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Kellen Winden

Showing results (1-10 of 9) with videos related to

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Human Molecular Genetics|March 24, 2016
Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophyMary H Wertz, Kellen Winden, Pierre Neveu, et al.
Nature Reviews. Disease Primers|March 13, 2026
Tuberous sclerosis complexKellen Winden, E Martina Bebin, Shafali Jeste, et al.
The Journal of Experimental Medicine|February 11, 2017
Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complexEbru Ercan, Juliette M Han, Alessia Di Nardo, et al.
Nature|November 13, 2009
Human-specific transcriptional regulation of CNS development genes by FOXP2Genevieve Konopka, Jamee M Bomar, Kellen Winden, et al.
Neuron|August 28, 2012
Human-specific transcriptional networks in the brainGenevieve Konopka, Tara Friedrich, Jeremy Davis-Turak, et al.
Molecular Psychiatry|February 17, 2018
Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycinMaria Sundberg, Ivan Tochitsky, David E Buchholz, et al.
Research Square|July 3, 2023
High-Content Small Molecule Screen Identifies a Novel Compound That Restores AP-4-Dependent Protein Trafficking in Neuronal Models of AP-4-Associated Hereditary Spastic ParaplegiaAfshin Saffari, Barbara Brechmann, Cedric Boeger, et al.
Nature Communications|January 17, 2024
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegiaAfshin Saffari, Barbara Brechmann, Cedric Böger, et al.
Nature Neuroscience|February 24, 2025
PTEN mutations impair CSF dynamics and cortical networks by dysregulating periventricular neural progenitorsTyrone DeSpenza, Emre Kiziltug, Garrett Allington, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|March 24, 2016
Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophyMary H Wertz, Kellen Winden, Pierre Neveu, et al.
Nature Reviews. Disease Primers|March 13, 2026
Tuberous sclerosis complexKellen Winden, E Martina Bebin, Shafali Jeste, et al.
The Journal of Experimental Medicine|February 11, 2017
Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complexEbru Ercan, Juliette M Han, Alessia Di Nardo, et al.
Nature|November 13, 2009
Human-specific transcriptional regulation of CNS development genes by FOXP2Genevieve Konopka, Jamee M Bomar, Kellen Winden, et al.
Neuron|August 28, 2012
Human-specific transcriptional networks in the brainGenevieve Konopka, Tara Friedrich, Jeremy Davis-Turak, et al.
Molecular Psychiatry|February 17, 2018
Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycinMaria Sundberg, Ivan Tochitsky, David E Buchholz, et al.
Research Square|July 3, 2023
High-Content Small Molecule Screen Identifies a Novel Compound That Restores AP-4-Dependent Protein Trafficking in Neuronal Models of AP-4-Associated Hereditary Spastic ParaplegiaAfshin Saffari, Barbara Brechmann, Cedric Boeger, et al.
Nature Communications|January 17, 2024
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegiaAfshin Saffari, Barbara Brechmann, Cedric Böger, et al.
Nature Neuroscience|February 24, 2025
PTEN mutations impair CSF dynamics and cortical networks by dysregulating periventricular neural progenitorsTyrone DeSpenza, Emre Kiziltug, Garrett Allington, et al.
Pageof 1