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Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 20, 2024
Loss of hepatocyte Usp53 protects mice from a form of xenobiotic-induced liver injuryJian Ding, Hao Chi, Yi-Ling Qiu, et al.Orphanet Journal of Rare Diseases|October 10, 2021
Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ5-C27-steroid oxidoreductase (HSD3B7) deficiency in ChinaJing Zhao, Kenneth D R Setchell, Ying Gong, et al.Human Mutation|April 14, 2025
Splicing Analysis of MYO5B Noncanonical Variants in Patients with Low Gamma-Glutamyltransferase CholestasisLi Wang, Yi-Ling Qiu, Kuerbanjiang Abuduxikuer, et al.BMC Gastroenterology|June 21, 2017
Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective studyJia-Qi Li, Yi-Ling Qiu, Jing-Yu Gong, et al.Journal of Medical Genetics|June 27, 2025
Biallelic pathogenic TULP3 variants presenting as neonatal cholestasis, liver fibrosis and neurological manifestationsJia-Qi Li, Yan Li, Ruida He, et al.Journal of Pediatric Gastroenterology and Nutrition|October 23, 2020
Abnormal Bilirubin Metabolism in Patients With Sodium Taurocholate Cotransporting Polypeptide DeficiencyYan Yan Yan, Meng Xuan Wang, Jing Yu Gong, et al.The Journal of Molecular Diagnostics : JMD|February 5, 2023
Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ4-3-Oxosteroid-5β-Reductase DeficiencyJing Zhao, Yi-Ling Qiu, Li Wang, et al.Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|September 3, 2005
[Effect of heat shock response on the cleavage of nucleolin induced by oxidative stress]Kang-kai Wang, Lei Jiang, Yu-xin Yi, et al.Human Mutation|September 4, 2019
Novel missense mutation in VPS33B is associated with isolated low gamma-glutamyltransferase cholestasis: Attenuated, incomplete phenotype of arthrogryposis, renal dysfunction, and cholestasis syndromeYi-Ling Qiu, Teng Liu, Kuerbanjiang Abuduxikuer, et al.Liver International : Official Journal of the International Association for the Study of the Liver|May 14, 2022
Defining pathogenicity of NOTCH2 variants for diagnosis of Alagille syndrome type 2 using a large cohort of patientsZhong-Die Li, Kuerbanjiang Abuduxikuer, Li Wang, et al.Pageof 13