Search research articles
Contact Us
Filters
Showing results (11-20 of 51) with videos related to
Page
of 6
Sort By:
American Journal of Medical Genetics. Part A
|
April 3, 2026
Cardiovascular Defects as the Initial Presentation in Two Prenatal Cases of De Novo Heterozygous PBX1 Variants
Zhu Lan, Bocheng Xu, Hao Wang, et al.
The Science of the Total Environment
|
June 25, 2022
Exposure to BDE-47 causes female infertility risk and induces oxidative stress and lipotoxicity-mediated ovarian hormone secretion disruption in mice
Weike Shaoyong, Yalin Liu, Bocheng Xu, et al.
Journal of Hazardous Materials
|
June 15, 2023
Benzo [a] pyrene-loaded aged polystyrene microplastics promote colonic barrier injury via oxidative stress-mediated notch signalling
Weike Shaoyong, Hongli Jin, Xiao Jiang, et al.
Nutrition Reviews
|
May 17, 2021
The effects of nondigestible fermentable carbohydrates on adults with overweight or obesity: a meta-analysis of randomized controlled trials
Bocheng Xu, Jinping Cao, Jie Fu, et al.
International Journal of Legal Medicine
|
September 26, 2024
Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysis
Yu Tan, Huan Tian, Yuanyuan Xiao, et al.
Microbial Biotechnology
|
October 7, 2020
Bacillus subtilis and Enterococcus faecium co-fermented feed regulates lactating sow's performance, immune status and gut microbiota
Cheng Wang, Siyu Wei, Bocheng Xu, et al.
Journal of Clinical Laboratory Analysis
|
August 17, 2021
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing
Mei Yang, Hanbing Xie, Bocheng Xu, et al.
Frontiers in Genetics
|
April 3, 2025
Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3
Jingqun Mai, Zhu Zhang, Bocheng Xu, et al.
BMC Medical Genomics
|
July 8, 2022
Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family
Jing Chen, Qinqin Xiang, Xiao Xiao, et al.
Molecular Genetics & Genomic Medicine
|
November 6, 2023
Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case report
Jing Chen, Qinqin Xiang, Xiao Xiao, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics. Part A
|
April 3, 2026
Cardiovascular Defects as the Initial Presentation in Two Prenatal Cases of De Novo Heterozygous PBX1 Variants
Zhu Lan, Bocheng Xu, Hao Wang, et al.
The Science of the Total Environment
|
June 25, 2022
Exposure to BDE-47 causes female infertility risk and induces oxidative stress and lipotoxicity-mediated ovarian hormone secretion disruption in mice
Weike Shaoyong, Yalin Liu, Bocheng Xu, et al.
Journal of Hazardous Materials
|
June 15, 2023
Benzo [a] pyrene-loaded aged polystyrene microplastics promote colonic barrier injury via oxidative stress-mediated notch signalling
Weike Shaoyong, Hongli Jin, Xiao Jiang, et al.
Nutrition Reviews
|
May 17, 2021
The effects of nondigestible fermentable carbohydrates on adults with overweight or obesity: a meta-analysis of randomized controlled trials
Bocheng Xu, Jinping Cao, Jie Fu, et al.
International Journal of Legal Medicine
|
September 26, 2024
Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysis
Yu Tan, Huan Tian, Yuanyuan Xiao, et al.
Microbial Biotechnology
|
October 7, 2020
Bacillus subtilis and Enterococcus faecium co-fermented feed regulates lactating sow's performance, immune status and gut microbiota
Cheng Wang, Siyu Wei, Bocheng Xu, et al.
Journal of Clinical Laboratory Analysis
|
August 17, 2021
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing
Mei Yang, Hanbing Xie, Bocheng Xu, et al.
Frontiers in Genetics
|
April 3, 2025
Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3
Jingqun Mai, Zhu Zhang, Bocheng Xu, et al.
BMC Medical Genomics
|
July 8, 2022
Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family
Jing Chen, Qinqin Xiang, Xiao Xiao, et al.
Molecular Genetics & Genomic Medicine
|
November 6, 2023
Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case report
Jing Chen, Qinqin Xiang, Xiao Xiao, et al.
Page
of 6