An In Vitro Analysis of Ligament Reconstruction or Extension Osteotomy on Trapeziometacarpal Joint Stability and Contact Area

Object Expandable cages are becoming more popular due in large part to their versatility, but subsidence and catastrophic failure remain a concern. One of the proposed reasons of failure is edge loading of the endplate caused by a mismatch between the sagittal alignment of the motion segment and cage. This in vitro analysis investigates the endplate forces characteristic of expandable and fixed interbody cages in a single-level human cadaver corpectomy model. Methods Ten human thoracolumbar spines (T10–L2, L3–5) were biomechanically evaluated following a single-level corpectomy that was reconstructed with an expandable or fixed cage. Fixed cages were deployed with the best-fitting end cap combination, whereas expandable cages were deployed in normal, hypolordotic, and hyperlordotic alignment scenarios. The endplate forces and contact area were measured with a pressure measurement system, and the expansion torque applied by the surgeon was measured with a custom-made insertion device. Results The contact areas of the expandable cages were, in general, higher than those of the fixed cages. The endplate forces of the expandable cages were similar to those of the fixed cages in the normal alignment scenario. Higher endplate forces were observed in the hyperlordotic scenario, whereas the endplate forces in the hypolordotic and normal alignment scenarios were similar. There was no correlation with the expansion torque and the final endplate forces. Conclusions Expandable cages resulted in consistently higher contact area and endplate forces when compared with the fixed cages. Because the expansion torque does not correlate with the final endplate forces, surgeons should not rely solely on tactile feedback during deployment of these cages.

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Labral Reconstruction with Iliotibial Band Autograft and Semitendinosus Allograft Improves Hip Joint Contact Area and Contact Pressure: An In-Vitro Analysis

Arthroscopy The Journal of Arthroscopic and Related Surgery ◽

10.1016/j.arthro.2015.04.037 ◽

2015 ◽

Vol 31 (6) ◽

pp. e13

Author(s):

Shane Nho ◽

Simon Lee ◽

Thomas Wuerz ◽

Elizabeth Shewman ◽

Frank McCormick ◽

...

Keyword(s):

Contact Pressure ◽

Hip Joint ◽

Contact Area ◽

Iliotibial Band ◽

Joint Contact ◽

Vitro Analysis ◽

In Vitro Analysis

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The native structure of the eukaryotic ribosome

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100075890 ◽

1983 ◽

Vol 41 ◽

pp. 432-433

Author(s):

R.A. Milligan ◽

P.N.T. Unwin

Keyword(s):

Ribosomal Proteins ◽

Crystal Form ◽

Native Structure ◽

X Ray Diffraction ◽

Eukaryotic Ribosome ◽

Vitro Analysis ◽

In Vitro Analysis ◽

Resolution Structure ◽

Stable Unit

A detailed understanding of the mechanism of protein synthesis will ultimately depend on knowledge of the native structure of the ribosome. Towards this end we have investigated the low resolution structure of the eukaryotic ribosome embedded in frozen buffer, making use of a system in which the ribosomes crystallize naturally.The ribosomes in the cells of early chicken embryos form crystalline arrays when the embryos are cooled at 4°C. We have developed methods to isolate the stable unit of these arrays, the ribosome tetramer, and have determined conditions for the growth of two-dimensional crystals in vitro, Analysis of the proteins in the crystals by 2-D gel electrophoresis demonstrates the presence of all ribosomal proteins normally found in polysomes. There are in addition, four proteins which may facilitate crystallization. The crystals are built from two oppositely facing P4 layers and the predominant crystal form, accounting for >80% of the crystals, has the tetragonal space group P4212, X-ray diffraction of crystal pellets demonstrates that crystalline order extends to ~ 60Å.

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1163: Radial Dilation of Ureteral Balloons: A Comparative in-Vitro Analysis

The Journal of Urology ◽

10.1016/s0022-5347(18)35308-4 ◽

2005 ◽

Vol 173 (4S) ◽

pp. 315-316

Author(s):

Kari Hendlin ◽

Brynn Lund ◽

Manoj Monga

Keyword(s):

Vitro Analysis ◽

In Vitro Analysis

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Role of the 807 C/T Polymorphism of the α2 Gene in Platelet GP Ia Collagen Receptor Expression and Function

Thrombosis and Haemostasis ◽

10.1055/s-0037-1614605 ◽

1999 ◽

Vol 81 (06) ◽

pp. 951-956 ◽

Cited By ~ 59

Author(s):

J. Corral ◽

R. González-Conejero ◽

J. Rivera ◽

F. Ortuño ◽

P. Aparicio ◽

...

Keyword(s):

Venous Thrombosis ◽

Cell Types ◽

Receptor Expression ◽

Case Control Studies ◽

Platelet Surface ◽

Vitro Analysis ◽

And Function ◽

In Vitro Analysis

SummaryThe variability of the platelet GP Ia/IIa density has been associated with the 807 C/T polymorphism (Phe 224) of the GP Ia gene in American Caucasian population. We have investigated the genotype and allelic frequencies of this polymorphism in Spanish Caucasians. The T allele was found in 35% of the 284 blood donors analyzed. We confirmed in 159 healthy subjects a significant association between the 807 C/T polymorphism and the platelet GP Ia density. The T allele correlated with high number of GP Ia molecules on platelet surface. In addition, we observed a similar association of this polymorphism with the expression of this protein in other blood cell types. The platelet responsiveness to collagen was determined by “in vitro” analysis of the platelet activation and aggregation response. We found no significant differences in these functional platelet parameters according to the 807 C/T genotype. Finally, results from 3 case/control studies involving 302 consecutive patients (101 with coronary heart disease, 104 with cerebrovascular disease and 97 with deep venous thrombosis) determined that the 807 C/T polymorphism of the GP Ia gene does not represent a risk factor for arterial or venous thrombosis.

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