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Human Genomics|November 14, 2023
Genetic evidence for the causal association between type 1 diabetes and the risk of polycystic ovary syndromeShuwen Chen, Zaixin Guo, Qi YuHuman Genomics|November 10, 2023
The burden of rare variants in DPYS gene is a novel predictor of the risk of developing severe fluoropyrimidine-related toxicityElena De Mattia, Jerry Polesel, Marco Silvestri, et al.Human Genomics|August 4, 2023
Total RNA sequencing reveals gene expression and microbial alterations shared by oral pre-malignant lesions and cancerMohammed Muzamil Khan, Jennifer Frustino, Alessandro Villa, et al.Human Genomics|August 25, 2023
The RNA m6A modification might participate in microglial activation during hypoxic-ischemic brain damage in neonatal miceXiaojuan Su, Lingyi Huang, Shiping Li, et al.Human Genomics|August 16, 2023
Developing neural network diagnostic models and potential drugs based on novel identified immune-related biomarkers for celiac diseaseTao Shen, Haiyang Wang, Rongkang Hu, et al.Human Genomics|July 31, 2023
Transcriptome and proteome analysis reveals the anti-cancer properties of Hypnea musciformis marine macroalga extract in liver and intestinal cancer cellsRodiola Begolli, Myrto Chatziangelou, Martina Samiotaki, et al.Human Genomics|October 27, 2023
The complex impact of cancer-related missense mutations on the stability and on the biophysical and biochemical properties of MAPK1 and MAPK3 somatic variantsMaria Petrosino, Leonore Novak, Alessandra Pasquo, et al.Human Genomics|October 14, 2023
FGFR1 variants contributed to families with tooth agenesisSiyue Yao, Xi Zhou, Min Gu, et al.Human Genomics|July 10, 2023
Smoking-related dysregulation of plasma circulating microRNAs: the Rotterdam studyIrma Karabegović, Silvana C E Maas, Yu Shuai, et al.Human Genomics|July 14, 2023
Pharmacovariome scanning using whole pharmacogene resequencing coupled with deep computational analysis and machine learning for clinical pharmacogenomicsAlireza Tafazoli, John Mikros, Faeze Khaghani, et al.Pageof 112