Showing results (931-940 of 2,182) with videos related to

Sort By:
Pageof 219
The Journal of Gene Medicine|January 20, 2019
Ankyrin repeat domain 1: A novel gene for cardiac septal defectsYongchao Yang, Yu Xia, Yueheng Wu, et al.
The Journal of Gene Medicine|February 12, 2019
Genetic polymorphism of methylenetetrahydrofolate reductase is associated with insulin resistance in Egyptian women with polycystic ovary syndromeAyman Am Nsrallah, Azza H Abd-El Fatah, Hanan S Ahmed
The Journal of Gene Medicine|October 28, 2017
Genetic factors are stressed variably by onset age-based sample selection in psoriasis: A hint from major histocompatibility complex region-based analysisLei Ye, Chao Yang, Jin-Fa Dou, et al.
The Journal of Gene Medicine|January 12, 2018
Association of IGFN1 variant with polypoidal choroidal vasculopathyXiaofeng Wen, Yu Liu, Qi Yan, et al.
The Journal of Gene Medicine|July 22, 2021
MicroRNA-145-5p targeting of TRIM2 mediates the apoptosis of retinal ganglion cells via the PI3K/AKT signaling pathway in glaucomaKai Xu, Sizhen Li, Qingsong Yang, et al.
The Journal of Gene Medicine|June 30, 2021
Inhibition of circ_0081234 reduces prostate cancer tumor growth and metastasis via the miR-1/MAP 3 K1 axisGuangyao Zhang, Yibin Liu, Jianhui Yang, et al.
The Journal of Gene Medicine|April 5, 2020
A homozygous missense variant in the homeobox domain of the NKX6-2 results in progressive spastic ataxia type 8 associated with lower limb weakness and neurological manifestationsAhmad Almatrafi, Muhammad Umair, Amr Eldardear, et al.
The Journal of Gene Medicine|April 5, 2020
Triple diagnosis of Wiedemann-Steiner, Waardenburg and DLG3-related intellectual disability association found by WES: A case reportThibaut Matis, Vincent Michaud, Julien Van-Gils, et al.
The Journal of Gene Medicine|January 7, 2020
miR-142-5p protects against osteoarthritis through competing with lncRNA XISTPengfei Sun, Yunpeng Wu, Xuezhou Li, et al.
The Journal of Gene Medicine|September 29, 2020
Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun familyMuhammad Ismail Khan, Muhammad Latif, Maria Saif, et al.
Pageof 219