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Published in 2020 at "Acta Pharmacologica Sinica"
DOI: 10.1038/s41401-020-0454-y
Abstract: GM1 ganglioside is particularly abundant in the mammalian central nervous system and has shown beneficial effects on neurodegenerative diseases. In this study, we investigated the therapeutic effect of GM1 ganglioside in experimental models of Parkinson’s… read more here.
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Published in 2019 at "Autophagy"
DOI: 10.1080/15548627.2019.1632623
Abstract: ABSTRACT The age-induced deterioration of the organism results in detrimental and ultimately lethal pathologies. The process of aging itself involves a plethora of different mechanisms that should be subverted concurrently to delay and/or prevent age-related… read more here.
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Published in 2020 at "Autophagy"
DOI: 10.1080/15548627.2020.1714209
Abstract: ABSTRACT KRAS is the most frequently mutated oncogene in human neoplasia. Despite a large investment to understand the effects of KRAS mutation in cancer cells, the direct effects of the oncogenetic KRAS activation on immune… read more here.
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Published in 2022 at "American journal of respiratory cell and molecular biology"
DOI: 10.1165/rcmb.2022-0282oc
Abstract: The pathogenesis of bronchopulmonary dysplasia (BPD) remains incompletely understood. Recent studies suggest insufficient adenosine monophosphate-activated protein kinase (AMPK) activation as a potential cause of impaired autophagy in rodent and non-human primate (NHP) models of BPD.… read more here.
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Published in 2022 at "International Journal of General Medicine"
DOI: 10.2147/ijgm.s343046
Abstract: Background Ferroptosis is an autophagy-dependent form of cell death, sometimes called “ferritinophagy”. Its related pathway has been proven to regulate the programmed death of glioma stem cells. Mining autophagy-dependent ferroptosis-related gene (AD-FRG) signature could facilitate… read more here.
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Published in 2022 at "Frontiers in Molecular Biosciences"
DOI: 10.3389/fmolb.2022.952608
Abstract: Niemann–Pick type C disease (NPCD) is a rare genetic syndrome characterized by cholesterol accumulation in multiple organelles. NPCD is mainly caused by gene deficiency of NPC intracellular cholesterol transporter 1 (NPC1). It has been reported… read more here.
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Published in 2022 at "Frontiers in Oncology"
DOI: 10.3389/fonc.2022.756117
Abstract: Wilms tumor is the most common renal malignancy in children. Known gene mutations account for about 40% of all wilms tumor cases, but the full map of genetic mutations in wilms tumor is far from… read more here.
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Published in 2023 at "Frontiers in Oncology"
DOI: 10.3389/fonc.2023.1091118
Abstract: Glioblastoma (GBM) is the most common malignant primary brain tumor with a poor 5-year survival rate. Autophagy is a conserved intracellular degradation system that plays a dual role in GBM pathogenesis and therapy. On one… read more here.
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Published in 2022 at "Cancers"
DOI: 10.3390/cancers14020339
Abstract: Simple Summary Glioblastoma is the most common primary brain cancer in adults. One reason for the development and malignancy of this tumor is the misregulation of certain cellular proteins. The oncoprotein STAT3 that is frequently… read more here.
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Published in 2022 at "International Journal of Biological Sciences"
DOI: 10.7150/ijbs.76134
Abstract: It is emerging that autophagy-related proteins regulate the adaptive response to DNA damage in maintaining genome stability at multiple pathways. Here, we discuss recent insights into how autophagy-related proteins participate in DNA damage repair processes,… read more here.
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Published in 2022 at "PeerJ"
DOI: 10.7717/peerj.14180
Abstract: According to mounting evidence, long noncoding RNAs (lncRNAs) play a vital role in regulated cell death (RCD). A potential strategy for cancer therapy involves triggering ferroptosis, a novel form of RCD. Although it is thought… read more here.