Results 211 to 220 of about 23,678,950 (225)

Fibrillin-1 expression in normal and fibrotic rat liver and in cultured hepatic fibroblastic cells: modulation by mechanical stress and role in cell adhesion

Laboratory Investigation, 2004
Dieter P Reinhardt, Jean Rosenbaum, Chia-wei Tsai   +2 more
exaly  

The Fibrillin-1 RGD Integrin Binding Site Regulates Gene Expression and Cell Function through microRNAs.

Journal of Molecular Biology, 2019
Karina A. Zeyer, Rong-Mo Zhang, H. Kumra, Amani Hassan, D. Reinhardt   +4 more
semanticscholar   +1 more source

Microfibrils and fibrillin-1 induce integrin-mediated signaling, proliferation and migration in human endothelial cells

American Journal of Physiology - Cell Physiology, 2010
Yves Usson, Philippe Huber
exaly  

Aberrant fibrillin-1 expression in early emphysematous human lung: a proposed predisposition for emphysema

Modern Pathology, 2008
Johan Bulten
exaly  

Fibrillin-1, a novel TGF-beta-induced factor, is preferentially expressed in metaplastic carcinoma with spindle sarcomatous metaplasia.

Pathology (Sydney), 2019
H. Lien, Yi-Hsuan Lee, Yu-Lin Juang, Yueh-Tong Lu   +3 more
semanticscholar   +1 more source

Early Fibrillin-1 Assembly Monitored through a Modifiable Recombinant Cell Approach

Biomacromolecules, 2014
Dirk Hubmacher, Dieter P Reinhardt
exaly  

Fibrillin-1 insufficiency alters periodontal wound healing failure in a mouse model of Marfan syndrome.

Archives of Oral Biology, 2018
K. Handa, Syouta Abe, V. Suresh, Y. Fujieda, M. Ishikawa, Ai Orimoto, Yoko Kobayashi, S. Yamada, S. Yamaba, S. Murakami, M. Saito   +10 more
semanticscholar   +1 more source

Homocysteine Modifies Structural and Functional Properties of Fibronectin and Interferes with the Fibronectin–Fibrillin-1 Interaction

Biochemistry, 2011
Dirk Hubmacher, Dieter P Reinhardt
exaly  

The value of plasma fibrillin-1 level in patients with spontaneous coronary artery dissection.

International Journal of Cardiology, 2019
Peng Hui, Yang Bai, Xing Su, N. Quan, Bokang Qiao, Yang Zheng, Jiangcheng Shi, Xiaoyu Du, Jie Lu   +8 more
semanticscholar   +1 more source

Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome

Science Translational Medicine, 2010
Ilídio J Correia
exaly