scholarly journals 640 Single-cell transcriptomics of human pressure ulcers reveals MHCII expressing keratinocytes in patients with a worse healing outcome

2021 ◽  
Vol 141 (5) ◽  
pp. S111
Author(s):  
D. Li ◽  
S. Cheng ◽  
Q. Deng ◽  
N. Xu Landén
2018 ◽  
Vol 15 (11) ◽  
pp. 1105-1112 ◽  
Author(s):  
Jakub Taradaj ◽  
Barbara Shay ◽  
Robert Dymarek ◽  
Mirosław Sopel ◽  
Karolina Walewicz ◽  
...  

Author(s):  
Dongqing Li ◽  
Shangli Cheng ◽  
Yu Pei ◽  
Pehr Sommar ◽  
Jaanika Kärner ◽  
...  

2021 ◽  
Vol 2137 (1) ◽  
pp. 012038
Author(s):  
Xianyu Meng ◽  
Qi Wang ◽  
Hongsheng Liu ◽  
Xiquan Yu

Abstract At present, skin pressure ulcers are a common problem in the care of bedridden patients. Solving this problem usually involves turning the patient over regularly, which requires a lot of manpower and material resources. This paper designs a human body pressure recognition model, which can solve the problem of human pressure ulcers very well in combination with intelligent nursing beds. This paper collects the bone data of the human body by using the Kinect sensor, and then processes the collected data. The film pressure sensor is used to collect the pressure information of the human body, and the pressure information is matched with the bone data of the human body, so as to obtain the pressure of the corresponding part of the human body, and judge the current posture of the human body through the pressure information. When the pressure of the compression part of the human body reaches the threshold, the intelligent nursing bed automatically turns over to reduce the pressure of the compression part of the human body.


1996 ◽  
Vol 107 (5) ◽  
pp. 743-748 ◽  
Author(s):  
Dorne R. Yager ◽  
Liang-Y. Zhang ◽  
Hui-Xiu Liang ◽  
Robert F. Diegelmann ◽  
I. Kelman Cohen

Author(s):  
Debby A. Jennings ◽  
Michael J. Morykwas ◽  
Louis C. Argenta

Grafts of cultured allogenic or autogenic keratlnocytes have proven to be an effective treatment of chronic wounds and burns. This study utilized a collagen substrate for keratinocyte and fibroblast attachment. The substrate provided mechanical stability and augmented graft manipulation onto the wound bed. Graft integrity was confirmed by light and transmission electron microscopy.Bovine Type I dermal collagen sheets (100 μm thick) were crosslinked with 254 nm UV light (13.5 Joules/cm2) to improve mechanical properties and reduce degradation. A single cell suspension of third passage neonatal foreskin fibroblasts were plated onto the collagen. Five days later, a single cell suspension of first passage neonatal foreskin keratinocytes were plated on the opposite side of the collagen. The grafts were cultured for one month.The grafts were fixed in phosphate buffered 4% formaldehyde/1% glutaraldehyde for 24 hours. Graft pieces were then washed in 0.13 M phosphate buffer, post-fixed in 1% osmium tetroxide, dehydrated, and embedded in Polybed 812.


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