Zobrazeno 1 - 10
of 173
pro vyhledávání: '"Huijun, Yuan"'
Autor:
Xicui Long, Wenyu Xiong, Xuegang Wang, Jia Geng, Mingjun Zhong, Yu Huang, Man Liu, Fengxiao Bu, Jing Cheng, Yu Lu, Huijun Yuan
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background A comprehensive understanding of the genetic basis of rare diseases and their regulatory mechanisms is essential for human molecular genetics. However, the genetic mutant spectrum of pathogenic genes within the Chinese population
Externí odkaz:
https://doaj.org/article/e9a03254ab4e479e9ed0efd5ccfed104
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Pseudoaneurysm of the internal iliac artery is a very rare complication of intertrochanteric fracture. Here, the case of an 88-year-old female patient, who presented with intense pain following surgery for intertrochanteric fracture of the femur, is
Externí odkaz:
https://doaj.org/article/cb3a6e437d1546f5a3fa97bbccca3fb9
Autor:
Yu Huang, Jia Geng, Yang Long, Wenyu Xiong, Lu Kang, Meilin Chen, Ting Tang, Mingjun Zhong, Fengxiao Bu, Yu Lu, Jing Cheng, Huijun Yuan
Publikováno v:
Frontiers in Audiology and Otology, Vol 2 (2024)
IntroductionWaardenburg syndrome (WS) is a genetic disorder characterized by hearing loss, hypopigmentation, and distinct facial features. Despite > 60% molecular diagnosis rate for WS patients, pathogenic variants within coding regions are predomina
Externí odkaz:
https://doaj.org/article/17eef314b5b24edeaeb3e2d38adeddb4
Autor:
Sihan Liu, Mingjun Zhong, Yu Huang, Qian Zhang, Ting Chen, Xiaofei Xu, Wan Peng, Xiaolu Wang, Xiaoshu Feng, Lu Kang, Yu Lu, Jing Cheng, Fengxiao Bu, Huijun Yuan
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-14 (2023)
Abstract Background The American College of Medical Genetics and Genomics (ACMG)/Association for Molecular Pathology (AMP) guidelines recommend using variant enrichment among cases as "strong" evidence for pathogenicity per the PS4 criterion. However
Externí odkaz:
https://doaj.org/article/cde1251227894591acb952b830dfdbce
Autor:
Jieyu Qi, Fangzhi Tan, Liyan Zhang, Ling Lu, Hongyang Wang, Wenyan Li, Wenwen Liu, Xiaolong Fu, Zuhong He, Xiaoqiong Ding, Shan Sun, Qiaojun Fang, Yaodong Dong, Xuewei Zhu, Busheng Tong, Xianbao Cao, Min Guo, Xinmiao Fan, Qin Wang, Lu Ma, Tianhong Zhang, Yafeng Yu, Yongxin Li, Jiangang Fan, Yong Cui, Peina Wu, Hongzheng Zhang, Jie Tang, Weiwei Guo, Dingjun Zha, Fanglei Ye, Shuangba He, Wei Cao, Jianming Yang, Xiaoyun Qian, Yu Zhao, Jingwu Sun, Xiaowei Chen, Yu Sun, Ming Xia, Qiuju Wang, Huijun Yuan, Yong Feng, Weijia Kong, Shiming Yang, Haibo Wang, Maoli Duan, Xia Gao, Huawei Li, Lei Xu, Renjie Chai
Publikováno v:
Interdisciplinary Medicine, Vol 2, Iss 2, Pp n/a-n/a (2024)
Abstract Hereditary deafness is a common neurosensory disorder, and 148 non‐syndromic deafness genes have been identified to date. Gene therapy has been used to treat a variety of genetic diseases, but no gene therapy drug for hereditary deafness h
Externí odkaz:
https://doaj.org/article/ea0f2a4230db4684af2f3df943975776
Autor:
Naga Venkata Divya Challa, Shaoyi Chen, Huijun Yuan, Matthew R. Duncan, William Javier Moreno, Helen Bramlett, W. Dalton Dietrich, Merline Benny, Augusto F. Schmidt, Karen Young, Shu Wu
Publikováno v:
Journal of Neuroinflammation, Vol 20, Iss 1, Pp 1-15 (2023)
Abstract Background Neonatal hyperoxia exposure is associated with brain injury and poor neurodevelopment outcomes in preterm infants. Our previous studies in neonatal rodent models have shown that hyperoxia stimulates the brain’s inflammasome path
Externí odkaz:
https://doaj.org/article/b0eed5498d1f4ee88059914f8de125fa
Autor:
Sarah Sonny, Huijun Yuan, Shaoyi Chen, Matthew R. Duncan, Pingping Chen, Merline Benny, Karen Young, Kevin K. Park, Augusto F. Schmidt, Shu Wu
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-18 (2023)
Abstract Bronchopulmonary dysplasia (BPD) and retinopathy of prematurity (ROP) are among the most common morbidities affecting extremely premature infants who receive oxygen therapy. Many clinical studies indicate that BPD is associated with advanced
Externí odkaz:
https://doaj.org/article/8543ce01487746539f9d42dbd91313d9
Publikováno v:
Applied Sciences, Vol 13, Iss 20, p 11496 (2023)
Displacement monitoring systems play a crucial role in ensuring the safety of tunnels. Existing sensing technologies and analysis methods may be insufficient for monitoring tunnel displacement, particularly vertical displacement, due to the harshness
Externí odkaz:
https://doaj.org/article/b285163498aa4f5fbd9a209aa5465fd3
Autor:
Huijun Yuan, Keith A. Webster, Muhammad Tariq Bhatti, William W. Hauswirth, Alfred S. Lewin, John Guy
Publikováno v:
Clinical and Translational Discovery, Vol 2, Iss 3, Pp n/a-n/a (2022)
Abstract Background Mutation of the m. 8993 T > G ATP6 subunit of ATP synthase causes a maternally inherited Leigh Syndrome (LS), a rapidly fatal encephalomyelopathy in childhood called and related Neuropathy, Ataxia and Retinitis Pigmentosa (NARP) i
Externí odkaz:
https://doaj.org/article/6ccb0d57256b4c32af337b310ee758c0
Hyperoxia-activated circulating extracellular vesicles induce lung and brain injury in neonatal rats
Autor:
Anum Ali, Ronald Zambrano, Matthew R. Duncan, Shaoyi Chen, Shihua Luo, Huijun Yuan, Pingping Chen, Merline Benny, Augusto Schmidt, Karen Young, Nadine Kerr, Juan Pablo de Rivero Vaccari, Robert W. Keane, W. Dalton Dietrich, Shu Wu
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Hyperoxia-induced lung injury plays a key role in the development of bronchopulmonary dysplasia (BPD), characterized by inflammatory injury and impaired lung development in preterm infants. Although BPD is a predictor of poor neurodevelopmen
Externí odkaz:
https://doaj.org/article/15155bae7ccb4cd9aba80857a69a7304