Vipendra Kumar
Gurgaon, HR, India
Last Updated: 09/26/2026
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Found 10 publications
Withaferin A Induces Heat Shock Response and Ameliorates Disease Progression in a Mouse Model of Huntington's Disease.
Journal: Molecular neurobiology
Published: February 20, 2021
Simvastatin Restores HDAC1/2 Activity and Improves Behavioral Deficits in Angelman Syndrome Model Mouse.
Journal: Frontiers in molecular neuroscience
Published: August 15, 2019
Down-Regulation of miRNA-708 Promotes Aberrant Calcium Signaling by Targeting Neuronatin in a Mouse Model of Angelman Syndrome.
Journal: Frontiers in molecular neuroscience
Published: October 31, 2018
Azadiradione Restores Protein Quality Control and Ameliorates the Disease Pathogenesis in a Mouse Model of Huntington's Disease.
Journal: Molecular neurobiology
Published: October 05, 2017
Glycogen synthase protects neurons from cytotoxicity of mutant huntingtin by enhancing the autophagy flux.
Journal: Cell death & disease
Published: September 01, 2017
Ube3a deficiency inhibits amyloid plaque formation in APPswe/PS1δE9 mouse model of Alzheimer's disease.
Journal: Human molecular genetics
Published: May 10, 2017
Rescue of altered HDAC activity recovers behavioural abnormalities in a mouse model of Angelman syndrome.
Journal: Neurobiology of disease
Published: March 14, 2017
Topoisomerase 1 inhibitor topotecan delays the disease progression in a mouse model of Huntington's disease.
Journal: Human molecular genetics
Published: October 31, 2016
Environmental Enrichment Improves Behavioral Abnormalities in a Mouse Model of Angelman Syndrome.
Journal: Molecular neurobiology
Published: June 04, 2016
Deficiency of Ube3a in Huntington's disease mice brain increases aggregate load and accelerates disease pathology.
Journal: Human molecular genetics
Published: July 17, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026