Showing results (111-120 of 132) with videos related to
Sort By:
Pageof 14
Science China. Life Sciences|June 23, 2017
The clinical and genetic characteristics in children with mitochondrial disease in ChinaFang Fang, Zhimei Liu, Hezhi Fang, et al.Journal of Human Genetics|September 3, 2024
Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural historyHuafang Jiang, Chaolong Xu, Ruoyu Duan, et al.Cell Reports|March 8, 2025
Ectopic protein lysine methacrylation contributes to defects caused by loss of HIBCH or ECHS1Yawen Li, Ting Wu, Yaoyao Li, et al.Current Medical Research and Opinion|August 9, 2014
Comparative effectiveness of second-line targeted therapies for metastatic renal cell carcinoma: synthesis of findings from two multi-practice chart reviews in the United StatesJames E Signorovitch, Nicholas J Vogelzang, Sumanta K Pal, et al.Expert Opinion on Pharmacotherapy|March 14, 2015
Prognostic factors for survival following initiation of second-line treatment with everolimus for metastatic renal cell carcinoma: evidence from a nationwide sample of clinical practice in the United StatesMichael K Wong, Eric Jonasch, Sumanta K Pal, et al.Life (Basel, Switzerland)|February 25, 2022
A 90-Day Safety Study of Meat from MSTN and FGF5 Double-Knockout Sheep in Wistar RatsYue Zhao, Mingming Chen, Yao Li, et al.Frontiers in Veterinary Science|April 17, 2023
Reproduction and viscera organ characteristics of MSTN and FGF5 dual-gene knockout sheepMingming Chen, Yue Zhao, Yao Li, et al.Journal of Child Neurology|April 4, 2015
Caring for Children With Tuberous Sclerosis Complex: What Is the Physical and Mental Health Impact on Caregivers?Anne M Rentz, Anne M Skalicky, Chris L Pashos, et al.Mitochondrion|November 20, 2021
Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center studyYuqing Shi, Guohong Chen, Dan Sun, et al.Frontiers in Genetics|July 19, 2021
Report of the Largest Chinese Cohort With SLC19A3 Gene Defect and Literature ReviewJiaping Wang, Junling Wang, Xiaodi Han, et al.Pageof 14