Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
Plos Genetics|May 12, 2016
BOD1 Is Required for Cognitive Function in Humans and DrosophilaSahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 11, 2015
Converging evidence does not support GIT1 as an ADHD risk geneMarieke Klein, Monique van der Voet, Benjamin Harich, et al.
Human Molecular Genetics|April 12, 2013
CEP89 is required for mitochondrial metabolism and neuronal function in man and flyBregje W M van Bon, Merel A W Oortveld, Leo G Nijtmans, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Neuroscience and Biobehavioral Reviews|March 26, 2014
Drosophila models of early onset cognitive disorders and their clinical applicationsMonique van der Voet, Bonnie Nijhof, Merel A W Oortveld, et al.
Frontiers in Neuroscience|December 25, 2014
Age-related decreased inhibitory vs. excitatory gene expression in the adult autistic brainLouie N van de Lagemaat, Bonnie Nijhof, Daniëlle G M Bosch, et al.
Plos Computational Biology|March 22, 2016
A New Fiji-Based Algorithm That Systematically Quantifies Nine Synaptic Parameters Provides Insights into Drosophila NMJ MorphometryBonnie Nijhof, Anna Castells-Nobau, Louis Wolf, et al.
Journal of Visualized Experiments : Jove|May 19, 2017
Two Algorithms for High-throughput and Multi-parametric Quantification of Drosophila Neuromuscular Junction MorphologyAnna Castells-Nobau, Bonnie Nijhof, Ilse Eidhof, et al.
American Journal of Human Genetics|January 11, 2016
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent ModulesKorinna Kochinke, Christiane Zweier, Bonnie Nijhof, et al.
Plos One|December 5, 2013
Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disabilityJoke Vandewalle, Marion Langen, Marlen Zschätzsch, et al.
Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
Plos Genetics|May 12, 2016
BOD1 Is Required for Cognitive Function in Humans and DrosophilaSahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 11, 2015
Converging evidence does not support GIT1 as an ADHD risk geneMarieke Klein, Monique van der Voet, Benjamin Harich, et al.
Human Molecular Genetics|April 12, 2013
CEP89 is required for mitochondrial metabolism and neuronal function in man and flyBregje W M van Bon, Merel A W Oortveld, Leo G Nijtmans, et al.
Pageof 2