Search research articles
Contact Us
Filters
Showing results (41-50 of 132) with videos related to
Page
of 14
Sort By:
Cytogenetic and Genome Research
|
June 29, 2017
A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Hui Zeng, Jian-Guang Tang, Yi-Feng Yang, et al.
Journal of Human Genetics
|
June 12, 2022
A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient
Heng Gu, Zhuang-Zhuang Yuan, Xiao-Hui Xie, et al.
The Journal of Trauma and Acute Care Surgery
|
May 24, 2014
Improvement of ventilation-induced lung injury in a rodent model by inhibition of inhibitory κB kinase
Yu-Sheng Shu, Wei Tao, Qian-Bing Miao, et al.
BMC Genomics
|
February 18, 2025
Whole exome sequence reveals genetic profiles of primary cardiomyopathy and genotype-phenotype association in Chinese population
Rui-Lin Liu, Yi-Feng Yang, Ke Gong, et al.
Heart, Lung & Circulation
|
November 18, 2015
An Isolated Congenital Left Ventricular Diverticulum with Mitral Valve Endocarditis
Bo Jiang, Yi-feng Yang, Xi Wang, et al.
Applied Optics
|
August 12, 2025
Theoretical and experimental study on PRBS time-domain characteristic effects: stimulated Brillouin scattering in silica-based optical fiber
Kai Yuan Wang, He Wang, Yi Feng Yang, et al.
Biomicrofluidics
|
December 25, 2014
An enzyme-linked immunosorbent assay on a centrifugal platform using magnetic beads
Chih-Hsin Shih, Ho-Chin Wu, Chong-Yi Chang, et al.
Annals of General Psychiatry
|
December 20, 2024
Mood instability and risk of gastrointestinal diseases - a univariable and multivariable mendelian randomization study
Rui-Lin Liu, Qing-Chun Song, Li-Ming Liu, et al.
Bioscience, Biotechnology, and Biochemistry
|
January 24, 2019
Expression and characterization of recombinant human lactoferrin in edible alga Chlamydomonas reinhardtii
Xiaonan Pang, Yuxi Tong, Wenzhi Xue, et al.
Gene
|
July 30, 2013
576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy
Xin Zhu, Yi Zhang, Jian Wang, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 132) with videos related to
Sort By:
Page
of 14
Cytogenetic and Genome Research
|
June 29, 2017
A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Hui Zeng, Jian-Guang Tang, Yi-Feng Yang, et al.
Journal of Human Genetics
|
June 12, 2022
A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient
Heng Gu, Zhuang-Zhuang Yuan, Xiao-Hui Xie, et al.
The Journal of Trauma and Acute Care Surgery
|
May 24, 2014
Improvement of ventilation-induced lung injury in a rodent model by inhibition of inhibitory κB kinase
Yu-Sheng Shu, Wei Tao, Qian-Bing Miao, et al.
BMC Genomics
|
February 18, 2025
Whole exome sequence reveals genetic profiles of primary cardiomyopathy and genotype-phenotype association in Chinese population
Rui-Lin Liu, Yi-Feng Yang, Ke Gong, et al.
Heart, Lung & Circulation
|
November 18, 2015
An Isolated Congenital Left Ventricular Diverticulum with Mitral Valve Endocarditis
Bo Jiang, Yi-feng Yang, Xi Wang, et al.
Applied Optics
|
August 12, 2025
Theoretical and experimental study on PRBS time-domain characteristic effects: stimulated Brillouin scattering in silica-based optical fiber
Kai Yuan Wang, He Wang, Yi Feng Yang, et al.
Biomicrofluidics
|
December 25, 2014
An enzyme-linked immunosorbent assay on a centrifugal platform using magnetic beads
Chih-Hsin Shih, Ho-Chin Wu, Chong-Yi Chang, et al.
Annals of General Psychiatry
|
December 20, 2024
Mood instability and risk of gastrointestinal diseases - a univariable and multivariable mendelian randomization study
Rui-Lin Liu, Qing-Chun Song, Li-Ming Liu, et al.
Bioscience, Biotechnology, and Biochemistry
|
January 24, 2019
Expression and characterization of recombinant human lactoferrin in edible alga Chlamydomonas reinhardtii
Xiaonan Pang, Yuxi Tong, Wenzhi Xue, et al.
Gene
|
July 30, 2013
576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy
Xin Zhu, Yi Zhang, Jian Wang, et al.
Page
of 14