Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jin-Yuan Yang"'
Autor:
Lang Zhang, Jin-Yuan Yang, Qiu-Quan Wang, Xue Gao, Guo-Jian Wang, Ming-Yu Han, Dong-Yang Kang, Dong-Yi Han, Sha-Sha Huang, Yong-Yi Yuan
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background Mutations in MPZL2, the characteristic genetic etiology of autosomal recessive deafness loci 111 (DFNB111), cause non-syndromic and moderate sensorineural hearing loss. Methods In this study, we analyzed the phenotype and genotype
Externí odkaz:
https://doaj.org/article/9056a91342b84ef7b12cc530b53a6390
Autor:
Jin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jin-Cao Xu, Ying Fu, Dong-Yang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yong-Yi Yuan, Pu Dai
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-16 (2022)
Abstract Pathogenic variants in MYO15A are known to cause autosomal recessive nonsyndromic hearing loss (ARNSHL), DFNB3. We have previously reported on one ARNSHL family including two affected siblings and identified MYO15A c.5964+3G > A and c.8375 T
Externí odkaz:
https://doaj.org/article/ee9185e4b81c4596b2cae7e39d7fd8bc
Autor:
Kun Yang, Xi Wang, Wei‐Qian Wang, Ming‐Yu Han, Li‐Min Hu, Dong‐Yang Kang, Jin‐Yuan Yang, Min Liu, Xue Gao, Yong‐Yi Yuan, Jin‐Cao Xu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Background Myhre syndrome is a rare multisystem genetic disorder that is caused by de novo heterozygous gain‐of‐function variants in SMAD4. Patients with Myhre syndrome exhibit several phenotypes at different ages such as small size, aut
Externí odkaz:
https://doaj.org/article/72523bacc75d4f989e2a04bb15ec1358
Autor:
Jin-Yuan Yang, 楊金源
94
This research focuses on the study of potential administration risks in the current domestic futures market. Contemporary cases are analyzed from the risk perspective with useful outcomes that might be helpful in both promoting the degrees an
This research focuses on the study of potential administration risks in the current domestic futures market. Contemporary cases are analyzed from the risk perspective with useful outcomes that might be helpful in both promoting the degrees an
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/93676446051602219290
Autor:
Kun Yang, Xi Wang, Wei‐Qian Wang, Ming‐Yu Han, Li‐Min Hu, Dong‐Yang Kang, Jin‐Yuan Yang, Min Liu, Xue Gao, Yong‐Yi Yuan, Jin‐Cao Xu
Publikováno v:
Molecular geneticsgenomic medicineREFERENCES.
Myhre syndrome is a rare multisystem genetic disorder that is caused by de novo heterozygous gain-of-function variants in SMAD4. Patients with Myhre syndrome exhibit several phenotypes at different ages such as small size, autism, developmental delay
Publikováno v:
Desalination. 320:49-55
A new system of chemical cleaning and repairing of the used reverse osmosis membranes (CCR-ROM) has been designed and used for researching. The results indicate that the average salt rejection of the cleaned membranes was increased from 67.5% (32.3%,
Autor:
Jin Yuan Yang
Publikováno v:
2008 IEEE International Conference on Industrial Technology.
The aim of the bridge health monitoring system reveals that the potential safety problems promptly. Because of huge number of sensors and high-frequency data acquisition in the long-term health monitoring systems, mass raw data are produced. Therefor