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Tissue recombination is a powerful method to evaluate the paracrine-signaling events that orchestrate the development of organs using the in vivo environment of a host rodent. Studies have reported the successful generation of primary cultures of rodent bladder urothelium, but none have reported their use to recapitulate bladder tissue with tissue recombination. We propose that primary cultured bladder urothelium, when recombined with inductive embryonic bladder mesenchyme, will form bladder tissue in a recombination model. Adult rat bladders were isolated and urothelium obtained. Sheets of bladder urothelium were re-suspended in collagen and maintained in tissue culture. After expansion (>20 passages), the urothelium was recombined with embryonic day-14 mouse bladder mesenchyme, then grafted beneath the renal capsule of immunocompromised mouse hosts. Grafts were harvested after 28 days. Control grafts were performed with bladder mesenchyme alone, cultured bladder urothelium alone, and collagen matrix alone. Final tissues were evaluated with staining and immunohistochemistry (H&E, Gomori's trichrome, broad-spectrum uroplakin, and smooth muscle actin alpha and gamma). Immunocytochemistry on cultured urothelium for broad-spectrum keratin, vimentin, and broad-spectrum uroplakin confirmed pure populations, void of mesenchymal contaminants. Staining of recombinant grafts demonstrated bladder tissue with mature urothelium and stromal differentiation. Control tissues were void of bladder tissue formation. We have successfully demonstrated that a chimeric bladder is formed from primary cultured bladder urothelium recombined with embryonic bladder mesenchyme. This is a powerful new tool for investigating the molecular mechanisms of bladder development and disease. Future applications may include the in vitro genetic manipulation of urothelium and examining those effects on growth and development in an in vivo environment.  相似文献   
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Deep learning is becoming increasingly popular and available to new users, particularly in the medical field. Deep learning image segmentation, outcome analysis, and generators rely on presentation of Digital Imaging and Communications in Medicine (DICOM) images and often radiation therapy (RT) structures as masks. Although the technology to convert DICOM images and RT structures into other data types exists, no purpose-built Python module for converting NumPy arrays into RT structures exists. The 2 most popular deep learning libraries, Tensorflow and PyTorch, are both implemented within Python, and we believe a set of tools built in Python for manipulating DICOM images and RT structures would be useful and could save medical researchers large amounts of time and effort during the preprocessing and prediction steps. Our module provides intuitive methods for rapid data curation of RT-structure files by identifying unique region of interest (ROI) names and ROI structure locations and allowing multiple ROI names to represent the same structure. It is also capable of converting DICOM images and RT structures into NumPy arrays and SimpleITK Images, the most commonly used formats for image analysis and inputs into deep learning architectures and radiomic feature calculations. Furthermore, the tool provides a simple method for creating a DICOM RT-structure from predicted NumPy arrays, which are commonly the output of semantic segmentation deep learning models. Accessing DicomRTTool via the public Github project invites open collaboration, and the deployment of our module in PyPi ensures painless distribution and installation. We believe our tool will be increasingly useful as deep learning in medicine progresses.  相似文献   
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Background

There is a sizable proportion of elderly, both men and women, with fragility fractures, approximately 2 million fractures per year in the United States.

Methods

A retrospective chart review of 365 patient presented between January 2012 and December 2017 with vertebral compression fractures. Pre-post study design to determine refracture between Group A (before Fracture Liaison Service (FLS)) and Group B, after. Calcium, Vitamin D, DEXA scans, FRAX scores, and refracture rates were measured.

Results

Mean age for group A and B were 79.0 and 74.9 years, respectively, and predominantly females. Serum calcium was higher in group B (9.51?mg/d/L versus 9.40?mg/dL) but not significant (p?=?0.19). Fracture score among the groups was similar (20% versus 22%; p?=?0.44). The total refracture rate for both vertebral and other fracture was significantly less in the post FLS patients, 36.5% versus 56% p-value?=?0.01.

Conclusion

FLS program benefited patients with fragility fractures by decreasing the incidence of all refracture rates.  相似文献   
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