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The Journal of Gene Medicine|September 25, 2025
Exploring Potential Hub Genes and Molecular Mechanisms Linking Cardia Carcinoma With Sjögren's Syndrome Based on Comprehensive Bioinformatics Analysis and Machine LearningMeng Qian, Ying Chen, Zhenxiang Wang, et al.
The Journal of Gene Medicine|December 28, 2020
A novel missense mutation in the UBE2A gene causes intellectual disability in the large X-linked familySaide Betül Arslan Satılmış, Emin Emre Kurt, Ebru Perim Akçay, et al.
The Journal of Gene Medicine|January 5, 2020
AAVS1 site-specific integration of the CAR gene into human primary T cells using a linear closed-ended AAV-based DNA vectorWei Chen, Liang Tan, Qungang Zhou, et al.
The Journal of Gene Medicine|December 13, 2019
TNNT1, negatively regulated by miR-873, promotes the progression of colorectal cancerYu Chen, Jinsong Wang, Donghua Wang, et al.
The Journal of Gene Medicine|November 22, 2022
Evaluation of CRISPR/Cas9 exon-skipping vector for choroideremia using human induced pluripotent stem cell-derived RPEToshiro Iwagawa, Hiroki Masumoto, Hitoshi Tabuchi, et al.
The Journal of Gene Medicine|April 5, 2020
Zinc finger protein 750(ZNF750), negatively regulated by miR-17-5p, inhibits proliferation, motility and invasion of colonic cancer cellsJie Qu, Xiuqin Zhang, Xiying Lv
The Journal of Gene Medicine|March 30, 2020
A novel UBE2A mutation in a Chinese family with X-linked intellectual disabilityWeimin Jia, Qi Hu, Yanling Wu, et al.
The Journal of Gene Medicine|March 12, 2020
MicroRNA-1249 targets four-jointed box kinase 1 and reduces cell proliferation, migration and invasion of colon adenocarcinomaWen Dang, Zhen Zhu
The Journal of Gene Medicine|March 24, 2020
The impact of catalase and glutathione peroxidase-1 genetic polymorphisms on their enzyme activities among Egyptian patients with keratoconusRehab S Abdul-Maksoud, Rania A Fouad, Tamer G Elsayed, et al.
The Journal of Gene Medicine|January 28, 2020
Implementation of high-resolution melting analysis of the porcupine (PORCN) gene for molecular diagnosis of focal dermal hypoplasia: Identification of a novel mutationMirna Martínez-Saucedo, Carolina Ornelas-Fuentes, Mark Dedden, et al.
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