Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Qifei Li

Showing results (61-70 of 87) with videos related to

Pageof 9
Sort By:
Biorxiv : the Preprint Server for Biology|May 10, 2023
Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complexQifei Li, Jasmine Lin, Shiyu Luo, et al.
Journal of Cachexia, Sarcopenia and Muscle|May 10, 2024
Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complexQifei Li, Jasmine Lin, Shiyu Luo, et al.
Nutrition in Clinical Practice : Official Publication of the American Society for Parenteral and Enteral Nutrition|November 5, 2024
Global Leadership Initiative on Malnutrition criteria: Clinical benefits for patients with gastric cancerJingxian Zheng, Xiaojie Wang, Jiami Yu, et al.
Molecular Genetics & Genomic Medicine|May 12, 2021
A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8Sheng Yi, Yue Zhang, Zailong Qin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 4, 2018
Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformationsChunyun Fu, Shiyu Luo, Yue Zhang, et al.
Scientific Reports|January 18, 2018
Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonatesChunyun Fu, Shiyu Luo, Qifei Li, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|January 30, 2025
Clinical and prognostic insights into Chlamydia trachomatis in pediatric acute respiratory infections: evidence from targeted next-generation sequencing of 5,021 casesChunyun Fu, Huan Zhang, Xiangjun Lu, et al.
European Journal of Medicinal Chemistry|June 16, 2026
Discovery of 1-(3-phenoxybenzyl)-4-(1-phenyl-1H-1,2,3-triazol-4-yl)piperidine analogues as potent and selective agonists of the human CC chemokine receptor 8Qifei Li, Wout Van Eynde, Tom Van Loy, et al.
Molecular Genetics and Metabolism Reports|July 11, 2018
Novel <i>ETFDH</i> mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiencyXin Fan, Bobo Xie, Jun Zou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 18, 2017
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidismChunyun Fu, Shiyu Luo, Xigui Long, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Biorxiv : the Preprint Server for Biology|May 10, 2023
Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complexQifei Li, Jasmine Lin, Shiyu Luo, et al.
Journal of Cachexia, Sarcopenia and Muscle|May 10, 2024
Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complexQifei Li, Jasmine Lin, Shiyu Luo, et al.
Nutrition in Clinical Practice : Official Publication of the American Society for Parenteral and Enteral Nutrition|November 5, 2024
Global Leadership Initiative on Malnutrition criteria: Clinical benefits for patients with gastric cancerJingxian Zheng, Xiaojie Wang, Jiami Yu, et al.
Molecular Genetics & Genomic Medicine|May 12, 2021
A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8Sheng Yi, Yue Zhang, Zailong Qin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 4, 2018
Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformationsChunyun Fu, Shiyu Luo, Yue Zhang, et al.
Scientific Reports|January 18, 2018
Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonatesChunyun Fu, Shiyu Luo, Qifei Li, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|January 30, 2025
Clinical and prognostic insights into Chlamydia trachomatis in pediatric acute respiratory infections: evidence from targeted next-generation sequencing of 5,021 casesChunyun Fu, Huan Zhang, Xiangjun Lu, et al.
European Journal of Medicinal Chemistry|June 16, 2026
Discovery of 1-(3-phenoxybenzyl)-4-(1-phenyl-1H-1,2,3-triazol-4-yl)piperidine analogues as potent and selective agonists of the human CC chemokine receptor 8Qifei Li, Wout Van Eynde, Tom Van Loy, et al.
Molecular Genetics and Metabolism Reports|July 11, 2018
Novel <i>ETFDH</i> mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiencyXin Fan, Bobo Xie, Jun Zou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 18, 2017
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidismChunyun Fu, Shiyu Luo, Xigui Long, et al.
Pageof 9