Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vaibhav S. Marde"'
Autor:
Vaibhav S. Marde, Prerna L. Tiwari, Nitu L. Wankhede, Brijesh G. Taksande, Aman B. Upaganlawar, Milind J. Umekar, Mayur B. Kale
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-8 (2021)
Abstract Background Over the last decade, aggregating evidences suggested that there is a causative link between mutation in gene associated with mitochondrial dysfunction and development of several neurodegenerative disorders. Main text Recent struc
Externí odkaz:
https://doaj.org/article/4e920affe7f1410b923a8b86d690d375
Autor:
Baijayantimala Swain, Abrar Khan, Priti Singh, Vaibhav S. Marde, Andrea Angeli, Krishna Kartheek Chinchilli, Venkata Madhavi Yaddanapudi, Simone Carradori, Claudiu T. Supuran, Mohammed Arifuddin
Publikováno v:
Molecules, Vol 27, Iss 22, p 8028 (2022)
A novel series of twenty-five rhodamine-linked benzenesulfonamide derivatives (7a–u and 9a–d) were synthesized and screened for their inhibitory action against four physiologically relevant human (h) carbonic anhydrase (CA) isoforms, namely hCA I
Externí odkaz:
https://doaj.org/article/a422a55ee080449dab1df6c758b9bb1d
Autor:
Aman B. Upaganlawar, Shweta V. Gawali, Vaibhav S. Marde, Nandini B. Kale, Mrunali D. Dhokne, Mayur B. Kale, Nitu L. Wankhede, Brijesh G. Taksande, Milind J. Umekar
Publikováno v:
Current Indian Science. 1
Background: Neurodevelopmental disorders (NDDs) are types of disorders that are marked by a wide range of genetic and clinical mutability which will affect the development and function of the brain. Mitochondria are increasingly associated with vario
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaeea55200988f700c392793816705d0
https://doi.org/10.2174/2210299x02666221107151717
https://doi.org/10.2174/2210299x02666221107151717
Autor:
Brijesh G. Taksande, Aman B. Upaganlawar, Milind J. Umekar, Nitu L. Wankhede, Mayur B. Kale, Vaibhav S. Marde, Prerna L. Tiwari
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-8 (2021)
Background Over the last decade, aggregating evidences suggested that there is a causative link between mutation in gene associated with mitochondrial dysfunction and development of several neurodegenerative disorders. Main text Recent structural and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6276525720a42210f737510bca665946
https://doaj.org/article/4e920affe7f1410b923a8b86d690d375
https://doaj.org/article/4e920affe7f1410b923a8b86d690d375
Autor:
Nitu L. Wankhede, Brijesh G. Taksande, Milind J. Umekar, Aman B. Upaganlawar, Saurabh P. Badole, Utkarsha A. Atkare, Vaibhav S. Marde, Mayur B. Kale, Prerna L. Tiwari, Shweta V. Gawali
Publikováno v:
Asian journal of psychiatry. 68
One of the comorbid conditions in an individual with Alzheimer’s disease is a sleep disorder. Clinical features of sleep disorders involve various sleep disturbances such as Obstructive Sleep Apnea (OSAS), Excessive Daytime Sleepiness (EDS), Rapid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad40dcc4e7bfaadb66f5b09ba3915bda
https://pubmed.ncbi.nlm.nih.gov/34890930
https://pubmed.ncbi.nlm.nih.gov/34890930