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LiFeng Tian

Showing results (71-80 of 142) with videos related to

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Frontiers in Neurology|December 5, 2022
Indentification of novel <i>MSTO1</i> compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxiaJia Chen, Junfang Xiao, Ge Chen, et al.
Frontiers in Cellular and Infection Microbiology|April 1, 2024
Causal associations between <i>Helicobacter pylori</i> infection and pregnancy and neonatal outcomes: a two-sample Mendelian randomization studyJialyu Huang, Yuxin Liu, Dingfei Xu, et al.
Case Reports in Genetics|April 13, 2016
Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain FunctionDong Li, Elizabeth Bhoj, Elizabeth McCormick, et al.
Frontiers in Immunology|May 23, 2022
PD1 Expression in EGFRvIII-Directed CAR T Cell Infusion Product for Glioblastoma Is Associated with Clinical ResponseOliver Y Tang, Lifeng Tian, Todd Yoder, et al.
Cell Cycle (Georgetown, Tex.)|January 5, 2011
PACSIN 2 represses cellular migration through direct association with cyclin D1 but not its alternate splice form cyclin D1bHui Meng, Lifeng Tian, Jie Zhou, et al.
American Journal of Medical Genetics. Part A|June 26, 2015
Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndromeElizabeth J Bhoj, Dong Li, Margaret H Harr, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated HypoparathyroidismDong Li, Elizabeth A Streeten, Alice Chan, et al.
Metabolism: Clinical and Experimental|November 6, 2020
Association of DLL1 with type 1 diabetes in patients characterized by low polygenic risk scoreJingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|May 3, 2023
Mutational analysis of minichromosome maintenance complex component (<i>MCM</i>) family genes in Chinese Han women with polycystic ovarian syndromeJiangyan Zhou, Faying Liu, Lifeng Tian, et al.
Biochemical and Biophysical Research Communications|April 25, 2006
Ubc9 interacts with SOX4 and represses its transcriptional activityXin Pan, Huiyan Li, Peijing Zhang, et al.
Pageof 15

Showing results (71-80 of 142) with videos related to

Sort By:
Pageof 15
Frontiers in Neurology|December 5, 2022
Indentification of novel <i>MSTO1</i> compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxiaJia Chen, Junfang Xiao, Ge Chen, et al.
Frontiers in Cellular and Infection Microbiology|April 1, 2024
Causal associations between <i>Helicobacter pylori</i> infection and pregnancy and neonatal outcomes: a two-sample Mendelian randomization studyJialyu Huang, Yuxin Liu, Dingfei Xu, et al.
Case Reports in Genetics|April 13, 2016
Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain FunctionDong Li, Elizabeth Bhoj, Elizabeth McCormick, et al.
Frontiers in Immunology|May 23, 2022
PD1 Expression in EGFRvIII-Directed CAR T Cell Infusion Product for Glioblastoma Is Associated with Clinical ResponseOliver Y Tang, Lifeng Tian, Todd Yoder, et al.
Cell Cycle (Georgetown, Tex.)|January 5, 2011
PACSIN 2 represses cellular migration through direct association with cyclin D1 but not its alternate splice form cyclin D1bHui Meng, Lifeng Tian, Jie Zhou, et al.
American Journal of Medical Genetics. Part A|June 26, 2015
Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndromeElizabeth J Bhoj, Dong Li, Margaret H Harr, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated HypoparathyroidismDong Li, Elizabeth A Streeten, Alice Chan, et al.
Metabolism: Clinical and Experimental|November 6, 2020
Association of DLL1 with type 1 diabetes in patients characterized by low polygenic risk scoreJingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|May 3, 2023
Mutational analysis of minichromosome maintenance complex component (<i>MCM</i>) family genes in Chinese Han women with polycystic ovarian syndromeJiangyan Zhou, Faying Liu, Lifeng Tian, et al.
Biochemical and Biophysical Research Communications|April 25, 2006
Ubc9 interacts with SOX4 and represses its transcriptional activityXin Pan, Huiyan Li, Peijing Zhang, et al.
Pageof 15