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Pullani Shashidharan - Publications

Affiliations: 
Icahn School of Medicine at Mount Sinai, New York, NY, United States 
Area:
Neuroscience Biology
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 Armata IA, Diplas AI, Ozelius LJ, Shashidharan P. Allelic Imbalance in TOR1A mRNA Expression in Manifesting and Non-Manifesting Carriers of the GAG-Deletion. Journal of Nucleic Acids. 2012: 985260. PMID 22988486 DOI: 10.1155/2012/985260  0.622
2011 Nambu A, Chiken S, Shashidharan P, Nishibayashi H, Ogura M, Kakishita K, Tanaka S, Tachibana Y, Kita H, Itakura T. Reduced pallidal output causes dystonia. Frontiers in Systems Neuroscience. 5: 89. PMID 22164134 DOI: 10.3389/fnsys.2011.00089  0.317
2011 Lange N, Hamann M, Shashidharan P, Richter A. Behavioural and pharmacological examinations in a transgenic mouse model of early-onset torsion dystonia. Pharmacology, Biochemistry, and Behavior. 97: 647-55. PMID 21078339 DOI: 10.1016/J.Pbb.2010.11.005  0.524
2010 Giannakopoulou D, Armata I, Mitsacos A, Shashidharan P, Giompres P. Modulation of the basal ganglia dopaminergic system in a transgenic mouse exhibiting dystonia-like features. Journal of Neural Transmission (Vienna, Austria : 1996). 117: 1401-9. PMID 21136125 DOI: 10.1007/S00702-010-0521-5  0.631
2010 Bao L, Patel JC, Walker RH, Shashidharan P, Rice ME. Dysregulation of striatal dopamine release in a mouse model of dystonia. Journal of Neurochemistry. 114: 1781-91. PMID 20626557 DOI: 10.1111/j.1471-4159.2010.06890.x  0.374
2008 Armata IA, Ananthanarayanan M, Balasubramaniyan N, Shashidharan P. Regulation of DYT1 gene expression by the Ets family of transcription factors. Journal of Neurochemistry. 106: 1052-65. PMID 18466338 DOI: 10.1111/j.1471-4159.2008.05465.x  0.614
2005 Shashidharan P, Sandu D, Potla U, Armata IA, Walker RH, McNaught KS, Weisz D, Sreenath T, Brin MF, Olanow CW. Transgenic mouse model of early-onset DYT1 dystonia. Human Molecular Genetics. 14: 125-33. PMID 15548549 DOI: 10.1093/hmg/ddi012  0.641
1993 Andreas P, Panayiotis F, Anastasia BN, Shashidharan P. Glutamate Dehydrogenase Deficiency in Cerebellar Degenerations: Clinical, Biochemical and Molecular Genetic Aspects Canadian Journal of Neurological Sciences / Journal Canadien Des Sciences Neurologiques. 20: S109-S116. DOI: 10.1017/S0317167100048617  0.3
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