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

Yun-Fei An

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|July 16, 2021
[Gene editing for the treatment of primary immunodeficiency disease]Shan Liu, Shu-Yu Fang, Yun-Fei An
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|August 21, 2014
[MonoMAC syndrome]Zhao-Long Chen, Yun-Fei An, Xiao-Dong Zhao
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 19, 2010
[A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child]Yun-fei An, Xiao-dong Zhao, Feng Xu, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|June 10, 2017
[Genotype of Thalassemia in Han Chinese and Tibetans in Sichuan Province,China.]Qian Niu, Xun-Bei Huang, Yun-Fei An, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 14, 2012
[Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells]Jing Wang, Zheng Liu, Li-ping Jiang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|September 20, 2011
[Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives]Xi Yang, Jing Wang, Yun-fei An, et al.
Pediatric Blood & Cancer|July 22, 2014
Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1Yun-Fei An, Xiao-Bo Luo, Xi Yang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 22, 2009
[A compound heterozygosity mutation in the interleukin-7 receptor-alpha gene resulted in severe combined immunodeficiency in a Chinese patient]Zhi-yong Zhang, Xiao-dong Zhao, Mo Wang, et al.
Pharmacogenomics|January 20, 2016
Donor ABCB1 3435 C>T genetic polymorphisms influence early renal function in kidney transplant recipients treated with tacrolimusLin Yan, Yi Li, Jiang-Tao Tang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|October 15, 2013
[Expression and significance of interleukin-6, interferon-inducible protein-10 and interleukin-17 in serum and synovial fluid of patients with juvenile idiopathic arthritis]Rui-juan Li, Xue-mei Tang, Wei Liu, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|July 16, 2021
[Gene editing for the treatment of primary immunodeficiency disease]Shan Liu, Shu-Yu Fang, Yun-Fei An
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|August 21, 2014
[MonoMAC syndrome]Zhao-Long Chen, Yun-Fei An, Xiao-Dong Zhao
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 19, 2010
[A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child]Yun-fei An, Xiao-dong Zhao, Feng Xu, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|June 10, 2017
[Genotype of Thalassemia in Han Chinese and Tibetans in Sichuan Province,China.]Qian Niu, Xun-Bei Huang, Yun-Fei An, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 14, 2012
[Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells]Jing Wang, Zheng Liu, Li-ping Jiang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|September 20, 2011
[Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives]Xi Yang, Jing Wang, Yun-fei An, et al.
Pediatric Blood & Cancer|July 22, 2014
Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1Yun-Fei An, Xiao-Bo Luo, Xi Yang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 22, 2009
[A compound heterozygosity mutation in the interleukin-7 receptor-alpha gene resulted in severe combined immunodeficiency in a Chinese patient]Zhi-yong Zhang, Xiao-dong Zhao, Mo Wang, et al.
Pharmacogenomics|January 20, 2016
Donor ABCB1 3435 C>T genetic polymorphisms influence early renal function in kidney transplant recipients treated with tacrolimusLin Yan, Yi Li, Jiang-Tao Tang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|October 15, 2013
[Expression and significance of interleukin-6, interferon-inducible protein-10 and interleukin-17 in serum and synovial fluid of patients with juvenile idiopathic arthritis]Rui-juan Li, Xue-mei Tang, Wei Liu, et al.
Pageof 2