Visualisation Technique for Trabecular Architecture of Bone Using Ultrasound Signals

2004 ◽  
Vol 1-2 ◽  
pp. 99-106
Author(s):  
Fumio Nogata
Keyword(s):  
Bone Marrow ◽  
Attenuation Factor ◽  
Bovine Bone ◽  
Trabecular Architecture ◽  
Pixel Size ◽  
Image Size ◽  
Heel Bone ◽  
The Difference ◽  
A New Technique ◽  
Visualisation Technique

We have proposed a new technique for visualising trabecular architecture of spongy bone using ultrasound A-mode signals from a transducer of medical ultrasound system. The technique can be established by finding a method to distinguish between bone and bone marrow. Firstly, the A-mode signal intensity was fitted by the form, A=A0exp(-ax), where A, A0, a, and x represent echo intensity, initial value of echo, attenuation factor, and distance, respectively. Then the curve was moved slightly downward or upward by multiplying with the coefficient k (0.9~1.2), and it was used as an index line to distinguish between bone and bone marrow. To clarify the validity of the proposed technique, we examined bovine bone specimen and a spongy-shaped specimen made by ceramics. The pixel size for creating architecture was 0.2 (width) × 0.15 (depth) mm for bone marrow and 0.2 × 0.3 mm for bone substance, and the pixel size differs due to the difference in wave speeds. The visualisation technique was capable to create an image size of ~10 mm depths from the surface of cortical bone. We also tried to visualise the heel bone.

scholarly journals Annual Spread Rate of Tomentosus Root Disease

Plant Disease ◽  
1997 ◽  
Vol 81 (9) ◽  
pp. 1053-1056 ◽  
Author(s):  
R. S. Hunt ◽  
F. G. Peet
Keyword(s):  
British Columbia ◽  
Tree Ring ◽  
Root Disease ◽  
Uninfected Control ◽  
Radial Increment ◽  
Spread Rate ◽  
Annual Increment ◽  
Temporal Differences ◽  
The Difference ◽  
A New Technique

The spread rate of tomentosus root disease, caused by Inonotus tomentosus, was investigated by a new technique employing temporal differences in the initiation of the reduced annual radial increment between pairs of diseased trees. Pairs of infected trees (stumps) located on the periphery of disease centers were selected in each of six widely separated spruce (Picea spp.) stands in British Columbia. Distances between 12 pairs of stumps were measured, and disks were collected from each stump. Similarly, disks from four additional pairs were collected from trees in a younger stand. Uninfected control disks were collected for all sites. Tree-ring measurements were determined for all disk samples and the year in which the reduction of the annual increment attributable to I. tomentosus began was determined for infected trees. The difference between initiation years for pairs of infected trees divided into the distance between them produced an average annual spread rate of 20 cm/yr. This rate will be used in developing a model for the disease.

scholarly journals A Stochastic Model for Block Segmentation of Images Based on the Quadtree and the Bayes Code for It

Entropy ◽  
2021 ◽  
Vol 23 (8) ◽  
pp. 991
Author(s):  
Yuta Nakahara ◽  
Toshiyasu Matsushima
Keyword(s):  
Computational Cost ◽  
Block Size ◽  
Input Image ◽  
Generative Model ◽  
Image Size ◽  
Variable Block ◽  
General Data ◽  
The Difference ◽  
Segmentation Of Images ◽  
Target Data

In information theory, lossless compression of general data is based on an explicit assumption of a stochastic generative model on target data. However, in lossless image compression, researchers have mainly focused on the coding procedure that outputs the coded sequence from the input image, and the assumption of the stochastic generative model is implicit. In these studies, there is a difficulty in discussing the difference between the expected code length and the entropy of the stochastic generative model. We solve this difficulty for a class of images, in which they have non-stationarity among segments. In this paper, we propose a novel stochastic generative model of images by redefining the implicit stochastic generative model in a previous coding procedure. Our model is based on the quadtree so that it effectively represents the variable block size segmentation of images. Then, we construct the Bayes code optimal for the proposed stochastic generative model. It requires the summation of all possible quadtrees weighted by their posterior. In general, its computational cost increases exponentially for the image size. However, we introduce an efficient algorithm to calculate it in the polynomial order of the image size without loss of optimality. As a result, the derived algorithm has a better average coding rate than that of JBIG.

scholarly journals Functional and aesthetic outcomes of spreader graft and auto-spreader flap after nasal hump removal

2020 ◽  
Vol 36 (1) ◽  
Author(s):  
Maged Baher Naguib ◽  
Mohamed Rifaat Ahmed ◽  
Yasser Taha Madian ◽  
Tarek Mohamady Elnahriry ◽  
Wael Elshahat Eldeeb
Keyword(s):  
Nasal Obstruction ◽  
Operative Time ◽  
Nasal Valve ◽  
Spreader Graft ◽  
Spreader Flap ◽  
The Mean ◽  
The Difference ◽  
A New Technique ◽  
Nasal Valve Collapse ◽  
Duration Of Operation

Abstract Background Following the reduction of the nasal hump to a desired level, spreader grafts are usually positioned to prevent the complication of nasal valve collapse. Auto-spreader flap is a new technique that gained more popularity recently and can be used as an alternative to spreader graft. This RCCT compared between both techniques aesthetically and functionally as well as the operative time. Results Forty patients, 17 males (42.5%) and 23 females (57.5%), were included. The mean duration of operation in auto-spreader flap was 11.8 ± 3.4 min, while it was 19.2 ± 3.2 min in spreader graft. The difference between the two procedures was statistically significant (P < 0.05). Functional assessment of nasal obstruction was done for all patients in both groups preoperative that was (75.6 ± 19.9) which showed marked improvement when re-evaluated 3 moths postoperatively (18.9 ± 14.7), and after 6 months NOSE scale was (29.1 ± 20.2). The overall aesthetic satisfaction was 62.5% (25 of 40) irrespective of the surgery done. Sixteen out of 20 patients in spreader group and 9 out of 20 in auto-spreader flap group. Conclusion Auto-spreader flap and spreader graft are very effective surgical procedure for treatment of nasal obstruction due to internal nasal valve dysfunction, but the auto-spreader flap had shorter operative time. However, spreader graft has a superior aesthetic outcome.

ACCURATE ANALYSIS OF GLOBAL INTERCONNECTS IN NANO-FPGAs

NANO ◽  
2009 ◽  
Vol 04 (03) ◽  
pp. 171-176 ◽  
Author(s):  
DAVOOD FATHI ◽  
BEHJAT FOROUZANDEH
Keyword(s):  
Propagation Delay ◽  
Modeling Method ◽  
Accurate Analysis ◽  
Proposed Model ◽  
Simulation Results ◽  
The Difference ◽  
A New Technique ◽  
Global Interconnects ◽  
Technology Nodes ◽  
Model Technique

This paper introduces a new technique for analyzing the behavior of global interconnects in FPGAs, for nanoscale technologies. Using this new enhanced modeling method, new enhanced accurate expressions for calculating the propagation delay of global interconnects in nano-FPGAs have been derived. In order to verify the proposed model, we have performed the delay simulations in 45 nm, 65 nm, 90 nm, and 130 nm technology nodes, with our modeling method and the conventional Pi-model technique. Then, the results obtained from these two methods have been compared with HSPICE simulation results. The obtained results show a better match in the propagation delay computations for global interconnects between our proposed model and HSPICE simulations, with respect to the conventional techniques such as Pi-model. According to the obtained results, the difference between our model and HSPICE simulations in the mentioned technology nodes is (0.29–22.92)%, whereas this difference is (11.13–38.29)% for another model.

THE FATE OF BOVINE BONE MARROW STROMAL CELLS IN HYDROGELS

2008 ◽  
Vol 41 ◽  
pp. S130 ◽  
Author(s):  
Stephan Zeiter ◽  
Marije van der Werf ◽  
Keita Ito
Keyword(s):  
Bone Marrow ◽  
Stromal Cells ◽  
Bone Marrow Stromal Cells ◽  
Marrow Stromal Cells ◽  
Bovine Bone

scholarly journals Species Identification and Quantification of Bovine Bone Marrow from Non-Bovine Products using DNA and Protein Fingerprints

2021 ◽  
Author(s):  
Yize Guan ◽  
Nan Li ◽  
Tancheng Li ◽  
Liyuan Sun ◽  
Li Ming Cheng
Keyword(s):  
Bone Marrow ◽  
Multiplex Pcr ◽  
High Sensitivity ◽  
Bovine Bone ◽  
Assay Sensitivity ◽  
Conserved Sequence ◽  
Specific Pcr ◽  
Modified Method ◽  
Sds Page ◽  
Mitochondrial Cytochrome B

Abstract Bovine bone marrow is traditionally regarded as a highly nutritious food that has been widely used as a medicinal and healthy food for several decades in China. A large number of adulterated and counterfeit bone marrows from pigs and donkeys have been used in place of bovine bone marrow in commercial products, which are almost identical morphologically to species. Therefore, we explored a feasibility of fingerprinting of multiplex PCR gels combined with imaged SDS-PAGE gels of proteins. Three pairs of specific primers for bovine, pig and donkey were designed according to the conserved sequence in mitochondrial cytochrome b. The optimal reaction conditions for triple PCR were optimized. A modified method was used to extract total proteins and SDS-PAGE gels of proteins were set up. A three-fold PCR detection assay was successfully established to identify three species of bovine, pig and donkey. Three primers have good specificity and high sensitivity. Additionally, the assay sensitivity test confirmed that the extracted DNA concentration was the lowest of bovine bone marrow at 0.1 pg. The assay also showed 100% specificity. The electrophoretogram of SDS-PAGE showed distinct electrophoresis profiles among three species. The established fingerprint of multiplex PCR DNA gels combined with imaged SDS-PAGE gels of proteins has strong specificity and can be quickly and accurately used for the identification of bovine bone marrow. Rapid authentication of bovine bone marrow and differentiation from non-bovine products can be achieved using an improved SDS alkali denaturation method, species-specific PCR assay combined with imaged SDS-PAGE gels of proteins.

scholarly journals Hematopoietic Recovery after Transplantation CD117+B220- (lacZ+) Bone Marrow Cells in Lethally Irradiated Mice

2008 ◽  
Vol 51 (1) ◽  
pp. 37-41 ◽  
Author(s):  
Miroslav Hodek ◽  
Jiřina Vávrová ◽  
Zuzana Šinkorová ◽  
Jaroslav Mokrý ◽  
Stanislav Filip
Keyword(s):  
Bone Marrow ◽  
Bone Marrow Cells ◽  
Repair Process ◽  
Whole Body ◽  
Lacz Gene ◽  
Colony Forming Units ◽  
The Difference ◽  
Macrophage Colony ◽  
Marrow Cells

Experiments presented here were aimed at the description of hematopoiesis repair and in vivo homing of transplanted separated CD117+B220–bone marrow cells after whole-body lethal irradiation at LD 9Gy. ROSA 26 mice were used as donors of marrow cells for transplantation [B6;129S/Gt (ROSA)26Sor] and were tagged with lacZ gene, and F2 hybrid mice [B6129SF2/J] were used as recipients of bone marrow transplanted cells. Hematopoiesis repair was provided by transplantation, both suspension of whole bone marrow cells (5x106) and isolated CD117+B220–cells (5x104). Mice survived up to thirty days after irradiation. We demonstrated that transplantation of suspension of whole bone marrow cells led to faster recovery of CFU-GM (Granulocyte-macrophage colony forming units) in bone marrow and in the spleen too. It is not clear what the share of residential and transplanted cells is in the repair process. Our results demonstrate that sufficient hematopoietic repair occurs after transplantation of CD117+B220–(lacZ+) in lethally irradiated mice, and the difference in CFU-GM numbers in the bone marrow and spleen found on day 8 posttransplant has no influence on the survival of lethally irradiated mice (30 days follow-up).

A NEW TECHNIQUE: SERIAL BONE MARROW BIOPSIES FOR MONITORING CHROMOSOMAL CHANGES IN RATS

Abstracts ◽  
1977 ◽  
pp. 168
Author(s):  
Aurelio Pasi ◽  
Jesus Nemenzo ◽  
Gaye H. Eisenlord ◽  
Charles H. Hine
Keyword(s):  
Bone Marrow ◽  
New Technique ◽  
Bone Marrow Biopsies ◽  
Chromosomal Changes ◽  
A New Technique
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