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pro vyhledávání: '"Bhupender Verma"'
Autor:
Anshika Goenka, Fatima Khan, Bhupender Verma, Priyanka Sinha, Crismita C. Dmello, Manasi P. Jogalekar, Prakash Gangadaran, Byeong‐Cheol Ahn
Publikováno v:
Cancer Communications, Vol 43, Iss 5, Pp 525-561 (2023)
Abstract Tumor development and metastasis are facilitated by the complex interactions between cancer cells and their microenvironment, which comprises stromal cells and extracellular matrix (ECM) components, among other factors. Stromal cells can ado
Externí odkaz:
https://doaj.org/article/d8791161e3824e2a8f6f16b55281fab8
Publikováno v:
Journal of Ayurveda and Integrative Medicine, Vol 13, Iss 4, Pp 100636- (2022)
Background: Emerging reports indicate that age-associated cognitive decline begins with the transition from young to middle-aged, and this neurological condition manifests mainly due to the progressive impairment in the adaptive homeostasis process.
Externí odkaz:
https://doaj.org/article/40f78c5d804e46b6b34d92b493fe6ee7
Publikováno v:
Molecular Neurobiology. 59:5532-5548
Brain aging is characterized by a gradual decline in cellular homeostatic processes, thereby losing the ability to respond to physiological stress. At the anatomical level, the aged brain is characterized by degenerating neurons, proteinaceous plaque
Publikováno v:
Journal of Ayurveda and integrative medicine. 13(4)
Emerging reports indicate that age-associated cognitive decline begins with the transition from young to middle-aged, and this neurological condition manifests mainly due to the progressive impairment in the adaptive homeostasis process. Moreover, co
Publikováno v:
Experimental neurology. 340
Heat shock response (HSR) is a conserved cytoprotective pathway controlled by the master transcriptional regulator, the heat shock factor 1 (HSF1), that activates the expression of heat shock proteins (HSPs). HSPs, as chaperones, play essential roles
Publikováno v:
Molecular neurobiology. 58(3)
Lafora disease (LD) is one of the progressive and fatal forms of a neurodegenerative disorder and is characterized by teenage-onset myoclonic seizures. Neuropathological changes in LD include the formation of abnormal glycogen as Lafora bodies, glios