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Fan Lin

Showing results (981-990 of 1,046) with videos related to

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BMC Cardiovascular Disorders|September 30, 2025
A novel NOTCH1 nonsense variant in a bicuspid aortic valve family with intrafamilial clinical heterogeneityQian Chen, Zi-Yan Xu, Wu Chi, et al.
Scientific Reports|April 1, 2024
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutationDan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Cell Reports|June 3, 2026
HSPA6 maintains IMPDH2 phosphorylation to regulate GTP synthesis for driving radioresistance of glioblastoma stem cellsJunlei Yang, Qiankun Lin, Danling Gu, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 10, 2021
Changes in the clinical phenotype and behavior of pediatric luminal Crohn's disease at diagnosis in the last decadeSamuel Sassine, Mathieu Savoie Robichaud, Yi Fan Lin, et al.
JGH Open : an Open Access Journal of Gastroenterology and Hepatology|December 24, 2021
Factors associated with time to clinical remission in pediatric luminal Crohn's disease: A retrospective cohort studySamuel Sassine, Souhila Zekhnine, Marwa Qaddouri, et al.
Frontiers in Neuroscience|August 15, 2024
<i>In vitro</i> study of <i>ATP1A3</i> p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonismDan-Dan Ruan, Jing Zou, Li-Sheng Liao, et al.
British Journal of Haematology|June 26, 2024
Recent infection with SARS-CoV-2 in donors was associated with a higher incidence of acute graft-versus-host disease in recipients undergoing allogeneic haematopoietic stem cell transplantationFan Lin, Lanping Xu, Tingting Han, et al.
NPJ Genomic Medicine|March 28, 2018
Improving imputation in disease-relevant regions: lessons from cystic fibrosisNaim Panjwani, Bowei Xiao, Lizhen Xu, et al.
BMC Cancer|August 11, 2020
OncoPDSS: an evidence-based clinical decision support system for oncology pharmacotherapy at the individual levelQuan Xu, Jin-Cheng Zhai, Cai-Qin Huo, et al.
Scientific Reports|September 10, 2024
Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutationDan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Pageof 105

Showing results (981-990 of 1,046) with videos related to

Sort By:
Pageof 105
BMC Cardiovascular Disorders|September 30, 2025
A novel NOTCH1 nonsense variant in a bicuspid aortic valve family with intrafamilial clinical heterogeneityQian Chen, Zi-Yan Xu, Wu Chi, et al.
Scientific Reports|April 1, 2024
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutationDan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Cell Reports|June 3, 2026
HSPA6 maintains IMPDH2 phosphorylation to regulate GTP synthesis for driving radioresistance of glioblastoma stem cellsJunlei Yang, Qiankun Lin, Danling Gu, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 10, 2021
Changes in the clinical phenotype and behavior of pediatric luminal Crohn's disease at diagnosis in the last decadeSamuel Sassine, Mathieu Savoie Robichaud, Yi Fan Lin, et al.
JGH Open : an Open Access Journal of Gastroenterology and Hepatology|December 24, 2021
Factors associated with time to clinical remission in pediatric luminal Crohn's disease: A retrospective cohort studySamuel Sassine, Souhila Zekhnine, Marwa Qaddouri, et al.
Frontiers in Neuroscience|August 15, 2024
<i>In vitro</i> study of <i>ATP1A3</i> p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonismDan-Dan Ruan, Jing Zou, Li-Sheng Liao, et al.
British Journal of Haematology|June 26, 2024
Recent infection with SARS-CoV-2 in donors was associated with a higher incidence of acute graft-versus-host disease in recipients undergoing allogeneic haematopoietic stem cell transplantationFan Lin, Lanping Xu, Tingting Han, et al.
NPJ Genomic Medicine|March 28, 2018
Improving imputation in disease-relevant regions: lessons from cystic fibrosisNaim Panjwani, Bowei Xiao, Lizhen Xu, et al.
BMC Cancer|August 11, 2020
OncoPDSS: an evidence-based clinical decision support system for oncology pharmacotherapy at the individual levelQuan Xu, Jin-Cheng Zhai, Cai-Qin Huo, et al.
Scientific Reports|September 10, 2024
Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutationDan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Pageof 105