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International Journal of Molecular Sciences|September 9, 2022
A Novel Pathway of Chlorimuron-Ethyl Biodegradation by Chenggangzhangella methanolivorans Strain CHL1 and Its Molecular MechanismsZhixiong Yu, Yumeng Dai, Tingting Li, et al.Natural Product Research|September 29, 2025
Investigating the anti-atherosclerotic effect and potential mechanism of Sanzi San in ApoE-defcient mice by UHPLC-ESI-QE-Orbitrap-MS based non-targeted metabonomicsShuai Liu, Hongyu Zheng, Jianye Wang, et al.Orphanet Journal of Rare Diseases|October 8, 2020
Biochemical and genetic approaches to the prenatal diagnosis of propionic acidemia in 78 pregnanciesMengyao Dai, Bing Xiao, Huiwen Zhang, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 23, 2023
C-kit controls blood-brain barrier permeability by regulating caveolae-mediated transcytosis after chronic cerebral hypoperfusionJunkui Shang, Wei Li, Huiwen Zhang, et al.Nature Communications|December 31, 2024
GATD3A-deficiency-induced mitochondrial dysfunction facilitates senescence of fibroblast-like synoviocytes and osteoarthritis progressionKai Shen, Hao Zhou, Qiang Zuo, et al.Frontiers in Genetics|December 26, 2022
Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, ChinaSiyu Chang, Yi Yang, Feng Xu, et al.Journal of Human Genetics|October 11, 2020
Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arraysYanjie Fan, Lili Wang, Yu Sun, et al.Scientific Reports|March 16, 2017
Diagnostic Application of Targeted Next-Generation Sequencing of 80 Genes Associated with Disorders of Sexual DevelopmentYanjie Fan, Xia Zhang, Lili Wang, et al.Prenatal Diagnosis|November 8, 2019
Noninvasive prenatal diagnosis of cobalamin C (cblC) deficiency through target region sequencing of cell-free DNA in maternal plasmaLianshu Han, Chao Chen, Fengyu Guo, et al.The Journal of Clinical Endocrinology and Metabolism|July 25, 2024
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency CohortRuifang Wang, Xiaomei Luo, Yu Sun, et al.Pageof 33