Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Xiongzheng Mu"'
Autor:
Yun Xie, MD, Sufan Wu, MD, Lei Wang, MD, Xiongzheng Mu, MD, Maoguo Shu, MD, Matthias Hofmann, PhD, Gudrun Klein, PhD, Qingfeng Li, MD, PhD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 11, Iss 11, p e5423 (2023)
Background:. Soft-tissue fillers, specifically hyaluronic acid fillers, can reduce many signs of aging by treating the associated loss of subcutaneous fat and midfacial contour deficiencies. The objective of this study was to investigate whether the
Externí odkaz:
https://doaj.org/article/c65d188f28a44294a183ad2400fb12e6
Autor:
Jieyi Chen, Ping Zhang, Meifang Peng, Bo Liu, Xiao Wang, Siyuan Du, Yao Lu, Xiongzheng Mu, Yulan Lu, Sijia Wang, Yingzhi Wu
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Craniosynostosis (CRS) is a disease with prematurely fused cranial sutures. In the last decade, the whole-exome sequencing (WES) was widely used in Caucasian populations. The WES largely contributed in genetic diagnosis and exploration on new genetic
Externí odkaz:
https://doaj.org/article/0af426616d2342a5afc97107e5b4d93a
Publikováno v:
Proteome Science, Vol 16, Iss 1, Pp 1-9 (2018)
Abstract Background Fibroblast growth factor receptor 2 (FGFR2) play a vital role in skeletogenesis. However, the molecular mechanisms triggered by FGFR2 in osteoblasts are still not fully understood. In this study, proteomics and bioinformatics anal
Externí odkaz:
https://doaj.org/article/46d18a02da3540a29986a9536d7f1766
Autor:
Weiguo Zou, Andrew O.M. Wilkie, Xiongzheng Mu, Jieyi Chen, Meifang Peng, Jinlong Suo, Yanqing Xu, Sihai Zou, Sijia Wang, Yingzhi Wu
Publikováno v:
Journal of Genetics and Genomics. 48:167-171
Publikováno v:
Journal of cosmetic dermatologyREFERENCES. 21(12)
Soft-tissue augmentation of the midface is increasingly requested by patients, and hyaluronic acid (HA) fillers are frequently used in treatment.To evaluate the efficacy and safety of treatment of midface volume/contour deficit with a firm HA filler
Autor:
Wei Qian, Manfei Zhang, Kaiwen Wan, Yunxia Xie, Siyuan Du, Jiarui Li, Xiongzheng Mu, Jiange Qiu, Xiangyang Xue, Xiahai Zhuang, Yingzhi Wu, Fan Liu, Sijia Wang
Publikováno v:
Journal of genetics and genomics = Yi chuan xue bao. 49(10)
Facial and cranial variation represent a multidimensional set of highly correlated and heritable phenotypes. Little is known about the genetic basis explaining this correlation. We develop a software package ALoSFL for simultaneous localization of fa
Publikováno v:
Journal of the American Academy of Dermatology. 85:AB84
Publikováno v:
Journal of Craniofacial Surgery. 28:1481-1485
Craniosynostosis is a complex disease condition, which involves premature fusion of cranial vault sutures and lacks desirable treatment. Previous studies have demonstrated decreased proliferation rate of osteoblasts and downregulated expression of gl
Autor:
Bin, Yang, Zuoliang, Qi, Min, Wei, Xiongzheng, Mu, Li, Teng, Zhiyong, Zhang, Xiaolei, Jin, Kai, Tao, Weiming, Shen, Guoping, Wu, Zhengxue, Han, Maoguo, Shu, Xiaoping, Chen, Nan, Bao
Publikováno v:
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi
The authors made a profound review on the development and the recent status of craniomaxillofacial surgery in China during past three decades. The emphases were placed on the following aspects: the modifications of the reconstructive procedure and mi
Publikováno v:
Journal of Craniofacial Surgery. 26:336-339
Purpose The aim of this study was to correct facial disharmony with or without occlusal dysfunction. Methods Based on computed tomography and presurgical design, restoration of normal skeleton relationship is a priority for selected facial deformitie