Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Beihong Liu"'
Autor:
Licheng Gong, Beihong Liu, Jing Wang, Hong Pan, Anhui Qi, Siyang Zhang, Jinyi Wu, Ping Yang, Binbin Wang
Publikováno v:
BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Hashimoto’s thyroiditis is a complex autoimmune thyroid disease, the onset of which is associated with environmental exposures and specific susceptibility genes. Its incidence in females is higher than its incidence in males. Th
Externí odkaz:
https://doaj.org/article/d16fd69ae21e43bdade8cbc908b8c1fe
Autor:
Beili Chen, Lin Li, Jing Wang, Tengyan Li, Hong Pan, Beihong Liu, Yiran Zhou, Yunxia Cao, Binbin Wang
Publikováno v:
Journal of Ovarian Research, Vol 11, Iss 1, Pp 1-6 (2018)
Abstract Background To dissect the genetic alteration in two sisters with premature ovarian insufficiency (POI) from a consanguineous family. Methods Whole-exome sequencing technology was used in the POI proband, bioinformatics analysis was carried o
Externí odkaz:
https://doaj.org/article/0ce0099d7b5b46ffa64f62a6f25ced23
Autor:
Xuehan Qian, Beihong Liu, Jing Wang, Nan Wei, Xiaoli Qi, Xue Li, Jing Li, Ying Zhang, Ning Hua, Yuxian Ning, Gang Ding, Xu Ma, Binbin Wang
Publikováno v:
BMC Ophthalmology, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background The prevalence of adolescent eye disease in remote areas of the Qinghai-Tibet Plateau has rarely been reported. To understand the prevalence of common eye diseases in Tibet, we performed ocular-disease screening on students from p
Externí odkaz:
https://doaj.org/article/6b009165251a4e9487ac8cf6c9430197
Autor:
Ying Zhu, Zhi Cheng, Jing Wang, Beihong Liu, Longfei Cheng, Beili Chen, Yunxia Cao, Binbin Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-6 (2017)
Abstract Background The etiology of Müllerian duct anomalies (MDAs) is poorly understood at present. The HOXA11 gene is crucial for the development of the Müllerian duct. The objective of this study is to report a unique case of MDAs with a novel m
Externí odkaz:
https://doaj.org/article/e95cafc817474b86ac5676c403eea6ed
Publikováno v:
Eighth Symposium on Novel Photoelectronic Detection Technology and Applications.
Autor:
Tingting Liu, Genfu Zhao, Beihong Liu, Shubiao Xia, Xiang Gao, Huani Li, Yuhao Zhang, Hong Guo, Zhihui Gao
Publikováno v:
Sustainable Energy & Fuels. 4:2208-2219
Phosphorus-based materials can be used to construct promising anodes for sodium-ion batteries (SIBs) due to their high theoretical capacity (2596 mA h g−1) and safe working potential. However, their disadvantages are severe volume changes as well a
Autor:
Hong Pan, Bo Wan, Binbin Wang, Xu Ma, Shijing Wu, Jing Wang, Tian Zhu, Yan Luo, Ruifang Sui, Tengyan Li, Beihong Liu
Publikováno v:
Journal of Medical Genetics. 56:671-677
BackgroundHigh myopia (HM) is one of the leading causes of vision impairment worldwide, accompanied by a series of pathological ocular complications. Studies have shown that genetic factors play an important role in the pathogenesis of HM. The aim of
Autor:
Genfu Zhao, Hui Liu, Mengfang Liang, Timur Borjigin, Hong Guo, Xiaofei Yang, Beihong Liu, Yuhao Zhang
Publikováno v:
Sustainable Energy & Fuels. 3:2312-2320
A facile and clean strategy is developed here to synthesize the Au@HP5@SWCNT nanocomposite via in-site loading of Au nanoparticles onto the surface of hydroxyl pillar[5]arene (HP5) functionalized single-walled carbon nanotubes (SWCNT). The process is
Autor:
Wangwei Cai, Siyang Zhang, Binbin Wang, Hong Pan, Yunxia Zhang, Tengyan Li, Xianshou Wang, Beihong Liu, Dongjing Yan
Publikováno v:
Genetic Testing and Molecular Biomarkers. 23:12-15
There has been recent recognition that the GSTM1 gene is associated with successful aging and longevity. It has been hypothesized that individuals with a GSTM1 deletion are at a greater risk for developing a plethora of diseases. This study was carri
Autor:
Tengyan Li, Yunxia Cao, Yiran Zhou, Xu Ma, Binbin Wang, Hong Pan, Zhaolian Wei, Beihong Liu, Huifen Xiang, Jing Wang
Publikováno v:
The American Journal of Pathology. 189:124-131
Recurrent pregnancy loss (RPL) is a major concern for women's reproductive health. Several studies have proved that genetics is a major factor leading to unexplained RPL, but the maternal pathogenic genes involved in RPL remain largely unknown. A con