AbstractWe quantitatively compare data obtained from imaging two-dimensional slices of three-dimensional unlabeled and fluorescently labeled collagen gels with confocal reflectance microscopy (CRM) and/or confocal fluorescence microscopy (CFM). Different network structures are obtained by assembling the gels over a range of concentrations at various temperatures. Comparison between CRM and CFM shows that the techniques are not equally sensitive to details of network structure, with CFM displaying higher fidelity in imaging fibers parallel to the optical axis. Comparison of CRM of plain and labeled collagen gels shows that labeling itself induces changes in gel structure, chiefly through inhibition of fibril bundling. Despite these differenc...
We describe a robust method for determining morphological properties of filamentous biopolymer netwo...
We study the micromechanics of collagen-I gel with the goal of bridging the gap between theory and e...
<p>SCMF were grown in gels of 1.0, 1.5, 2.0, or 2.5 mg/ml collagen for 2 days. A) Confocal reflectio...
Cellularized collagen gels are a common model in tissue engineering, but the relationship between th...
Multiphoton microscopy of collagen hydrogels produces second harmonic generation (SHG) and two-photo...
We investigate the dependence of fiber brightness on three-dimensional fiber orientation when imagin...
Recent evidence supports the notion that biological functions of extracellular matrix (ECM) are high...
AbstractWe investigate the dependence of fiber brightness on three-dimensional fiber orientation whe...
AbstractMultiphoton microscopy of collagen hydrogels produces second harmonic generation (SHG) and t...
AbstractType I collagen gels are routinely used in biophysical studies and bioengineering applicatio...
Multiphoton microscopy (MPM) holds promise as a noninvasive imaging technique for characterizing col...
We describe a robust method for determining morphological properties of filamentous biopolymer netwo...
AbstractMultiphoton microscopy (MPM) holds promise as a noninvasive imaging technique for characteri...
Multiphoton microscopy (MPM) holds promise as a noninvasive imaging technique for characterizing col...
Collagen microstructure is closely related to the mechanical properties of tissues and affects cell ...
We describe a robust method for determining morphological properties of filamentous biopolymer netwo...
We study the micromechanics of collagen-I gel with the goal of bridging the gap between theory and e...
<p>SCMF were grown in gels of 1.0, 1.5, 2.0, or 2.5 mg/ml collagen for 2 days. A) Confocal reflectio...
Cellularized collagen gels are a common model in tissue engineering, but the relationship between th...
Multiphoton microscopy of collagen hydrogels produces second harmonic generation (SHG) and two-photo...
We investigate the dependence of fiber brightness on three-dimensional fiber orientation when imagin...
Recent evidence supports the notion that biological functions of extracellular matrix (ECM) are high...
AbstractWe investigate the dependence of fiber brightness on three-dimensional fiber orientation whe...
AbstractMultiphoton microscopy of collagen hydrogels produces second harmonic generation (SHG) and t...
AbstractType I collagen gels are routinely used in biophysical studies and bioengineering applicatio...
Multiphoton microscopy (MPM) holds promise as a noninvasive imaging technique for characterizing col...
We describe a robust method for determining morphological properties of filamentous biopolymer netwo...
AbstractMultiphoton microscopy (MPM) holds promise as a noninvasive imaging technique for characteri...
Multiphoton microscopy (MPM) holds promise as a noninvasive imaging technique for characterizing col...
Collagen microstructure is closely related to the mechanical properties of tissues and affects cell ...
We describe a robust method for determining morphological properties of filamentous biopolymer netwo...
We study the micromechanics of collagen-I gel with the goal of bridging the gap between theory and e...
<p>SCMF were grown in gels of 1.0, 1.5, 2.0, or 2.5 mg/ml collagen for 2 days. A) Confocal reflectio...