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Stuart R Cobb

Showing results (21-30 of 33) with videos related to

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Neurochemistry International|September 14, 2016
Kynurenine pathway metabolism following prenatal KMO inhibition and in Mecp2<sup>+/-</sup> mice, using liquid chromatography-tandem mass spectrometryCaroline M Forrest, Peter G E Kennedy, Jean Rodgers, et al.
Nature|October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defectsRebekah Tillotson, Jim Selfridge, Martha V Koerner, et al.
Molecular Therapy. Methods & Clinical Development|May 13, 2017
Development of a Novel AAV Gene Therapy Cassette with Improved Safety Features and Efficacy in a Mouse Model of Rett SyndromeKamal K E Gadalla, Thishnapha Vudhironarit, Ralph D Hector, et al.
Synapse (New York, N.Y.)|January 20, 2006
Inhibition of Ih reduces epileptiform activity in rodent hippocampal slicesCatherine H Gill, Jon T Brown, Nadia Shivji, et al.
Brain : a Journal of Neurology|April 25, 2012
Morphological and functional reversal of phenotypes in a mouse model of Rett syndromeLianne Robinson, Jacky Guy, Leanne McKay, et al.
Molecular Therapy. Nucleic Acids|August 28, 2023
Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7Yu-Ting Huang, Hannah R Crick, Helena Chaytow, et al.
Nature Reviews. Disease Primers|March 25, 2025
Publisher Correction: Rett syndromeWendy A Gold, Alan K Percy, Jeffrey L Neul, et al.
Molecular Therapy. Methods & Clinical Development|May 13, 2017
Improved <i>MECP2</i> Gene Therapy Extends the Survival of MeCP2-Null Mice without Apparent Toxicity after Intracisternal DeliverySarah E Sinnett, Ralph D Hector, Kamal K E Gadalla, et al.
Nature Reviews. Disease Primers|November 7, 2024
Rett syndromeWendy A Gold, Alan K Percy, Jeffrey L Neul, et al.
Neurology. Genetics|December 22, 2017
<i>CDKL5</i> variants: Improving our understanding of a rare neurologic disorderRalph D Hector, Vera M Kalscheuer, Friederike Hennig, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Neurochemistry International|September 14, 2016
Kynurenine pathway metabolism following prenatal KMO inhibition and in Mecp2<sup>+/-</sup> mice, using liquid chromatography-tandem mass spectrometryCaroline M Forrest, Peter G E Kennedy, Jean Rodgers, et al.
Nature|October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defectsRebekah Tillotson, Jim Selfridge, Martha V Koerner, et al.
Molecular Therapy. Methods & Clinical Development|May 13, 2017
Development of a Novel AAV Gene Therapy Cassette with Improved Safety Features and Efficacy in a Mouse Model of Rett SyndromeKamal K E Gadalla, Thishnapha Vudhironarit, Ralph D Hector, et al.
Synapse (New York, N.Y.)|January 20, 2006
Inhibition of Ih reduces epileptiform activity in rodent hippocampal slicesCatherine H Gill, Jon T Brown, Nadia Shivji, et al.
Brain : a Journal of Neurology|April 25, 2012
Morphological and functional reversal of phenotypes in a mouse model of Rett syndromeLianne Robinson, Jacky Guy, Leanne McKay, et al.
Molecular Therapy. Nucleic Acids|August 28, 2023
Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7Yu-Ting Huang, Hannah R Crick, Helena Chaytow, et al.
Nature Reviews. Disease Primers|March 25, 2025
Publisher Correction: Rett syndromeWendy A Gold, Alan K Percy, Jeffrey L Neul, et al.
Molecular Therapy. Methods & Clinical Development|May 13, 2017
Improved <i>MECP2</i> Gene Therapy Extends the Survival of MeCP2-Null Mice without Apparent Toxicity after Intracisternal DeliverySarah E Sinnett, Ralph D Hector, Kamal K E Gadalla, et al.
Nature Reviews. Disease Primers|November 7, 2024
Rett syndromeWendy A Gold, Alan K Percy, Jeffrey L Neul, et al.
Neurology. Genetics|December 22, 2017
<i>CDKL5</i> variants: Improving our understanding of a rare neurologic disorderRalph D Hector, Vera M Kalscheuer, Friederike Hennig, et al.
Pageof 4