نتایج جستجو برای: glycosylation end products

تعداد نتایج: 686733  

2013
Ifat Cohen-Or Chen Katz Eliora Z. Ron

Advanced Glycation End Products (AGEs) are the final products of non-enzymatic protein glycation that results in loss of protein structure and function. We have previously shown that in E. coli AGEs are continually formed as high-molecular weight protein complexes. Moreover, we showed that AGEs are removed from the cells by an active, ATP-dependent secretion and that these secreted molecules ha...

2017
Tarek Ahmed Anthony Nash Kristina EN Clark Marion Ghibaudo Nora H de Leeuw Anne Potter Richard Stratton Helen L Birch Ramona Enea Casse Laurent Bozec

The extracellular matrix of the dermis is a complex, dynamic system with the various dermal components undergoing individual physiologic changes as we age. Age-related changes in the physical properties of collagen were investigated in particular by measuring the effect of aging, most likely due to the accumulation of advanced glycation end product (AGE) cross-links, on the nanomechanical prope...

Journal: :Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis 2005
Paul J Thornalley

Protein glycation adducts, early glycation adducts, such as N(epsilon)-fructosyl-lysine, and advanced glycation end products (AGEs) are uremic toxins. Glycation adducts are found in plasma and tissue proteins (glycation adduct residues), in peptides (glycation adduct peptide residues), and glycated amino acids (glycation free adducts). The latter two analyte groups arise from proteolysis of gly...

2015
Louise J. N. Jensen Allan Flyvbjerg Mette Bjerre

The receptor of advanced glycation end products (RAGE) and its ligands are linked to the pathogenesis of coronary artery disease (CAD), and circulating soluble receptor of advanced glycation end products (sRAGE), reflecting the RAGE activity, is suggested as a potential biomarker. Elevated sRAGE levels are reported in relation to acute ischemia and this review focuses on the role of sRAGE as a ...

2015
Florence Boyer Jennifer Baraka Vidot Alexis Guerin Dubourg Philippe Rondeau M Faadiel Essop Emmanuel Bourdon

Diabetes is a major health problem that is usually associated with obesity, together with hyperglycemia and increased advanced glycation endproducts (AGEs) formation. Elevated AGEs elicit severe downstream consequences via their binding to receptors of AGEs (RAGE). This includes oxidative stress and oxidative modifications of biological compounds together with heightened inflammation. For examp...

2017
Gözde Hondur Emre Göktaş Xiangjun Yang Lama Al-Aswad James D. Auran Dana M. Blumberg George A. Cioffi Jeffrey M. Liebmann Leejee H. Suh Danielle Trief Gülgün Tezel

Purpose Glaucoma-related molecular biomarkers can improve clinical testing to diagnose the disease early, predict its prognosis, and monitor treatment responses. Based on the evidence of increased oxidative stress in glaucomatous tissues, this study analyzed oxidative stress-related biomarker candidates in blood and aqueous humor samples with or without glaucoma. Methods The blood and aqueous...

2017
Sebastian Brings Thomas Fleming Marc Freichel Martina U. Muckenthaler Stephan Herzig Peter P. Nawroth

Advanced glycation end-products (AGEs) are non-enzymatic protein and amino acid adducts as well as DNA adducts which form from dicarbonyls and glucose. AGE formation is enhanced in diabetes and is associated with the development of diabetic complications. In the current review, we discuss mechanisms that lead to enhanced AGE levels in the context of diabetes and diabetic complications. The meth...

2013
Philip J. Vernon Herbert J. Zeh III Michael T. Lotze

We identified a critical role for receptor for advanced glycation end products (RAGE) in the intratumoral accumulation of myeloid-derived suppressor cells (MDSCs) during pancreatic carcinogenesis. The absence of RAGE markedly delayed neoplasia and limited MDSC accumulation in mice expressing an oncogenic variant of Kras. In spite of MDSCs, these mice accumulated non-immunosuppressive macrophage...

2012
Gen-Xiang Mao Ling-Di Zheng Yong-Bao Cao Zhuo-Mei Chen Yuan-Dong Lv Ya-Zhen Wang Xi-Lian Hu Guo-Fu Wang Jing Yan

The present paper was designed to investigate the effect of pine pollen against aging in human diploid fibroblast 2BS cells and in an accelerated aging model, which was established by subcutaneous injections with D-galactose daily for 8 weeks in C57BL/6J mice. Pine pollen (1 mg/mL and 2 mg/mL) is proved to delay the replicative senescence of 2BS cells as evidenced by enhanced cell proliferation...

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