Search research articles
Contact Us
Filters
Showing results (651-660 of 680) with videos related to
Page
of 68
Sort By:
JCI Insight
|
January 26, 2018
Mutations in Hnrnpa1 cause congenital heart defects
Zhe Yu, Paul Lf Tang, Jing Wang, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Scientific Reports
|
February 18, 2015
Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9)
Yu Chen, Jie Zhou, Zhongshan Cheng, et al.
The Journal of Clinical Investigation
|
November 14, 2023
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis
Xiaolu Wang, Ming Yue, Jason Pui Yin Cheung, et al.
Clinical and Translational Medicine
|
September 14, 2022
Mitochondrial regulation of acute extrafollicular B-cell responses to COVID-19 severity
Tianyu Cao, Li Liu, Kelvin Kai-Wang To, et al.
BMC Cancer
|
May 9, 2023
Radiographic and α-fetoprotein response predict pathologic complete response to immunotherapy plus a TKI in hepatocellular carcinoma: a multicenter study
Cheng Huang, Xiao-Dong Zhu, Ying-Hao Shen, et al.
Archives of Dermatological Research
|
December 25, 2019
Etanercept biosimilar (recombinant human tumor necrosis factor-α receptor II: IgG Fc fusion protein) and methotrexate combination therapy in Chinese patients with moderate-to-severe plaque psoriasis: a multicentre, randomized, double-blind, placebo-controlled trial
Lun-Fei Liu, Ji-Su Chen, Jun Gu, et al.
Ebiomedicine
|
June 22, 2021
DAGM: A novel modelling framework to assess the risk of HER2-negative breast cancer based on germline rare coding mutations
Mei Yang, Yanhui Fan, Zhi-Yong Wu, et al.
Human Molecular Genetics
|
November 6, 2018
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci
Anas M Khanshour, Ikuyo Kou, Yanhui Fan, et al.
Cancer Medicine
|
August 26, 2022
Comparison of the long-term outcomes of patients with hepatocellular carcinoma within the Milan criteria treated by ablation, resection, or transplantation
Ning-Ning Zhang, Jian Zheng, Ying Wu, et al.
Page
of 68
Search research articles
Search
Showing results (651-660 of 680) with videos related to
Sort By:
Page
of 68
JCI Insight
|
January 26, 2018
Mutations in Hnrnpa1 cause congenital heart defects
Zhe Yu, Paul Lf Tang, Jing Wang, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Scientific Reports
|
February 18, 2015
Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9)
Yu Chen, Jie Zhou, Zhongshan Cheng, et al.
The Journal of Clinical Investigation
|
November 14, 2023
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis
Xiaolu Wang, Ming Yue, Jason Pui Yin Cheung, et al.
Clinical and Translational Medicine
|
September 14, 2022
Mitochondrial regulation of acute extrafollicular B-cell responses to COVID-19 severity
Tianyu Cao, Li Liu, Kelvin Kai-Wang To, et al.
BMC Cancer
|
May 9, 2023
Radiographic and α-fetoprotein response predict pathologic complete response to immunotherapy plus a TKI in hepatocellular carcinoma: a multicenter study
Cheng Huang, Xiao-Dong Zhu, Ying-Hao Shen, et al.
Archives of Dermatological Research
|
December 25, 2019
Etanercept biosimilar (recombinant human tumor necrosis factor-α receptor II: IgG Fc fusion protein) and methotrexate combination therapy in Chinese patients with moderate-to-severe plaque psoriasis: a multicentre, randomized, double-blind, placebo-controlled trial
Lun-Fei Liu, Ji-Su Chen, Jun Gu, et al.
Ebiomedicine
|
June 22, 2021
DAGM: A novel modelling framework to assess the risk of HER2-negative breast cancer based on germline rare coding mutations
Mei Yang, Yanhui Fan, Zhi-Yong Wu, et al.
Human Molecular Genetics
|
November 6, 2018
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci
Anas M Khanshour, Ikuyo Kou, Yanhui Fan, et al.
Cancer Medicine
|
August 26, 2022
Comparison of the long-term outcomes of patients with hepatocellular carcinoma within the Milan criteria treated by ablation, resection, or transplantation
Ning-Ning Zhang, Jian Zheng, Ying Wu, et al.
Page
of 68