نتایج جستجو برای: hmgb proteins

تعداد نتایج: 555827  

2015
R. Sánchez-Giraldo F. J. Acosta-Reyes C. S. Malarkey N. Saperas M. E. A. Churchill J. L. Campos

High-mobility group protein 1 (HMGB1) is an essential and ubiquitous DNA architectural factor that influences a myriad of cellular processes. HMGB1 contains two DNA-binding domains, box A and box B, which have little sequence specificity but have remarkable abilities to underwind and bend DNA. Although HMGB1 box A is thought to be responsible for the majority of HMGB1-DNA interactions with pre-...

2016
Hyong Woo Choi Murli Manohar Patricia Manosalva Miaoying Tian Magali Moreau Daniel F. Klessig

Damage-associated molecular pattern molecules (DAMPs) signal the presence of tissue damage to induce immune responses in plants and animals. Here, we report that High Mobility Group Box 3 (HMGB3) is a novel plant DAMP. Extracellular HMGB3, through receptor-like kinases BAK1 and BKK1, induced hallmark innate immune responses, including i) MAPK activation, ii) defense-related gene expression, iii...

2012
Theodore G. Liou Frederick R. Adler Ruth H. Keogh Yanping Li Judy L. Jensen William Walsh Kristyn Packer Teresa Clark Holly Carveth Jun Chen Shaunessy L. Rogers Christen Lane James Moore Anne Sturrock Robert Paine David R. Cox John R. Hoidal

Lung function, acute pulmonary exacerbations (APE), and weight are the best clinical predictors of survival in cystic fibrosis (CF); however, underlying mechanisms are incompletely understood. Biomarkers of current disease state predictive of future outcomes might identify mechanisms and provide treatment targets, trial endpoints and objective clinical monitoring tools. Such CF-specific biomark...

2012
Thiruvengadam Arumugam Vijaya Ramachandran Sobeyda B Gomez Ann M Schmidt Craig D Logsdon

Author manuscripts have been peer reviewed and accepted for publication but have not yet been edited. Abstract Purpose: The receptor for advanced glycation end products (RAGE) contributes to multiple pathologies, including diabetes, arthritis, neurodegenerative diseases, and cancer. Despite the obvious need, no RAGE inhibitors are in common clinical use. Therefore, we developed a novel small RA...

Journal: :American journal of physiology. Cell physiology 2010
Narayanam V Rao Brian Argyle Xiaoyu Xu Paul R Reynolds Jeanine M Walenga Margaret Prechel Glenn D Prestwich Robert B MacArthur Bradford B Walters John R Hoidal Thomas P Kennedy

While heparin has been used almost exclusively as a blood anticoagulant, important literature demonstrates that it also has broad anti-inflammatory activity. Herein, using low anti-coagulant 2-O,3-O-desulfated heparin (ODSH), we demonstrate that most of the anti-inflammatory pharmacology of heparin is unrelated to anticoagulant activity. ODSH has low affinity for anti-thrombin III, low anti-Xa,...

2015
Man-Wah Li Liang Zhou Hon-Ming Lam Jörg Langowski

Arabidopsis High Mobility Group Box (HMBG) proteins were previously found associated with the interphase chromatin but not the metaphase chromosome. However, these studies are usually based on immunolocalization analysis involving paraformaldehyde fixation. Paraformaldehyde fixation has been widely adapted to preserved cell morphology before immunofluorescence staining. On one hand, the process...

Journal: :International journal of molecular medicine 2010
Mian Zhou Rongqian Wu Weifeng Dong Jennifer Leong Ping Wang

Sepsis is associated with an increase in circulating levels of bacterial endotoxin. Sepsis is a particularly serious problem in the geriatric population due to the associated high mortality rate. However, it remains unknown whether this phenomenon is related to an increase in apoptosis in splenic cells. To investigate this issue, male Fischer-344 rats (young, 3 months old; aged, 24 months old) ...

2013
Fabricio S. Belgrano Isabel C. de Abreu da Silva Francisco M. Bastos de Oliveira Marcelo R. Fantappié Ronaldo Mohana-Borges

High mobility group box (HMGB) proteins are abundant nonhistone proteins found in all eukaryotic nuclei and are capable of binding/bending DNA. The human HMGB1 is composed of two binding motifs, known as Boxes A and B, are L-shaped alpha-helix structures, followed by a random-coil acidic tail that consists of 30 Asp and Glu residues. This work aimed at evaluating the role of the acidic tail of ...

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