[HTML][HTML] Glyoxalase system: A systematic review of its biological activity, related-diseases, screening methods and small molecule regulators
Y He, C Zhou, M Huang, C Tang, X Liu, Y Yue… - Biomedicine & …, 2020 - Elsevier
The glyoxalase system is a ubiquitous enzymatic network which plays important roles in
biological life. It consists of glyoxalase 1 (GLO1), glyoxalase 2 (GLO2), and reduced …
biological life. It consists of glyoxalase 1 (GLO1), glyoxalase 2 (GLO2), and reduced …
Vitamin D deficiency and the risk of cerebrovascular disease
HA Kim, A Perrelli, A Ragni, F Retta, TM De Silva… - Antioxidants, 2020 - mdpi.com
Vitamin D deficiency has been clearly linked to major chronic diseases associated with
oxidative stress, inflammation, and aging, including cardiovascular and neurodegenerative …
oxidative stress, inflammation, and aging, including cardiovascular and neurodegenerative …
Biological activities, health benefits, and therapeutic properties of avenanthramides: from skin protection to prevention and treatment of cerebrovascular diseases
A Perrelli, L Goitre, AM Salzano… - Oxidative medicine …, 2018 - Wiley Online Library
Oat (Avena sativa) is a cereal known since antiquity as a useful grain with abundant
nutritional and health benefits. It contains distinct molecular components with high …
nutritional and health benefits. It contains distinct molecular components with high …
Vitamin D as therapeutic modulator in cerebrovascular diseases: a mechanistic perspectives
Vitamin D deficiency has been linked to several major chronic diseases, such as
cardiovascular and neurodegenerative diseases, diabetes, and cancer, linked to oxidative …
cardiovascular and neurodegenerative diseases, diabetes, and cancer, linked to oxidative …
Polymorphisms in genes related to oxidative stress and inflammation: Emerging links with the pathogenesis and severity of Cerebral Cavernous Malformation disease
A Perrelli, SF Retta - Free Radical Biology and Medicine, 2021 - Elsevier
Abstract Cerebral Cavernous Malformation (CCM) is a cerebrovascular disease of genetic
origin affecting 0.5% of the population and characterized by abnormally enlarged and leaky …
origin affecting 0.5% of the population and characterized by abnormally enlarged and leaky …
Association of nanoparticles and Nrf2 with various oxidative stress-mediated diseases
R Thiruvengadam, B Venkidasamy… - Chemico-Biological …, 2023 - Elsevier
Nuclear factor erythroid 2-related factor 2 (Nrf2) is a transcription factor that regulates the
cellular antioxidant defense system at the posttranscriptional level. During oxidative stress …
cellular antioxidant defense system at the posttranscriptional level. During oxidative stress …
[HTML][HTML] KRIT1 loss-of-function induces a chronic Nrf2-mediated adaptive homeostasis that sensitizes cells to oxidative stress: Implication for Cerebral Cavernous …
Abstract KRIT1 (CCM1) is a disease gene responsible for Cerebral Cavernous
Malformations (CCM), a major cerebrovascular disease of proven genetic origin affecting 0.3 …
Malformations (CCM), a major cerebrovascular disease of proven genetic origin affecting 0.3 …
Glyoxalase system as a therapeutic target against diabetic retinopathy
G Aragonès, S Rowan, SG Francisco, W Yang… - Antioxidants, 2020 - mdpi.com
Hyperglycemia, a defining characteristic of diabetes, combined with oxidative stress, results
in the formation of advanced glycation end products (AGEs). AGEs are toxic compounds that …
in the formation of advanced glycation end products (AGEs). AGEs are toxic compounds that …
KRIT1: A traffic warden at the busy crossroads between redox signaling and the pathogenesis of Cerebral Cavernous Malformation disease
A Perrelli, C Ferraris, E Berni, AJ Glading… - Antioxidants & Redox …, 2023 - liebertpub.com
Significance: KRIT1 (Krev interaction trapped 1) is a scaffolding protein that plays a critical
role in vascular morphogenesis and homeostasis. Its loss-of-function has been …
role in vascular morphogenesis and homeostasis. Its loss-of-function has been …
KRIT1 Loss-Of-Function Associated with Cerebral Cavernous Malformation Disease Leads to Enhanced S-Glutathionylation of Distinct Structural and Regulatory …
L Cianfruglia, A Perrelli, C Fornelli, A Magini, S Gorbi… - Antioxidants, 2019 - mdpi.com
Loss-of-function mutations in the KRIT1 gene are associated with the pathogenesis of
cerebral cavernous malformations (CCMs), a major cerebrovascular disease still awaiting …
cerebral cavernous malformations (CCMs), a major cerebrovascular disease still awaiting …