Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/9835
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dc.contributor.authorDanani, Jessica-
dc.contributor.authorPatel, Khushboo-
dc.contributor.authorDesai, Priyanshi-
dc.contributor.authorPrajapati, Riyaben-
dc.contributor.authorChabhadia, Rupal-
dc.contributor.authorSagathia, Vrunda-
dc.date.accessioned2021-07-27T08:51:42Z-
dc.date.available2021-07-27T08:51:42Z-
dc.date.issued2021-05-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/9835-
dc.description.abstractHsps are important chaperone molecules participating in regulation of various processes in the body including the central nervous system. Studies have shown hsps having an integral role in many CNS disorders. Several hsps like Hsp 40, Hsp 27, Hsp 60, Hsp 90, Hsp 70 etc have been found to be effective as a target in CNS diseases. Therefore it is believed that targeting these hsps, can be a novel treatment option for treating those diseases and also several studies have supported the same. In this review, the role of hsps in various CNS disorders like Alzheimer's disease, Parkinson’s disease, Neuro inflammation, Huntington's disease and Psychiatric disorders are given along with the possible therapeutic options available targeting hsps. Also we have demonstrated the pathophysiology of all the above mentioned CNS diseases, with that a clear description of the roles of different hsps and their mechanism of action for the treatment of the CNS Diseases. Hence, collectively it suggests that hsps can be a novel target for CNS disorders and can pave a new way for treating these deadly CNS diseases.en_US
dc.publisherInstitute of Pharmacy, Nirma University, A'baden_US
dc.relation.ispartofseriesPPR01051;-
dc.subjectPPR01051en_US
dc.subjectB. Pharm Project Reporten_US
dc.subjectPharmacologyen_US
dc.subjectProteinen_US
dc.subjectCNS Disorderen_US
dc.subjectcentral nervous systemen_US
dc.titleHeat Shock Proteins: Novel Targets for CNS Disordersen_US
dc.typeProject Reporten_US
Appears in Collections:B. Pharm Project Reports

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