scholarly journals Tissue Source Site

2020 ◽  
Author(s):  
Keyword(s):  
2016 ◽  
Vol 41 (12) ◽  
pp. 1543-1547 ◽  
Author(s):  
Leonard G. Heydenrych ◽  
Donald F. du Toit ◽  
Colleen M. Aldous

1994 ◽  
Vol 84 (1) ◽  
pp. 1-15 ◽  
Author(s):  
John Boatwright

Abstract The vertical components of the S wave trains recorded on the Eastern Canadian Telemetered Network (ECTN) from 1980 through 1990 have been spectrally analyzed for source, site, and propagation characteristics. The data set comprises some 1033 recordings of 97 earthquakes whose magnitudes range from M ≈ 3 to 6. The epicentral distances range from 15 to 1000 km, with most of the data set recorded at distances from 200 to 800 km. The recorded S wave trains contain the phases S, SmS, Sn, and Lg and are sampled using windows that increase with distance; the acceleration spectra were analyzed from 1.0 to 10 Hz. To separate the source, site, and propagation characteristics, an inversion for the earthquake corner frequencies, low-frequency levels, and average attenuation parameters is alternated with a regression of residuals onto the set of stations and a grid of 14 distances ranging from 25 to 1000 km. The iteration between these two parts of the inversion converges in about 60 steps. The average attenuation parameters obtained from the inversion were Q = 1997 ± 10 and γ = 0.998 ± 0.003. The most pronounced variation from this average attenuation is a marked deamplification of more than a factor of 2 at 63 km and 2 Hz, which shallows with increasing frequency and increasing distance out to 200 km. The site-response spectra obtained for the ECTN stations are generally flat. The source spectral shape assumed in this inversion provides an adequate spectral model for the smaller events (Mo < 3 × 1021 dyne-cm) in the data set, whose Brune stress drops range from 5 to 150 bars. For the five events in the data set with Mo ≧ 1023 dyne-cm, however, the source spectra obtained by regressing the residuals suggest that an ω2 spectrum is an inadequate model for the spectral shape. In particular, the corner frequencies for most of these large events appear to be split, so that the spectra exhibit an intermediate behavior (where |ü(ω)| is roughly proportional to ω).


2018 ◽  
Vol 24 (23-24) ◽  
pp. 1733-1741 ◽  
Author(s):  
Hui-Yi Hsiao ◽  
Chin-Yu Yang ◽  
Jia-Wei Liu ◽  
Eric M. Brey ◽  
Ming-Huei Cheng
Keyword(s):  

Author(s):  
Sean Dennis Christie ◽  
Damaso Sadi ◽  
Ivar Mendez

Background:The role of neural transplantation as a restorative strategy for spinal cord injury continues to be intensely investigated. Ideally, the tissue source for transplantation must be readily available, free of disease and able to survive and mature following implantation into the adverse environment created by the injury. We have studied the use of a commercially available cell line of cultured human neurons (hNT neurons) as a tissue source for neural transplantation in spinal cord injury.Methods:Following a left lateral thoracic hemisection, 54 immunosuppressed, female Wistar rats were randomly allocated into different treatment groups; hemisection only or hemisection and hNT cell transplantation (via a bridge, double or triple graft). Grafting occurred three days after spinal cord injury. After thirteen weeks the animals were sacrificed and tissue sections were stained with human neuron specific enolase and human specific neural cell adhesion molecule.Results:Immunohistochemical evidence of graft survival was displayed in 66.7% of the surviving, grafted animals. Fibre outgrowth, greatest in the bridge and triple grafts, was observed in both rostral and caudal directions essentially bridging the lesion. Double grafts were smaller, displaying less fibre outgrowth, which did not cross the lesion. Long fibre outgrowth was evident up to 2 cm from the graft as assessed by tracing and immunohistochemical studies.Conclusion:Bridge and triple grafts displayed greater growth and enabled the hNT graft to essentially bridge the lesion. This suggests that hNT neurons have the potential to structurally reconnect the proximal and distal spinal cord across the region of injury.


The Lancet ◽  
1968 ◽  
Vol 291 (7536) ◽  
pp. 230-231 ◽  
Author(s):  
J.H. Cort ◽  
V. Pliska ◽  
T. DOU&Sbreve;A

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