Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the FKRP Gene

von Xie, Zhiying, Xiao, Jiangxi, Zheng, Yiming, Wang, Zhaoxia, Yuan, Yun
Veröffentlicht in Biomed Res Int (2018)

Spatial and temporal heterogeneities of capillary hemodynamics and its functional coupling during neural activation

von Wei, Wei, Li, Yuandong, Xie, Zhiying, Deegan, Anthony, Wang, Ruikang K.
Veröffentlicht in IEEE Trans Med Imaging (2018)

Dynamic imaging and quantification of subcellular motion with ED-OCT based variance analysis

von Wei, Wei, Tang, Peijun, Xie, Zhiying, Li, Yuandong, Wang, Ruikang K.
Veröffentlicht in J Biophotonics (2019)

Measurement and visualization of stimulus-evoked tissue dynamics in mouse barrel cortex using phase-sensitive optical coherence tomography

von Tang, Peijun, Li, Yuandong, Rakymzhan, Adiya, Xie, Zhiying, Wang, Ruikang K.
Veröffentlicht in Biomed Opt Express (2020)

Appendicular skeletal muscle mass: A more sensitive biomarker of disease severity than BMI in adults with mitochondrial diseases

von Hou, Yue, Xie, Zhiying, Zhao, Xutong, Yuan, Yun, Dou, Pan, Wang, Zhaoxia
Veröffentlicht in PLoS One (2019)

A deep learning model for diagnosing dystrophinopathies on thigh muscle MRI images

von Yang, Mei, Zheng, Yiming, Xie, Zhiying, Wang, Zhaoxia, Xiao, Jiangxi, Zhang, Jue, Yuan, Yun
Veröffentlicht in BMC Neurol (2021)

Optical coherence tomography angiography measures blood pulsatile waveforms at variable tissue depths

von Xie, Zhiying, Wang, Geng, Cheng, Yuxuan, Zhang, Qinqin, Le, Minh Nhan, Wang, Ruikang K.
Veröffentlicht in Quant Imaging Med Surg (2021)

Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients

von Xie, Zhiying, Hou, Yue, Yu, Meng, Liu, Yilin, Fan, Yanbin, Zhang, Wei, Wang, Zhaoxia, Xiong, Hui, Yuan, Yun
Veröffentlicht in Orphanet J Rare Dis (2019)

Novel TTN mutations and muscle imaging characteristics in congenital titinopathy

von Yu, Meng, Zhu, Ying, Xie, Zhiying, Zheng, Yiming, Xiao, Jiangxi, Zhang, Wei, Nishino, Ichizo, Yuan, Yun, Wang, Zhaoxia
Veröffentlicht in Ann Clin Transl Neurol (2019)

Erythrocytic α-Synuclein as a potential biomarker for Parkinson’s disease

von Tian, Chen, Liu, Genliang, Gao, Liyan, Soltys, David, Pan, Catherine, Stewart, Tessandra, Shi, Min, Xie, Zhiying, Liu, Na, Feng, Tao, Zhang, Jing
Veröffentlicht in Transl Neurodegener (2019)

Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex

von Xie, Zhiying, Xie, Zhihao, Yu, Meng, Zheng, Yiming, Sun, Chengyue, Liu, Yilin, Ling, Chen, Zhu, Ying, Zhang, Wei, Xiao, Jiangxi, Wang, Zhaoxia, Yuan, Yun
Veröffentlicht in Orphanet J Rare Dis (2019)

Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral Sclerosis

von Deng, Jianwen, Wu, Wei, Xie, Zhiying, Gang, Qiang, Yu, Meng, Liu, Jing, Wang, Qingqing, Lv, He, Zhang, Wei, Huang, Yining, Wang, Tao, Yuan, Yun, Hong, Daojun, Wang, Zhaoxia
Veröffentlicht in Front Neurosci (2019)

Splicing Characteristics of Dystrophin Pseudoexons and Identification of a Novel Pathogenic Intronic Variant in the DMD Gene

von Xie, Zhiying, Tang, Liuqin, Xie, Zhihao, Sun, Chengyue, Shuai, Haoyue, Zhou, Chao, Liu, Yilin, Yu, Meng, Zheng, Yiming, Meng, Lingchao, Zhang, Wei, Leal, Suzanne M., Wang, Zhaoxia, Schrauwen, Isabelle, Yuan, Yun
Veröffentlicht in Genes (Basel) (2020)

Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies

von Xie, Zhiying, Sun, Chengyue, Zhang, Siwen, Liu, Yilin, Yu, Meng, Zheng, Yiming, Meng, Lingchao, Acharya, Anushree, Cornejo‐Sanchez, Diana M, Wang, Gao, Zhang, Wei, Schrauwen, Isabelle, Leal, Suzanne M., Wang, Zhaoxia, Yuan, Yun
Veröffentlicht in Ann Clin Transl Neurol (2020)

Erythrocytic α-synuclein contained in microvesicles regulates astrocytic glutamate homeostasis: a new perspective on Parkinson’s disease pathogenesis

von Sheng, Lifu, Stewart, Tessandra, Yang, Dishun, Thorland, Eric, Soltys, David, Aro, Patrick, Khrisat, Tarek, Xie, Zhiying, Li, Na, Liu, Zongran, Tian, Chen, Bercow, Matthew, Matsumoto, Junichi, Zabetian, Cyrus P., Peskind, Elaine, Quinn, Joseph F., Shi, Min, Zhang, Jing
Veröffentlicht in Acta Neuropathol Commun (2020)

The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3

von Yu, Jiaxi, Deng, Jianwen, Guo, Xueyu, Shan, Jingli, Luan, Xinghua, Cao, Li, Zhao, Juan, Yu, Meng, Zhang, Wei, Lv, He, Xie, Zhiying, Meng, LingChao, Zheng, Yiming, Zhao, Yawen, Gang, Qiang, Wang, Qingqing, Liu, Jing, Zhu, Min, Zhou, Binbin, Li, Pidong, Liu, Yinzhe, Wang, Yang, Yan, Chuanzhu, Hong, Daojun, Yuan, Yun, Wang, Zhaoxia
Veröffentlicht in Brain (2021)

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy

von Deng, Jianwen, Yu, Jiaxi, Li, Pidong, Luan, Xinghua, Cao, Li, Zhao, Juan, Yu, Meng, Zhang, Wei, Lv, He, Xie, Zhiying, Meng, LingChao, Zheng, Yiming, Zhao, Yawen, Gang, Qiang, Wang, Qingqing, Liu, Jing, Zhu, Min, Guo, Xueyu, Su, Yanan, Liang, Yu, Liang, Fan, Hayashi, Tomohiro, Maeda, Meiko Hashimoto, Sato, Tatsuro, Ura, Shigehisa, Oya, Yasushi, Ogasawara, Masashi, Iida, Aritoshi, Nishino, Ichizo, Zhou, Chang, Yan, Chuanzhu, Yuan, Yun, Hong, Daojun, Wang, Zhaoxia
Veröffentlicht in Am J Hum Genet (2020)