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LiFeng Tian

Showing results (121-130 of 142) with videos related to

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Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.
Scientific Reports|March 29, 2018
Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathiesIker Sanchez-Navarro, Luciana R J da Silva, Fiona Blanco-Kelly, et al.
Nature Immunology|May 27, 2014
The transcription factor Foxp1 is a critical negative regulator of the differentiation of follicular helper T cellsHaikun Wang, Jianlin Geng, Xiaomin Wen, et al.
American Journal of Human Genetics|September 13, 2016
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel BlockersDong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, et al.
Scientific Reports|August 23, 2017
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Scientific Reports|June 21, 2017
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Nature Biotechnology|April 12, 2016
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseasesRong Chen, Lisong Shi, Jörg Hakenberg, et al.
Nature Medicine|July 3, 2019
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorDong Li, Michael E March, Alvaro Gutierrez-Uzquiza, et al.
The Journal of Clinical Investigation|February 11, 2021
CCR5-edited CD4+ T cells augment HIV-specific immunity to enable post-rebound control of HIV replicationPablo Tebas, Julie K Jadlowsky, Pamela A Shaw, et al.
Nature|November 13, 2015
Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphismDerek A Oldridge, Andrew C Wood, Nina Weichert-Leahey, et al.
Pageof 15

Showing results (121-130 of 142) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.
Scientific Reports|March 29, 2018
Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathiesIker Sanchez-Navarro, Luciana R J da Silva, Fiona Blanco-Kelly, et al.
Nature Immunology|May 27, 2014
The transcription factor Foxp1 is a critical negative regulator of the differentiation of follicular helper T cellsHaikun Wang, Jianlin Geng, Xiaomin Wen, et al.
American Journal of Human Genetics|September 13, 2016
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel BlockersDong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, et al.
Scientific Reports|August 23, 2017
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Scientific Reports|June 21, 2017
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingDong Li, Xiao Chang, John J Connolly, et al.
Nature Biotechnology|April 12, 2016
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseasesRong Chen, Lisong Shi, Jörg Hakenberg, et al.
Nature Medicine|July 3, 2019
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorDong Li, Michael E March, Alvaro Gutierrez-Uzquiza, et al.
The Journal of Clinical Investigation|February 11, 2021
CCR5-edited CD4+ T cells augment HIV-specific immunity to enable post-rebound control of HIV replicationPablo Tebas, Julie K Jadlowsky, Pamela A Shaw, et al.
Nature|November 13, 2015
Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphismDerek A Oldridge, Andrew C Wood, Nina Weichert-Leahey, et al.
Pageof 15