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Redox Biology|February 19, 2026
Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure developmentUmesh Bhattarai, Ziru Niu, Lihong Pan, et al.Journal of Immunology (Baltimore, Md. : 1950)|January 22, 2004
p47phox deficiency impairs NF-kappa B activation and host defense in Pseudomonas pneumoniaRuxana T Sadikot, Heng Zeng, Fiona E Yull, et al.Chinese Medical Journal|January 5, 2017
Association of Chronic Kidney Disease with Coronary Heart Disease and Stroke Risks in Patients with Type 2 Diabetes Mellitus: An Observational Cross-sectional Study in Hangzhou, ChinaXue Sun, Jie He, Xiao-Li Ji, et al.Blood|May 21, 2026
Biallelic loss-of-function mutations in BPNT1 cause vitamin B12-dependent megaloblastic anemiaYi-Heng Zeng, Yun-Hong Li, Ru-Ying Yuan, et al.Clinical Genetics|March 21, 2019
Identification of SLC20A2 deletions in patients with primary familial brain calcificationXin-Xin Guo, Hui-Zhen Su, Xiao-Huan Zou, et al.BMJ Open|January 12, 2022
Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort studyYu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, et al.Annals of Clinical and Translational Neurology|November 1, 2024
Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutationJingjing Lin, Yun-Lu Li, Bo-Li Chen, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2023
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular CharacterizationXiang Lin, Jun-Yi Jiang, Dao-Jun Hong, et al.Annals of Neurology|June 14, 2022
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal MyopathyYi-Heng Zeng, Kang Yang, Gan-Qin Du, et al.Journal of Human Genetics|June 12, 2024
Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxiaZe-Hong Zheng, Chun-Yan Cao, Bi Cheng, et al.Pageof 14