نتایج جستجو برای: cuzn superoxide dismutase 1 sod1

تعداد نتایج: 2775979  

Journal: :The Tohoku journal of experimental medicine 2003
Ender Inci Sabiha Civelek Arzu Seven Figen Inci Nazim Korkut Gülden Burçax

This study was designed to investigate the oxidative stress parameters in laryngeal cancer and cancer-free adjacent tissues. Lipid peroxidation end product and the endogenous antioxidant components-CuZn superoxide dismutase (CuZn SOD) glutathione peroxidase (GSH Px), glutathione reductase (GSSG Rd) and glutathione (GSH)-were analysed by spectrophotometric and kinetic methods. Laryngeal cancer t...

Journal: :Investigative ophthalmology & visual science 2011
Kenya Yuki Yoko Ozawa Tetsu Yoshida Toshihide Kurihara Manabu Hirasawa Naoki Ozeki Daisuke Shiba Kousuke Noda Susumu Ishida Kazuo Tsubota

PURPOSE To investigate the influence of deficiency in superoxide dismutase (SOD) 1, a major antioxidative enzyme, on retinal ganglion cells (RGCs). METHODS In the SOD1 total knockout (SOD1-deficient) mice, the level of superoxide anion was measured using dihydroethidium. The number of RGCs was counted in both the retinal sections and the flat-mount retinas after retrograde labeling. Thickness...

2013
Yoshiaki Furukawa

Dominant mutations in Cu,Zn-superoxide dismutase (SOD1) cause a familial form of amyotrophic lateral sclerosis (fALS). Misfolding and aggregation of mutant SOD1 proteins are a pathological hallmark of SOD1-related fALS cases; however, the molecular mechanism of SOD1 aggregation remains controversial. Here, I have used E. coli as a model organism and shown multiple distinct pathways of SOD1 aggr...

Journal: :The Journal of Cell Biology 2007
Jihong Kang Serge Rivest

Increasing evidence suggests that neurotoxicity of secreted superoxide dismutase 1 (SOD1) mutants is associated with amyotrophic lateral sclerosis (ALS). We show here that mutant SOD1 protein activates microglia via a myeloid differentiation factor 88 (MyD88)-dependent pathway. This inflammatory response is also associated with a marked recruitment of bone marrow-derived microglia (BMDM) in the...

Journal: :The EMBO journal 2014
Benjamin M Schwenk Dieter Edbauer

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease leading to selective death of upper and lower motoneurons. Clinically, the ALS syndrome is linked to pathogenic mutations in superoxide dismutase 1 (SOD1), though actual molecular mechanisms remain ill understood. Two papers recently published in Cell Stem Cell and Cell Reports employ syngenic, iPSC-derived cell lines of o...

Journal: :Journal of immunology 2009
Ricardo Khouri André Bafica Maria da Purificação Pereira Silva Almerio Noronha Jean-Pierre Kolb Juana Wietzerbin Aldina Barral Manoel Barral-Netto Johan Van Weyenbergh

Type I IFNs (IFN-alpha/beta) have only recently gained considerable attention as immunomodulators in nonviral infectious diseases. IFN-beta has been shown to protect, in a NO-dependent manner, against murine Old World leishmaniasis caused by Leishmania major, but data in New World leishmaniasis are lacking. We found that IFN-beta dose-dependently increases parasite burden in Leishmania amazonen...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
T L Williamson L I Bruijn Q Zhu K L Anderson S D Anderson J P Julien D W Cleveland

Mutations in superoxide dismutase 1 (SOD1), the only proven cause of amyotrophic lateral sclerosis (ALS), provoke disease through an unidentified toxic property. Neurofilament aggregates are pathologic hallmarks of both sporadic and SOD1-mediated familial ALS. By deleting NF-L, the major neurofilament subunit required for filament assembly, onset and progression of disease caused by familial AL...

2009
Pilar Larrodé Pedro Iñarrea José L. Capablo Cristina Iñiguez José R. Ara Jesús Martin Enrique Mostacero

Background: Evidence suggests that mitochondrial dysfunction and oxidative stress may be involved in the pathogenesis of Amyotrophic Lateral Sclerosis (ALS). Some studies show the presence of altered anti-oxidative defence enzyme activity in the blood of ALS patients. It has also been demonstrated that a superoxide-dismutase-1 (SOD1) enzyme fraction is located in the mitochondria. Objective: To...

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