Search research articles
Contact Us
Filters
Showing results (91-100 of 158) with videos related to
Page
of 16
Sort By:
Molecular Human Reproduction
|
February 2, 2011
A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro
Hui Wang, Qiaoli Li, Teng Wang, et al.
Obesity Surgery
|
October 24, 2022
Combination of Single-Nucleotide Polymorphisms and Preoperative Body Mass Index to Predict Weight Loss After Laproscopic Sleeve Gastrectomy in Chinese Patients with Body Mass Index ≥ 32.5 kg/m<sup>2</sup>
Liang Wang, Guangzhong Xu, Chenxu Tian, et al.
Plos One
|
February 8, 2014
Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome
Qing Sang, Xin Li, Haojue Wang, et al.
Genome Biology
|
September 10, 2025
High-resolution time-series transcriptomic and metabolomic profiling reveals the regulatory mechanism underlying salt tolerance in maize
Fei Zhang, Boming Ji, Si Wu, et al.
Human Reproduction (Oxford, England)
|
December 20, 2016
Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development
Biaobang Chen, Bin Li, Da Li, et al.
American Journal of Obstetrics and Gynecology
|
April 17, 2026
Biallelic mutations in ANAPC13 cause female infertility characterized by oocyte maturation arrest both in humans and mice
Yu Wang, Zhiming Ding, Xuemei Liu, et al.
Journal of Assisted Reproduction and Genetics
|
February 21, 2021
A novel splicing variant in DNAH8 causes asthenozoospermia
Zhou Zhou, Xiaoyan Mao, Biaobang Chen, et al.
Plos One
|
February 6, 2013
Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)
Qing Sang, Xukun Yan, Huan Wang, et al.
Journal of Assisted Reproduction and Genetics
|
November 22, 2025
Novel missense variants in COX15 cause oocyte degeneration and female infertility
Ran Yu, Xuelin Zhang, Qian Dou, et al.
The American Surgeon
|
March 25, 2024
Prevalence, Risk Factors, and Metabolic Characteristics of Metabolically Healthy Obesity in Patients Seeking Bariatric Surgery: A Cohort Study
Xuejing Zheng, Chenxu Tian, Guangzhong Xu, et al.
Page
of 16
Search research articles
Search
Showing results (91-100 of 158) with videos related to
Sort By:
Page
of 16
Molecular Human Reproduction
|
February 2, 2011
A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro
Hui Wang, Qiaoli Li, Teng Wang, et al.
Obesity Surgery
|
October 24, 2022
Combination of Single-Nucleotide Polymorphisms and Preoperative Body Mass Index to Predict Weight Loss After Laproscopic Sleeve Gastrectomy in Chinese Patients with Body Mass Index ≥ 32.5 kg/m<sup>2</sup>
Liang Wang, Guangzhong Xu, Chenxu Tian, et al.
Plos One
|
February 8, 2014
Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome
Qing Sang, Xin Li, Haojue Wang, et al.
Genome Biology
|
September 10, 2025
High-resolution time-series transcriptomic and metabolomic profiling reveals the regulatory mechanism underlying salt tolerance in maize
Fei Zhang, Boming Ji, Si Wu, et al.
Human Reproduction (Oxford, England)
|
December 20, 2016
Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development
Biaobang Chen, Bin Li, Da Li, et al.
American Journal of Obstetrics and Gynecology
|
April 17, 2026
Biallelic mutations in ANAPC13 cause female infertility characterized by oocyte maturation arrest both in humans and mice
Yu Wang, Zhiming Ding, Xuemei Liu, et al.
Journal of Assisted Reproduction and Genetics
|
February 21, 2021
A novel splicing variant in DNAH8 causes asthenozoospermia
Zhou Zhou, Xiaoyan Mao, Biaobang Chen, et al.
Plos One
|
February 6, 2013
Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)
Qing Sang, Xukun Yan, Huan Wang, et al.
Journal of Assisted Reproduction and Genetics
|
November 22, 2025
Novel missense variants in COX15 cause oocyte degeneration and female infertility
Ran Yu, Xuelin Zhang, Qian Dou, et al.
The American Surgeon
|
March 25, 2024
Prevalence, Risk Factors, and Metabolic Characteristics of Metabolically Healthy Obesity in Patients Seeking Bariatric Surgery: A Cohort Study
Xuejing Zheng, Chenxu Tian, Guangzhong Xu, et al.
Page
of 16