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Novel reno-protective mechanism of Aspirin involves H2AK119 monoubiquitination and Set7 in preventing type 1 diabetic nephropathy

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dc.contributor.author Gaikwad, Anil Bhanudas
dc.date.accessioned 2023-12-21T06:47:39Z
dc.date.available 2023-12-21T06:47:39Z
dc.date.issued 2018-06
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S1734114017304310
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13483
dc.description.abstract Even after several novel therapeutic approaches, the number of people with diabetic nephropathy (DN) still continues to increase globally, this suggest to find novel therapeutic strategies to prevent it completely. Recent reports, are indicating the ubiquitin proteasome system alterations in DN. Recently, we also showed that, histone H2AK119 mono-ubiquitination (H2AK119-Ub) found to regulate Set7, a key epigenetic enzyme in the development of renal fibrosis under type 1 diabetic condition. Hence, we aimed to study the role of a known 20 s proteasome inhibitor Aspirin, on histone ubiquitination in the progression of DN. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Pharmacy en_US
dc.subject Diabetic nephropathy (DN) en_US
dc.subject H2AK119 mono-ubiquitination en_US
dc.title Novel reno-protective mechanism of Aspirin involves H2AK119 monoubiquitination and Set7 in preventing type 1 diabetic nephropathy en_US
dc.type Article en_US


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