A Comparison of Death Domain-Associated Protein 6 in Different Endometrial Carcinomas Histotypes

por Jin, Cao, Hacking, Sean, Komforti, Miglena K, Nasim, Mansoor
Publicado 2019

Multiple recurrent aneurysms with angiitis of the central nervous system in a girl: A case report

por Wen, Jiayu, Ye, Shengda, Yang, Bin, Liu, Xi, Chen, JinCao
Publicado 2022

Plasma heat shock protein 27 is associated with coronary artery disease, abdominal aortic aneurysm and peripheral artery disease

por Jin, Cao, Phillips, Victoria L, Williams, Michael JA, van Rij, Andre M, Jones, Gregory T
Publicado 2014

Long Noncoding RNA PVT1 Promotes Stemness and Temozolomide Resistance through miR-365/ELF4/SOX2 Axis in Glioma

por Gong, Rui, Li, Zhi-Qiang, Fu, Kai, Ma, Chao, Wang, Wei, Chen, Jin-Cao
Publicado 2021

Endovascular embolization for basal ganglia and thalamic arteriovenous malformations

por Lan, Jing, Ma, Yi-hui, Feng, Yu, Zhang, Ting-Bao, Zhao, Wen-yuan, Chen, Jin-cao
Publicado 2023

Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment

por Gao, Xue, Yuan, Yong-Yi, Wang, Guo-Jian, Xu, Jin-Cao, Su, Yu, Lin, Xi, Dai, Pu
Publicado 2017

Moyamoya Disease Associated With Morning Glory Disc Anomaly and Other Ophthalmic Findings: A Mini-Review

por Wang, Yue-ye, Zhou, Ke-yao, Ye, Yang, Song, Fan, Yu, Jin, Chen, Jin-cao, Yao, Ke
Publicado 2020

Development and Validation of a Deep Learning Predictive Model Combining Clinical and Radiomic Features for Short-Term Postoperative Facial Nerve Function in Acoustic Neuroma Patie...

por Wang, Meng-yang, Jia, Chen-guang, Xu, Huan-qing, Xu, Cheng-shi, Li, Xiang, Wei, Wei, Chen, Jin-cao
Publicado 2023

Differentiating non-lactating mastitis and malignant breast tumors by deep-learning based AI automatic classification system: A preliminary study

por Zhou, Ying, Feng, Bo-Jian, Yue, Wen-Wen, Liu, Yuan, Xu, Zhi-Feng, Xing, Wei, Xu, Zhao, Yao, Jin-Cao, Wang, Shu-Rong, Xu, Dong
Publicado 2022

A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4

por Yang, Kun, Wang, Xi, Wang, Wei‐Qian, Han, Ming‐Yu, Hu, Li‐Min, Kang, Dong‐Yang, Yang, Jin‐Yuan, Liu, Min, Gao, Xue, Yuan, Yong‐Yi, Xu, Jin‐Cao
Publicado 2022

Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss

por Wang, Wei-Qian, Gao, Xue, Huang, Sha-Sha, Kang, Dong-Yang, Xu, Jin-Cao, Yang, Kun, Han, Ming-Yu, Zhang, Xin, Yang, Su-Yan, Yuan, Yong-Yi, Dai, Pu
Publicado 2022

Glycine Potentiates AMPA Receptor Function through Metabotropic Activation of GluN2A-Containing NMDA Receptors

por Li, Li-Jun, Hu, Rong, Lujan, Brendan, Chen, Juan, Zhang, Jian-Jian, Nakano, Yasuko, Cui, Tian-Yuan, Liao, Ming-Xia, Chen, Jin-Cao, Man, Heng-Ye, Feng, Hua, Wan, Qi
Publicado 2016

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

por Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Xu, Jin-Cao, Gu, Ping, Bai, Dan, Kang, Dong-Yang, Han, Ming-Yu, Wang, Guo-Jian, Zhang, Mei-Guang, Li, Jia, Dai, Pu
Publicado 2017

A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

por Wang, Rui, Wang, Wei-Qian, Li, Xiao-Qin, Zhao, Juan, Yang, Kun, Feng, Yong, Guo, Meng-Meng, Liu, Min, Liu, Xing, Wang, Xi, Yuan, Yong-Yi, Gao, Xue, Xu, Jin-Cao
Publicado 2021

Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

por Gao, Xue, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Han, Ming-Yu, Lu, Jing-Qiao, Zhao, Hui, Yu, Fei, Xu, Jin-Cao, Zhang, Mei-Guang, Dong, Jiang, Lin, Xi, Dai, Pu
Publicado 2014

Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

por Gao, Xue, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Han, Ming-Yu, Lu, Jing-Qiao, Zhao, Hui, Yu, Fei, Xu, Jin-Cao, Zhang, Mei-Guang, Dong, Jiang, Lin, Xi, Dai, Pu
Publicado 2015

Comparison of Body, Auricular, and Abdominal Acupuncture Treatments for Insomnia Differentiated as Internal Harassment of Phlegm-Heat Syndrome: An Orthogonal Design

por Jiao, Yue, Han, Ying, Li, Xin, Fang, Yi-gong, Liu, Zhao-hui, Zhou, Wen-na, Zhou, Jin-cao, Wu, Zhong-chao, Yang, Jin-hong, Li, Shao-yuan, Meng, Fan-ying, Xu, Wei-wei
Publicado 2015

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

por Gao, Xue, Xu, Jin-Cao, Wang, Wei-Qian, Yuan, Yong-Yi, Bai, Dan, Huang, Sha-Sha, Wang, Guo-Jian, Su, Yu, Li, Jia, Kang, Dong-Yang, Zhang, Mei-Guang, Lin, Xi, Dai, Pu
Publicado 2018

Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations

por Gao, Xue, Zhao, Juan, Li, Guan-Hua, Wang, Xi, Wang, Wei, Liu, Xing, Liu, Min, Guo, Meng-Meng, Wang, Zhen-Dong, Lu, Ya-Yan, Li, Jia, Feng, Yong, Yang, Kun, Xu, Jin-Cao, Dai, Pu
Publicado 2023

Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

por Gao, Xue, Su, Yu, Chen, Yu-Lan, Han, Ming-Yu, Yuan, Yong-Yi, Xu, Jin-Cao, Xin, Feng, Zhang, Mei-Guang, Huang, Sha-Sha, Wang, Guo-Jian, Kang, Dong-Yang, Guan, Li-Ping, Zhang, Jian-Guo, Dai, Pu
Publicado 2015