Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Yong Feng"'
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0306994 (2024)
BackgroundSpeckle Type POZ Protein (SPOP), despite its tumor type-dependent role in tumorigenesis, primarily as a tumor suppressor gene is associated with a variety of different cancers. However, its function in pancreatic cancer remains uncertain.Me
Externí odkaz:
https://doaj.org/article/d21bf50c577b47b99256a1f08421a507
Autor:
Xiankun Zhao, Xinyu Cheng, Jing Ye, Jiaqing Ren, Bin Li, Dongmei Tan, Tangshan Li, Kai Zhou, Jing Pu, Xia Luo, Yong Feng
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0301686 (2024)
BackgroundFunctional dyspepsia (FD) refers to a group of clinical symptoms caused by gastric and duodenal dysfunction. Which is a chronic functional disorder of the gastrointestinal tract with no cure. Zhishixiaopi decoction (ZSXP) is a type of Chine
Externí odkaz:
https://doaj.org/article/912b8149d76642f2ab103010cbaed3bb
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0302414 (2024)
PurposeInvestigating the association between red cell distribution width (RDW) and all-cause mortality in patients with breast cancer, to evaluate the potential clinical prognostic value of RDW.MethodsBased on the RDW index, patients with breast canc
Externí odkaz:
https://doaj.org/article/5f1c2b67d032460cb46f637ad92a872e
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0302468 (2024)
In order to further clarify the shale oil accumulation period of the Chang 7 member of the Mesozoic Triassic Yanchang Formation in the Zhijing-Ansai area of the central Ordos Basin, Using fluid inclusion petrography analysis, microscopic temperature
Externí odkaz:
https://doaj.org/article/0da12e56b11a404f9089beeac497cf1b
Autor:
Xianlin Liu, Jie Wen, Xuezhong Liu, Anhai Chen, Sijun Li, Jing Liu, Jie Sun, Wei Gong, Xiaoming Kang, Zhili Feng, Chufeng He, Lingyun Mei, Jie Ling, Yong Feng
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0288640 (2023)
The ELMOD3 gene is implicated in causing autosomal recessive/dominant non-syndromic hearing loss in humans. However, the etiology has yet to be completely elucidated. In this study, we generated a patient-derived iPSC line carrying ELMOD3 c.512A>G mu
Externí odkaz:
https://doaj.org/article/adce9d9495d24721b446265975dd91ca
Autor:
Li Xia, Gang He, Yong Feng, Xiaoxu Yu, Xiaolong Zhao, Shankai Yin, Zhengnong Chen, Jian Wang, Jiangang Fan, Chuan Dong
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0246328 (2021)
To investigate if the anxiety associated with coronavirus disease 2019 (COVID-19) is a promoting factor to tinnitus. A retrospective research design collected from 188 tinnitus patients, was used to compare the clinical characteristics of tinnitus be
Externí odkaz:
https://doaj.org/article/0cc8c55827e442de9a8335bbf93daaee
Autor:
Yalan Liu, Chang Hu, Chang Liu, Deyuan Liu, Lingyun Mei, Chufeng He, Lu Jiang, Hong Wu, Hongsheng Chen, Yong Feng
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0215212 (2019)
Hearing loss (HL) is a common sensory disorder. More than half of HL cases can be attributed to genetic causes. There is no effective therapy for genetic HL at present, early diagnosis to reduce the incidence of genetic HL is important for clinical i
Externí odkaz:
https://doaj.org/article/ea8271589eb245ffadce8f072e2672e7
Autor:
Zhijie Niu, Yong Feng, Lingyun Mei, Jie Sun, Xueping Wang, Juncheng Wang, Zhengmao Hu, Yunpeng Dong, Hongsheng Chen, Chufeng He, Yalan Liu, Xinzhang Cai, Xuezhong Liu, Lu Jiang
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0178384 (2017)
X-linked hearing impairment is the rarest form of genetic hearing loss (HL) and represents only a minor fraction of all cases. The aim of this study was to investigate the cause of X-linked inherited sensorineural HL in a four-generation Chinese fami
Externí odkaz:
https://doaj.org/article/029ac6b4b6c6470da8d46cbef595c21d
Autor:
Hong Wu, Yong Feng, Lu Jiang, Qian Pan, Yalan Liu, Chang Liu, Chufeng He, Hongsheng Chen, Xueming Liu, Chang Hu, Yiqiao Hu, Lingyun Mei
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151909 (2016)
The aim of this study was to evaluate the GoldenGate microarray as a diagnostic tool and to elucidate the contribution of the genes on this array to the development of both nonsyndromic and syndromic sensorineural hearing loss in China.We developed a
Externí odkaz:
https://doaj.org/article/a380810b8182407082c67f3d9b871ed3
Autor:
Yalan Liu, Lili Wang, Yong Feng, Chufeng He, Deyuan Liu, Xinzhang Cai, Lu Jiang, Hongsheng Chen, Chang Liu, Hong Wu, Lingyun Mei
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168508 (2016)
Enlarged vestibular aqueduct (EVA) is one of the most common congenital inner ear malformations and accounts for 1-12% of sensorineural deafness in children and adolescents. Multiple genetic defects contribute to EVA; therefore, early molecular diagn
Externí odkaz:
https://doaj.org/article/85ceec7b84fa49a8ba487f78af7bf120