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Hereditas|November 22, 2025
RBM15 mediates m6A methylation modification of FOSB mRNA to promote dysfunction of trophoblast cells-a potential link to preeclampsiaYan Li, Fei Li, Qian Gao
Hereditas|November 22, 2025
Challenges of ECMO use for severe trauma: a narrative reviewXin-Liang Zhang, Ying-Qi Zhang, Zhi-Yong Hou, et al.
Hereditas|November 19, 2025
The diagnostic value of miR-340-5p in pediatric ulcerative colitis and its molecular mechanism by targeting MAP3K2 to modulate intestinal epithelial cell dysfunctionFanting Meng, Xianlong Han, Lingxia Ge, et al.
Hereditas|December 21, 2024
Inhibition of microRNA-660-5p decreases breast cancer progression through direct targeting of TMEM41BValeria Villarreal-García, José Roberto Estupiñan-Jiménez, Vianey Gonzalez-Villasana, et al.
Hereditas|February 1, 2025
Association between chronic obstructive pulmonary disease and osteoporosis: Mendelian randomization combined with bibliometric analysisFangjun Yang, Huaming Wang, Miaomiao Liu, et al.
Hereditas|December 31, 2024
Association between bone mineral density and scoliosis: a two-sample mendelian randomization study in european populationsFangjun Yang, Jiantao Wen
Hereditas|September 28, 2024
A novel approach for breast cancer treatment: the multifaceted antitumor effects of rMeV-Hu191Xiao-Yu Zheng, Yao Lv, Ling-Yan Xu, et al.
Hereditas|September 10, 2024
Mir-150-5p distinguishes acute pulmonary embolism, predicts the occurrence of pulmonary arterial hypertension, and regulates ox-LDL-induced endothelial cell injuryYue Wu, Xin Sun, Guangqiang Cui, et al.
Hereditas|February 19, 2024
A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese familyXiaoying Xie, Juan Du, Shunkang Geng, et al.
Hereditas|June 22, 2023
Enhancer-driven transcription of MCM8 by E2F4 promotes ATR pathway activation and glioma stem cell characteristicsYu-Meng Sun, Yi-Meng Zhang, Hai-Liang Shi, et al.
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