نتایج جستجو برای: cartilage oligomeric matrix protein comp

تعداد نتایج: 1574030  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Chung-Hyun Cho Richard A Kammerer Hyuek Jong Lee Michel O Steinmetz Young Shin Ryu Sung Ho Lee Kunio Yasunaga Kyung-Tae Kim Injune Kim Han-Ho Choi Won Kim Sung Hyun Kim Sung Kwang Park Gyun Min Lee Gou Young Koh

Angiopoietin-1 (Ang1) has potential therapeutic applications in inducing angiogenesis, enhancing endothelial cell survival, and preventing vascular leakage. However, production of Ang1 is hindered by aggregation and insolubility resulting from disulfide-linked higher-order structures. Here, by replacing the N-terminal portion of Ang1 with the short coiled-coil domain of cartilage oligomeric mat...

Journal: :Circulation research 2009
Li Wang Jingang Zheng Xue Bai Bo Liu Chuan-Ju Liu Qingbo Xu Yi Zhu Nanping Wang Wei Kong Xian Wang

The migration of vascular smooth muscle cells (VSMCs) plays an essential role during the development of atherosclerosis and restenosis. Extensive studies have implicated the importance of extracellular matrix (ECM)-degrading proteinases in VSMC migration. A recently described family of proteinases, a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTs), is capable of degrading ...

2017
Wei Qin Yide Cao Liangpeng Li Wen Chen Xin Chen

Aortic aneurysm (AA) remains a fatal condition with high rates of morbidity and mortality, and the associated underlying mechanism influencing its pathology remains to be elucidated. A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)‑7 has previously been demonstrated to be involved in the pathogenesis of vascular atherosclerosis via degradation of cartilage oligomeric matr...

2010
Karen L. Posey Peiman Liu Huiqiu R. Wang Alka C. Veerisetty Joseph L. Alcorn Jacqueline T. Hecht

Mutations in cartilage oligomeric matrix protein (COMP), a large extracellular glycoprotein expressed in musculoskeletal tissues, cause two skeletal dysplasias, pseudoachondroplasia and multiple epiphyseal dysplasia. These mutations lead to massive intracellular retention of COMP, chondrocyte death and loss of growth plate chondrocytes that are necessary for linear growth. In contrast, COMP nul...

Journal: :Blood 2015
Ying Liang Yi Fu Ruomei Qi Meili Wang Nan Yang Li He Fang Yu Jian Zhang Cai-Hong Yun Xian Wang Junling Liu Wei Kong

Thrombin is an effector enzyme for hemostasis and thrombosis; however, endogenous regulators of thrombin remain elusive. Cartilage oligomeric matrix protein (COMP), a matricellular protein also known as thrombospondin-5, is essential for maintaining vascular homeostasis. Here, we asked whether COMP is involved in the process of blood coagulation. COMP deficiency shortened tail-bleeding and clot...

Journal: :Human molecular genetics 1999
E Délot L M King M D Briggs W R Wilcox D H Cohn

Pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED) are two human autosomal dominant skeletal dysplasias characterized by variable short stature, joint laxity and early-onset degenerative joint disease. Both disorders can result from mut-ations in the gene for cartilage oligomeric matrix protein (COMP), an extracellular matrix glycoprotein. About one-third of PSACH cases result...

Journal: :Arthritis Research & Therapy 2004
Helena Forsblad d'Elia Stephan Christgau Lars-Åke Mattsson Tore Saxne Claes Ohlsson Elisabeth Nordborg Hans Carlsten

This study aimed to evaluate the effects of hormone replacement therapy (HRT), known to prevent osteoporosis and fractures, on markers of bone and cartilage metabolism. Furthermore, we assessed whether changes in these markers corresponded to alterations in bone mineral density and radiographic joint destructions in postmenopausal women with rheumatoid arthritis. Eighty-eight women were randomi...

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