Zobrazeno 1 - 10
of 591
pro vyhledávání: '"Guixing, Qiu"'
Autor:
Sen Zhao, Hengqiang Zhao, Lina Zhao, Xi Cheng, Zhifa Zheng, Mengfan Wu, Wen Wen, Shengru Wang, Zixiang Zhou, Haibo Xie, Dengfeng Ruan, Qing Li, Xinquan Liu, Chengzhu Ou, Guozhuang Li, Zhengye Zhao, Guilin Chen, Yuchen Niu, Xiangjie Yin, Yuhong Hu, Xiaochen Zhang, Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study, Pengfei Liu, Guixing Qiu, Wanlu Liu, Chengtian Zhao, Zhihong Wu, Jianguo Zhang, Nan Wu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract Congenital vertebral malformation, affecting 0.13–0.50 per 1000 live births, has an immense locus heterogeneity and complex genetic architecture. In this study, we analyze exome/genome sequencing data from 873 probands with congenital vert
Externí odkaz:
https://doaj.org/article/5d2439648d9a4a0c8a930156c25c0a91
Akademický článek
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Autor:
Guixing Qiu
Publikováno v:
The Spine Journal. 14:1059
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::927c4cf8bbe75f6f051c7a111afe1ec5
https://doi.org/10.1016/j.spinee.2014.03.021
https://doi.org/10.1016/j.spinee.2014.03.021
Autor:
Wen Wen, Zhengye Zhao, Zhifa Zheng, Sen Zhao, Hengqiang Zhao, Xi Cheng, Huakang Du, Ziquan Li, Shengru Wang, Guixing Qiu, Zhihong Wu, Terry Jianguo Zhang, Nan Wu
Publikováno v:
Journal of Medical Genetics; Jul2024, Vol. 61 Issue 7, p666-676, 25p
Autor:
Yipeng Wang, Xiaoyang Liu
Publikováno v:
European Spine Journal. 23:935-937
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19592ef68549f1ed96b4ae09139b904e
https://doi.org/10.1007/s00586-014-3172-7
https://doi.org/10.1007/s00586-014-3172-7
Autor:
Xi Chen, Yiou Wang, Ruichen Ma, Huiming Peng, Shibai Zhu, Shanni Li, Songlin Li, Xiying Dong, Guixing Qiu, Wenwei Qian
Publikováno v:
Orthopaedic Surgery, Vol 14, Iss 6, Pp 1152-1160 (2022)
Objective This study aims to compare the accuracy of CT‐based preoperative planning with that of acetate templating in predicting implant size, neck length, and neck cut length, and to evaluate the reproducibility of the two methods. Methods This p
Externí odkaz:
https://doaj.org/article/40edef0909894ed598da687a6fd3f4c0
Autor:
Muchuan Wang, Ziquan Li, Sen Zhao, Zhifa Zheng, Yipeng Wang, Guixing Qiu, Zhihong Wu, Nan Wu, Terry Jianguo Zhang, Siyi Cai
Publikováno v:
Cell Regeneration, Vol 11, Iss 1, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/a844a0a9a765409e8965b903925bce31
Autor:
Di Wu, Xiao Chang, Jingjing Tian, Lin Kang, Yuanhao Wu, Jieying Liu, Xiangdong Wu, Yue Huang, Bo Gao, Hai Wang, Guixing Qiu, Zhihong Wu
Publikováno v:
Journal of Nanobiotechnology, Vol 21, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/638e0d4f864e4aa884bb6d21c05d69ef
Autor:
Lian Liu, Liying Sun, Yujun Chen, Muchuan Wang, Chenxi Yu, Yingzhao Huang, Sen Zhao, Huakang Du, Shaoke Chen, Xin Fan, Wen Tian, Zhihong Wu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study group, Guixing Qiu, Terry Jianguo Zhang, Nan Wu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background Skeletal deformity is characterized by an abnormal anatomical structure of bone and cartilage. In our previous studies, we have found that a substantial proportion of patients with skeletal deformity could be explained by monogeni
Externí odkaz:
https://doaj.org/article/10847cd3fdaa467197acb54b9ee82b40
Autor:
Sen Zhao, Yuanqiang Zhang, Sigrun Hallgrimsdottir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte, Sen Liu, Hillevi Lindelöf, Shengru Wang, Anna Hammarsjö, Yang Yang, Yongyu Ye, Lianlei Wang, Zihui Yan, Jiachen Lin, Chenxi Yu, Zefu Chen, Yuchen Niu, Huizi Wang, Zhi Zhao, Pengfei Liu, Guixing Qiu, Jennifer E. Posey, Zhihong Wu, James R. Lupski, Ieva Micule, Britt-Marie Anderlid, Ulrika Voss, Dennis Sulander, Ekaterina Kuchinskaya, Ann Nordgren, Ola Nilsson, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Giedre Grigelioniene, Nan Wu
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-11 (2022)
Abstract Pathogenic variants in MYH3 cause distal arthrogryposis type 2A and type 2B3 as well as contractures, pterygia and spondylocarpotarsal fusion syndromes types 1A and 1B. These disorders are ultra-rare and their natural course and phenotypic v
Externí odkaz:
https://doaj.org/article/0de9e51627714482a09108f93d1360a8