Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Yingzhao Hu"'
Autor:
Haoran Fu, Qingxu Ma, Zhengbo Ma, Yingzhao Hu, Fan Liu, Kaijun Chen, Wankun Pan, Sheng Tang, Xin Zhang, Lianghuan Wu
Publikováno v:
HortScience, Vol 56, Iss 11, Pp 1395-1401 (2021)
Pear (Pyrus spp.) is the third-largest economic crop in China after apples (Malus pumila Mill.) and citrus (Citrus reticulata Blanco), and it is mainly cultivated by smallholders. Currently, the yield of Chinese pear ranks midlevel globally, with onl
Externí odkaz:
https://doaj.org/article/c66dd0c0ff4c4c39b8b1393bcb98ad7a
Autor:
Yaohui Hu, Yadong Chen, Xiaobin Yi, Jiquan Zhong, Xing Wang, Zhiyong Yao, Yingzhao Hu, Tao Zhang, Yong Fang
Publikováno v:
Sensors & Materials; 2021, Vol. 33 Issue 8,Part 3, p2825-2833, 9p
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundThe surge in the number of publications on psoriasis has posed significant challenges for researchers in effectively managing the vast amount of information. However, due to the lack of tools to process metadata, no comprehensive bibliometr
Externí odkaz:
https://doaj.org/article/df1c0ed8516e47c5bd373b779e989e82
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:
Liying Sun, Yingzhao Huang, Sen Zhao, Junhui Zhao, Zihui Yan, Yang Guo, Mao Lin, Wenyao Zhong, Yuehan Yin, Zefu Chen, Nan Zhang, Yuanqiang Zhang, Zongxuan Zhao, Qingyang Li, Lianlei Wang, Xiying Dong, Yaqi Li, Xiaoxin Li, Guixing Qiu, Terry Jianguo Zhang, Zhihong Wu, Wen Tian, Nan Wu
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 24, Iss , Pp 961-970 (2021)
Congenital limb malformations (CLMs) affect 1 in 500 live births. However, the value of exome sequencing (ES) for CLM is lacking. The purpose of this study was to decipher the mutational signature of CLM on an exome level. We enrolled a cohort of 66
Externí odkaz:
https://doaj.org/article/17f87b72e2f24cc3bb479e7ddcc1d2c8
Autor:
Zhou Jiang, Chenzhou Wu, Shoushan Hu, Nailin Liao, Yingzhao Huang, Haoran Ding, Ruohan Li, Yi Li
Publikováno v:
International Journal of Oral Science, Vol 13, Iss 1, Pp 1-7 (2021)
Abstract Neck dissection for oral squamous-cell carcinoma (OSCC) is a clinically controversial issue and has therefore been the subject of abundant research. However, no one has performed a bibliometric study on this topic to date. The aim of this st
Externí odkaz:
https://doaj.org/article/56330f6ae7c3410ba87a2b18d18437ea
Autor:
Yingzhao Huang, Qi Zhan, Chenzhou Wu, Nailin Liao, Zhou Jiang, Haoran Ding, Kunyu Wang, Yi Li
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Nanoparticles for the gene therapy field have seen remarkable progress over the last 10 years; however, low delivery efficiency and other reasons impede the clinical translation of nanocarriers. Therefore, a summary of hotspots and trends in this fie
Externí odkaz:
https://doaj.org/article/4b7096a184a94dd89d2e3181916f53a7
Autor:
Liying Sun, Yingzhao Huang, Sen Zhao, Wenyao Zhong, Jile Shi, Yang Guo, Junhui Zhao, Ge Xiong, Yuehan Yin, Zefu Chen, Nan Zhang, Zongxuan Zhao, Qingyang Li, Dan Chen, Yuchen Niu, Xiaoxin Li, Guixing Qiu, Zhihong Wu, Terry Jianguo Zhang, Wen Tian, Nan Wu
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Congenital contractural arachnodactyly (CCA) is a rare autosomal dominant disorder of connective tissue characterized by crumpled ears, arachnodactyly, camptodactyly, large joint contracture, and kyphoscoliosis. The nature course of CCA has not been
Externí odkaz:
https://doaj.org/article/dd71cbe7517b4d9ea945ab22c554e427
Autor:
Wen Tian, Yingzhao Huang, Liying Sun, Yang Guo, Sen Zhao, Mao Lin, Xiying Dong, Wenyao Zhong, Yuehan Yin, Zefu Chen, Nan Zhang, Yuanqiang Zhang, Lianlei Wang, Jiachen Lin, Zihui Yan, Xinzhuang Yang, Junhui Zhao, Guixing Qiu, Jianguo Zhang, Zhihong Wu, Nan Wu, (Deciphering Disorders Involving Scoliosis, COmorbidities) study group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Background Isolated macrodactyly is a severe congenital hand anomaly with functional and physiological impact. Known causative genes include PIK3CA, AKT1 and PTEN. The aim of this study is to gain insights into the genetics basis of isolated
Externí odkaz:
https://doaj.org/article/a62046b0c2114c88ac5c13072584d84c
Autor:
Zefu Chen, Zihui Yan, Chenxi Yu, Jiaqi Liu, Yanbin Zhang, Sen Zhao, Jiachen Lin, Yuanqiang Zhang, Lianlei Wang, Mao Lin, Yingzhao Huang, Xiaoxin Li, Yuchen Niu, Shengru Wang, Zhihong Wu, DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group, Guixing Qiu, Terry Jianguo Zhang, Nan Wu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background We previously reported a novel clinically distinguishable subtype of congenital scoliosis (CS), namely, TBX6-associated congenital scoliosis (TACS). We further developed the TBX6-associated CS risk score (TACScore), a multivariate
Externí odkaz:
https://doaj.org/article/0855793f02cf4a4ca530dbca6ded8948