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Article

Kumar, V and Joshi, T and Vatsa, N and Singh, BK and Jana, NR (2019) Simvastatin Restores HDAC1/2 Activity and Improves Behavioral Deficits in Angelman Syndrome Model Mouse. Front Mol Neurosci, 12 (289).

Vatsa, N and Kumar, V and Singh, BK and Kumar, SS and Sharma, A and Jana, NR (2019) Down-Regulation of Mirna-708 Promotes Aberrant Calcium Signaling by Targeting Neuronatin in a Mouse Model of Angelman Syndrome. Frontiers in Molecular Neuroscience, 12 (35).

Singh, BK and Vatsa, N and Nelson, VK and Kumar, V and Kumar, SS and Mandal, SC and Pal, M and Jana, NR (2018) Azadiradione Restores Protein Quality Control and Ameliorates the Disease Pathogenesis in a Mouse Model of Huntington’s Disease. Molecular Neurobiology, 55 (8). pp. 6337-6346.

Vatsa, N and Jana, NR (2018) Ube3a and Its Link with Autism. Front Mol Neurosci, 11 (448).

Shekhar, S and Vatsa, N and Kumar, V and Singh, BK and Jamal, I and Sharma, A and Jana, NR (2017) Topoisomerase 1 inhibitor topotecan delays the disease progression in a mouse model of Huntington's disease. Human Molecular Genetics, 26 (2). pp. 420-429.

Jamal, I and Kumar, V and Vatsa, N and Singh, BK and Shekhar, S and Sharma, A and Jana, NR (2017) Environmental Enrichment Improves Behavioral Abnormalities in a Mouse Model of Angelman Syndrome. Molecular Neurobiology, 54 (7). pp. 5319-5326.

Jamal, I and Kumar, V and Vatsa, N and Shekhar, S and Singh, BK and Sharma, A and Jana, NR (2017) Rescue of altered HDAC activity recovers behavioural abnormalities in a mouse model of Angelman syndrome. Neurobiology of Disease, 105. pp. 99-108.

Singh, BK and Vatsa, N and Kumar, V and Shekhar, S and Sharma, A and Jana, NR (2017) Ube3a deficiency inhibits amyloid plaque formation in APPswe/PS1δE9 mouse model of Alzheimer's disease. Human Molecular Genetics, 26 (20). pp. 4042-4054.

Maheshwari, M and Shekhar, S and Singh, BK and Jamal, I and Vatsa, N and Kimar, V and Sharma, A and Jana, NR (2014) Deficiency of Ube3a in Huntington's disease mice brain increases aggregate load and accelerates disease pathology. Hum Mol Genet, 23 (23). pp. 6235-6245.

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